The views and lived experiences of individuals with intellectual and developmental disabilities who live in secure services: a meta-ethnography

Objectives In the United Kingdom, numerous scandals of abuse in in-patient services for individuals with intellectual and/or developmental disabilities (IDD) have prompted major policy reforms in service delivery, including a move towards reducing long-stay hospital beds and increasing community living. Despite widespread critiques and concerns about their effectiveness, secure settings continue to be commissioned for individuals with complex forensic or mental health needs, often due to limitations in community provision. To avoid repeating past failures, changes to the current service models are warranted. An initial step is understanding first-hand perspectives to inform more effective and supportive care. This meta-ethnography aimed to synthesise the literature relating to the lived experiences of people with IDD living in secure services. Methods Using Noblit and Hare’s meta-ethnographic model, a systematic search of the literature was conducted on Embase, PsychInfo, and Ovid Medline. To evaluate the methodological quality of studies, the Critical Appraisal Skills Programme framework was used. Results Eleven studies were included. Four primary themes were formulated: sense of self; where is my power?; navigating social relationships; and necessary evil. Of these, subthemes were formed to explore shared and contrasting views on belonging and identity, powerlessness, and meaningful social contact. Conclusions The findings reveal shared narratives from people with IDD that highlight areas for improvement in in-patient care services. While insights can guide service redesign, the methodological quality of several studies was low, underscoring the need for more rigorous research. Clinical and research implications are discussed.

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Publication Details

Journal
International Journal of Developmental Disabilities
Published
2026-02-26
DOI
https://doi.org/10.1080/20473869.2026.2632854
Primary Topic
Down syndrome and intellectual disability research
Type
article
Field-Weighted Citation Impact
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article

The views and lived experiences of individuals with intellectual and developmental disabilities who live in secure services: a meta-ethnography

John Rose, Franca Chidera Onyema, Lisa Richardson
International Journal of Developmental Disabilities
Down syndrome and intellectual disability research
article

The views and lived experiences of individuals with intellectual and developmental disabilities who live in secure services: a meta-ethnography

John Rose, Franca Chidera Onyema, Lisa Richardson
article en

Abstract

Objectives In the United Kingdom, numerous scandals of abuse in in-patient services for individuals with intellectual and/or developmental disabilities (IDD) have prompted major policy reforms in service delivery, including a move towards reducing long-stay hospital beds and increasing community living. Despite widespread critiques and concerns about their effectiveness, secure settings continue to be commissioned for individuals with complex forensic or mental health needs, often due to limitations in community provision. To avoid repeating past failures, changes to the current service models are warranted. An initial step is understanding first-hand perspectives to inform more effective and supportive care. This meta-ethnography aimed to synthesise the literature relating to the lived experiences of people with IDD living in secure services. Methods Using Noblit and Hare’s meta-ethnographic model, a systematic search of the literature was conducted on Embase, PsychInfo, and Ovid Medline. To evaluate the methodological quality of studies, the Critical Appraisal Skills Programme framework was used. Results Eleven studies were included. Four primary themes were formulated: sense of self; where is my power?; navigating social relationships; and necessary evil. Of these, subthemes were formed to explore shared and contrasting views on belonging and identity, powerlessness, and meaningful social contact. Conclusions The findings reveal shared narratives from people with IDD that highlight areas for improvement in in-patient care services. While insights can guide service redesign, the methodological quality of several studies was low, underscoring the need for more rigorous research. Clinical and research implications are discussed.

International Journal of Developmental Disabilities
University of Kent (GB), University of Birmingham (GB)
Reduced inequalities
Openalex Percentile: Top 37%
Down syndrome and intellectual disability research
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