Evidence map›Paper›PMID 39642783›Full record

Trial reportDrug and alcohol dependence2025

A novel prolonged exposure therapy protocol for improving therapy session attendance and PTSD symptoms among adults receiving buprenorphine or methadone treatment.

Kelly R Peck, Jillian Giannini, Gary J Badger, Rebecca Cole, Stacey C Sigmon

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Drug and alcohol dependence, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04104022 (Treating Posttraumatic Stress Disorder in Patients With Opioid Use Disorder), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

NCT04104022 nacompletednot on this map

Treating Posttraumatic Stress Disorder in Patients With Opioid Use Disorder

TypeinterventionalSponsorUniversity of VermontRan2019 to 2023Enrolled82ConditionsPost Traumatic Stress Disorder, Opioid-use DisorderArmsProlonged Exposure Therapy, Attendance-based monetary incentives
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Trial
  2. Article
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

5 authors.

Kelly R PeckDepartment of Psychiatry, University of Vermont, Burlington, VT 05401, United States; Department of Psychology, University of Vermont, United States. Electronic address: Kelly.Peck@uvm.edu.
Jillian GianniniDepartment of Psychiatry, University of Vermont, Burlington, VT 05401, United States; Department of Psychology, University of Vermont, United States.
Gary J BadgerDepartment of Medical Biostatistics, University of Vermont, Burlington, VT 05405, United States.
Rebecca ColeDepartment of Psychiatry, University of Vermont, Burlington, VT 05401, United States.
Stacey C SigmonDepartment of Psychiatry, University of Vermont, Burlington, VT 05401, United States; Department of Psychology, University of Vermont, United States.

Funding

Vermont Center on Behavior and HealthP20GM103644 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI HIGGINS, STEPHEN T · 2013 to 2022
$21.3M
TRAINING IN BEHAV. PHARMACOLOGY OF HUMAN DRUG DEPENDENCET32DA007242 · NIDA · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI HEIL, SARAH H, HIGGINS, STEPHEN T · 1990 to 2025
$8.2M
Novel Telemedicine-Delivered Prolonged Exposure Therapy for Treating PTSD in Individuals with OUDR01DA057308 · NIDA · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI Kelly R. Peck · 2023 to 2026
$2.8M
NIDA NIH HHS R01 DA057308NIDA NIH HHS T32 DA007242NIGMS NIH HHS P20 GM103644
6 · The paper itself

Abstract

backgroundAmong individuals with opioid use disorder (OUD), the prevalence of posttraumatic stress disorder (PTSD) is higher than in the general population. Prolonged exposure (PE) therapy is highly efficacious for improving PTSD symptoms. However, few studies have evaluated PE in individuals receiving medications for OUD (MOUD) and treatment completion rates have been low. This randomized trial evaluated the efficacy of a novel protocol for improving PE attendance and PTSD symptoms among adults receiving buprenorphine or methadone treatment.

methodsEligible participants (n=52) were randomized to one of three 12-week experimental conditions: (a) continued MOUD treatment as usual (TAU; n=17), (b) Prolonged Exposure Therapy (PE; n=17), or (c) PE with financial incentives contingent upon PE session attendance (PE+; n=18). Primary outcomes included percent of PE sessions attended and Clinician Administered PTSD Scale for DSM-5 (CAPS-5).

resultsPE+ participants attended significantly more therapy sessions than PE participants (88 % vs 33 %; p<.001). All three groups reported significant (p<.05) improvements in CAPS-5 scores between intake and week 12, with no significant group differences. However, PE+ participants achieved significantly greater improvements in self-reported PTSD symptoms (p=.02) than TAU participants, as well as higher rates of diagnostic remission compared to TAU and PE participants (p<.001). Participants in the two PE groups did not exhibit an increase in non-prescribed drug use.

conclusionsIn this study of adults receiving MOUD treatment, PE+ was efficacious for increasing PE attendance. Our findings also provide promising support for the efficacy of PE+ for improving PTSD symptoms without exacerbating substance use. CLINICAL TRIAL NUMBER: NCT04104022.

Indexed as

BuprenorphineImplosive TherapyMethadoneOpiate Substitution TreatmentOpioid-Related DisordersStress Disorders, Post-TraumaticAdultFemaleHumansMaleMiddle AgedPatient ComplianceTreatment OutcomeBuprenorphineMethadoneFinancial incentivesMedications for opioid use disorderOpioid use disorderPosttraumatic stress disorderProlonged exposure therapy

Identifiers

PMID39642783
PMCPMC11685033

What OpenQuestion holds

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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.