The effectiveness of peer support in increasing hope and quality of life in psychiatric patients discharged from hospital

ISRCTN ISRCTN74852771
DOI https://doi.org/10.1186/ISRCTN74852771
Protocol serial number 8516
Sponsor East London NHS Foundation Trust (UK)
Funder National Institute for Health Research (NIHR) - Research for Patient Benefit (RfPB) (UK) (Ref: Grant Codes: PB-PG-0408-16151)
Submission date
23/02/2011
Registration date
23/02/2011
Last edited
06/02/2014
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Mental and Behavioural Disorders
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data

Plain English summary of protocol

Not provided at time of registration

Contact information

Prof Alan Simpson
Scientific

School Community & Health Sciences, Philpot Street
London
E1 2EA
United Kingdom

Email a.simpson@city.ac.uk

Study information

Primary study designInterventional
Study designRandomised interventional treatment
Secondary study designRandomised controlled trial
Study type Participant information sheet
Scientific titleA pilot randomised controlled trial to measure the effectiveness of peer support in increasing hope and quality of life in psychiatric patients discharged from hospital
Study acronymPeer Support Project
Study objectivesA pilot randomised controlled trial to compare effectiveness and cost effectiveness of peer support provided by Peer Support Workers (PSW) alongside usual aftercare to patients discharged from psychiatric units, with patients receiving usual aftercare alone.
Ethics approval(s)East London & The City REC Alpha on 26/03/2011 (REC Ref: 10/H0704/9)
Health condition(s) or problem(s) studiedTopic: Mental Health Research Network; Subtopic: All Diagnoses; Disease: Not Applicable
InterventionPeer Support, Peer Support Workers (PSW) will provide peer support for six weeks to patients discharged from four psychiatric wards over a seven month period. Peer support will be in addition to usual aftercare, described in the control condition. Initial contact will be made while the user is an inpatient. Follow up length: 3 months, study entry : single randomisation only
Intervention typeOther
Primary outcome measure(s)Beck Hopelessness Scale (BHS); Timepoints: One month (T1) and three months (T2) after discharge
Key secondary outcome measure(s)1. EuroQol, Timepoints: One month (T1) and three-months (T2) post-discharge
2. UCLA Loneliness Scale (V3) Timepoints: One month (T1) and three-months (T2) post-discharge
Completion date31/05/2011

Eligibility

Participant type(s)Patient
Age groupAdult
Lower age limit18 Years
SexAll
Target sample size at registration143
Key inclusion criteria1. Gender: Male & Female, age between 18 and 65 years
2. Diagnosed mental illness, approaching discharge/extended leave
Key exclusion criteria1. Considered a risk to others, alcohol or drug dependent/problematic substance user or primary diagnosis of substance use
2. Serious personality disorder
3. Pregnant or caring for children
Date of first enrolment01/10/2010
Date of final enrolment31/05/2011

Locations

Countries of recruitment

  • United Kingdom
  • England

Study participating centre

School Community & Health Sciences, Philpot Street
London
E1 2EA
United Kingdom

Results and Publications

Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
IPD sharing plan

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Results article results 05/02/2014 Yes No
Participant information sheet Participant information sheet 11/11/2025 11/11/2025 No Yes