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Study Protocol

Protocol for an exploratory, longitudinal single case study of a novel palliative care rehabilitative service

[version 1; peer review: 1 approved, 2 approved with reservations]
PUBLISHED 20 Dec 2021
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Abstract

Background: Early access to rehabilitation can improve quality of life for those with life-limiting illnesses and is highlighted as a core component of the Adult Palliative Care Services Model of Care for Ireland. Despite this, palliative rehabilitation remains under-utilised and under-developed. In 2020, the Sláintecare Integration Fund provided opportunity to pilot a novel rehabilitative palliative care service, “Palliat Rehab”. This protocol proposes a case study, which aims to advance understanding of the form, content, and delivery of the pilot service.
Methods: A prospective, longitudinal, mixed-methods, case study design will be used to describe the service and to explore the experiences of patients, informal carers and clinicians. Additionally, data collection instruments will be tested and the utility of outcome measures will be examined. Data will be collected from documentary, survey, and interview sources.
Quantitative data will be analysed using descriptive statistics, including chi-square tests for categorical variables, Mann-Whitney U tests for ordinal data, and t-tests/ ANOVA for continuous data. Qualitative data will be analysed using thematic analysis.
Conclusions: New pathways are required to advance service provision to ensure that patients receive the ‘right care, in the right place, at the right time’. The development of ‘‘Palliat Rehab’’ offers opportunity to study an innovative service and consider its potential contribution to the achievement of Sláintecare goals. Investigating the service within its environmental context will lead to a better understanding of ‘how’ and ‘why’ things happen. Findings will be of value in assessing whether there is evidence that supports the service, and will be used to inform efforts to further develop and tailor the intervention.

Keywords

Palliative Care, Rehabilitation, Study protocol, Quality of Life 

Introduction

The number of older people living with a palliative care need in Ireland is projected to increase by 89% between 2016 to 20461. The population will account disproportionately for disability burden, pain prevalence and health care use, leading to increased population health burdens and health care utilisation. It is estimated, for example, that there will be a 106% increase in requirement for the hours of healthcare delivered at home1. Rehabilitative care offers an important way for the health system to re-tool to meet these challenges, yet it is an under-developed component of palliative care for all adults receiving services in Ireland2.

Rehabilitative palliative care has been defined as a paradigm integrating rehabilitation, enablement, self-management, and self-care into the model of palliative care to provide patients with support to enjoy the fullest possible life until death3. The unmet rehabilitative needs of those with serious illness are increasingly recognised- that is, the need to be normal and in control, the need for better every day functioning and mobility, and the need to alleviate the fear of being a burden4. Despite the growing evidence base, the literature guiding service provision remains limited. In 2016, the authors of a narrative synthesis concluded that there remained a lack of consensus on when and how rehabilitative palliative care should be offered and recommended that further research was required with regards to methods, activities, frameworks, and practice guidelines for service provision5.

Since the publication of Thuesen et al.5, further studies have pointed to the benefit of an exercise programme for patients with cancer-related fatigue6 and advanced non-small cell lung cancer7. An interdisciplinary rehabilitation programme has also demonstrated benefit for patients newly diagnosed with advanced cancer8. However, the few studies which have been conducted to date in Ireland on palliative care rehabilitation have been descriptive or exploratory in nature911, and the only interventional study that has been published has focused on health and social care professional education12.

The Adult Palliative Care Services Model of Care for Ireland recognises the importance of rehabilitative palliative care as a core part of service provision, while acknowledging the deficits that exist in staffing and development of services2. The publication of the Sláintecare Report from the Oireachtas Committee on the Future of Healthcare offers the promise of addressing these deficits with its commitment to develop universal palliative care13. Responding to the urgent need to provide support to the healthcare system to test and scale ideas that meet Sláintecare goals, the Sláintecare Integration Fund was established in 2019. The Fund aims to support projects that:

  • Demonstrate innovative ways in which citizens can engage in their own health,

  • Represent best practice in the management of chronic diseases and caring for older people, and

  • Encourage innovations in shift of care to the community or promoting hospital avoidance.

Following application to the Fund, our team was awarded a grant to deliver an integrated rehabilitation service for patients with palliative care needs and to conduct an exploratory, longitudinal case study. The case study aims to advance understanding of the form, content, and delivery of the novel rehabilitative palliative care service (‘‘Palliat Rehab’’) in the provision of specialist palliative care for academic, policy and practice purposes.

Objectives

The specific study objectives are:

  • To describe the novel rehabilitative palliative care service that spans hospital and community settings.

  • To explore the experiences of patients, informal carers and clinicians while receiving or providing the service.

  • To test data collection instruments and examine the utility of selected outcome measures.

Methods

Design

This study adopts a prospective longitudinal, case study design that will collect data from documentary, survey, and interview sources. ‘Palliat Rehab’ is a new service initiative, and a case study design was chosen because of the need to capture information to answer ‘how’, ‘what’ and ‘why’ questions using a naturalistic method. Case studies allow for investigation of a contemporary phenomenon within its real-life context when the boundaries between phenomenon and context are not clearly evident14 and provide an in-depth, multi-faceted understanding of issues that can help develop or refine theory15.

Guided by an exploratory case study framework16, and adopting a post-positivist approach17, this case study will examine the novel service as delivered by one hospital organisation and one community-based organisation for an 18-month period of service provision and will provide insight into the delivery of palliative care rehabilitation. In doing so, the study will contribute to opening the ‘black box’ of palliative care rehabilitation interventions and provide transferable knowledge that will be of value to the future development of interventional studies of service delivery.

Study setting

This study defines a single, holistic case as the rehabilitation service, the staff delivering the service, and the direct and indirect recipients of the service (patients and family members). The rehabilitation service will be provided by the Mater Misericordiae University Hospital (Mater Hospital) and St Francis Hospice for a 15-month period.

The Mater Hospital is a 630-bed teaching hospital providing local services for its catchment population of Dublin’s north inner city and a range of specialist services on a regional and national level. St Francis Hospice Dublin is a specialist palliative care service organisation providing in-patient, out-patient, and home-based services to people with progressive, life-limiting illness in the North Dublin area. The rehabilitation service will be delivered by a hospital-based Senior Occupational Therapist and a community-based Senior Physiotherapist, both of whom work as members of specialist palliative care teams. A description of the service based on TIDIER criteria is available in the Extended data. The case study population comprises patients who receive the palliative care rehabilitation service, their caregivers and clinicians managing or working with the rehabilitation service.

Sample

The study will recruit participants from the specialist palliative care services of the Mater Misericordiae University Hospital (Mater Hospital) and the community palliative care services of St Francis Hospice Dublin to contribute to the case study.

Three groups of participants are identified according to the nature and method of data collection that will be conducted:

  • 1. All patients receiving the novel service. Anonymised, routine data relating to service utilisation and outcomes will be collected as a usual part of service provision for all patients receiving the novel service.

  • 2. Patients who consent to provide survey data relating to satisfaction and outcomes. Additional information will be collected from patients who meet eligibility criteria (see Table 1) and who consent to complete a short survey on satisfaction with service and outcomes.

  • 3. Patients, caregivers, and staff who consent to participate in semi-structured qualitative interviews to gather information on their experience of the service. Additional information on experience of the service will collected from a purposive sample of patients, caregivers and staff who consent to participate in semi-structured interviews (see Table 1).

Table 1. Eligibility criteria for interview participation.

Patient inclusion criteriaCaregiver inclusion criteriaStaff inclusion criteria
    1.   Receiving the novel palliative
         care rehabilitation service due
         to identification of rehabilitation
         need
    2.   ≥ 18 years of age
    3.   English speaking
    4.   Able to provide informed consent
    5.   Patients do not need a caregiver
         willing to participate in the study
    1.   Self-endorsing or identified
         by the patient as a primary
         caregiver
    2.   ≥ 18 years of age
    3.   English speaking
    4.   Able to provide informed
         consent
    5.   Caregivers related to a
         participating patient are
         eligible for inclusion if the
         above criteria are satisfied,
         regardless whether their
         loved one participates in the
         research element or receives
         the intervention only.
    1.   Identified as a clinical
         staff member who has
         been involved in the
         design and/or delivery
         of the palliative care
         rehabilitation service
Patient exclusion criteriaCaregiver exclusion criteria
    1.   Unable to complete the study
         measures and/ or participate in
         an interview in the opinion of
         attending clinician. Patients may
         be unable to complete measures
         or participate due to ill-health,
         symptom burden or cognitive
         impairment.
    1.   Patient does not wish
         caregiver to be invited to
         participate in the study

Sample size

The sample size for a case study methodology described by Yin (2018) depends on the number of participants that is sufficient to describe the phenomenon18.

As sample size estimation for qualitative interview samples is an area of conceptual debate and practical uncertainty19, the projected sample size is based on the concepts of data adequacy and research practicality. The population included within this case study is relatively homogeneous, as participants will be availing of one single palliative care rehabilitation service. A purposive sample of 16-22 individuals will therefore be recruited for qualitative data analysis across three stakeholder groups; patients receiving the service (n= 4-6), family members of individuals receiving the service (n= 4-6), and clinicians involved in the design and/or delivery of the new service (n= 8-10).

The aim of the case study is not to test the rehabilitation service, therefore, it would not be appropriate to use traditional power calculations when considering sample size for the quantitative data collection component of the case study20. The purpose of quantitative data collection in the case study is to contribute to the understanding of care delivery and stakeholder experience and to test data collection instruments and examine the utility of selected outcome measures. Considering the issue of justification of sample adequacy, anonymised, routine data will be collected on all patients who receive the service, and all eligible patients will be offered the opportunity to participate in survey data collection.

Participation selection and recruitment

Patients. A palliative care needs assessment is conducted as a usual part of service provision when a patient is first seen by the specialist palliative care teams of either the Mater Hospital or St Francis Hospice. Needs assessments comprise holistic assessments of individual need that include, but are not limited to, assessment of physical condition, appraisals of pain, examination of function and mobility, discussion of potential difficulties completing activities of daily living, and identifying goals patients may have for their care. During usual assessment, consideration will be given by the Palliative Medicine consultant and palliative care team as to whether patients would benefit from involvement with ‘Palliat Rehab’. Referral to the service will depend on this palliative care needs assessment, where severe ill-health, symptom burden and/or cognitive deficit may preclude individuals from taking part. As rehabilitation needs can vary substantially between individuals and their conditions, however, inclusion will be determined on a case-by-case basis. If the specialist palliative team think that an individual has a rehabilitation need that could be met by the service, then the new service will be explained and offered to the patient by a team member.

Should the patient avail of the service, then demographic, service use and health and symptom data necessary for the delivery of care will be collected. Additionally, the physiotherapist (PT), occupational therapist (OT) and consultant will consider whether the patient meets eligibility criteria (Table 1) to be invited to take part in a survey and/or interview that focuses on their experiences of the service. The interview may take place in person or remotely according to patient preference, although only an audio recording will be made regardless of method of interview. Interviews are estimated to last approximately 30–40 minutes and protocols will be piloted with volunteers in St. Francis Hospice to ensure question clarity, in addition to monitoring time demand. As discussions involving an individual’s experience with a life-limiting illness may incur distress or negative emotions, patients will be assured that they are free to end the interview at any moment without providing a reason for stopping. Moreover, for any instances of distress, support mechanisms such as ready access to nursing, medical or social work members of the specialist palliative care teams will be readily available, if required.

Eligible patients will be invited to participate by any of the PT, OT, or consultant. Potential participants will be reassured that their care will be unaffected by their decision, and that individuals can receive ‘Palliat Rehab’ without participating in either the survey or interview.

All potential participants will be provided with an information leaflet detailing the purpose of the additional data collection, the potential risks and benefits to participation, and data protection rights. Following a minimum of 24 hours, potential participants will be asked whether they are interested in being contacted by a researcher to discuss participation further. A researcher will make telephone contact with individuals who indicate that they are willing to be contacted and answer questions and provide information, as needed. Following this, when potential participants are satisfied that they have been given sufficient time, written informed consent will be obtained prior to holding the interview for those who agree to take part. Confirmation of verbal consent will be sought again at time of interview.

Caregivers. Patients receiving ‘Palliat Rehab’ will also be asked by either the PT, OT, or consultant to consider whether they wish for their primary caregiver to also be invited to participate in a separate Zoom or telephone interview. It will be explained that the reason for inviting their caregiver to participate is to include caregiver perspectives in the research study. It will again be emphasised that their decision or that of their caregiver will not influence the patient’s care in any way. Following a minimum of 24 hours and allowing sufficient time for the patient to discuss the matter with his/her caregiver, the patient will be asked whether their caregiver is interested in being contacted by a researcher to discuss participation. A researcher will telephone individuals who indicate that they are willing to be contacted and answer questions and provide information, as needed. Following this, allowing a minimum of 24 hours, written informed consent will be obtained for those caregivers who agree to take part. Confirmation of verbal consent will be sought again at time of interview.

Staff. Clinical staff who have been involved in the design and/or delivery of the palliative care rehabilitation service will be invited to take part in two interviews by the Principal Investigator (PI). Both interviews will be separated by a minimum of 6 months to contrast learnings and applications of developed knowledge during the piloting of the intervention. It will be explained that the reason for inviting the staff member to participate is to include the perspectives of health and social care professionals in the study. Information will be provided to them regarding the study, the potential risks and benefits to participation, and data protection rights. It will be emphasised that the decision of the staff member will not influence or affect their career or work relationships in any way. If the staff member expresses interest in participating, the PI will send an individualised email introducing the staff member to the researcher. The researcher will provide the potential participant with written information on the study and the consent form and will be available to answer further questions as needed. Following this, allowing a minimum of 24 hours, written informed consent will be obtained for those staff members who agree to take part. Confirmation of verbal consent will be sought again at time of interview.

Data collection

Using a mixed-methods approach, description of the service will be informed by multiple sources of quantitative and qualitative data which will be collected in a sequential manner. Quantitative data collection will take place from service commencement, while qualitative interviewing will take place at two time points – approximately 4–6 months after commencement of the service and in the final two months of service provision.

It has been observed that rehabilitation is best described as a process containing specific actions21, and for this reason, the bundle of interventions will be investigated rather than specific components.

Quantitative data. Quantitative measures will include data that is recorded as a necessary or usual part of palliative care or rehabilitative palliative care service provision during patient assessments in patient charts or electronic patient records. All quantitative measures are summarised in Table 2 under three category headings: demographic data, service-usage data and, health and symptom data.

Table 2. Quantitative data and measures.

Demographic dataService-usage dataHealth and symptom data
    1.   Gender Identity
    2.   Age
    3.   Marital status
    4.   Primary diagnosis
    5.   Primary care
         network
    6.   Current living
         conditions including
         home supports
    1.   Response times between
         referral and service enrolment
    2.   The number, type,
         nd period of clinical
         interactions with the
         rehabilitative palliative care
         service
    3.   Length of hospital stay (for
         hospitalised patients only)
    4.   Whether re-admitted to
         hospital within 30-days
         of discharge or receipt of
         services
         enrolment
    2.   The number, type,
         and period of clinical
         interactions with the
         rehabilitative palliative care
         service
    3.   Length of hospital stay (for
         hospitalised patients only)
    4.   Whether re-admitted to
         hospital within 30-days
         of discharge or receipt of
         services
    1.   The Palliative Care Outcomes
         Collaborative (PCOC) scale22
    2.   Charlson Comorbidities
         Index (CCI)23
    3.   The Clinical Frail Scale24
    4.   Palmar Grip Strength
    5.   5x Sit-to-Stand test25

The routine, anonymised data will be collected at baseline (on enrolment in the programme) and at each interaction with the rehabilitation service. The survey data will be collected on completion of engagement with the rehabilitation service intervention.

Qualitative data. Semi-structured interview schedules for the first set of interviews for each group of participants were developed using a five-step framework of design26. The five steps are as follows: (1) identifying the prerequisites for using semi-structured interviews; (2) retrieving and using previous knowledge; (3) formulating the preliminary semi-structured interview guide; (4) pilot testing the guide; and (5) presenting the complete semi-structured interview guide.

Data management

Potential participants personal data will be processed under article 6 (1)(e) Public Interest and under article 9 (2)(j) Scientific Research of the General Data Protection Regulation (GDPR) 201627, and data will be secured in accordance with the requirements of the Data Protection Act (2015). Data will be anonymised and where applicable, pseudonyms will be used in reports and publications.

Analytic plan. Data analysis will be iterative and will continue over the course of the study.

Descriptive statistics will be generated using R28 to summarize participant characteristics across demographic and service usage domains, where categorical variables will be reported as raw numbers and percentages. Reports of continuous variables will include mean, median, range and standard deviation values. For repeated measures analysis of health and symptom data pre- and post-service engagement, significance of variations will be determined using x2 tests or Fisher’s Exact Test, when required, for categorical data, Mann-Whitney U tests for ordinal data, and t-tests/ ANOVA for continuous data. 95% confidence intervals (CI) will be used, and significance levels will be assessed at the alpha level of .05.

Interview audio will be transcribed using Happy Scribe (2021) transcription software and reviewed using original audio-recordings to ensure accuracy, the removal of identifiable information and to engage in data familiarity. For qualitative data, reflexive thematic analysis2931 will be used to generate descriptive themes related to the experiences and perspectives of stakeholders on the novel service. Thematic analysis was selected for analysis given its flexibility in application, enabling the collation of differing perspectives and the iterative construction of common themes.

Coding will be conducted both inductively and deductively using the open-source QDA Miner programme (version Lite), where inductive coding will entail annotating similarities and intriguing features across the dataset. Deductive coding will comprise the construction of a deductive codebook based on the core foundations of the Adult Palliative Care Services Model of Care2, and contemporary literature on rehabilitation, integration and palliative care3234.

Coding will be completed by three researchers forming a coding team with diverse academic backgrounds in health economics, rehabilitative palliative care, and psychology. These researchers will not be involved in the provision of the rehabilitative service. Coding will be completed through individual coding sessions and facilitatory discussions to gauge differences in interpretation and to fully explore the breadth of data collected. As the dataset will be coded progressively, base codes will be continually revised and refined in response to new facets of data. Theme construction will then be facilitated by the design of a coding tree to identify similar concepts generated during the coding process. To ensure regular reflection during the analytic process, a reflexive log will be maintained to track and detail aspects of the coding process to identify potential assumptions underlying their approach31. Qualitative analysis will be reported in line with the COREQ reporting guidelines45.

The construct validity, internal validity, external validity, and reliability of the data will be established through use of the following methods. First, the use of a protocol and exact documentation of each step of the process facilitates traceability35. Second, the use of multiple methods increases validity by providing multiple perspectives on the same phenomenon35. Third, a researcher diary will be used to record thoughts, feelings, and expectations that may at a later stage be used for data analysis36. Fourth, a well-structured database will be used for data management and will serve as the evidentiary source of conclusions35. Fifth, analytical techniques during data analysis such as explanation building and addressing rival explanations will be employed37. Sixth, the multidisciplinary composition of the team will allow the researchers to raise questions throughout the course of the study, particularly regarding the fit between the methods used and the results obtained, and study conclusions37. Finally, thick description will establish transferability38. Convergence of quantitative and qualitative data will be undertaken to describe the service and its implementation from the perspectives of patients, informal carers and clinicians.

Ethics

The research protocol has been approved by the Mater Misericordiae University Hospital (IRB Ref 1/378/2113) and St Francis Hospice Dublin (Rec. approval 16/1/20).

The case study will be conducted in accordance with the ethical standards of the organisations and with the 1964 Helsinki declaration and its later amendments39. The protocol was designed giving consideration to best practice in palliative and rehabilitative care and ensuring that risks (e.g., participant distress occurring during interview) will be minimised to the greatest possible degree for patients, carers and staff. The autonomy of participants will be respected by providing informed choice. All participants will receive oral and written information prior to the interview, and written informed consent will be obtained prior to interview. All participants will be informed that they may withdraw from the study, and/or withdraw their data, at any point without affecting their access to services. All data will be anonymized and will not be identifiable and will be managed securely.

Public and patient involvement

Due to required timeframes and available resources, public involvement in the development of the case study protocol has been at level one of the Public Participation Spectrum40 developed by the International Association for Public Participation. A virtual meeting was held with members of Voices4Care in March 2021 where the study protocol was presented, and a question-and-answer session held. Voices4Care is an initiative of All Ireland Institute of Hospice and Palliative Care (AIIHPC) – an all-island organisation working to improve palliative and end-of-life care for patients and their families. Voices4Care is a volunteer group with members comprising people living with a life-limiting illness/with palliative care needs, informal carers of adults with palliative care needs, and people from the wider community interested in palliative care.

Dissemination plans

In keeping with the mission of the research to develop service provision and meet patient needs, knowledge exchange activities will be undertaken to support a dissemination plan that reaches the public, health and social care professionals and policy makers. Dissemination materials will be developed to meet the needs of individual groups and a final project report will be provided to the Sláintecare Programme Implementation Office. Additionally, the case study will be submitted for publication in a peer-reviewed journal. Findings will be presented at national and international meetings. A project webpage has been created and may be accessed at https://palliativerehab.ie/. Information will also be shared via the Rehabilitative Palliative Care Slaintecare Project Twitter feed (@PalliativeRehab).

Study status

Data collection commenced in February 2020 but was interrupted by the COVID-19 pandemic. The palliative care rehabilitation service was suspended for a three-month period and data collection re-commenced in July 2020. Data collection is due to finish on December 31st, 2021.

Discussion

The Sláintecare Report set the vision of the all-party Committee on the Future of Healthcare to achieve a universal single-tier health and social care system where everyone has equitable access to services based on need, and not ability to pay. Core Sláintecare goals are the achievement of a shift in care from the acute to the community setting to bring care closer to home for service users, and a focus on enablement and well-being. Palliative rehabilitation aligns well with these objectives as it seeks to integrate enablement, self-management, and self-care into the holistic model of palliative care. Despite being recognised as an essential part of palliative care service provision2, rehabilitation services remain under-developed and under-utilised in Ireland and beyond. New pathways and models of care are required to advance service provision to ensure that patients receive the ‘right care, in the right place, at the right time, by the right people’. The development of ‘‘Palliat Rehab’’ offers opportunity to study an innovative service and consider its potential contribution to the achievement of Sláintecare goals. Investigating the rehabilitation service in-depth and within its environmental context will lead to a better understanding of ‘how’ and ‘why’ things happen. Case study findings will be of value in assessing whether there is evidence that supports the rehabilitation service, and will be used to inform efforts to further develop and tailor the intervention.

Limitations

Several limitations should be considered. The rehabilitation intervention is being delivered during a period of great change within health services that has been precipitated by the pandemic. This has resulted in a period of suspension of the service but has also impacted on usual ways of working (e.g., the requirement for physical distancing, utilisation of remote forms of communication). Detailed contextual description will be provided to enable others to understand the effect of the pandemic on service provision.

The study will appraise the suitability of selected outcome measures for use within the rehabilitation service. This is of particular importance given that the clinical usefulness of function and mobility-based outcome measures for individuals receiving specialist palliative care are currently a topic of debate41,42. Selecting an appropriate outcome measure is a critical step in designing valid and useful clinical trials and outcome studies, as the best design cannot make up for the use of an inappropriate measure. It is possible that the quantitative measures may have limited utility in contributing to knowledge of effectiveness. However, the application of mixed methods methodology will ensure that the strengths of one approach complements the restrictions of another and qualitative data will be used to understand the meaningfulness, or otherwise, of the quantitative outcomes. While the design of the Palliat Rehab service was informed by expert opinion and the evidence base, the staffing of the team was limited by funding availability and the required timelines of the project. Case study findings will provide important data on this issue.

Conclusion

This study aims to advance our knowledge of the implementation and delivery of a novel rehabilitative palliative care service. By providing an in-depth description of the experiences of patients, carers and health and social care professionals, a better understanding of the ‘how’ and ‘why’ (or ‘why not’) of the service’s perceived effectiveness will be obtained. Findings will be used to develop and tailor the intervention and will inform the development of future interventional studies as part of the journey towards evidence-based service provision.

Data availability

Underlying data

No data is associated with this article.

Extended data

Open Science Framework: Palliat Rehab Service, https://doi.org/10.17605/OSF.IO/RA93N47

This project contains a description of the novel service in line with the TIDieR checklist and interview schedules for each sample.

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

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Ní Chéileachair FN, Johnston BM, Payne C et al. Protocol for an exploratory, longitudinal single case study of a novel palliative care rehabilitative service [version 1; peer review: 1 approved, 2 approved with reservations]. HRB Open Res 2021, 4:131 (https://doi.org/10.12688/hrbopenres.13461.1)
NOTE: If applicable, it is important to ensure the information in square brackets after the title is included in all citations of this article.
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Reviewer Report 25 Jan 2022
Mai-Britt Guldin, REHPA, The Danish Knowledge Centre for Rehabilitation and Palliative Care, Odense University Hospital, Odense, Denmark 
Jette Thuesen, Department of Public Health, Unit for User Perspectives and Community Interventions, University of Southern Denmark, Odense, Denmark;  Center for Nutrition and Rehabilitation, Absalon University College, Holbæk, Denmark 
Approved with Reservations
VIEWS 46
Dear Colleagues,

Thank you for this manuscript. We were excited to read that you had undertaken developing a protocol on a case study of a novel palliative care rehabilitation service. We think this is exactly the type ... Continue reading
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Guldin MB and Thuesen J. Reviewer Report For: Protocol for an exploratory, longitudinal single case study of a novel palliative care rehabilitative service [version 1; peer review: 1 approved, 2 approved with reservations]. HRB Open Res 2021, 4:131 (https://doi.org/10.21956/hrbopenres.14672.r31107)
NOTE: it is important to ensure the information in square brackets after the title is included in all citations of this article.
  • Author Response 25 May 2022
    Fódhla Ní Chéileachair, Department of Palliative Care, Mater Misericordiae University Hospital, Dublin, Dublin, Ireland
    25 May 2022
    Author Response
    Dear Dr. Guldin and Dr. Thuesen, 
    Many thanks for taking the time to review the protocol for the Palliat Rehab case study. We are delighted you feel this study can ... Continue reading
COMMENTS ON THIS REPORT
  • Author Response 25 May 2022
    Fódhla Ní Chéileachair, Department of Palliative Care, Mater Misericordiae University Hospital, Dublin, Dublin, Ireland
    25 May 2022
    Author Response
    Dear Dr. Guldin and Dr. Thuesen, 
    Many thanks for taking the time to review the protocol for the Palliat Rehab case study. We are delighted you feel this study can ... Continue reading
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Reviewer Report 19 Jan 2022
JongKyu Kim, Department of Physical Medicine and Rehabilitation, Seoul Medical Center, Seoul, South Korea 
Approved with Reservations
VIEWS 53
Thank you for your great study protocol. It is very interesting and I am looking forward to the result from this study protocol.

Major recommendations:
  1. This study protocol is for the program of
... Continue reading
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CITE
HOW TO CITE THIS REPORT
Kim J. Reviewer Report For: Protocol for an exploratory, longitudinal single case study of a novel palliative care rehabilitative service [version 1; peer review: 1 approved, 2 approved with reservations]. HRB Open Res 2021, 4:131 (https://doi.org/10.21956/hrbopenres.14672.r31110)
NOTE: it is important to ensure the information in square brackets after the title is included in all citations of this article.
  • Author Response 31 Jan 2022
    Fódhla Ní Chéileachair, Department of Palliative Care, Mater Misericordiae University Hospital, Dublin, Dublin, Ireland
    31 Jan 2022
    Author Response
    Dear Dr. Kim,

    We are delighted you took the time to review the article and welcome your comments!
    In relation to the key components of Palliat Rehab, we would ... Continue reading
  • Author Response 25 May 2022
    Fódhla Ní Chéileachair, Department of Palliative Care, Mater Misericordiae University Hospital, Dublin, Dublin, Ireland
    25 May 2022
    Author Response
    Dear Dr. Kim, 

    Many thanks again for your helpful comments. We agree that it would be helpful to summarise the components of ‘Palliat Rehab’ and  we have restructured the ... Continue reading
COMMENTS ON THIS REPORT
  • Author Response 31 Jan 2022
    Fódhla Ní Chéileachair, Department of Palliative Care, Mater Misericordiae University Hospital, Dublin, Dublin, Ireland
    31 Jan 2022
    Author Response
    Dear Dr. Kim,

    We are delighted you took the time to review the article and welcome your comments!
    In relation to the key components of Palliat Rehab, we would ... Continue reading
  • Author Response 25 May 2022
    Fódhla Ní Chéileachair, Department of Palliative Care, Mater Misericordiae University Hospital, Dublin, Dublin, Ireland
    25 May 2022
    Author Response
    Dear Dr. Kim, 

    Many thanks again for your helpful comments. We agree that it would be helpful to summarise the components of ‘Palliat Rehab’ and  we have restructured the ... Continue reading
Views
45
Cite
Reviewer Report 12 Jan 2022
Lubayna Fawcett, Physical Therapy Department, Mayo Clinic, Scottsdale, AZ, USA;  Arizona State University, Tempe, AZ, USA 
Approved
VIEWS 45
This article will contribute to the much needed 'way forward' in palliative rehabilitation. The study settings and sampling as well as the outcome measures tools can all be easily implemented/replicated even in low income countries. 

In addition, ... Continue reading
CITE
CITE
HOW TO CITE THIS REPORT
Fawcett L. Reviewer Report For: Protocol for an exploratory, longitudinal single case study of a novel palliative care rehabilitative service [version 1; peer review: 1 approved, 2 approved with reservations]. HRB Open Res 2021, 4:131 (https://doi.org/10.21956/hrbopenres.14672.r31108)
NOTE: it is important to ensure the information in square brackets after the title is included in all citations of this article.
  • Author Response 31 Jan 2022
    Fódhla Ní Chéileachair, Department of Palliative Care, Mater Misericordiae University Hospital, Dublin, Dublin, Ireland
    31 Jan 2022
    Author Response
    Dear Dr. Fawcett,

    We're delighted with your comments on the protocol. Many thanks for taking the time to review this publication.

    With best wishes,
    Fódhla Ní Chéileachair
    Competing Interests: Corresponding author of the protocol.
COMMENTS ON THIS REPORT
  • Author Response 31 Jan 2022
    Fódhla Ní Chéileachair, Department of Palliative Care, Mater Misericordiae University Hospital, Dublin, Dublin, Ireland
    31 Jan 2022
    Author Response
    Dear Dr. Fawcett,

    We're delighted with your comments on the protocol. Many thanks for taking the time to review this publication.

    With best wishes,
    Fódhla Ní Chéileachair
    Competing Interests: Corresponding author of the protocol.

Comments on this article Comments (0)

Version 2
VERSION 2 PUBLISHED 20 Dec 2021
Comment
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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