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Developing and testing a strategy to prevent involuntary psychiatric hospital admissions

Development, feasibility testing and pilot trial of a crisis planning and monitoring intervention to reduce compulsory hospital readmissions (the FINCH study)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN11627644
Enrollment
91
Registered
2022-05-25
Start date
2022-05-27
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Mental health Mental and Behavioural Disorders

Interventions

One way to try and reduce use of the Mental Health Act is to offer people a bespoke form of support after they are discharged to prevent them from being readmitted again. Therefore, the aim of this st

Sponsors

University College London
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Service user participants: Eligible participants will: 1. Have been compulsorily detained under section of the Mental Health Act (section 2 or 3) during their current hospital admission 2. Be due to receive community mental health care locally post-discharge 3. Be aged 18+ years 4. Have the capacity to consent at the time of recruitment Clinician participants (for intervention development and evaluation): Eligible participants will be 1. Currently working in an NHS mental health service as a nurse, psychiatrist, psychologist, social worker, occupational therapist, support worker or assistant psychologist 2. Currently working with service users who are currently or recently (in the last year) detained under section of the Mental Health Act (section 2 or 3) Personal mental health worker (for intervention evaluation): 1. Eligible participants will have delivered the adapted intervention to participants in the trial

Exclusion criteria

Exclusion criteria: Service user participants: Participants will be excluded if they: 1. Are already receiving an intensive psychosocial intervention that focuses on crisis reduction (for example, assertive outreach services) 2. Have a diagnosis of dementia or a brain injury 3. Do not speak sufficient English to take part without an interpreter 4. Lack capacity to consent Staff participants and personal mental health workers: Does not meet the inclusion criteria

Design outcomes

Primary

MeasureTime frame
Compulsory readmission to psychiatric in-patient services measured by checking the medical records of participants at 12 months

Secondary

MeasureTime frame
Measured at baseline, 6 months post-randomisation, and 12 months post-randomisation unless stated otherwise: 1. Satisfaction with services assessed using the Client Satisfaction Questionnaire 2. Personal recovery assessed using the Process of Recovery Questionnaire 3. Self-management confidence assessed using the Mental Health Confidence Scale 4. Symptoms of mental illness assessed using the Brief Psychiatric Rating Scale 5. Quality of life assessed using Recovering Quality of Life (REQOL-10) 6. Economic costs assessed using an adapted version of the “generic UK mental health” version of the Client Service Receipt Inventory 7. Service engagement measured through routinely collected data from patient records about all service use during data-collection periods at 12 and 24 months post randomisation 8. Compulsory readmission to hospital measured by checking the medical records of participants at 24 months 9. Demographic and clinical/service user characteristics, including Community Treatment Order status, previous admission history and clinical diagnosis

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 9, 2026