Psychosocial interventions for community-dwelling individuals with schizophrenia: study protocol for a systematic review and meta-analysis.
Author
Shikuri, YukiTanoue, Hiroki
Imai, Hissei
Nakamura, Hideki
Yamaguchi, Fumitake
Goto, Taichi
Kido, Yoshifumi
Tajika, Aran
Sawada, Hirotake
Ishida, Yasushi
Yoshinaga, Naoki
Date
2022-04-29Journal
BMJ OpenPublisher
BMJ Publishing GroupType
Article
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Introduction: Despite the recent global mental health movement of the transition from hospital-centred to integrated community-based services, comprehensive evidence of psychosocial interventions focusing on community-dwelling individuals with schizophrenia is still lacking. To overcome this gap in the current knowledge, we will conduct a systematic review and meta-analysis to assess the efficacy of all types of psychosocial interventions for community-dwelling (non-hospitalised) individuals with schizophrenia when compared with non-active control conditions (eg, treatment as usual). Methods and analysis: This study protocol has been developed according to the Preferred Reporting Items for Systematic Review and Meta-Analysis Protocols guidelines. By March 2022, the following sources will have been searched, without restrictions for language or publication period: Embase, PubMed, PsycINFO, CINAHL, the Cochrane Central Register of Controlled Trials, ClinicalTrials.gov and the WHO International Clinical Trials Registry Platform. We will also try to identify other potentially eligible studies by searching the reference lists of included studies, other relevant systematic reviews and grey literature. All relevant randomised controlled trials from both high-income and low-income to middle-income countries will be allowed. Two independent reviewers will conduct the selection/screening of studies, data extraction and methodological quality assessment of included studies. The primary outcomes are quality of life and psychiatric hospital admission. Standard pairwise meta-analyses with a random-effects model will be conducted. Subgroup and sensitivity analyses will be performed to assess the robustness of the findings. Risk of bias will be assessed with the Revised Cochrane Risk-of-Bias Tool for Randomised Trials. The Grades of Recommendation Assessment, Development and Evaluation approach will be used to assess the quality of evidence. Ethics and dissemination: Ethics approval is not required for this study. The study findings will be disseminated through conference presentations as well as peer-reviewed publications. Prospero registration number: CRD42021266187.Rights/Terms
© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.Identifier to cite or link to this item
http://hdl.handle.net/10713/18723ae974a485f413a2113503eed53cd6c53
10.1136/bmjopen-2021-057286
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