Prolonged Exposure and Sertraline Treatments for Posttraumatic Stress Disorder Also Improve Multiple Indicators of Social Functioning.


Journal

Journal of traumatic stress
ISSN: 1573-6598
Titre abrégé: J Trauma Stress
Pays: United States
ID NLM: 8809259

Informations de publication

Date de publication:
08 2020
Historique:
received: 25 11 2019
revised: 23 03 2020
accepted: 29 04 2020
pubmed: 15 7 2020
medline: 1 9 2021
entrez: 15 7 2020
Statut: ppublish

Résumé

Trauma survivors with posttraumatic stress disorder (PTSD) frequently also suffer from difficulties in social functioning that range across emotional, cognitive, and environmental domains. A detailed evaluation of the differential impacts of effective PTSD treatments on social functioning is needed. Men and women (N = 200) with chronic PTSD received 10 weeks of prolonged exposure (PE) or sertraline in a randomized clinical trial and were followed for 24 months. A secondary data analysis examined changes in social functioning with regard to fear of intimacy; receipt of social support; and distress, avoidance, and negative cognitions in social situations. Effects were examined between treatments over time, controlling for baseline functioning. There were large, durable improvements across all indices. Compared to sertraline, PE was more efficient at reducing fear of intimacy and distress from negative social cognitions by posttreatment, ds = 0.94-1.14. Patients who received sertraline continued to improve over the course of follow-up, ds = 0.54-1.17. The differential speed of therapeutic effects may argue for more direct mechanisms in cognitive behavioral interventions versus cascade effects in serotonin reuptake inhibitors. Notably, both treatments produced substantial social benefits for trauma survivors with social functioning difficulties, and effect sizes were comparable to typical reductions in PTSD, depression, and anxiety.

Identifiants

pubmed: 32662191
doi: 10.1002/jts.22570
pmc: PMC7719061
mid: NIHMS1620520
doi:

Substances chimiques

Serotonin Uptake Inhibitors 0
Sertraline QUC7NX6WMB

Banques de données

ClinicalTrials.gov
['NCT00127673']

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

488-499

Subventions

Organisme : NCRR NIH HHS
ID : UL1 RR024989
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002548
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH066348
Pays : United States
Organisme : Wellcome Trust
ID : 205156
Pays : United Kingdom
Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : NIMH NIH HHS
ID : R01 MH066347
Pays : United States

Informations de copyright

© 2020 The Authors. Journal of Traumatic Stress published by Wiley Periodicals, Inc. on behalf of International Society for Traumatic Stress Studies.

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Auteurs

Belinda Graham (B)

Department of Psychology, University of Washington, Seattle, Washington, USA.

Natalia M Garcia (NM)

Department of Psychology, University of Washington, Seattle, Washington, USA.

Hannah E Bergman (HE)

Department of Psychological Sciences, Case Western Reserve University, Cleveland, Ohio, USA.

Norah C Feeny (NC)

Department of Psychological Sciences, Case Western Reserve University, Cleveland, Ohio, USA.

Lori A Zoellner (LA)

Department of Psychology, University of Washington, Seattle, Washington, USA.

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