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Maximizing Treatment Outcome in Post-Traumatic Stress Disorder (PTSD)

Primary Purpose

Post-Traumatic Stress Disorder

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Prolonged Exposure
Exercise
Sponsored by
University of Texas at Austin
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Post-Traumatic Stress Disorder focused on measuring PTSD, Anxiety, Behavior Therapy, Prolonged Exposure, Exercise, Wellness, Post-traumatic, Stress

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • You have PTSD.
  • You are between the ages of 18 and 65.
  • You have written physician approval/medical clearance to participate in an exercise protocol.
  • You are currently taking no psychotropic medications or are able and willing to discontinue these medications prior to the first PE session.

Exclusion Criteria:

  • You are currently participating in a structured exercise program.
  • You have severe depression.
  • You have any history of bipolar disorder, psychotic disorder, or obsessive compulsive disorder.
  • You have a diagnosis of eating disorder, or substance abuse or dependence (excluding nicotine) within the past six months.
  • You have any history of a suicide attempt, or are at a significant risk or self-harm or harm to others.
  • You have ever been diagnosed with organic brain syndrome, mental retardation, or other cognitive dysfunction.

Sites / Locations

  • The University of Texas at Austin
  • Southern Methodist University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Prolonged Exposure + Exercise

Prolonged Exposure Alone

Arm Description

Outcomes

Primary Outcome Measures

PTSD Symptoms
Self-report measure that assesses PTSD symptoms. Will be assessed at each visit throughout the three month protocol.

Secondary Outcome Measures

BDNF (by blood sample)
Small blood sample taken twice (at the beginning and end of the 3 month protocol).
General Mood and Anxiety Symptoms
Self-report measures that assesses mood and anxiety. Will be assessed at each visit throughout the 3 month protocol.

Full Information

First Posted
November 22, 2013
Last Updated
December 28, 2015
Sponsor
University of Texas at Austin
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1. Study Identification

Unique Protocol Identification Number
NCT01998100
Brief Title
Maximizing Treatment Outcome in Post-Traumatic Stress Disorder (PTSD)
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Completed
Study Start Date
September 2010 (undefined)
Primary Completion Date
July 2013 (Actual)
Study Completion Date
July 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Texas at Austin

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to examine the efficacy of exercise + therapy to therapy alone to determine if they can improve the effects of prolonged exposure therapy (PE) in reducing symptoms of anxiety associated with Post-traumatic Stress Disorder (PTSD). In addition the two strategies (i.e., exercise + therapy and therapy alone condition) will be compared in terms of levels of brain-derived neurotrophic factor (BDNF). BDNF is a protein that helps to support the survival of existing neurons and stimulate the growth of new neurons and synapses. BDNF is important to learning and memory in general and therefore may be associated with the learning and memory as it relates to PE and corresponding symptoms PTSD improvement.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post-Traumatic Stress Disorder
Keywords
PTSD, Anxiety, Behavior Therapy, Prolonged Exposure, Exercise, Wellness, Post-traumatic, Stress

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
28 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Prolonged Exposure + Exercise
Arm Type
Experimental
Arm Title
Prolonged Exposure Alone
Arm Type
Active Comparator
Intervention Type
Behavioral
Intervention Name(s)
Prolonged Exposure
Intervention Description
75-90 minute weekly psychotherapy sessions x 12 weeks, focused on gradually confronting distressing trauma-related memories and reminders.
Intervention Type
Behavioral
Intervention Name(s)
Exercise
Intervention Description
30 minutes of moderate-intensity treadmill exercise prior to the Prolonged Exposure
Primary Outcome Measure Information:
Title
PTSD Symptoms
Description
Self-report measure that assesses PTSD symptoms. Will be assessed at each visit throughout the three month protocol.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
BDNF (by blood sample)
Description
Small blood sample taken twice (at the beginning and end of the 3 month protocol).
Time Frame
3 months
Title
General Mood and Anxiety Symptoms
Description
Self-report measures that assesses mood and anxiety. Will be assessed at each visit throughout the 3 month protocol.
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: You have PTSD. You are between the ages of 18 and 65. You have written physician approval/medical clearance to participate in an exercise protocol. You are currently taking no psychotropic medications or are able and willing to discontinue these medications prior to the first PE session. Exclusion Criteria: You are currently participating in a structured exercise program. You have severe depression. You have any history of bipolar disorder, psychotic disorder, or obsessive compulsive disorder. You have a diagnosis of eating disorder, or substance abuse or dependence (excluding nicotine) within the past six months. You have any history of a suicide attempt, or are at a significant risk or self-harm or harm to others. You have ever been diagnosed with organic brain syndrome, mental retardation, or other cognitive dysfunction.
Facility Information:
Facility Name
The University of Texas at Austin
City
Austin
State/Province
Texas
ZIP/Postal Code
78712
Country
United States
Facility Name
Southern Methodist University
City
Dallas
State/Province
Texas
ZIP/Postal Code
75206
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
25706090
Citation
Powers MB, Medina JL, Burns S, Kauffman BY, Monfils M, Asmundson GJ, Diamond A, McIntyre C, Smits JA. Exercise Augmentation of Exposure Therapy for PTSD: Rationale and Pilot Efficacy Data. Cogn Behav Ther. 2015;44(4):314-27. doi: 10.1080/16506073.2015.1012740. Epub 2015 Feb 23.
Results Reference
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Maximizing Treatment Outcome in Post-Traumatic Stress Disorder (PTSD)

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