Skip to content

Assessing volunteering in mental health care for people with psychosis

An exploratory randomised controlled trial assessing volunteering in mental health care for people with psychosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN14021839
Enrollment
159
Registered
2015-07-23
Start date
2015-07-24
Completion date
Unknown
Last updated
2021-03-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Topic: Mental Health

Interventions

Befriending scheme: Patient participants will be individually matched with a volunteer companion. During the 12 months of the intervention, the patient and companion volunteer will meet on a weekly ba

Sponsors

Queen Mary University of London (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: For patient participants: 1. A diagnosis of schizophrenia or a related disorder (ICD-10:F20-29) 2. Being socially isolated i.e. spending on average less than 60 mins a day in social activities as measured by the TUS (Time Use Scale) 3. Willingness to receive regular one-to-one input from a volunteer participant over a period of 12 months 4. Aged between 18-65 5. Sufficient spoken and written English to converse with a volunteer participant on a regular basis and ability to fill in any necessary paperwork and forms 6. Being in the care of the community mental health team for a minimum of two months 7. Capacity to provide informed consent For volunteer participants: 1. 18 or more years of age 2. Willingness to provide regular one-to-one input to a patient with mental illness over a one year period 3. Willingness to participate in appropriate training and supervision 4. Sufficient command of English to be interviewed/fill out forms in English and to regularly converse with the patient 5. DBS checks show no major criminal convictions (e.g., sexual offences)

Exclusion criteria

Exclusion criteria: For patient participants: 1. Severe physical disability sufficient to prevent them in participating in community activities. 2. Learning disability 3. Having received a one to one volunteer input scheme in the last 2 years in the community (e.g., befriending, companion, peer support) 4. Currently receiving inpatient care from mental health care services 5. Evidence of history of physical violence 6. Currently in another research study For volunteer participants: 1. Having received care for a mental health illness from secondary or primary care services in the last 12 months 2. Current professional role in secondary mental health service 3. Severe physical disability sufficient to prevent them in participating in community activities 4. Lack of understanding of the responsibilities and characteristics of the volunteer role despite having received appropriate training 5. Unspent convictions of fraud, theft, violent assault or sexual offenses as identified on the DBS check

Design outcomes

Primary

MeasureTime frame
Time use; Timepoint(s): Baseline; 6 months; 12 months (i.e. end of the intervention); 18 months (i.e. 6 months follow-up)

Secondary

MeasureTime frame
1. Assessment of therapeutic relationship STAR; Timepoint(s): 6 month, 12 month (i.e. end of the intervention), 18 months (i.e. 6 month follow-up) 2. Attitudes to mental health; Timepoint(s): Baseline, 6 month, 12 month (i.e. end of the intervention), 18 months (i.e. 6 month follow-up) 3. Beck Depression Inventory BDI-II; Timepoint(s): Baseline, 6 month, 12 month (i.e. end of the intervention), 18 months (i.e. 6 month follow-up) 4. CAINS; Timepoint(s): Baseline, 6 month, 12 month (i.e. end of the intervention), 18 months (i.e. 6 month follow-up) 5. CSRI; Timepoint(s): Baseline, 6 month, 12 month (i.e. end of the intervention), 18 months (i.e. 6 month follow-up) 6. EQ-5D-5L; Timepoint(s): Baseline, 6 month, 12 month (i.e. end of the intervention), 18 months (i.e. 6 month follow-up) 7. PANSS; Timepoint(s): Baseline, 6 month, 12 month (i.e. end of the intervention), 18 months (i.e. 6 month follow-up) 8. Self-esteem; Timepoint(s): Baseline, 6 month, 12 month (i.e. end of the intervention), 18 months (i.e. 6 month follow-up) 9. Social contacts; Timepoint(s): Baseline, 6 month, 12 month (i.e. end of the intervention), 18 months (i.e. 6 month follow-up) 10. Subjective Quality of Life; Timepoint(s): Baseline, 6 month, 12 month (i.e. end of the intervention), 18 months (i.e. 6 month follow-up)

Countries

United Kingdom

Contacts

Public ContactHana Pavlickova

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 1, 2026