Evidence map›Paper›PMID 22491790›Full record

Trial reportBMJ (Clinical research ed.)2012

Early detection and intervention evaluation for people at risk of psychosis: multisite randomised controlled trial.

Anthony P Morrison, Paul French, Suzanne L K Stewart, Max Birchwood, David Fowler, Andrew I Gumley, Peter B Jones, Richard P Bentall, Shôn W Lewis, Graham K Murray and 8 more

Open access · hybridAbstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in BMJ (Clinical research ed.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 116 papers, 12 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed, 12 pooled it
22.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

116 citing papers in PubMed, 12 syntheses or guidelines pooled it, 329 citations in OpenAlex.

  1. Quality of life in individuals at clinical high risk for psychosis: A systematic review and meta-analysis.European psychiatry : the journal of the Association of European Psychiatrists · 2026
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  6. Interventions for prodromal stage of psychosis.The Cochrane database of systematic reviews · 2019
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56 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 10 institutions in 1 country.

Anthony P MorrisonSchool of Psychological Sciences, University of Manchester, Manchester M13 9PL, UK. tony.morrison@manchester.ac.uk
Paul French
Suzanne L K Stewart
Max Birchwood
David Fowler
Andrew I Gumley
Peter B Jones
Richard P Bentall
Shôn W Lewis
Graham K Murray
Paul Patterson
Kat Brunet
Jennie Conroy
Sophie Parker
Tony Reilly
Rory Byrne
Linda M Davies
Graham Dunn
Greater Manchester Mental Health NHS Foundation Trust · GBUniversity of Manchester · GBUniversity of Birmingham · GBUniversity of Cambridge · GBBirmingham and Solihull Mental Health NHS Foundation Trust · GBCambridgeshire and Peterborough NHS Foundation Trust · GBNorfolk and Suffolk NHS Foundation Trust · GBUniversity of East Anglia · GBUniversity of Glasgow · GBUniversity of Liverpool · GB

Funding

Department of HealthMedical Research Council G0500264Medical Research Council G0701911
6 · The paper itself

Abstract

objectiveTo determine whether cognitive therapy is effective in preventing the worsening of emerging psychotic symptoms experienced by help seeking young people deemed to be at risk for serious conditions such as schizophrenia.

designMultisite single blind randomised controlled trial.

settingDiverse services at five UK sites.

participants288 participants aged 14-35 years (mean 20.74, SD 4.34 years) at high risk of psychosis: 144 were assigned to cognitive therapy plus monitoring of mental state and 144 to monitoring of mental state only. Participants were followed-up for a minimum of 12 months and a maximum of 24 months.

interventionCognitive therapy (up to 26 (mean 9.1) sessions over six months) plus monitoring of mental state compared with monitoring of mental state only.

main outcome measuresPrimary outcome was scores on the comprehensive assessment of at risk mental states (CAARMS), which provides a dichotomous transition to psychosis score and ordinal scores for severity of psychotic symptoms and distress. Secondary outcomes included emotional dysfunction and quality of life.

resultsTransition to psychosis based on intention to treat was analysed using discrete time survival models. Overall, the prevalence of transition was lower than expected (23/288; 8%), with no significant difference between the two groups (proportional odds ratio 0.73, 95% confidence interval 0.32 to 1.68). Changes in severity of symptoms and distress, as well as secondary outcomes, were analysed using random effects regression (analysis of covariance) adjusted for site and baseline symptoms. Distress from psychotic symptoms did not differ (estimated difference at 12 months -3.00, 95% confidence interval -6.95 to 0.94) but their severity was significantly reduced in the group assigned to cognitive therapy (estimated between group effect size at 12 months -3.67, -6.71 to -0.64, P=0.018).

conclusionsCognitive therapy plus monitoring did not significantly reduce transition to psychosis or symptom related distress but reduced the severity of psychotic symptoms in young people at high risk. Most participants in both groups improved over time. The results have important implications for the at risk mental state concept.

trial registrationCurrent Controlled Trials ISRCTN56283883.

Indexed as

Cognitive Behavioral TherapyAdolescentAdultEarly DiagnosisHumansMental DisordersPsychotic DisordersSingle-Blind MethodTreatment OutcomeYoung Adult

Identifiers

PMID22491790
PMCPMC3320714
OpenAlexW2095692398

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.