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Systematic review of study designs and methods in health transition research for young people with intellectual
Axel Kaehne1, Joann Kiernan1, James Ridley1
1Faculty of Health, Social Care and Medicine, Edge Hill University, Ormskirk, United Kingdom.
Insights
Health care transition research for young people with intellectual disabilities is limited, with a focus on experiences rather than robust evidence. Future research needs to involve young people more directly.
Area of Science:
- Health Services Research
- Disability Studies
- Pediatric to Adult Transition
Background:
- Healthcare transition for young people with intellectual disabilities is challenging.
- Existing evidence on interventions, methodologies, and study designs is limited.
- This systematic review focuses on published evidence in healthcare transitions.
Purpose of the Study:
- To assess interventions, methodological approaches, study designs, and locations of published evidence on healthcare transitions.
- To provide a comprehensive overview of the current research landscape.
- To identify gaps in the evidence base for this vulnerable population.
Main Methods:
- Systematic review adhering to the PRISMA protocol.
- Utilized an amended quality appraisal tool.
- Explored the nature of published evidence on healthcare transitions for young people.
Main Results:
- Health transition research for this population lacks a robust evidence base.
- Researchers predominantly favor exploratory studies on the experiential aspects of transition.
- There is a significant absence of genuinely participatory research involving young people.
Conclusions:
- This is the first systematic review of empirical studies on health transitions for young people with intellectual disabilities.
- The findings highlight the need for more rigorous and participatory research.
- Results will inform future research priorities in this critical area.
Background:
Transition for young people with intellectual disabilities from paediatric or adolescent services into adult health care services remains a difficult process for all stakeholders. The study assessed the type of interventions, the methodological approaches, study designs and location of existing published evidence in health care transitions.
Methods:
A systematic review utilising the PRISMA protocol with an amended quality appraisal tool to explore the nature of published evidence on health care transitions for young people.
Results:
Findings demonstrate that health transition research for this population lacks a robust evidence base and researchers favour exploratory studies investigating the experiential dimension of transition. The lack of involvement of young people in the studies indicates a problematic absence of genuinely participatory research.
Conclusion:
The study is the first systematic review of empirical studies in health transition of young people with intellectual disabilities exploring the nature of existing evidence. The results will support setting priorities for future research.
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