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Trauma Management Therapy and Prolonged Exposure Therapy for PTSD in an active duty sample: Design and methodology of a randomized clinical trial

Posttraumatic stress disorder (PTSD) resulting from military service is a common, yet often chronic condition. Treatment outcome often is attenuated by programs that are (a) lengthy in nature and (b) constricted in their target outcomes. These limitations leave much of the emotional and behavioral i...

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Autores principales: Beidel, Deborah C., Neer, Sandra M., Bowers, Clint A., Newins, Amie R., Tuerk, Peter W., Cunningham, Craig A., Mooney, Scott R., Hauck, Heather N., Jett, Marti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881668/
https://www.ncbi.nlm.nih.gov/pubmed/31799476
http://dx.doi.org/10.1016/j.conctc.2019.100491
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author Beidel, Deborah C.
Neer, Sandra M.
Bowers, Clint A.
Newins, Amie R.
Tuerk, Peter W.
Cunningham, Craig A.
Mooney, Scott R.
Hauck, Heather N.
Jett, Marti
author_facet Beidel, Deborah C.
Neer, Sandra M.
Bowers, Clint A.
Newins, Amie R.
Tuerk, Peter W.
Cunningham, Craig A.
Mooney, Scott R.
Hauck, Heather N.
Jett, Marti
author_sort Beidel, Deborah C.
collection PubMed
description Posttraumatic stress disorder (PTSD) resulting from military service is a common, yet often chronic condition. Treatment outcome often is attenuated by programs that are (a) lengthy in nature and (b) constricted in their target outcomes. These limitations leave much of the emotional and behavioral impairment that accompanies PTSD unaddressed and/or unassessed. Typical PTSD treatment programs are 3–4 months in length, which is challenging for the pace of the nation's military. In this investigation, we will compare two treatments, Trauma Management Therapy (TMT) and Prolonged Exposure (PE), both redesigned to address the needs of active duty personnel (300 participants at 3 military installations). Specifically, we will compare the TMT Intensive Outpatient Program (IOP; 3 weeks) to PE's compressed (2 week) format. Both interventions will be compared to a standard course of PE (12 weeks). In addition to PTSD symptomatology, outcome measurement includes other aspects of psychopathology as well as changes in social, occupational, and familial impairment. Potential negative outcomes of massed treatment, such as increased suicidal ideation or increased alcohol use, will be assessed, as will genetic predictors of PTSD subtype and treatment outcome. This study will inform the delivery of care for military-related PTSD and particularly the use of intensive or compressed treatments for active duty personnel.
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spelling pubmed-68816682019-12-03 Trauma Management Therapy and Prolonged Exposure Therapy for PTSD in an active duty sample: Design and methodology of a randomized clinical trial Beidel, Deborah C. Neer, Sandra M. Bowers, Clint A. Newins, Amie R. Tuerk, Peter W. Cunningham, Craig A. Mooney, Scott R. Hauck, Heather N. Jett, Marti Contemp Clin Trials Commun Article Posttraumatic stress disorder (PTSD) resulting from military service is a common, yet often chronic condition. Treatment outcome often is attenuated by programs that are (a) lengthy in nature and (b) constricted in their target outcomes. These limitations leave much of the emotional and behavioral impairment that accompanies PTSD unaddressed and/or unassessed. Typical PTSD treatment programs are 3–4 months in length, which is challenging for the pace of the nation's military. In this investigation, we will compare two treatments, Trauma Management Therapy (TMT) and Prolonged Exposure (PE), both redesigned to address the needs of active duty personnel (300 participants at 3 military installations). Specifically, we will compare the TMT Intensive Outpatient Program (IOP; 3 weeks) to PE's compressed (2 week) format. Both interventions will be compared to a standard course of PE (12 weeks). In addition to PTSD symptomatology, outcome measurement includes other aspects of psychopathology as well as changes in social, occupational, and familial impairment. Potential negative outcomes of massed treatment, such as increased suicidal ideation or increased alcohol use, will be assessed, as will genetic predictors of PTSD subtype and treatment outcome. This study will inform the delivery of care for military-related PTSD and particularly the use of intensive or compressed treatments for active duty personnel. Elsevier 2019-11-15 /pmc/articles/PMC6881668/ /pubmed/31799476 http://dx.doi.org/10.1016/j.conctc.2019.100491 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Beidel, Deborah C.
Neer, Sandra M.
Bowers, Clint A.
Newins, Amie R.
Tuerk, Peter W.
Cunningham, Craig A.
Mooney, Scott R.
Hauck, Heather N.
Jett, Marti
Trauma Management Therapy and Prolonged Exposure Therapy for PTSD in an active duty sample: Design and methodology of a randomized clinical trial
title Trauma Management Therapy and Prolonged Exposure Therapy for PTSD in an active duty sample: Design and methodology of a randomized clinical trial
title_full Trauma Management Therapy and Prolonged Exposure Therapy for PTSD in an active duty sample: Design and methodology of a randomized clinical trial
title_fullStr Trauma Management Therapy and Prolonged Exposure Therapy for PTSD in an active duty sample: Design and methodology of a randomized clinical trial
title_full_unstemmed Trauma Management Therapy and Prolonged Exposure Therapy for PTSD in an active duty sample: Design and methodology of a randomized clinical trial
title_short Trauma Management Therapy and Prolonged Exposure Therapy for PTSD in an active duty sample: Design and methodology of a randomized clinical trial
title_sort trauma management therapy and prolonged exposure therapy for ptsd in an active duty sample: design and methodology of a randomized clinical trial
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881668/
https://www.ncbi.nlm.nih.gov/pubmed/31799476
http://dx.doi.org/10.1016/j.conctc.2019.100491
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