Mobile phone applications to support psychotropic tapering: a scoping review protocol

Miriam Boland; Agnes Higgins; Gavin Doherty; Greg Sheaf; Adele Framer; Cathal Cadogan

doi:10.12688/hrbopenres.13501.2

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Study Protocol

Revised

Mobile phone applications to support psychotropic tapering: a scoping review protocol

[version 2; peer review: 2 approved]

Miriam Boland¹, Agnes Higgins², Gavin Doherty³, Greg Sheaf⁴, Adele Framer⁵, Cathal Cadogan ¹

Miriam Boland¹, Agnes Higgins², [...] Gavin Doherty³, Greg Sheaf⁴, Adele Framer⁵, Cathal Cadogan ¹

PUBLISHED 19 Aug 2022

Author details Author details

¹ School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin, Dublin, Ireland
² School of Nursing and Midwifery, Trinity College Dublin, Dublin, Ireland
³ School of Computer Science and Statistics, Trinity College Dublin, Dublin, Ireland
⁴ The Library of Trinity College, Trinity College Dublin, Dublin, Ireland
⁵ SurvivingAntidepressants.org, San Francisco, California, USA

Miriam Boland
Roles: Conceptualization, Funding Acquisition, Investigation, Methodology, Project Administration, Writing – Original Draft Preparation

Agnes Higgins
Roles: Conceptualization, Investigation, Methodology, Writing – Original Draft Preparation

Gavin Doherty
Roles: Methodology, Writing – Review & Editing

Greg Sheaf
Roles: Methodology, Writing – Review & Editing

Adele Framer
Roles: Writing – Review & Editing

Cathal Cadogan
Roles: Conceptualization, Funding Acquisition, Investigation, Methodology, Project Administration, Writing – Original Draft Preparation

OPEN PEER REVIEW

REVIEWER STATUS

Abstract

Background: In the context of a recovery-oriented approach to mental healthcare, the role of psychotropic medication over extended or indefinite periods is increasingly being called into question. To minimise the risks of withdrawal symptoms and relapse, it is crucial that service users who want to discontinue psychotropic medication are supported throughout the tapering process. However, in the absence of effective interventions and supports, service users are increasingly relying on online resources for guidance and support. To date, the evidence base for mobile phone applications (‘apps’) and app-based interventions supporting discontinuation of psychotropic use has not been examined. This scoping review aims to examine the content, underpinning evidence base and impact of available mobile phone apps and app-based interventions to support psychotropic tapering.

Methods: A scoping review will be conducted using the Joanna Briggs Institute guidance and results will be reported using the Preferred Reporting Items for Systematic Reviews and Meta‐Analyses extension for Scoping Reviews (PRISMA-ScR) guideline. Several electronic databases (MEDLINE, EMBASE, CINAHL, PsycINFO, Web of Science, ACM and IEEE Xplore) will be searched from 2008 onwards. Searches of the major app stores will also be conducted, specifically Apple's App Store (iOS) and Google Play Store (Android). Following screening, key information will be extracted from the included studies and apps. Identified apps will be coded using the Behaviour Change Technique (BCT) Taxonomy. The findings will be described using narrative synthesis.

Conclusions: This scoping review will provide a broad overview of available apps to support psychotropic tapering, including a summary of their content using the BCT Taxonomy. The review findings will guide future research relating to the development, implementation and evaluation of app-based interventions to support the tapering of psychotropic medication.

Keywords

Psychotropic, antidepressants, benzodiazepines, antipsychotics, withdrawal, tapering, discontinuation, smartphone apps, mental disorders, scoping review

Corresponding author: Cathal Cadogan

Competing interests: No competing interests were disclosed.

Grant information: Health Research Board Ireland [LP-HSR-2019-012]. Miriam Boland was supported by a 1252 Scholarship from the School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin.
The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Copyright: © 2022 Boland M et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to cite: Boland M, Higgins A, Doherty G et al. Mobile phone applications to support psychotropic tapering: a scoping review protocol [version 2; peer review: 2 approved]. HRB Open Res 2022, 5:18 (https://doi.org/10.12688/hrbopenres.13501.2) First published: 08 Mar 2022, 5:18 (https://doi.org/10.12688/hrbopenres.13501.1) Latest published: 19 Aug 2022, 5:18 (https://doi.org/10.12688/hrbopenres.13501.2)

Revised Amendments from Version 1

This protocol has been revised based on reviewer's valuable feedback. While there are no major differences between this version of the manuscript and the first published version, the following amendments were made:
In the introduction section, the controversy that exists around the safety and efficacy of psychotropic medication was acknowledged. So too was the lack of understanding of their mechanism of action.

See the authors' detailed response to the review by Mark Horowitz
See the authors' detailed response to the review by Luke Molloy

Introduction

Psychotropic medications, including antidepressants, anxiolytics, hypnotics, mood stabilisers and antipsychotics, are frequently prescribed for people experiencing mental health problems, with notable increases in prescribing rates observed year on year^1,2. Globally, the total consumption of psychotropic medication increased by 4% annually from 2008 to 2019³. This surge in the use of psychotropic medication has contributed to the ongoing debate surrounding the over-prescribing of these medications and the potentially inappropriate treatment of mental health disorders. While guidelines published by the National Institute for Health and Care Excellence (NICE) support the use of psychotropic medication in the treatment of various mental disorders for a limited duration, evidence on long-term outcomes is lacking^4,5.

The safety and efficacy of psychotropic medication is increasingly being debated, particularly in terms of the extent of any clinically meaningful improvements in symptoms when compared to placebo, and the potential for adverse effects, such as dependence and withdrawal symptoms⁶. Studies have shown that 30–60% of long-term antidepressant prescriptions lack an indication for continued use and therefore may be inappropriate^7,8. Similar concerns have been raised about antipsychotic and benzodiazepine use and their known potential risks. While evidence supports the use of antipsychotics in acute psychosis, evidence on their long-term use is lacking⁹. This is acknowledged by other studies which estimate that approximately 40% of those taking antipsychotics would remain well (i.e. would achieve a good outcome in the long term) without them⁹. With respect to benzodiazepine receptor agonists, while guidelines recommend that they should be limited to short‐term use (i.e., ≤4 weeks) to minimise the risk of adverse outcomes, long-term use of these medications is common¹⁰. It is estimated that 3% of the general population use benzodiazepines for extended periods (>6 months)¹¹.

The role of psychotropic medication, particularly over extended or indefinite periods, is also being called into question with increasing advocacy of a recovery-oriented approach to mental healthcare. Despite the widespread use of psychotropic medication in treating mental health problems for many years, the mechanisms of action for drugs such as antidepressants and antipsychotics are still not fully understood. Previous theories that these drugs address an underlying chemical imbalance have found to be lacking any supporting evidence^12,13. While recovery in mental health is difficult to define, personal recovery is about living a satisfying, meaningful and hopeful life despite the presence of challenges or the on-going limitations caused by mental health problems^14–16. As such, a recovery-oriented approach is underpinned by values of service user engagement, respect for autonomy and personhood, including the right to be involved in decision making about care. Service users nationally and internationally have reported a high focus on medication adherence in their treatment, as well as a lack of collaboration in medication-related decisions, resulting in inability to make fully informed decisions with respect to their treatment^17,18. This does not align with a rights-based, recovery-oriented approach to mental healthcare, which seeks to promotes open discussion about medication, including risks and benefits¹⁹.

Psychotropic medications have various adverse effects. Examples include akathisia, involuntary movements, weight gain, and sexual dysfunction²⁰. Additionally, the use of psychotropic medication can lead to the development of physiological dependence with long-term use and withdrawal symptoms on discontinuation, which may ultimately play a role in extending their duration of use, even for those who have recovered during drug therapy or for whom there is no longer a valid indication to continue it²¹. Some service users decide to discontinue psychotropic medication to recapture lost personal autonomy, to live a life free of medication and, in some cases, because these medications have failed to manage the person’s distressful experience and symptoms²². However, these individuals have reported challenges in accessing professional support and having their autonomy and choice respected^22,23.

Several studies have been conducted to investigate interventions that support the discontinuation of psychotropic medication and identify effective interventions that minimise the risk of relapse and withdrawal symptoms^24–26. In many cases, the existing evidence base is limited. This can often be attributed to the lack of studies conducted over extended periods and the withdrawal confounding bias, i.e. misidentifying withdrawal symptoms as relapse^20,24. A slow tapering method is often reportedly employed by individuals attempting psychotropic discontinuation and involves gradually reducing the dose of the psychotropic medication over a prolonged period of time²⁷. A conservative 10% dose reduction per month of the most recent dose is a common approach with some successes reported^27,28. A similar approach involves switching to an alternative medication with a longer half-life before beginning gradual dosage reduction^20,29.

The potential for withdrawal symptoms exists both during gradual reduction and following discontinuation of psychotropic medications. This can be explained by the neurophysiologic readjustments that take place in the body in the absence of the psychotropic agent³⁰. While the frequency and severity of withdrawal symptoms are difficult to ascertain, their rate of occurrence is potentially more common than reported due to the potential for misdiagnosis as an emergence or recurrence of a mental health problem^31,32. While guidelines have previously suggested that withdrawal symptoms from psychotropic medications are limited to one to two weeks, this is increasingly contested, with evidence they may last for months³³. The list of withdrawal symptoms is extensive, with people reporting a range of symptoms (e.g. anxiety, tremors, lethargy) that range on a continuum of mild to severe^32,34. Withdrawal symptoms can be debilitating and protracted, and are one of the main barriers reported by service users to successful discontinuation of psychotropic medication³⁴.

In the absence of effective interventions and supports, service users are increasingly relying on online resources, such as discussion fora and Facebook groups, for guidance and support while tapering psychotropic medicationt^2,27,35. In addition, the use and acceptability of mobile ‘apps’ defined as “a software program that runs on a mobile phone” has been gaining momentum in healthcare³⁶. As of 2020, there were more than 10,000 mental health and wellness related apps available for download, which equates to one third of the app market³⁷. While the use and functioning of apps that promote adherence to psychotropic medication have been evaluated by several studies to date, the evidence base for apps and app-based interventions in supporting safe and effective discontinuation of psychotropic use has not been examined³⁸.

The aim of this scoping review is to examine the content, underpinning evidence base and impact of available mobile apps and app-based interventions to support psychotropic tapering. The objectives are to:

1. Identify the available apps;

2. Describe the apps in terms of functions, tapering recommendations and any linked services or supports to promote recovery;

3. Examine the app development process (i.e. underpinning evidence and theory);

4. Characterise the identified apps’ active components using the behaviour change technique (BCT) taxonomy³⁹;

5. Characterise the study populations included in evaluations of the apps;

6. Identify the outcome measures that have been used to evaluate the apps;

7. Summarise the impact of the identified apps based on the available evidence.

Methods

Given that the aim of this review is to provide a broad overview of the existing literature, a scoping review was deemed the more suitable review methodology, in comparison to a systematic review which tends to be more specific in nature. Scoping reviews explore the depth of existing literature, identify knowledge gaps and inform future research⁴⁰. The scoping review protocol presented in this manuscript has been developed in accordance with the Joanna Briggs Institute (JBI) guidance^40,41. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines for scoping reviews (PRISMA-ScR) will be used to guide the reporting of the final review⁴².

Eligibility criteria

The Population-Intervention-Comparison-Outcome (PICO) framework will be used to guide study selection and to align the eligibility criteria with the aims of this review.

Types of participants. This review will include apps and app-based interventions targeting individuals who want to discontinue psychotropic medication use. For the purpose of this review, studies and apps that include or target adults (≥18 years) taking any form of psychotropic medication will be included (e.g. antidepressants, anxiolytics, antipsychotics and/or mood stabilisers).

Types of interventions. Eligible apps and app-based interventions must focus on supporting the process of psychotropic tapering. Tapering-related guidance can come from any source. Eligible apps will include those available from publicly available commercial apps, as well as those identified through electronic database searching. Apps and interventions which only focus on medication adherence will be excluded.

Types of outcome measures. Given the lack of existing reviews evaluating app-based interventions to support psychotropic tapering, all outcomes for studies that meet the pre-specified inclusion criteria will be included in this review. These will include quantitative outcome measures and qualitative feedback reported by service users and/or service providers, as well as proximal outcomes such as engagement and usage. This will enable a comprehensive overview of outcome measures to be generated.

Types of studies. All studies evaluating apps and app-based interventions meeting the above criteria will be included in this review. This will include quantitative evaluations (e.g. randomised controlled trials, before and after studies) and qualitative evaluations (e.g. interview studies). Apps identified solely through online stores that have not undergone any formal evaluation will also be eligible for inclusion. Only studies and apps published in the English language will be considered for inclusion.

Search strategy

The search strategy will consist of two components: (1) a search of electronic databases to identify empirical research; and (2) a search of mobile phone application stores (‘app stores’) to identify commercially available apps⁴³.

Component one will include a search of the following electronic databases and digital libraries: MEDLINE, EMBASE, CINAHL, PsycINFO, Web of Science, ACM and IEEE Xplore. All databases and libraries will be searched from 2008, the year the first app store (Apple) was introduced. The electronic database searches will consist of three steps:

1. A preliminary search of one electronic database (Web of Science) will be undertaken to identify articles relevant to the review topic. This will enable the identification of keywords and index terms from the titles and abstracts of relevant articles.
2. Based on the above, a comprehensive search strategy will be designed and refined in collaboration with a research/medical librarian (GS), with expertise in information retrieval and systematic reviews.
3. A search of the databases listed above will be conducted using all identified keywords and index terms, modified to each database accordingly.

Component two will include a search of the following app stores from their inception: Apple's App Store (iOS) and Google Play Store (Android). This will involve:

1. A preliminary search of Apple’s app store to identify keywords and apps relevant to the review topic. This initial search will enable the identification of the names and descriptions of relevant apps and guide future searches.

2. Informed by these findings, a comprehensive search strategy will be designed and refined in conjunction with a co-author with expertise in app searching (GD).

3. A systematic search of the two platforms will be conducted using the identified keywords. Separate searches for each keyword will be conducted on each platform, across all categories of apps. Search results will be downloaded and stored for screening.

Initial search terms for online peer-reviewed papers will include: antidepressants, benzodiazepines, anxiolytics, taper, psychotropic, withdrawal, discontinuation, depression, anxiety, psychosis, mobile phone applications, apps. The complete list of search terms will be included in the final review manuscript. Reference lists of included studies will be screened for additional studies.

Study selection

Following completion of the electronic database searches, identified references will be imported into Covidence (reference management software platform; https://www.covidence.org/) and undergo deduplication. A two-step screening process will be used:

1. Two researchers (MB, CC) will independently screen titles and abstracts for inclusion based on the pre-specified inclusion criteria outlined above.
2. If a study appears to meet inclusion criteria or a decision cannot be made based on the title and abstract alone, the full-text article will be retrieved. All full-text articles will be screened independently by both researchers. Any disagreements throughout the screening process will be resolved by consensus with the input of a third reviewer (AH) where required.

A similar process will be undertaken with the app store searches. Details of all potentially relevant apps identified from the app store searches will be entered into Microsoft Excel by the lead researcher (MB). The following details will be recorded for each app: the name, brief description of its functions, the app store and app store category, age category, author/creator and a link to access the app. All apps will be screened for inclusion by two researchers independently (MB, CC). The third reviewer (AH) will again be consulted in the event of any disagreements.

The study selection process will be described both narratively and using a PRISMA-ScR flow diagram, detailing all the steps involved. A list of excluded apps and articles will be provided as an appendix which will include reasons for exclusion.

Data extraction

Two researchers (MB, CC) will independently perform data extraction (‘data charting’) using a data extraction form/charting table that will be developed in Microsoft Excel. This will be developed in accordance with the relevant methodological guidance to record key information from each source. The data extraction form will be piloted on one study and one app meeting inclusion criteria and refined accordingly.

Key information to be extracted will include:

1. Study/App: author(s)/creator(s), year of publication/creation, origin/country of origin, aims/purpose;
2. Target population;
3. Intervention/App content (including BCTs, app functions and linked services/intervention);
4. App development process to ascertain quality (including details of any underpinning clinical evidence, theory and/or evidence of human-centred design process);
5. Study design, sample size and outcome measures (if available);
6. Outputs and reports;
7. Key findings of the evaluations of any identified apps.

Data analysis and synthesis

The JBI guidance recommends that the analysis of data be pre-specified within the protocol to ensure transparency and justification^40,41. Given that the aim of this scoping review is to provide a broad overview of the existing literature and commercially available apps and not to pool outcome data, narrative synthesis will be used to describe the key findings and how they relate to the review’s objectives. The approach to narrative synthesis will be informed by the Synthesis Without Meta-analysis (SWiM) guidelines⁴⁴. This will help to address the common issues that have been identified with narrative synthesis, including a lack of description of the methods used and inadequate reporting of the limitations of the synthesis. Key study and app information will be summarised and then presented in tabular form. This will be accompanied by a narrative summary which will describe how these results relate to the review objectives and questions. This process will be further developed and refined throughout the data extraction process.

App coding

Identified apps and app-based interventions will be coded using the Behaviour Change Technique Taxonomy version 1 (BCTTv1)³⁹. A BCT is defined as “observable, replicable, and irreducible component of an intervention designed to alter or redirect causal processes that regulate behaviour”³⁹. The BCT Taxonomy consists of 93 BCTs, grouped within 16 categories with detailed definitions of each BCT³⁹. The application of this taxonomy will enable the identification and characterisation of the identified apps’ active components using standardised terminology²⁵. This will ultimately allow for greater comparison and replication of any identified interventions⁴⁵.

Apps will be downloaded from the app stores by two researchers (MB, CC). This will enable the functionality of these apps to be assessed. To account for the potential of longitudinal features offered by apps, the researchers will set up a profile on each app using a sample patient case (e.g. tapering from 10 mg diazepam three times daily). This will enable them to fully explore the apps’ features and functionality, including any notifications and usage metrics over a fixed period of time (e.g. four weeks). Screenshots of the content and outputs of each app will be retained to facilitate app coding. The app coding process will consist of three stages.

1. Preliminary coding of a random sample of 20% of identified apps will be undertaken by two researchers (MB, CC) using the entire BCT taxonomy.
2. A coding manual will be developed which will include definitions for the subset of identified BCTs and examples of how they apply in the context of the identified app/interventions.
3. BCT coding of the apps/interventions will be conducted by two researchers (MB, CC) independently using the coding manual, which will be refined on an iterative basis.

Any disagreements will be resolved by consensus or through discussion with a third reviewer (AH).

Critical appraisal

Given that the aim of this scoping review is to provide a broad overview of the existing literature and apps and not to pool outcome data⁴⁰, the critical appraisal process will focus on the potential for bias and the extent to which it has been addressed by the included studies. Critical appraisal of included studies will be performed by two researchers (MB, CC) working independently using the relevant JBI Critical Appraisal Checklist for different study types⁴⁶. The critical appraisal process will not be used to exclude studies, but to help inform the synthesis and interpretation of the review findings.

Presentation of results

The JBI guidance recommends that scoping review protocols include a proposed plan for presenting results. This plan will be further refined at the review stage based on the identified studies and the charted data. The results will be collated and summarised according to the review objectives and eligibility criteria (PICO framework). Key findings will be presented under the following headings and using a PRISMA-ScR flow diagram:

1. Search results
2. Aims/purpose of identified apps
3. Target population
4. Intervention/App content (including BCTs, app functions and linked services/intervention)
5. App development process
6. Study design, sample size and outcome measures
7. Key findings

Discussion

The use of psychotropic medications is becoming more widespread, with about a third of service users receiving long-term treatment despite insufficient medical indication⁸. Although potential benefits are associated with the use of psychotropic medications in certain circumstances, they also have various associated adverse effects. Increasingly, it is recognised that psychotropic medication may not be needed or appropriate over extended periods, and service users are seeking support in safely discontinuing treatment.

This review will identify apps and app-based interventions to support the discontinuation of psychotropic medications. It will provide a broad overview of available apps, including a summary of their content using the BCT Taxonomy. The review will also provide a summary of existing evaluations of the effectiveness of these app. The review findings will guide future research relating to the development, implementation and evaluation of app-based interventions to support the tapering of psychotropic medications.

Dissemination of findings

The completed review will be submitted for publication in a peer-reviewed journal.

Study status

At the time of publication of this protocol, database searches have yet to be completed.

Data availability

Underlying data

No underlying data are associated with this article.

Extended data

Open Science Framework: A scoping review of mobile phone applications to support psychotropic tapering (protocol). https://doi.org/10.17605/OSF.IO/ZGBKF⁴³

This project contains the following extended data:

WebOfScience_Strategy_OSF.docx (Web of Science Search Strategy)

Reporting guidelines

Open Science Framework: PRISMA-P checklist for ‘Mobile phone applications to support psychotropic tapering: a scoping review protocol’. https://doi.org/10.17605/OSF.IO/ZGBKF⁴³

Data are available under the terms of the Creative Commons Zero "No rights reserved" data waiver (CC0 1.0 Public domain dedication).

Faculty Opinions recommended

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41. Aromataris E, Munn Z: JBI Manual for Evidence Synthesis. JBI. 2020; Accessed: 31.01.22. Reference Source
42. Tricco AC, Lillie E, Zarin W, et al.: PRISMA Extension for Scoping Reviews (PRISMA-ScR): Checklist and Explanation. Ann Intern Med. 2018; 169(7): 467–73. PubMed Abstract | Publisher Full Text
43. Boland M: A Scoping Review of Mobile Phone Applications to Support Psychotropic Tapering (protocol). OSF. 2022. http://www.doi.org/10.17605/OSF.IO/YFXWG
44. Campbell M, McKenzie JE, Sowden A, et al.: Synthesis without meta-analysis (SWiM) in systematic reviews: reporting guideline. BMJ. 2020; 368: l6890. PubMed Abstract | Publisher Full Text | Free Full Text
45. Presseau J, Ivers NM, Newham JJ, et al.: Using a behaviour change techniques taxonomy to identify active ingredients within trials of implementation interventions for diabetes care. Imp Sci. 2015; 10(1): 55. PubMed Abstract | Publisher Full Text | Free Full Text
46. Moola S, Munn Z, Tufanaru C, et al.: Chapter 7: Systematic reviews of etiology and risk. JBI Manual for Evidence Synthesis. In: Aromataris E, Munn Z (Editors). JBI. 2020. Publisher Full Text

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Version 2

VERSION 2 PUBLISHED 08 Mar 2022

Author details Author details

Miriam Boland
Roles: Conceptualization, Funding Acquisition, Investigation, Methodology, Project Administration, Writing – Original Draft Preparation

Agnes Higgins
Roles: Conceptualization, Investigation, Methodology, Writing – Original Draft Preparation

Gavin Doherty
Roles: Methodology, Writing – Review & Editing

Greg Sheaf
Roles: Methodology, Writing – Review & Editing

Adele Framer
Roles: Writing – Review & Editing

Cathal Cadogan
Roles: Conceptualization, Funding Acquisition, Investigation, Methodology, Project Administration, Writing – Original Draft Preparation

Competing interests

No competing interests were disclosed.

Grant information

Health Research Board Ireland [LP-HSR-2019-012]. Miriam Boland was supported by a 1252 Scholarship from the School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin.
The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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https://doi.org/10.12688/hrbopenres.13501.2

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© 2022 Boland M et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Boland M, Higgins A, Doherty G et al. Mobile phone applications to support psychotropic tapering: a scoping review protocol [version 2; peer review: 2 approved]. HRB Open Res 2022, 5:18 (https://doi.org/10.12688/hrbopenres.13501.2)

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Reviewer Report 04 Oct 2022

Mark Horowitz, Division of Psychiatry, University College London, London, UK

Approved

https://doi.org/10.21956/hrbopenres.14874.r32714

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Reviewer Report 29 Jul 2022

Luke Molloy, School of Nursing, University of Wollongong, Wollongong, NSW, Australia

Approved

https://doi.org/10.21956/hrbopenres.14726.r32384

There is a clear rationale for this proposed review. The area is of interest to mental health-related clinicians and academics, and I am sure there will be interest in its findings across disciplines. There is a clear narrative and excellent use of literature within the sections establishing this. A scoping review is established as the most appropriate approach to understanding this phenomenon, and the details of the methods are clear and would allow replication of the work to be undertaken. The findings of such a work will support quality recovery-focused mental health care.

Is the rationale for, and objectives of, the study clearly described?

Yes
Is the study design appropriate for the research question?

Yes
Are sufficient details of the methods provided to allow replication by others?

Yes
Are the datasets clearly presented in a useable and accessible format?

Yes

Competing Interests: No competing interests were disclosed.

Reviewer Expertise: Mental health care, trauma-informed care, strengths-based practice.

I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.

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Report a concern

Author Response 25 Aug 2022

Miriam Boland, School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin, Dublin, Ireland

25 Aug 2022

Author Response

There is a clear rationale for this proposed review. The area is of interest to mental health-related clinicians and academics, and I am sure there will be interest in its ... Continue reading There is a clear rationale for this proposed review. The area is of interest to mental health-related clinicians and academics, and I am sure there will be interest in its findings across disciplines. There is a clear narrative and excellent use of literature within the sections establishing this. A scoping review is established as the most appropriate approach to understanding this phenomenon, and the details of the methods are clear and would allow replication of the work to be undertaken. The findings of such a work will support quality recovery-focused mental health care.

Response: We are very grateful to the reviewer for reviewing our manuscript and for the positive feedback they have provided.
There is a clear rationale for this proposed review. The area is of interest to mental health-related clinicians and academics, and I am sure there will be interest in its findings across disciplines. There is a clear narrative and excellent use of literature within the sections establishing this. A scoping review is established as the most appropriate approach to understanding this phenomenon, and the details of the methods are clear and would allow replication of the work to be undertaken. The findings of such a work will support quality recovery-focused mental health care.

Response: We are very grateful to the reviewer for reviewing our manuscript and for the positive feedback they have provided.
Competing Interests: No competing interests were disclosed. Close
Report a concern
Respond or Comment

COMMENTS ON THIS REPORT

Author Response 25 Aug 2022

Miriam Boland, School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin, Dublin, Ireland

25 Aug 2022

Author Response

There is a clear rationale for this proposed review. The area is of interest to mental health-related clinicians and academics, and I am sure there will be interest in its ... Continue reading There is a clear rationale for this proposed review. The area is of interest to mental health-related clinicians and academics, and I am sure there will be interest in its findings across disciplines. There is a clear narrative and excellent use of literature within the sections establishing this. A scoping review is established as the most appropriate approach to understanding this phenomenon, and the details of the methods are clear and would allow replication of the work to be undertaken. The findings of such a work will support quality recovery-focused mental health care.

Response: We are very grateful to the reviewer for reviewing our manuscript and for the positive feedback they have provided.
There is a clear rationale for this proposed review. The area is of interest to mental health-related clinicians and academics, and I am sure there will be interest in its findings across disciplines. There is a clear narrative and excellent use of literature within the sections establishing this. A scoping review is established as the most appropriate approach to understanding this phenomenon, and the details of the methods are clear and would allow replication of the work to be undertaken. The findings of such a work will support quality recovery-focused mental health care.

Response: We are very grateful to the reviewer for reviewing our manuscript and for the positive feedback they have provided.
Competing Interests: No competing interests were disclosed. Close
Report a concern

Views

Reviewer Report 04 Apr 2022

Mark Horowitz, Division of Psychiatry, University College London, London, UK

Approved with Reservations

https://doi.org/10.21956/hrbopenres.14726.r31734

Is the rationale for, and objectives of, the study clearly described?

Yes
Is the study design appropriate for the research question?

Partly
Are sufficient details of the methods provided to allow replication by others?

Yes
Are the datasets clearly presented in a useable and accessible format?

Not applicable

References

1. Framer A: What I have learnt from helping thousands of people taper off antidepressants and other psychotropic medications.Ther Adv Psychopharmacol. 2021; 11: 2045125321991274 PubMed Abstract | Publisher Full Text
2. Sørensen A, Juhl Jørgensen K, Munkholm K: Clinical practice guideline recommendations on tapering and discontinuing antidepressants for depression: a systematic review.Ther Adv Psychopharmacol. 2022; 12: 20451253211067656 PubMed Abstract | Publisher Full Text

Competing Interests: No competing interests were disclosed.

Reviewer Expertise: I study rationale psychopharmacology and patient-centred deprescribing of psychotropic drugs

I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard, however I have significant reservations, as outlined above.

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Report a concern

Author Response 25 Aug 2022

Miriam Boland, School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin, Dublin, Ireland

25 Aug 2022

Author Response

Thank you for giving me the opportunity to review this timely proposed review. This study will produce a useful overview of existing mobile apps for the process of deprescribing psychiatric ... Continue reading Thank you for giving me the opportunity to review this timely proposed review. This study will produce a useful overview of existing mobile apps for the process of deprescribing psychiatric medication, a topic which has been until recently ignored, and this review is an important step forward, given how ubiquitous apps are for every facet of human life – and I congratulate the authors for taking on this project in this important area.

Response: We are very grateful to the reviewer for reviewing our manuscript and for the feedback they have provided. We have responded to each comment below and revised the manuscript accordingly. We have indicated the page numbers within the revised manuscript where revisions have been made (all visible as tracked changes).

1. Psychotropic medication has increased by 4% annually – over what time period?

Response: We have now clarified the time period in the introduction.
“Globally, the total consumption of psychotropic medication increased by 4% annually from 2008 to 2019 (3).” (Page 3)

2. There are several analyses which find that the difference between placebo and antidepressant is not clinically significant (though it is statistically significant), leading to queries from Cochrane reviews, and others about whether these drugs should be used at all. This should inform this introduction.

Response: We have amended this part in the introduction section to address this point. However, we do not wish to weigh in on the ongoing debate about whether antidepressants should be used as this is beyond the scope of this review:

“The safety and efficacy of psychotropic medication is increasingly being debated, particularly in terms of the extent of any clinically meaningful improvements in symptoms when compared to placebo, and the potential for adverse effects, such as dependence and withdrawal symptoms (6). Studies have shown that 30-60% of long-term antidepressant prescriptions lack an indication for continued use and therefore may be inappropriate (7, 8). Similar concerns have been raised about antipsychotic and benzodiazepine use and their known potential risks. While evidence supports the use of antipsychotics in acute psychosis, evidence on their long-term use is lacking (9). This is acknowledged by studies which estimate that approximately 40% of those taking antipsychotics would remain well (i.e., would achieve a good outcome in the long term) without them (9).” (Page 3)

3. It is also worth pointing out that the neurotransmitter deficiencies that are often cited as rationales for medication in mental health conditions are now generally rejected and so a biological rationale for the treatment of distressing experiences is not solid. A ‘recovery’ approach in this frame may simply represent a common sense, reality-based approach to care.

Response: We have amended this section, so that it reads as follows:

“Despite the widespread use of psychotropic medication in treating mental health problems for many years, the mechanisms of action for drugs such as antidepressants and antipsychotics are still not fully understood. Previous theories that these drugs address an underlying chemical imbalance have found to be lacking any supporting evidence (12,13).” (Page 3)

4. Discussion of BZRAs – this statement regarding the evidence for benefit in long-term use is lacking is not accurate: most guidelines recommend that they are not used for more than 2-4 weeks and people using them longer than this should stop them. Their harms and benefits are similar to benzos to which they are almost identical. This section should be less equivocal.

Response: We have reworded this sentence as follows:

“With respect to benzodiazepine receptor agonists, while guidelines recommend that they should be limited to short‐term use (i.e., ≤4 weeks) to minimise the risk of adverse outcomes, long-term use of these medications is common. It is estimated that 3% of the general population use benzodiazepines for extended periods (>6 months) (10,11).”(Page 3)

5. Each of the domains of withdrawal symptoms mentioned on p.3 could be mild, moderate and severe – there are mild tremors and severe anxiety (panic attacks) so please re-phrase this section.

Response: We have reworded this sentence as follows:

“The list of withdrawal symptoms is extensive, with people reporting a range of symptoms (e.g., anxiety, tremors, lethargy) that range on a continuum of mild to severe (32, 34).” (Page 5)

6. The major rationale to evaluate apps is to see which are most effective – given that a trial of the apps is not proposed, the next best criteria would be to assess which apps adhere most closely to accepted ‘best practice’ for tapering or which generate the greatest user satisfaction. I can see that outcomes if measured will be included in appraisal under ‘key findings’.

I am not sure that assessing the development process of an app allows this to be established. An app could be established through a very comprehensive process and still fail to generate an app that is useful to patients. Therefore I wonder whether an additional frame is used to evaluate the apps: namely, fidelity to best practice. Best practice is itself a quandary, in this under-studied area, but I would suggest RCPsych’s guidance on stopping antidepressants, or an approach as outlined in Framer (2021), with NICE guidance for the other relevant classes also applicable.

Perhaps, similarly to this appraisal of existing CPGs for deprescribing, some domains of good practice could be established, against which existing apps are evaluated: Sørensen et al. (2022).

Response: The purpose of this scoping review is to provide a broad overview of the existing literature on apps, as well as commercially available apps. We are interested in looking at the apps in terms of their content, as well as their development, evaluation and reporting. Equally, if we establish that there are deficits in terms of how apps/studies are developed, evaluated and reported, that will provide useful information to inform future research.

While we will be looking to describe the tapering recommendations and establish which sources of evidence, if any, the apps report as the basis for instructions on tapering, we have purposefully avoided selecting any single source as a gold standard to critique the recommendations as we realise that there is no universally accepted guidance on tapering. However, we do plan on putting the findings of the review on this topic in context and discussing different sources of guidance on tapering in the discussion section of the completed review.

7. Additionally, I see a major problem is with the approach of coding using the BCT taxonomy. In the introduction the authors state that the main cause of difficulty stopping these medications is physiological dependence that leads to withdrawal on stopping.

A BCT taxonomy seems to be a framework for changing behaviour. This seems to imply its relevance is most geared to modifying addictive behaviour – for example, stopping compulsive smoking. However with physiological dependence there is not a learned behaviour that needs to be modified – antidepressant, and antipsychotic users are not using these drugs compulsively or in an addictive manner, and this is also true for the majority of users of benzos and z-drugs. People who want to stop these medications mostly would like to throw them in the bin. But they are unable to do so because of the aversive physiological consequences that result.

It therefore does not make sense to me to apply a BCT approach to these apps that are trying to achieve something quite different. From my knowledge of these apps, they attempt to help patients make calculations regarding hyperbolic or exponential dose reductions, log withdrawal symptoms and provide motivation and reassurance through a physiologically unpleasant trajectory.

I fear applying a BCT lens to this implies that difficulty stopping comes down to a learnt behaviour i.e. a predominantly psychological process and that in doing so it will miss the main ingredients.

Perhaps a less rigid approach that does not bring to bear the assumptions of a BCT frame would be best, perhaps adapted from this framework if the authors believe there are elements that are useful?

Response: For this review, the core focus of the apps that we are interested in looking at is the tapering of psychotropic medication. Even if dependence itself is not a learned behaviour, identifying solutions for helping people to taper and framing them in terms of BCTs could help ensure that they are described using a common terminology. Applying the BCT taxonomy allows for the content of any intervention to be defined using standardised terminology which will aid both the comparison of any identified interventions, as well as potential for future replication.

As per the nature of a scoping review which is intended to be broad and exploratory, if we identify important features of any apps that cannot be coded using this taxonomy, then we will report that. This could ultimately help to stimulate future research on how best to describe the content of tapering apps using standardised terminology.

8. How will apps that were not developed through academic processes (the vast majority of them presumably) be evaluated? Mention is made of trialling with a user – will their satisfaction be measured? Is pretending to be someone on 10mg TDS of diazepam really likely to generate a useful output of what using the app is like? It may be better to either say you will simply list the elements of these apps or involve someone actually tapering to trial these apps (which might be a more involved and different study)? Will the developer of these apps be written to in order to inquire about their development process?

Response: The evaluation of apps that are available on the app stores will primarily focus on the app content and functions. Once these apps have been identified, we will attempt to contact the app developers via email to ask for more information on the app development process.

The purpose of trialling the apps with a sample user profile is not to assess the user satisfaction (this would require an actual research study with a sample of participants to gather quantitative and/or qualitative data), but to enable us as the reviewers to gain a better understanding of the features and functions offered by the apps.
Thank you for giving me the opportunity to review this timely proposed review. This study will produce a useful overview of existing mobile apps for the process of deprescribing psychiatric medication, a topic which has been until recently ignored, and this review is an important step forward, given how ubiquitous apps are for every facet of human life – and I congratulate the authors for taking on this project in this important area.

Response: We are very grateful to the reviewer for reviewing our manuscript and for the feedback they have provided. We have responded to each comment below and revised the manuscript accordingly. We have indicated the page numbers within the revised manuscript where revisions have been made (all visible as tracked changes).

1. Psychotropic medication has increased by 4% annually – over what time period?

Response: We have now clarified the time period in the introduction.
“Globally, the total consumption of psychotropic medication increased by 4% annually from 2008 to 2019 (3).” (Page 3)

2. There are several analyses which find that the difference between placebo and antidepressant is not clinically significant (though it is statistically significant), leading to queries from Cochrane reviews, and others about whether these drugs should be used at all. This should inform this introduction.

Response: We have amended this part in the introduction section to address this point. However, we do not wish to weigh in on the ongoing debate about whether antidepressants should be used as this is beyond the scope of this review:

“The safety and efficacy of psychotropic medication is increasingly being debated, particularly in terms of the extent of any clinically meaningful improvements in symptoms when compared to placebo, and the potential for adverse effects, such as dependence and withdrawal symptoms (6). Studies have shown that 30-60% of long-term antidepressant prescriptions lack an indication for continued use and therefore may be inappropriate (7, 8). Similar concerns have been raised about antipsychotic and benzodiazepine use and their known potential risks. While evidence supports the use of antipsychotics in acute psychosis, evidence on their long-term use is lacking (9). This is acknowledged by studies which estimate that approximately 40% of those taking antipsychotics would remain well (i.e., would achieve a good outcome in the long term) without them (9).” (Page 3)

3. It is also worth pointing out that the neurotransmitter deficiencies that are often cited as rationales for medication in mental health conditions are now generally rejected and so a biological rationale for the treatment of distressing experiences is not solid. A ‘recovery’ approach in this frame may simply represent a common sense, reality-based approach to care.

Response: We have amended this section, so that it reads as follows:

“Despite the widespread use of psychotropic medication in treating mental health problems for many years, the mechanisms of action for drugs such as antidepressants and antipsychotics are still not fully understood. Previous theories that these drugs address an underlying chemical imbalance have found to be lacking any supporting evidence (12,13).” (Page 3)

4. Discussion of BZRAs – this statement regarding the evidence for benefit in long-term use is lacking is not accurate: most guidelines recommend that they are not used for more than 2-4 weeks and people using them longer than this should stop them. Their harms and benefits are similar to benzos to which they are almost identical. This section should be less equivocal.

Response: We have reworded this sentence as follows:

“With respect to benzodiazepine receptor agonists, while guidelines recommend that they should be limited to short‐term use (i.e., ≤4 weeks) to minimise the risk of adverse outcomes, long-term use of these medications is common. It is estimated that 3% of the general population use benzodiazepines for extended periods (>6 months) (10,11).”(Page 3)

5. Each of the domains of withdrawal symptoms mentioned on p.3 could be mild, moderate and severe – there are mild tremors and severe anxiety (panic attacks) so please re-phrase this section.

Response: We have reworded this sentence as follows:

“The list of withdrawal symptoms is extensive, with people reporting a range of symptoms (e.g., anxiety, tremors, lethargy) that range on a continuum of mild to severe (32, 34).” (Page 5)

6. The major rationale to evaluate apps is to see which are most effective – given that a trial of the apps is not proposed, the next best criteria would be to assess which apps adhere most closely to accepted ‘best practice’ for tapering or which generate the greatest user satisfaction. I can see that outcomes if measured will be included in appraisal under ‘key findings’.

I am not sure that assessing the development process of an app allows this to be established. An app could be established through a very comprehensive process and still fail to generate an app that is useful to patients. Therefore I wonder whether an additional frame is used to evaluate the apps: namely, fidelity to best practice. Best practice is itself a quandary, in this under-studied area, but I would suggest RCPsych’s guidance on stopping antidepressants, or an approach as outlined in Framer (2021), with NICE guidance for the other relevant classes also applicable.

Perhaps, similarly to this appraisal of existing CPGs for deprescribing, some domains of good practice could be established, against which existing apps are evaluated: Sørensen et al. (2022).

Response: The purpose of this scoping review is to provide a broad overview of the existing literature on apps, as well as commercially available apps. We are interested in looking at the apps in terms of their content, as well as their development, evaluation and reporting. Equally, if we establish that there are deficits in terms of how apps/studies are developed, evaluated and reported, that will provide useful information to inform future research.

While we will be looking to describe the tapering recommendations and establish which sources of evidence, if any, the apps report as the basis for instructions on tapering, we have purposefully avoided selecting any single source as a gold standard to critique the recommendations as we realise that there is no universally accepted guidance on tapering. However, we do plan on putting the findings of the review on this topic in context and discussing different sources of guidance on tapering in the discussion section of the completed review.

7. Additionally, I see a major problem is with the approach of coding using the BCT taxonomy. In the introduction the authors state that the main cause of difficulty stopping these medications is physiological dependence that leads to withdrawal on stopping.

A BCT taxonomy seems to be a framework for changing behaviour. This seems to imply its relevance is most geared to modifying addictive behaviour – for example, stopping compulsive smoking. However with physiological dependence there is not a learned behaviour that needs to be modified – antidepressant, and antipsychotic users are not using these drugs compulsively or in an addictive manner, and this is also true for the majority of users of benzos and z-drugs. People who want to stop these medications mostly would like to throw them in the bin. But they are unable to do so because of the aversive physiological consequences that result.

It therefore does not make sense to me to apply a BCT approach to these apps that are trying to achieve something quite different. From my knowledge of these apps, they attempt to help patients make calculations regarding hyperbolic or exponential dose reductions, log withdrawal symptoms and provide motivation and reassurance through a physiologically unpleasant trajectory.

I fear applying a BCT lens to this implies that difficulty stopping comes down to a learnt behaviour i.e. a predominantly psychological process and that in doing so it will miss the main ingredients.

Perhaps a less rigid approach that does not bring to bear the assumptions of a BCT frame would be best, perhaps adapted from this framework if the authors believe there are elements that are useful?

Response: For this review, the core focus of the apps that we are interested in looking at is the tapering of psychotropic medication. Even if dependence itself is not a learned behaviour, identifying solutions for helping people to taper and framing them in terms of BCTs could help ensure that they are described using a common terminology. Applying the BCT taxonomy allows for the content of any intervention to be defined using standardised terminology which will aid both the comparison of any identified interventions, as well as potential for future replication.

As per the nature of a scoping review which is intended to be broad and exploratory, if we identify important features of any apps that cannot be coded using this taxonomy, then we will report that. This could ultimately help to stimulate future research on how best to describe the content of tapering apps using standardised terminology.

8. How will apps that were not developed through academic processes (the vast majority of them presumably) be evaluated? Mention is made of trialling with a user – will their satisfaction be measured? Is pretending to be someone on 10mg TDS of diazepam really likely to generate a useful output of what using the app is like? It may be better to either say you will simply list the elements of these apps or involve someone actually tapering to trial these apps (which might be a more involved and different study)? Will the developer of these apps be written to in order to inquire about their development process?

Response: The evaluation of apps that are available on the app stores will primarily focus on the app content and functions. Once these apps have been identified, we will attempt to contact the app developers via email to ask for more information on the app development process.

The purpose of trialling the apps with a sample user profile is not to assess the user satisfaction (this would require an actual research study with a sample of participants to gather quantitative and/or qualitative data), but to enable us as the reviewers to gain a better understanding of the features and functions offered by the apps.
Competing Interests: No competing interests were disclosed. Close
Report a concern
Respond or Comment

COMMENTS ON THIS REPORT

Author Response 25 Aug 2022

Miriam Boland, School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin, Dublin, Ireland

25 Aug 2022

Author Response

Thank you for giving me the opportunity to review this timely proposed review. This study will produce a useful overview of existing mobile apps for the process of deprescribing psychiatric ... Continue reading Thank you for giving me the opportunity to review this timely proposed review. This study will produce a useful overview of existing mobile apps for the process of deprescribing psychiatric medication, a topic which has been until recently ignored, and this review is an important step forward, given how ubiquitous apps are for every facet of human life – and I congratulate the authors for taking on this project in this important area.

Response: We are very grateful to the reviewer for reviewing our manuscript and for the feedback they have provided. We have responded to each comment below and revised the manuscript accordingly. We have indicated the page numbers within the revised manuscript where revisions have been made (all visible as tracked changes).

1. Psychotropic medication has increased by 4% annually – over what time period?

Response: We have now clarified the time period in the introduction.
“Globally, the total consumption of psychotropic medication increased by 4% annually from 2008 to 2019 (3).” (Page 3)

2. There are several analyses which find that the difference between placebo and antidepressant is not clinically significant (though it is statistically significant), leading to queries from Cochrane reviews, and others about whether these drugs should be used at all. This should inform this introduction.

Response: We have amended this part in the introduction section to address this point. However, we do not wish to weigh in on the ongoing debate about whether antidepressants should be used as this is beyond the scope of this review:

“The safety and efficacy of psychotropic medication is increasingly being debated, particularly in terms of the extent of any clinically meaningful improvements in symptoms when compared to placebo, and the potential for adverse effects, such as dependence and withdrawal symptoms (6). Studies have shown that 30-60% of long-term antidepressant prescriptions lack an indication for continued use and therefore may be inappropriate (7, 8). Similar concerns have been raised about antipsychotic and benzodiazepine use and their known potential risks. While evidence supports the use of antipsychotics in acute psychosis, evidence on their long-term use is lacking (9). This is acknowledged by studies which estimate that approximately 40% of those taking antipsychotics would remain well (i.e., would achieve a good outcome in the long term) without them (9).” (Page 3)

3. It is also worth pointing out that the neurotransmitter deficiencies that are often cited as rationales for medication in mental health conditions are now generally rejected and so a biological rationale for the treatment of distressing experiences is not solid. A ‘recovery’ approach in this frame may simply represent a common sense, reality-based approach to care.

Response: We have amended this section, so that it reads as follows:

“Despite the widespread use of psychotropic medication in treating mental health problems for many years, the mechanisms of action for drugs such as antidepressants and antipsychotics are still not fully understood. Previous theories that these drugs address an underlying chemical imbalance have found to be lacking any supporting evidence (12,13).” (Page 3)

4. Discussion of BZRAs – this statement regarding the evidence for benefit in long-term use is lacking is not accurate: most guidelines recommend that they are not used for more than 2-4 weeks and people using them longer than this should stop them. Their harms and benefits are similar to benzos to which they are almost identical. This section should be less equivocal.

Response: We have reworded this sentence as follows:

“With respect to benzodiazepine receptor agonists, while guidelines recommend that they should be limited to short‐term use (i.e., ≤4 weeks) to minimise the risk of adverse outcomes, long-term use of these medications is common. It is estimated that 3% of the general population use benzodiazepines for extended periods (>6 months) (10,11).”(Page 3)

5. Each of the domains of withdrawal symptoms mentioned on p.3 could be mild, moderate and severe – there are mild tremors and severe anxiety (panic attacks) so please re-phrase this section.

Response: We have reworded this sentence as follows:

“The list of withdrawal symptoms is extensive, with people reporting a range of symptoms (e.g., anxiety, tremors, lethargy) that range on a continuum of mild to severe (32, 34).” (Page 5)

6. The major rationale to evaluate apps is to see which are most effective – given that a trial of the apps is not proposed, the next best criteria would be to assess which apps adhere most closely to accepted ‘best practice’ for tapering or which generate the greatest user satisfaction. I can see that outcomes if measured will be included in appraisal under ‘key findings’.

I am not sure that assessing the development process of an app allows this to be established. An app could be established through a very comprehensive process and still fail to generate an app that is useful to patients. Therefore I wonder whether an additional frame is used to evaluate the apps: namely, fidelity to best practice. Best practice is itself a quandary, in this under-studied area, but I would suggest RCPsych’s guidance on stopping antidepressants, or an approach as outlined in Framer (2021), with NICE guidance for the other relevant classes also applicable.

Perhaps, similarly to this appraisal of existing CPGs for deprescribing, some domains of good practice could be established, against which existing apps are evaluated: Sørensen et al. (2022).

Response: The purpose of this scoping review is to provide a broad overview of the existing literature on apps, as well as commercially available apps. We are interested in looking at the apps in terms of their content, as well as their development, evaluation and reporting. Equally, if we establish that there are deficits in terms of how apps/studies are developed, evaluated and reported, that will provide useful information to inform future research.

While we will be looking to describe the tapering recommendations and establish which sources of evidence, if any, the apps report as the basis for instructions on tapering, we have purposefully avoided selecting any single source as a gold standard to critique the recommendations as we realise that there is no universally accepted guidance on tapering. However, we do plan on putting the findings of the review on this topic in context and discussing different sources of guidance on tapering in the discussion section of the completed review.

7. Additionally, I see a major problem is with the approach of coding using the BCT taxonomy. In the introduction the authors state that the main cause of difficulty stopping these medications is physiological dependence that leads to withdrawal on stopping.

A BCT taxonomy seems to be a framework for changing behaviour. This seems to imply its relevance is most geared to modifying addictive behaviour – for example, stopping compulsive smoking. However with physiological dependence there is not a learned behaviour that needs to be modified – antidepressant, and antipsychotic users are not using these drugs compulsively or in an addictive manner, and this is also true for the majority of users of benzos and z-drugs. People who want to stop these medications mostly would like to throw them in the bin. But they are unable to do so because of the aversive physiological consequences that result.

It therefore does not make sense to me to apply a BCT approach to these apps that are trying to achieve something quite different. From my knowledge of these apps, they attempt to help patients make calculations regarding hyperbolic or exponential dose reductions, log withdrawal symptoms and provide motivation and reassurance through a physiologically unpleasant trajectory.

I fear applying a BCT lens to this implies that difficulty stopping comes down to a learnt behaviour i.e. a predominantly psychological process and that in doing so it will miss the main ingredients.

Perhaps a less rigid approach that does not bring to bear the assumptions of a BCT frame would be best, perhaps adapted from this framework if the authors believe there are elements that are useful?

Response: For this review, the core focus of the apps that we are interested in looking at is the tapering of psychotropic medication. Even if dependence itself is not a learned behaviour, identifying solutions for helping people to taper and framing them in terms of BCTs could help ensure that they are described using a common terminology. Applying the BCT taxonomy allows for the content of any intervention to be defined using standardised terminology which will aid both the comparison of any identified interventions, as well as potential for future replication.

As per the nature of a scoping review which is intended to be broad and exploratory, if we identify important features of any apps that cannot be coded using this taxonomy, then we will report that. This could ultimately help to stimulate future research on how best to describe the content of tapering apps using standardised terminology.

8. How will apps that were not developed through academic processes (the vast majority of them presumably) be evaluated? Mention is made of trialling with a user – will their satisfaction be measured? Is pretending to be someone on 10mg TDS of diazepam really likely to generate a useful output of what using the app is like? It may be better to either say you will simply list the elements of these apps or involve someone actually tapering to trial these apps (which might be a more involved and different study)? Will the developer of these apps be written to in order to inquire about their development process?

Response: The evaluation of apps that are available on the app stores will primarily focus on the app content and functions. Once these apps have been identified, we will attempt to contact the app developers via email to ask for more information on the app development process.

The purpose of trialling the apps with a sample user profile is not to assess the user satisfaction (this would require an actual research study with a sample of participants to gather quantitative and/or qualitative data), but to enable us as the reviewers to gain a better understanding of the features and functions offered by the apps.
Thank you for giving me the opportunity to review this timely proposed review. This study will produce a useful overview of existing mobile apps for the process of deprescribing psychiatric medication, a topic which has been until recently ignored, and this review is an important step forward, given how ubiquitous apps are for every facet of human life – and I congratulate the authors for taking on this project in this important area.

Response: We are very grateful to the reviewer for reviewing our manuscript and for the feedback they have provided. We have responded to each comment below and revised the manuscript accordingly. We have indicated the page numbers within the revised manuscript where revisions have been made (all visible as tracked changes).

1. Psychotropic medication has increased by 4% annually – over what time period?

Response: We have now clarified the time period in the introduction.
“Globally, the total consumption of psychotropic medication increased by 4% annually from 2008 to 2019 (3).” (Page 3)

2. There are several analyses which find that the difference between placebo and antidepressant is not clinically significant (though it is statistically significant), leading to queries from Cochrane reviews, and others about whether these drugs should be used at all. This should inform this introduction.

Response: We have amended this part in the introduction section to address this point. However, we do not wish to weigh in on the ongoing debate about whether antidepressants should be used as this is beyond the scope of this review:

“The safety and efficacy of psychotropic medication is increasingly being debated, particularly in terms of the extent of any clinically meaningful improvements in symptoms when compared to placebo, and the potential for adverse effects, such as dependence and withdrawal symptoms (6). Studies have shown that 30-60% of long-term antidepressant prescriptions lack an indication for continued use and therefore may be inappropriate (7, 8). Similar concerns have been raised about antipsychotic and benzodiazepine use and their known potential risks. While evidence supports the use of antipsychotics in acute psychosis, evidence on their long-term use is lacking (9). This is acknowledged by studies which estimate that approximately 40% of those taking antipsychotics would remain well (i.e., would achieve a good outcome in the long term) without them (9).” (Page 3)

3. It is also worth pointing out that the neurotransmitter deficiencies that are often cited as rationales for medication in mental health conditions are now generally rejected and so a biological rationale for the treatment of distressing experiences is not solid. A ‘recovery’ approach in this frame may simply represent a common sense, reality-based approach to care.

Response: We have amended this section, so that it reads as follows:

“Despite the widespread use of psychotropic medication in treating mental health problems for many years, the mechanisms of action for drugs such as antidepressants and antipsychotics are still not fully understood. Previous theories that these drugs address an underlying chemical imbalance have found to be lacking any supporting evidence (12,13).” (Page 3)

4. Discussion of BZRAs – this statement regarding the evidence for benefit in long-term use is lacking is not accurate: most guidelines recommend that they are not used for more than 2-4 weeks and people using them longer than this should stop them. Their harms and benefits are similar to benzos to which they are almost identical. This section should be less equivocal.

Response: We have reworded this sentence as follows:

“With respect to benzodiazepine receptor agonists, while guidelines recommend that they should be limited to short‐term use (i.e., ≤4 weeks) to minimise the risk of adverse outcomes, long-term use of these medications is common. It is estimated that 3% of the general population use benzodiazepines for extended periods (>6 months) (10,11).”(Page 3)

5. Each of the domains of withdrawal symptoms mentioned on p.3 could be mild, moderate and severe – there are mild tremors and severe anxiety (panic attacks) so please re-phrase this section.

Response: We have reworded this sentence as follows:

“The list of withdrawal symptoms is extensive, with people reporting a range of symptoms (e.g., anxiety, tremors, lethargy) that range on a continuum of mild to severe (32, 34).” (Page 5)

6. The major rationale to evaluate apps is to see which are most effective – given that a trial of the apps is not proposed, the next best criteria would be to assess which apps adhere most closely to accepted ‘best practice’ for tapering or which generate the greatest user satisfaction. I can see that outcomes if measured will be included in appraisal under ‘key findings’.

I am not sure that assessing the development process of an app allows this to be established. An app could be established through a very comprehensive process and still fail to generate an app that is useful to patients. Therefore I wonder whether an additional frame is used to evaluate the apps: namely, fidelity to best practice. Best practice is itself a quandary, in this under-studied area, but I would suggest RCPsych’s guidance on stopping antidepressants, or an approach as outlined in Framer (2021), with NICE guidance for the other relevant classes also applicable.

Perhaps, similarly to this appraisal of existing CPGs for deprescribing, some domains of good practice could be established, against which existing apps are evaluated: Sørensen et al. (2022).

Response: The purpose of this scoping review is to provide a broad overview of the existing literature on apps, as well as commercially available apps. We are interested in looking at the apps in terms of their content, as well as their development, evaluation and reporting. Equally, if we establish that there are deficits in terms of how apps/studies are developed, evaluated and reported, that will provide useful information to inform future research.

While we will be looking to describe the tapering recommendations and establish which sources of evidence, if any, the apps report as the basis for instructions on tapering, we have purposefully avoided selecting any single source as a gold standard to critique the recommendations as we realise that there is no universally accepted guidance on tapering. However, we do plan on putting the findings of the review on this topic in context and discussing different sources of guidance on tapering in the discussion section of the completed review.

7. Additionally, I see a major problem is with the approach of coding using the BCT taxonomy. In the introduction the authors state that the main cause of difficulty stopping these medications is physiological dependence that leads to withdrawal on stopping.

A BCT taxonomy seems to be a framework for changing behaviour. This seems to imply its relevance is most geared to modifying addictive behaviour – for example, stopping compulsive smoking. However with physiological dependence there is not a learned behaviour that needs to be modified – antidepressant, and antipsychotic users are not using these drugs compulsively or in an addictive manner, and this is also true for the majority of users of benzos and z-drugs. People who want to stop these medications mostly would like to throw them in the bin. But they are unable to do so because of the aversive physiological consequences that result.

It therefore does not make sense to me to apply a BCT approach to these apps that are trying to achieve something quite different. From my knowledge of these apps, they attempt to help patients make calculations regarding hyperbolic or exponential dose reductions, log withdrawal symptoms and provide motivation and reassurance through a physiologically unpleasant trajectory.

I fear applying a BCT lens to this implies that difficulty stopping comes down to a learnt behaviour i.e. a predominantly psychological process and that in doing so it will miss the main ingredients.

Perhaps a less rigid approach that does not bring to bear the assumptions of a BCT frame would be best, perhaps adapted from this framework if the authors believe there are elements that are useful?

Response: For this review, the core focus of the apps that we are interested in looking at is the tapering of psychotropic medication. Even if dependence itself is not a learned behaviour, identifying solutions for helping people to taper and framing them in terms of BCTs could help ensure that they are described using a common terminology. Applying the BCT taxonomy allows for the content of any intervention to be defined using standardised terminology which will aid both the comparison of any identified interventions, as well as potential for future replication.

As per the nature of a scoping review which is intended to be broad and exploratory, if we identify important features of any apps that cannot be coded using this taxonomy, then we will report that. This could ultimately help to stimulate future research on how best to describe the content of tapering apps using standardised terminology.

8. How will apps that were not developed through academic processes (the vast majority of them presumably) be evaluated? Mention is made of trialling with a user – will their satisfaction be measured? Is pretending to be someone on 10mg TDS of diazepam really likely to generate a useful output of what using the app is like? It may be better to either say you will simply list the elements of these apps or involve someone actually tapering to trial these apps (which might be a more involved and different study)? Will the developer of these apps be written to in order to inquire about their development process?

Response: The evaluation of apps that are available on the app stores will primarily focus on the app content and functions. Once these apps have been identified, we will attempt to contact the app developers via email to ask for more information on the app development process.

The purpose of trialling the apps with a sample user profile is not to assess the user satisfaction (this would require an actual research study with a sample of participants to gather quantitative and/or qualitative data), but to enable us as the reviewers to gain a better understanding of the features and functions offered by the apps.
Competing Interests: No competing interests were disclosed. Close
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VERSION 2 PUBLISHED 08 Mar 2022

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Version 2 (revision) 19 Aug 22	read
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Mark Horowitz, University College London, London, UK
Luke Molloy, University of Wollongong, Wollongong, Australia

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Reviewer Report

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04 Oct 2022 | for Version 2

Mark Horowitz, Division of Psychiatry, University College London, London, UK

29 Views Cite this report Responses(0)

Approved

Thank you for incorporating my feedback into your protocol and for responding to my concerns.

Competing Interests

I am the co-founder of a company called Outro Health aiming to support people who wish to stop long-term antidepressants in Canada and the US. I confirm that this potential conflict of interest did not affect my ability to write an objective and unbiased review of the article.

Reviewer Expertise

I study rationale psychopharmacology and patient-centred deprescribing of psychotropic drugs

I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.

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Reviewer Report

42 Views

29 Jul 2022 | for Version 1

Luke Molloy, School of Nursing, University of Wollongong, Wollongong, NSW, Australia

42 Views Cite this report Responses(1)

Approved

Is the rationale for, and objectives of, the study clearly described?

Yes
Is the study design appropriate for the research question?

Yes
Are sufficient details of the methods provided to allow replication by others?

Yes
Are the datasets clearly presented in a useable and accessible format?

Yes

Competing Interests

No competing interests were disclosed.

Reviewer Expertise

Mental health care, trauma-informed care, strengths-based practice.

I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.

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Author Response

25 Aug 2022

Miriam Boland, School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin, Dublin, Ireland

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No competing interests were disclosed.

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67 Views

04 Apr 2022 | for Version 1

Mark Horowitz, Division of Psychiatry, University College London, London, UK

67 Views Cite this report Responses(1)

Approved With Reservations

Is the rationale for, and objectives of, the study clearly described?

Yes
Is the study design appropriate for the research question?

Partly
Are sufficient details of the methods provided to allow replication by others?

Yes
Are the datasets clearly presented in a useable and accessible format?

Not applicable

References

Competing Interests

No competing interests were disclosed.

Reviewer Expertise

I study rationale psychopharmacology and patient-centred deprescribing of psychotropic drugs

Respond to this report

Responses (1)

Author Response

25 Aug 2022

Miriam Boland, School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin, Dublin, Ireland

Thank you for giving me the opportunity to review this timely proposed review. This study will produce a useful overview of existing mobile apps for the process of deprescribing psychiatric medication, a topic which has been until recently ignored, and this review is an important step forward, given how ubiquitous apps are for every facet of human life – and I congratulate the authors for taking on this project in this important area.

Response: We are very grateful to the reviewer for reviewing our manuscript and for the feedback they have provided. We have responded to each comment below and revised the manuscript accordingly. We have indicated the page numbers within the revised manuscript where revisions have been made (all visible as tracked changes).

1. Psychotropic medication has increased by 4% annually – over what time period?

Response: We have now clarified the time period in the introduction.
“Globally, the total consumption of psychotropic medication increased by 4% annually from 2008 to 2019 (3).” (Page 3)

2. There are several analyses which find that the difference between placebo and antidepressant is not clinically significant (though it is statistically significant), leading to queries from Cochrane reviews, and others about whether these drugs should be used at all. This should inform this introduction.

Response: We have amended this part in the introduction section to address this point. However, we do not wish to weigh in on the ongoing debate about whether antidepressants should be used as this is beyond the scope of this review:

“The safety and efficacy of psychotropic medication is increasingly being debated, particularly in terms of the extent of any clinically meaningful improvements in symptoms when compared to placebo, and the potential for adverse effects, such as dependence and withdrawal symptoms (6). Studies have shown that 30-60% of long-term antidepressant prescriptions lack an indication for continued use and therefore may be inappropriate (7, 8). Similar concerns have been raised about antipsychotic and benzodiazepine use and their known potential risks. While evidence supports the use of antipsychotics in acute psychosis, evidence on their long-term use is lacking (9). This is acknowledged by studies which estimate that approximately 40% of those taking antipsychotics would remain well (i.e., would achieve a good outcome in the long term) without them (9).” (Page 3)

3. It is also worth pointing out that the neurotransmitter deficiencies that are often cited as rationales for medication in mental health conditions are now generally rejected and so a biological rationale for the treatment of distressing experiences is not solid. A ‘recovery’ approach in this frame may simply represent a common sense, reality-based approach to care.

Response: We have amended this section, so that it reads as follows:

“Despite the widespread use of psychotropic medication in treating mental health problems for many years, the mechanisms of action for drugs such as antidepressants and antipsychotics are still not fully understood. Previous theories that these drugs address an underlying chemical imbalance have found to be lacking any supporting evidence (12,13).” (Page 3)

4. Discussion of BZRAs – this statement regarding the evidence for benefit in long-term use is lacking is not accurate: most guidelines recommend that they are not used for more than 2-4 weeks and people using them longer than this should stop them. Their harms and benefits are similar to benzos to which they are almost identical. This section should be less equivocal.

Response: We have reworded this sentence as follows:

“With respect to benzodiazepine receptor agonists, while guidelines recommend that they should be limited to short‐term use (i.e., ≤4 weeks) to minimise the risk of adverse outcomes, long-term use of these medications is common. It is estimated that 3% of the general population use benzodiazepines for extended periods (>6 months) (10,11).”(Page 3)

5. Each of the domains of withdrawal symptoms mentioned on p.3 could be mild, moderate and severe – there are mild tremors and severe anxiety (panic attacks) so please re-phrase this section.

Response: We have reworded this sentence as follows:

“The list of withdrawal symptoms is extensive, with people reporting a range of symptoms (e.g., anxiety, tremors, lethargy) that range on a continuum of mild to severe (32, 34).” (Page 5)

6. The major rationale to evaluate apps is to see which are most effective – given that a trial of the apps is not proposed, the next best criteria would be to assess which apps adhere most closely to accepted ‘best practice’ for tapering or which generate the greatest user satisfaction. I can see that outcomes if measured will be included in appraisal under ‘key findings’.

I am not sure that assessing the development process of an app allows this to be established. An app could be established through a very comprehensive process and still fail to generate an app that is useful to patients. Therefore I wonder whether an additional frame is used to evaluate the apps: namely, fidelity to best practice. Best practice is itself a quandary, in this under-studied area, but I would suggest RCPsych’s guidance on stopping antidepressants, or an approach as outlined in Framer (2021), with NICE guidance for the other relevant classes also applicable.

Perhaps, similarly to this appraisal of existing CPGs for deprescribing, some domains of good practice could be established, against which existing apps are evaluated: Sørensen et al. (2022).

Response: The purpose of this scoping review is to provide a broad overview of the existing literature on apps, as well as commercially available apps. We are interested in looking at the apps in terms of their content, as well as their development, evaluation and reporting. Equally, if we establish that there are deficits in terms of how apps/studies are developed, evaluated and reported, that will provide useful information to inform future research.

While we will be looking to describe the tapering recommendations and establish which sources of evidence, if any, the apps report as the basis for instructions on tapering, we have purposefully avoided selecting any single source as a gold standard to critique the recommendations as we realise that there is no universally accepted guidance on tapering. However, we do plan on putting the findings of the review on this topic in context and discussing different sources of guidance on tapering in the discussion section of the completed review.

7. Additionally, I see a major problem is with the approach of coding using the BCT taxonomy. In the introduction the authors state that the main cause of difficulty stopping these medications is physiological dependence that leads to withdrawal on stopping.

A BCT taxonomy seems to be a framework for changing behaviour. This seems to imply its relevance is most geared to modifying addictive behaviour – for example, stopping compulsive smoking. However with physiological dependence there is not a learned behaviour that needs to be modified – antidepressant, and antipsychotic users are not using these drugs compulsively or in an addictive manner, and this is also true for the majority of users of benzos and z-drugs. People who want to stop these medications mostly would like to throw them in the bin. But they are unable to do so because of the aversive physiological consequences that result.

It therefore does not make sense to me to apply a BCT approach to these apps that are trying to achieve something quite different. From my knowledge of these apps, they attempt to help patients make calculations regarding hyperbolic or exponential dose reductions, log withdrawal symptoms and provide motivation and reassurance through a physiologically unpleasant trajectory.

I fear applying a BCT lens to this implies that difficulty stopping comes down to a learnt behaviour i.e. a predominantly psychological process and that in doing so it will miss the main ingredients.

Perhaps a less rigid approach that does not bring to bear the assumptions of a BCT frame would be best, perhaps adapted from this framework if the authors believe there are elements that are useful?

Response: For this review, the core focus of the apps that we are interested in looking at is the tapering of psychotropic medication. Even if dependence itself is not a learned behaviour, identifying solutions for helping people to taper and framing them in terms of BCTs could help ensure that they are described using a common terminology. Applying the BCT taxonomy allows for the content of any intervention to be defined using standardised terminology which will aid both the comparison of any identified interventions, as well as potential for future replication.

As per the nature of a scoping review which is intended to be broad and exploratory, if we identify important features of any apps that cannot be coded using this taxonomy, then we will report that. This could ultimately help to stimulate future research on how best to describe the content of tapering apps using standardised terminology.

8. How will apps that were not developed through academic processes (the vast majority of them presumably) be evaluated? Mention is made of trialling with a user – will their satisfaction be measured? Is pretending to be someone on 10mg TDS of diazepam really likely to generate a useful output of what using the app is like? It may be better to either say you will simply list the elements of these apps or involve someone actually tapering to trial these apps (which might be a more involved and different study)? Will the developer of these apps be written to in order to inquire about their development process?

Response: The evaluation of apps that are available on the app stores will primarily focus on the app content and functions. Once these apps have been identified, we will attempt to contact the app developers via email to ask for more information on the app development process.

The purpose of trialling the apps with a sample user profile is not to assess the user satisfaction (this would require an actual research study with a sample of participants to gather quantitative and/or qualitative data), but to enable us as the reviewers to gain a better understanding of the features and functions offered by the apps.

View more View less

Competing Interests

No competing interests were disclosed.

Alongside their report, reviewers assign a status to the article:

Approved - the paper is scientifically sound in its current form and only minor, if any, improvements are suggested

Approved with reservations - A number of small changes, sometimes more significant revisions are required to address specific details and improve the papers academic merit.

Not approved - fundamental flaws in the paper seriously undermine the findings and conclusions

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Mobile phone applications to support psychotropic tapering: a scoping review protocol

Abstract

Keywords

Revised Amendments from Version 1

Introduction

Methods

Eligibility criteria

Search strategy

Study selection

Data extraction

Data analysis and synthesis

App coding

Critical appraisal

Presentation of results

Discussion

Dissemination of findings

Study status

Data availability

Underlying data

Extended data

Reporting guidelines

References

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Mobile phone applications to support psychotropic tapering: a scoping review protocol

Abstract

Keywords

Revised Amendments from Version 1

Introduction

Methods

Eligibility criteria

Search strategy

Study selection

Data extraction

Data analysis and synthesis

App coding

Critical appraisal

Presentation of results

Discussion

Dissemination of findings

Study status

Data availability

Underlying data

Extended data

Reporting guidelines

References

Comments on this article Comments (0)

Open Peer Review

Comments on this article Comments (0)

Open Peer Review

Reviewer Status

Reviewer Reports

Comments on this article

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