Pyle, Melissa; Corrigan, Patrick; Wood, Lisa; Pilling, Stephen; Murphy, Elizabeth; Macafee, Gillian; Kelly, Kate; ... Morrison, Anthony P; + view all Pyle, Melissa; Corrigan, Patrick; Wood, Lisa; Pilling, Stephen; Murphy, Elizabeth; Macafee, Gillian; Kelly, Kate; Byrne, Rory; Dunbar, Eleanor; Hudson, Jemma; Jones, Wendy; Hazzard, Raj; Larson, Jon E; MacLennan, Graeme; Swingler, James; Peters, Sarah; Morrison, Anthony P; - view fewer (2024) A feasibility randomised controlled trial of an individually delivered, peer support intervention to reduce the impact of psychosis stigma and discrimination for people with psychosis: The Let’s Talk Study. Psychological Medicine (In press).

Text Wood_Let's Talk Main Trial Paper 04 09 2024 clean.pdf Access restricted to UCL open access staff until 16 April 2025. Download (343kB)

Abstract

Background: Stigma of mental health conditions hinders recovery and well-being. The Honest, Open, Proud (HOP) programme shows promise in reducing stigma but there is uncertainty about the feasibility of a randomised trial to evaluate a peer-delivered, individual adaptation of HOP for psychosis (Let’s Talk).// Methods: A multi-site, Prospective Randomised Open Blinded Evaluation (PROBE) design, feasibility randomised controlled trial (RCT) comparing the peer-delivered intervention (Let’s Talk) to treatment as usual (TAU). Follow-up was 2.5 and 6 months. Randomisation was via a web-based system, with permuted blocks of random size. Up to 10 sessions of the intervention over 10 weeks were offered. The primary outcome was feasibility data (recruitment, retention, intervention attendance). Primary outcomes were analysed by intention to treat. Safety outcomes were reported by as treated status. The study was prospectively registered: https://doi.org/10.1186/ISRCTN17197043.// Results: 149 patients were referred to the study and 70 were recruited. 35 were randomly assigned to intervention+ TAU and 35 to TAU. Recruitment was 93% of the target sample size. Retention rate was high (81% at 2.5 months primary endpoint), and intervention attendance rate was high (83%). 21% of 33 patients in Let’s talk + TAU had an adverse event and 16% of 37 patients in TAU. One serious adverse event (pre-randomisation) was partially related and expected.// Conclusions: This is the first trial to show that it is feasible and safe to conduct a RCT of HOP adapted for people with psychosis and individual delivery. An adequately powered trial is required to provide robust evidence.

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