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Feasibility trial of a structured intervention for expanding social networks in psychosis

Feasibility trial of a structured intervention for expanding social networks in psychosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN93047402
Enrollment
45
Registered
2018-12-11
Start date
2018-06-07
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

Specialty: Mental Health, Primary sub-specialty: Psychosis

Interventions

Patients will be randomised to either the intervention or control. The allocation ratio will be 2:1 in favour of the intervention. Randomisation will be stratified by NHS Trust, ensuring balance betwe
about once per month. The intervention should start with a sufficiently long first two meetings (about 60 minutes) in the first month to

Sponsors

Noclor, East London NHS Foundation Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients: 1. 18-65 years old 2. Diagnosis of psychosis-related condition (ICD-10 F20-29) 3. Capacity to provide informed consent 4. Ability to communicate in English 5. Limited social network size and low quality of life (Score less than 5 on MANSA quality of life assessment and less than 7 consecutive days with social contacts in the previous week) Clinicians: 1. Mental health professional with experience of providing community mental health care (e.g. psychiatrists, clinical psychologists, nurses, occupational therapists) 2. Aged 18-65 years old 3. Employed by participating NHS Trusts 4. Capacity to provide informed consent 5. Ability to communicate in English

Exclusion criteria

Exclusion criteria: Patients: 1. Does not meet inclusion criteria 2. Primary problem of current drug addiction 3. No capacity to provide written informed consent 4. An inpatient on a psychiatric ward at the time of recruitment Clinicians: 1. Does not meet inclusion criteria

Design outcomes

Primary

MeasureTime frame
Quality of life measured by the Manchester Short Assessment for Quality of Life (Priebe et al., 1999) at baseline and at 6 months

Secondary

MeasureTime frame
1. The number and quality of social contacts on each day of the previous week will be measured using Social Contacts (SCA) (Giacco et al., 2016), including detailed questions about social activities as developed in the ongoing PGfAR VOLUME (on volunteering in mental health) and including questions of the Time Use Survey (Priebe et al., 2016) at baseline and at 6 months 2. Positive and negative symptoms assessed using the Positive and Negative Syndrome Scale (PANSS, Kay 1991 and Clinical Assessment Interview for Negative Symptoms (CAINS, Kring et al., 2013) at baseline and at 6 months 3. Loneliness assessed using UCLA-8 (Hays and DiMateo, 1987) at baseline and at 6 months

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026