Randomised controlled trial of a psychotherapeutic intervention to improve quality of life and other outcomes in people who repeatedly self-harm : FReSH START study protocol

Farley, K. and Copsey, B. and Wright-Hughes, A. and Farrin, A. and Bojke, C. and McMillan, D. and Graham, C. D. and Mattock, R. and Brennan, CA. and Gates, C. and Martin, A. and Dowse, A. and Horrocks, J. and House, AO. and Guthrie, EA. (2024) Randomised controlled trial of a psychotherapeutic intervention to improve quality of life and other outcomes in people who repeatedly self-harm : FReSH START study protocol. Trials, 25 (1). 564. ISSN 1745-6215 (https://doi.org/10.1186/s13063-024-08369-2)

[thumbnail of Farley-etal-Trials-2024-A-randomised-controlled-trial-of-psychotherapeutic-intervention]
Preview
 Text. Filename: Farley-etal-Trials-2024-A-randomised-controlled-trial-of-psychotherapeutic-intervention.pdf
Final Published Version
License: Creative Commons Attribution 4.0 logo
Download (1MB)| Preview

Abstract

Background Self-harm is a major public health challenge and repeated self-harm is common in those attending hospital following an episode. Evidence suggests psychological interventions could help people who self-harm, but few definitive studies have assessed their clinical and cost-effectiveness. Repeated self-harm is associated with poor quality of life, depression, suicide and increased health service costs which justify the development of psychotherapeutic interventions tailored for people with repeated self-harm. Methods FReSH START is a multicentre individually 1:1 randomised controlled trial evaluating the clinical and cost-effectiveness of standard care plus psychological therapy or standard care alone for adults (>=18 years) presenting at an emergency department (ED) with repeated self-harm. Recruiting 630 participants, it includes an internal pilot, economic evaluation and process evaluation. The intervention will be delivered by mental health staff working in acute settings, with experience of assessing and managing risk in people presenting to emergency services with self-harm. Staff will be trained and supervised to deliver one of three specially adapted therapies: psychodynamic interpersonal therapy, cognitive behavioural therapy, or acceptance and commitment therapy. Participants allocated to the intervention will receive one of the adapted therapies according to therapist allocation for up to 6 months via 12 weekly, one to one, 45-50 minute sessions. The primary outcome is quality of life measured by the Clinical Outcomes in Routine Evaluation Outcome Measure at 12 months post-randomisation. Secondary outcomes include suicidal intent, depression, and cost-effectiveness. Data are collected using hospital attendance records and online/postal/telephone questionnaires at 6 and 12 months post-randomisation, with resource use additionally collected at 3 and 9 months). Discussion This protocol outlines a randomised controlled trial to investigate whether modified therapies are cost-effective and improve quality of life for people who repeatedly self-harm. Few interventions are proven to be deliverable in the NHS for this population. This study is strengthened by the involvement of qualified mental health workers experienced in managing risk as therapists.

ORCID iDs

Farley, K., Copsey, B., Wright-Hughes, A., Farrin, A., Bojke, C., McMillan, D., Graham, C. D. ORCID logoORCID: https://orcid.org/0000-0001-8456-9154, Mattock, R., Brennan, CA., Gates, C., Martin, A., Dowse, A., Horrocks, J., House, AO. and Guthrie, EA.;
CORE (COnnecting REpositories)