Evidence map›Paper›PMID 29344631›Full record

Trial reportJAMA psychiatry2018

A Brief Exposure-Based Treatment vs Cognitive Processing Therapy for Posttraumatic Stress Disorder: A Randomized Noninferiority Clinical Trial.

Denise M Sloan, Brian P Marx, Daniel J Lee, Patricia A Resick

2 registry-linked trialsOpen access · bronzeAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in JAMA psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 104 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed, 5 pooled it
25.0field-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.

NCT01800773 nacompletednot on this map

Written Exposure Therapy for Post Traumatic Stress Disorder: A Randomized Noninferiority Trial

TypeinterventionalSponsorBoston UniversityRan2013 to 2018Enrolled192ConditionsPosttraumatic Stress DisorderArmsWritten Exposure Therapy, Cognitive Processing Therapy
NCT03605693 naterminatednot on this map

Written Exposure Therapy to Prevent PTSD in Survivors of Acute Cardiovascular Events: A Pilot Randomized Clinical Trial

TypeinterventionalSponsorColumbia UniversityRan2018 to 2019Enrolled10ConditionsAcute Coronary Syndrome, TIA, Stroke, Cardiac ArrestArmsWritten Exposure Therapy
3 · Its place in the literature

Who cites it

104 citing papers in PubMed, 5 syntheses or guidelines pooled it, 216 citations in OpenAlex.

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  3. A systematic review of written exposure therapy for the treatment of posttraumatic stress symptoms.Psychological trauma : theory, research, practice and policy · 2024
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  18. The effect of time since index trauma on trauma-related beliefs.Psychological trauma : theory, research, practice and policy · 2024
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44 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 1 country.

Denise M SloanNational Center for PTSD, Veterans Affairs Boston Health Care System, Boston, Massachusetts.
Brian P MarxNational Center for PTSD, Veterans Affairs Boston Health Care System, Boston, Massachusetts.
Daniel J LeeNational Center for PTSD, Veterans Affairs Boston Health Care System, Boston, Massachusetts.
Patricia A ResickDepartment of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, North Carolina.
Boston University · USDuke University Hospital · USNational Center for PTSD · US

Funding

Written Exposure Therapy for PTSD: A Randomized Noninferiority TrialR01MH095737 · NIMH · BOSTON UNIVERSITY MEDICAL CAMPUS · PI SLOAN, DENISE M. · 2012 to 2016
$1.4M
NIMH NIH HHS R01 MH095737
6 · The paper itself

Abstract

Importance: Written exposure therapy (WET), a 5-session intervention, has been shown to efficaciously treat posttraumatic stress disorder (PTSD). However, this treatment has not yet been directly compared with a first-line PTSD treatment such as cognitive processing therapy (CPT). Objective: To determine if WET is noninferior to CPT in patients with PTSD. Design, Setting, and Participants: In this randomized clinical trial conducted at a Veterans Affairs medical facility between February 28, 2013, and November 6, 2016, 126 veteran and nonveteran adults were randomized to either WET or CPT. Inclusion criteria were a primary diagnosis of PTSD and stable medication therapy. Exclusion criteria included current psychotherapy for PTSD, high risk of suicide, diagnosis of psychosis, and unstable bipolar illness. Analysis was performed on an intent-to-treat basis. Interventions: Participants assigned to CPT (n = 63) received 12 sessions and participants assigned to WET (n = 63) received 5 sessions. The CPT protocol that includes written accounts was delivered individually in 60-minute weekly sessions. The first WET session requires 60 minutes while the remaining 4 sessions require 40 minutes. Main Outcomes and Measures: The primary outcome was the total score on the Clinician-Administered PTSD Scale for DSM-5; noninferiority was defined by a score of 10 points. Blinded evaluations were conducted at baseline and 6, 12, 24, and 36 weeks after the first treatment session. Treatment dropout was also examined. Results: For the 126 participants (66 men and 60 women; mean [SD] age, 43.9 [14.6] years), improvements in PTSD symptoms in the WET condition were noninferior to improvements in the CPT condition at each of the assessment periods. The largest difference between treatments was observed at the 24-week assessment (mean difference, 4.31 points; 95% CI, -1.37 to 9.99). There were significantly fewer dropouts in the WET vs CPT condition (4 [6.4%] vs 25 [39.7%]; χ21 = 12.84, Cramer V = 0.40). Conclusions and Relevance: Although WET involves fewer sessions, it was noninferior to CPT in reducing symptoms of PTSD. The findings suggest that WET is an efficacious and efficient PTSD treatment that may reduce attrition and transcend previously observed barriers to PTSD treatment for both patients and providers. Trial Registration: clinicaltrials.gov Identifier: NCT01800773.

Indexed as

WritingAdultBostonCognitive Behavioral TherapyEquivalence Trials as TopicFemaleHumansImplosive TherapyMaleMiddle AgedPatient DropoutsPsychotherapy, BriefStress Disorders, Post-TraumaticTreatment OutcomeVeterans

Identifiers

PMID29344631
PMCPMC5843538
OpenAlexW2784527080

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.