Keywords
childhood vaccination, childhood immunisation, vaccination, immunisation, primary series vaccination, booster vaccination
This article is included in the Maternal and Child Health collection.
Completion of childhood vaccination schedules is essential to prevent childhood morbidity and mortality and to protect population health. Despite improvements in first-dose coverage globally, uptake of second or subsequent dose vaccines remains suboptimal. Parents serve as the primary decision-makers for childhood vaccination, with both modifiable and non-modifiable parent-level factors influencing vaccination uptake. However, it remains unclear what parent-level barriers and facilitators specifically affect second or subsequent vaccine dose uptake. The objective of this mixed-methods systematic review is to identify and integrate the existing evidence regarding parent-level barriers and facilitators to second or subsequent dose uptake in childhood vaccination.
This mixed-methods systematic review will follow the methodological guidance from the Joanna Briggs Institute (JBI) Manual for Evidence Synthesis. This review will include both published and unpublished literature employing quantitative, qualitative, and mixed-method approaches. A comprehensive and systematic search of electronic databases will be conducted, including PubMed, CINAHL, Scopus, PsycINFO and Cochrane Library. No search limits on date or language of publication will be applied. Searches for grey literature or research published outside of the indexed journal article format will be searched to supplement the electronic database searches. The findings will be reported in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-analyses.
This mixed-methods systematic review will present integrated findings of parent-level barriers and facilitators to second or subsequent dose uptake in childhood vaccination. The findings are expected to inform the design of targeted, evidence-based interventions aimed at improving second or subsequent dose vaccine uptake and overall childhood vaccination coverage. In doing so, the review will support global immunisation priorities, including the World Health Organisation’s Immunisation Agenda 2030.
Systematic review registration number: PROSPERO 2026 CRD420261324738.
childhood vaccination, childhood immunisation, vaccination, immunisation, primary series vaccination, booster vaccination
Vaccines play a critical role in reducing childhood morbidity and mortality and in safeguarding global health and economic security.1 Since the rollout of the World Health Organisation’s (WHO) Expanded Programme on Immunisation, vaccines have saved over 154 million lives and generated more than 10 billion years of life lived in full health.2 Achieving and sustaining these benefits depends on adherence to recommended vaccination schedules, including the completion of multi-dose primary series and booster doses series where appropriate.3
Despite substantial efforts, global childhood vaccination coverage remains suboptimal, particularly for second and subsequent vaccine doses. In 2024, global coverage of the second measles-containing vaccine (MCV2) reached 76%, falling below the 95% coverage threshold recommended to prevent measles outbreaks.1,4 Similar drops in coverage have been observed across other multi-dose childhood vaccines, highlighting a persistent challenge in vaccine completion beyond the first dose and undermining population-level immunity.5
Parents and guardians play a crucial role in childhood vaccination uptake, positioning parent-level factors as critical targets for public health intervention. A myriad of parent-level factors shape vaccine uptake, influencing whether parents consciously decline certain doses or unintentionally miss them, with some accepting selected vaccines while not completing others.6,7 Existing research has identified both modifiable and non-modifiable parental determinants of childhood vaccination. Identifying these determinants is important for identifying high-risk populations and targeting modifiable factors, both of which can be addressed through vaccination intervention programmes.
A global umbrella review by Sacre et al. found mixed evidence regarding the association between socioeconomic status (SES) and initiation and/or completion of childhood vaccination uptake, with both lower and higher SES associated with lower and higher uptake, respectively, across different contexts.8 An earlier systematic review similarly reported inconsistent findings regarding SES, but identified associations between low maternal education and high birth order and incomplete or delayed vaccination.9 More recently, Adisu et al. conducted a systematic review examining determinants of MCV2 uptake among children under five years of age in Africa.10 Consistent with previous evidence, significant determinants included high maternal education, attendance to antenatal care follow-ups, and use of postnatal care services. The review also identified reduced waiting times at vaccination sites, greater awareness, and positive perceptions of the second dose vaccine as significant predictors of MCV2 uptake.10
Beyond non-modifiable risk factors, a substantial body of the literature focuses on modifiable parental determinants of vaccine uptake. A global umbrella review by Kaufman et al. synthesised evidence on modifiable parent-level determinants of vaccination uptake, identifying key access- and acceptance-related factors. These determinants were grouped into six categories: access, clinic or health system barriers, concerns and beliefs, health perceptions and experiences, knowledge and information, and social or influence.11
However, existing literature typically examines non-modifiable and modifiable parental determinants of childhood vaccine uptake using binary outcomes, such as completion versus non-completion of the entire childhood vaccination schedule. What remains unclear is how parent-level barriers and facilitators of vaccine uptake may vary by vaccine dose. As vaccinations are delivered over extended periods and at different stages of a child’s development, second or subsequent doses are typically administered at older ages, when parental circumstances and healthcare engagement and experiences likely differ from the early infancy period.
As a result, parents may encounter distinct barriers and facilitators across vaccine doses. For example, parents participating in a qualitative study in the United Kingdom reported differential barriers to the second dose of measles-containing vaccine and diphtheria, tetanus, pertussis and polio (dTaP) booster dose compared with initial doses. Parents reported reduced availability of information and less contact with healthcare professionals regarding subsequent doses. In addition, parents reported a more difficult emotional experience, characterised by increased apprehension and guilt when taking an older child for subsequent doses compared with taking younger infants for their primary vaccination.12 Similarly, parents from a study in Ethiopia identified lack of information about when to return for the second dose as a significant barrier to MCV2 uptake.13 This evidence suggests a waning of informational and other supports following initial vaccine doses.
To the best of our knowledge, no review has synthesised global evidence on parent-level barriers and facilitators to second or subsequent dose uptake in childhood vaccination. While most studies examine vaccination uptake at the level of the overall childhood schedule, which varies across countries, limited attention has been paid to parent-level barriers and facilitators specific to second or subsequent doses within multi-dose vaccine series. Given the substantial variation in study methodologies, a mixed-methods systematic review is the most appropriate approach to address this research question and systematically synthesise the existing evidence base.
Therefore, the objective of this mixed-methods systematic review is to identify and integrate the literature on parent-level barriers and facilitators to second or subsequent childhood vaccine dose uptake. In this review, parent-level barriers and facilitators are defined as both modifiable and non-modifiable determinants of second or subsequent dose childhood vaccination, which are directly relevant to parents. This review is vital to inform appropriate vaccination schedules and interventions, and supports the overarching goals of the WHO Immunisation Agenda.1
What are the parent-level barriers and facilitators to second or subsequent dose uptake in childhood vaccination?
Parents or legal guardians of children who are eligible to receive a second or subsequent dose of a routine childhood vaccination are eligible for inclusion in this review. Children in this review do not include adolescents, and all studies involving parents of adolescents will be excluded. Studies not reporting barriers relevant to parents or legal guardians of children will be excluded.
The primary concept of interest in this review is parent-level barriers and/or facilitators to second or subsequent dose uptake in childhood vaccinations. In this review, uptake is defined as receipt versus non-receipt of vaccine doses. Studies examining parental factors associated with dropout between the first and subsequent doses of the same routine childhood vaccine series (e.g. dropout from first measles dose vaccine to second dose measles vaccine) will also be eligible for inclusion.
Parent-level barriers and facilitators are defined as both modifiable and non-modifiable determinants directly related to parents which can inhibit or encourage childhood vaccination uptake.
For the purposes of this review, second or subsequent childhood vaccine doses are defined as all doses administered after the first dose within a multi-dose vaccine series, including doses in both the childhood primary series and booster series. Eligible multi-dose vaccines include all universally recommended childhood vaccines as outlined by the WHO Vaccine Position Papers.14 Studies examining vaccines which are not recommended for all children in line with the WHO’s Vaccine Position Papers will be excluded, including but not limited to COVID-19 vaccines, seasonal influenza vaccines and varicella vaccines.14 Human papillomavirus vaccines will be excluded as they are administered during early adolescence, where parent-level barriers and facilitators may significantly different to those experienced in early childhood.
The proposed mixed-methods systematic review was developed following the methodological guidance from the Joanna Briggs Institute (JBI) Manual for Evidence Synthesis guidelines.15 The review will report in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses.16
A preliminary search of the literature will be conducted to identify keywords and subject headings used across databases. The text words and subject headings used in relevant articles will be used to develop a search strategy in collaboration with a subject librarian at Dublin City University. The following electronic databases will be searched, chosen in collaboration with a subject librarian: PubMed, Scopus, CINAHL, PsycINFO and Cochrane Library. An example of the search strategy is available elsewhere.17 The reference list of all studies included for critical appraisal will be screened for additional studies. No language or date restrictions will be applied to the searches.
Following the search, all identified sources will be uploaded to Covidence and duplicates removed. Title and abstract screening will be conducted independently by two reviewers and assessed against the inclusion criteria. The full text of potentially relevant articles will be retrieved and assessed against inclusion criteria independently by two reviewers. Potentially relevant articles published in languages other than English will be translated using DeepL. Any conflicts that arise between reviewers will be resolved via team discussion and the inclusion of a third reviewer if necessary. The results of the search and study inclusion process will be reported in the proposed systematic review and illustrated in a PRISMA flow diagram.
Eligible studies for inclusion will be assessed by two independent reviewers for methodological quality using the JBI critical appraisal tools appropriate for the study design. Quantitative studies and quantitative components of mixed methods studies eligible for inclusion will be assessed using the standardised JBI quantitative critical appraisal tool.18 Qualitative studies and qualitative components of mixed methods studies eligible for inclusion will be assessed using the standardised JBI qualitative critical appraisal tool.19 Any conflicts that arise between reviewers will be resolved via team discussion and the inclusion of a third reviewer if necessary. The results of the critical appraisal will be displayed in a tabulated format accompanied by a narrative discussion. All studies, irrespective of their methodological quality, will undergo data extraction and synthesis.
Data will be extracted from studies included in the systematic review by two independent reviewers using the standardised JBI data extraction tool.15 The data extraction process will be pilot tested prior to full implementation. The data extracted will relate to the PICo framework, including study authors’ names, year of study publication, study setting, population, sample size, vaccine type, and dose. For quantitative studies, all descriptive and/or inferential statistics relevant to the review question will be extracted. For qualitative studies, themes or subthemes relevant to the review question will be extracted. Any disagreements between reviewers will be resolved through team discussion. Study authors will be contacted if reviewers require additional information or clarification about the study.
This mixed-methods systematic review will follow a convergent integrated approach whereby quantitative data will be transformed into qualitzed data following data extraction.15 To achieve this, quantitative data will be translated into textual descriptions to allow integration with qualitative data. Integrated findings will be grouped by identifying similarities in meanings.
Childhood vaccination coverage remains suboptimal, particularly for second and subsequent vaccine doses administered across early and later childhood.1,4 Poor vaccination coverage increases the risk of vaccine-preventable disease outbreaks and poses an ongoing threat to population health. This mixed-methods systematic review will integrate the existing literature on parent-level barriers and facilitators to second or subsequent dose uptake in childhood vaccination. Examining both modifiable and non-modifiable parent-level factors, this review will help to identify populations who may be at a higher risk of under-vaccination, as well as actionable barriers to vaccine uptake that can be addressed through tailored vaccination interventions. The findings of this review are expected to inform service providers and policy makers, and to contribute to the development of appropriate strategies to improve childhood vaccination coverage.
Search strategy
Zenodo: “Example of a search strategy for parent level barriers and facilitators to second or subsequent dose uptake in childhood vaccination: A mixed-methods systematic review protocol.” https://doi.org/10.5281/zenodo.18759416.17
Zenodo: “PRISMA-P checklist for a systematic review.” https://doi.org/10.5281/zenodo.18759416.17
Data are available under the terms of the Creative Commons Attribution 4.0 International license (CC-BY 4.0).
The authors would like to acknowledge Emma Stapleton, Subject Librarian for the School of Nursing, Psychotherapy and Community Health, Dublin City University for her assistance in the development of the search strategy.
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?
Partly
Are the datasets clearly presented in a useable and accessible format?
Not applicable
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Vaccinology, health systems, scoping and systematic reviews
Alongside their report, reviewers assign a status to the article:
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Version 1 26 Mar 26 |
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