Completed Mental Health Psychology & Behaviour

Randomised controlled trial of the clinical and cost-effectiveness of a contingency management intervention for reduction of cannabis use and of relapse in early psychosis

In plain English

AI plain-English summary

Young people with early psychosis who use cannabis will be offered vouchers or small cash rewards if they can stay drug-free, in a trial testing whether this approach delays relapse. Cannabis use is common among people experiencing a first episode of psychosis, and it sharply increases the risk of relapse, hospital readmission, and long-term disability. Standard treatments—talking therapies and medication—often fail to keep these patients away from the drug. Contingency management, which provides tangible incentives for verified abstinence, has worked for other addictions but has not been rigorously tested in this group. If the trial shows that the incentive scheme extends the time between relapses, it would give mental health services a practical, low-cost tool to improve outcomes for a notoriously hard-to-treat population. The researchers will also calculate whether the intervention saves the NHS money by reducing hospital stays and crisis care. If cost-effective, the approach could be rolled out across early intervention services in the UK, changing how clinicians address cannabis use in young people with psychosis.

View original technical description
Our aim is to establish whether an intervention based on contingency management for cannabis use in early psychosis is effective in increasing time to relapse in young people with early psychosis and problematic cannabis use. We will begin by conducting a feasibility pilot study, testing the feasibility and acceptability of the intervention and whether satisfactory numbers can be recruited. We will aim to recruit 68 participants from 3 early intervention services over a 6 month period. If the targets of the pilot study are met, we will recruit further participants in 12 services to complete a full randomised controlled trial. Participants will be randomly allocated to either the experimental condition, involving contingency management combined with a psychoeducational package, or the control condition, involving psychoeducation only. Outcomes will be assessed 3 months after the beginning of the intervention and 18 months afterwards. We will also assess costs associated with being in each arm of the trial.

Related Research

Grants with similar aims, by meaning.

PRODIGY: Prevention and treatment of long term social disability amongst young people with emerging severe mental illness: A randomised controlled trial
Comparative effectiveness, safety and acceptability of pharmacological and psychosocial interventions for the treatment of cannabis use disorders
COMPEERS: A cluster randomised feasibility study of COntingency Management and PEER Support to promote attendance, increase treatment engagement, and improve outcomes for people with dual diagnoses of psychosis and drug/alcohol problems (DDp).
Helping people cope with temptations to smoke to reduce relapse: A factorial randomised controlled trial
Low intensity intervention to promote recovery in psychosis: a pilot randomised controlled trial

Original classification

Research

Plain English summaries and category classifications on this site are generated by AI and may not perfectly reflect the original research.