Evidence map›Paper›PMID 34773928›Full record

Trial reportJournal of traumatic stress2022

Temporal dynamics of symptom change among veterans receiving an integrated treatment for posttraumatic stress disorder and substance use disorders.

Christal L Badour, Julianne C Flanagan, Nicholas P Allan, Amanda K Gilmore, Daniel F Gros, Therese Killeen, Kristina J Korte, Delisa G Brown, Kateryna Kolnogorova, Sudie E Back

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of traumatic stress, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Trial
  2. Trial
  3. 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

10 authors at 5 institutions in 1 country.

Christal L BadourDepartment of Psychology, University of Kentucky, Lexington, Kentucky, USA.ORCID 0000-0001-9985-8418
Julianne C FlanaganDepartment of Psychiatry & Behavioral Sciences, Medical University of South Carolina, Charleston, South Carolina, USA.
Nicholas P AllanDepartment of Psychology, Ohio University, Athens, Ohio, USA.
Amanda K GilmoreDepartment of Health Policy & Behavioral Sciences, School of Public Health, Georgia State University, Atlanta, Georgia, USA.
Daniel F GrosDepartment of Psychiatry & Behavioral Sciences, Medical University of South Carolina, Charleston, South Carolina, USA.
Therese KilleenDepartment of Psychiatry & Behavioral Sciences, Medical University of South Carolina, Charleston, South Carolina, USA.
Kristina J KortePsychiatry Department, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Delisa G BrownDepartment of Psychiatry & Behavioral Sciences, Medical University of South Carolina, Charleston, South Carolina, USA.
Kateryna KolnogorovaDepartment of Psychology, Ohio University, Athens, Ohio, USA.
Sudie E BackDepartment of Psychiatry & Behavioral Sciences, Medical University of South Carolina, Charleston, South Carolina, USA.ORCID 0000-0002-7683-8737
Medical University of South Carolina · USOhio University · USGeorgia State University · USHarvard University · USUniversity of Kentucky · US

Funding

The Impact of Stress and Craving on Return to Postpartum Cannabis UseU54DA016511 · NIDA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI CONSTANCE GUILLE · 2018 to 2026
$15.9M
Vocational Training for Drug Dependent WomenP50DA016511 · NIDA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T. · 2002 to 2017
$14.5M
Supplement for Kentucky BIRCWH Program: Training the Next Generation of Women's Health Scholars: Dr. ConnerK12DA035150 · NIDA · UNIVERSITY OF KENTUCKY · PI Thomas E Curry · 2012 to 2026
$9.0M
Drug Abuse Research Training (DART) ProgramR25DA020537 · NIDA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI KATHLEEN T. BRADY, Sudie E Back · 2006 to 2026
$6.3M
Randomized Controlled Trial of N-acetylcysteine for Alcohol Use Disorder and Comorbid PTSDR01AA025086 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BACK, SUDIE E, GRAY, KEVIN M · 2016 to 2020
$3.1M
Integrated Treatment of OEF/OIF Veterans with PTSD and Substance Use DisordersR01DA030143 · NIDA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BACK, SUDIE E · 2010 to 2014
$1.6M
Technology-Based Prevention for Adolescent Substance Use, Sexual Assault, and Sexual Risk in Primary CareK23DA042935 · NIDA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI GILMORE, AMANDA KATHERINE · 2017 to 2021
$1.1M
Effects of Oxytocin on Alcohol Craving and Intimate Partner AggressionK23AA023845 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI FLANAGAN, JULIANNE CHRISTINA · 2016 to 2019
$774k
Reducing Cardiovascular Risk in Perimenopausal Latinas: Pilot Study of a Multi-Component InterventionK23MD014767 · NIMHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CORTES, YAMNIA I · 2019 to 2022
$531k
Transdiagnostic Psychotherapy for Veterans with Mood and Anxiety DisordersIK2CX000845 · VA · RALPH H JOHNSON VA MEDICAL CENTER · PI GROS, DANIEL F. · 2014 to 2018
–
CSRD VA IK2 CX000845NIAAA NIH HHS K23 AA023845NIAAA NIH HHS R01 AA025086NIDA NIH HHS K12 DA035150NIDA NIH HHS K23 DA042935NIDA NIH HHS P50 DA016511NIDA NIH HHS R01 DA030143NIDA NIH HHS R25 DA020537NIDA NIH HHS U54 DA016511
6 · The paper itself

Abstract

The present study examined temporal patterns of symptom change during treatment for comorbid posttraumatic stress disorders (PTSD) and substance use disorders (SUDs). We hypothesized that PTSD symptom severity would predict subsequent-session substance use and that this association would be particularly strong among patients who received an integrated treatment versus SUD-only treatment. Participants were 81 United States military veterans with current PTSD and an SUD who were enrolled in a 12-week, randomized controlled trial examining the efficacy of an integrated treatment called Concurrent Treatment of PTSD and Substance Use Disorders Using Prolonged Exposure (COPE) compared with cognitive behavioral relapse prevention therapy (RP). Lagged multilevel models indicated that PTSD symptom improvement did not significantly predict the likelihood of next-session substance use (likelihood of use: B = 0.03, SE = 0.02, p = .141; percentage of days using B = -0.02, SE = 0.01, p = .172. Neither substance use, B = 1.53, SE = 1.79, p = .391, nor frequency of use, B = 0.26, SE = 0.50, p = .612, predicted next-session PTSD symptom severity in either treatment condition. Stronger associations between PTSD symptoms and next-session substance use were expected given the self-medication hypothesis. Additional research is needed to better understand the temporal dynamics of symptom change as well as the specific mediators and mechanisms underlying symptom change.

Indexed as

Implosive TherapyStress Disorders, Post-TraumaticSubstance-Related DisordersVeteransComorbidityHumansTreatment OutcomeUnited States

Identifiers

PMID34773928
PMCPMC9035042
OpenAlexW3213341099

What OpenQuestion holds

Textmetadata
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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.