Evidence map›Paper›PMID 40948050›Full record

ArticleWorld psychiatry : official journal of the World Psychiatric Association (WPA)2025

A pragmatic randomized controlled trial of cognitive therapy for post-traumatic stress disorder in children and adolescents exposed to multiple traumatic stressors: the DECRYPT trial.

Richard Meiser-Stedman, Leila Allen, Polly-Anna Ashford, Ella Beeson, Sarah Byford, Andrea Danese, Annie Farr, Jack Finn, Ben Goodall, Lauren Grainger and 20 more

Abstract read
In one paragraph

Article in World psychiatry : official journal of the World Psychiatric Association (WPA), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

30 authors.

Richard Meiser-StedmanDepartment of Clinical Psychology and Psychological Therapies, Norwich Medical School, University of East Anglia, Norwich, UK.
Leila AllenDepartment of Clinical Psychology and Psychological Therapies, Norwich Medical School, University of East Anglia, Norwich, UK.
Polly-Anna AshfordNorwich Clinical Trials Unit, Norwich Medical School, University of East Anglia, Norwich, UK.
Ella BeesonHertfordshire Partnership University NHS Foundation Trust, Hatfield, UK.
Sarah ByfordKing's Health Economics, King's College London, London, UK.
Andrea DaneseDepartment of Child and Adolescent Psychiatry, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Annie FarrPublic and Patient Involvement representative.
Jack FinnDepartment of Clinical Psychology and Psychological Therapies, Norwich Medical School, University of East Anglia, Norwich, UK.
Ben GoodallNorth East London NHS Foundation Trust, Rainham, UK.
Lauren GraingerDepartment of Clinical Psychology and Psychological Therapies, Norwich Medical School, University of East Anglia, Norwich, UK.
Matthew HammondNorwich Clinical Trials Unit, Norwich Medical School, University of East Anglia, Norwich, UK.
Rebecca HarmstonPublic and Patient Involvement representative.
Ayla HumphreyCambridgeshire and Peterborough NHS Foundation Trust, Cambridge, UK.
Dorothy KingDepartment of Psychology, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Katie LofthouseDepartment of Clinical Psychology and Psychological Therapies, Norwich Medical School, University of East Anglia, Norwich, UK.
Gerwyn Mahoney-DaviesCardiff and Vale University Health Board, Cardiff, UK.
Sarah MilesNational and Specialist CAMHS Clinic for Trauma, Anxiety and Depression, South London and Maudsley NHS Foundation Trust, London, UK.
Jessica MooreDepartment of Clinical Psychology and Psychological Therapies, Norwich Medical School, University of East Anglia, Norwich, UK.
Nicola MorantDivision of Psychiatry, Faculty of Brain Sciences, University College London, London, UK.
Sarah RobertsonDepartment of Clinical Psychology and Psychological Therapies, Norwich Medical School, University of East Anglia, Norwich, UK.
Lee ShepstoneNorwich Clinical Trials Unit, Norwich Medical School, University of East Anglia, Norwich, UK.
Erika SimsNorwich Clinical Trials Unit, Norwich Medical School, University of East Anglia, Norwich, UK.
Paul StallardDepartment for Health, University of Bath, Bath, UK.
Annie SwanepoelNorth East London NHS Foundation Trust, Rainham, UK.
David TrickeyDepartment of Clinical, Educational and Health Psychology, University College London, London, UK.
Katie TriggDepartment of Clinical Psychology and Psychological Therapies, Norwich Medical School, University of East Anglia, Norwich, UK.
Ramesh VishwakarmaNorwich Clinical Trials Unit, Norwich Medical School, University of East Anglia, Norwich, UK.
Jon WilsonNorfolk and Suffolk NHS Foundation Trust, Norwich, UK.
Tim DalgleishMRC Cognition and Brain Sciences Unit, Cambridge, UK.
Patrick SmithNational and Specialist CAMHS Clinic for Trauma, Anxiety and Depression, South London and Maudsley NHS Foundation Trust, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Trauma-focused cognitive-behavioral therapies (TF-CBTs) are efficacious in children and adolescents with post-traumatic stress disorder (PTSD). However, there is limited evidence in youth exposed to multiple traumas, especially in real-world settings. This paper reports on a pragmatic randomized controlled trial (RCT) evaluating whether one form of TF-CBT, cognitive therapy for PTSD (CT-PTSD), was effective for PTSD following multiple trauma exposure in 8-17 year-olds attending UK mental health services, relative to treatment-as-usual (TAU). Youth with PTSD (N=120) following multiple traumas were randomly allocated to receive CT-PTSD or TAU. At baseline, complex PTSD diagnosis was common (55.0% of cases), and a large proportion of youth had comorbid mental disorders. The primary outcome was the score on the Child Revised Impact of Event Scale, 8-item version (CRIES-8) at post-treatment. Secondary outcomes included the CRIES-8 score at 11 months post-randomization, and several measures of PTSD, anxiety, depression, suicidal ideation, affect regulation, irritability, and general functioning at post-treatment and 11 months post-randomization. CT-PTSD was not found to be significantly superior to TAU on the CRIES-8 at post-treatment (adjusted difference: -3.80, 95% CI: -7.56 to -0.06, p=0.095; Hedges' g=-0.37, 95% CI: -0.78 to 0.03), but it was superior to TAU when patients who had received TF-CBT were excluded from that arm (adjusted difference: -4.60, 95% CI: -8.36 to -0.81, p=0.047; g=-0.46, 95% CI: -0.89 to -0.04). CT-PTSD was also superior to TAU on the CRIES-8 at 11 months (adjusted difference: -5.38, 95% CI: -8.88 to -1.87, p=0.003; g=-0.46, 95% CI: -0.90 to -0.02), and in a mixed-effect model incorporating all time points (p=0.007). Evidence of superiority for CT-PTSD was observed on parent-reported emotional difficulties at post-treatment and 11 months; and on child-reported total anxiety and depression, total anxiety, panic and separation anxiety, and parent-reported affect dysregulation and irritability at 11 months. Treatment withdrawal rate was low. Despite high baseline levels of comorbidity and impairment not seen in previous trials, CT-PTSD was not associated with significant deterioration or adverse events. This pragmatic trial is likely to contribute to the optimization of psychological intervention in youth with PTSD following multiple traumas, accompanied by severe comorbid mental disorders, in routine settings.

Indexed as

children and adolescentscognitive therapy for PTSD (CT‐PTSD)multiple traumasPost‐traumatic stress disorder (PTSD)pragmatic trialtrauma‐focused cognitive‐behavioral therapies

Identifiers

PMID40948050
PMCPMC12434375

What OpenQuestion holds

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Registered trials

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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.