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Clinical Trials/ISRCTN10043328
ISRCTN10043328
Completed
未知

Enhanced discharge from inpatient to community health care (ENRICH): a programme of applied research to manualise, pilot and trial a Peer Worker intervention

St George's, University of London0 sites590 target enrollmentNovember 28, 2016

Overview

Phase
未知
Intervention
Not specified
Conditions
Mental health
Sponsor
St George's, University of London
Enrollment
590
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

2020 Protocol article in https://www.ncbi.nlm.nih.gov/pubmed/32150057 protocol (added 10/03/2020) 2021 Other publications in https://pubmed.ncbi.nlm.nih.gov/34419155/ Intervention development (added 23/08/2021) 2022 Results article in https://pubmed.ncbi.nlm.nih.gov/35065722/ (added 24/01/2022)

Registry
who.int
Start Date
November 28, 2016
End Date
August 31, 2019
Last Updated
4 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Inpatients of adult acute psychiatric wards (acute admission wards and their equivalents as termed locally) with at least one previous psychiatric admission in the preceding two years
  • 2\. Aged 18\+
  • 3\. Assessed by an appropriate member of the ward clinical team as having sufficient capacity to give informed consent to participate in the study
  • 4\. Assessed by ward clinical team as likely to be discharged within the next month
  • 5\. Given written, witnessed informed consent to participate in the study

Exclusion Criteria

  • 1\. Diagnosis of organic mental health conditions
  • 2\. Primary diagnosis of eating disorders, learning disability, or drug or alcohol dependency
  • 3\. Assessed by ward clinical team as lacking sufficient capacity to give informed consent to participate in the study
  • 4\. Assessed by ward clinical team as unlikely to be discharged within the next month
  • 5\. Assessed by ward clinical team as presenting a current, substantial risk to peer worker
  • 6\. Already participants in either arm of the study (having been readmitted during follow\-up)
  • 7\. Not having given written, witnessed informed consent to participate in the study

Outcomes

Primary Outcomes

Not specified

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