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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01892033
Other study ID # 10N17
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 2011
Est. completion date September 2013

Study information

Verified date April 2019
Source North Texas Veterans Healthcare System
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The overall aim of this pilot feasibility study is to determine if 12-week moderate intensity exercise can safely alleviate posttraumatic symptoms in premenopausal women veterans.

Specific aims of the study are to;

1. Determine the feasibility, safety, and tolerability of 12-week moderate intensity exercise

2. Explore potential therapeutic benefits of 12-week moderate intensity exercise. Outcome data will include posttraumatic and depressive symptoms.

3. Explore potential therapeutic effects of a 12-week moderate intensity exercise on comorbid pain syndrome and quality of life.


Recruitment information / eligibility

Status Completed
Enrollment 31
Est. completion date September 2013
Est. primary completion date September 2013
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

1. Women veterans ages 18 and older

2. Premenopausal women of childbearing potential with a negative pregnancy test

3. DSM IV-TR confirmed PTSD related to any traumatic event as measured by Clinician Administered PTSD Scale (CAPS) with a CAPS score of at least 45

4. Relatively low sedentary life style

5. Existing psychotropic medications are allowed if on a stable dose

6. Evidence-based psychotherapy (e.g. Cognitive Processing Therapy or Prolonged Exposure) is not allowed to start of the study. However supportive or educational groups that are not PTSD-focused are allowed.

Exclusion Criteria:

1. Other psychiatric diagnoses including bipolar disorder, schizophrenia, schizoaffective disorder, active substance dependence/abuse (use in the past 1 month), obsessive-compulsive disorder, and eating disorders.Comorbid major depressive disorder, dysthymia and generalized anxiety disorders are not excluded.

2. Serious psychopathology

3. Actively suicidal or homicidal

4. Psychiatric hospitalization within the past 30 days

5. Active medical conditions that preclude the use of aerobic exercise such as uncontrolled hypertension, active musculoskeletal degenerative conditions, and symptomatic cardiovascular or respiratory conditions.

Study Design


Intervention

Behavioral:
Aerobic Exercise
12 weeks of brisk walking

Locations

Country Name City State
United States Dallas VA Medical Center Dallas Texas

Sponsors (1)

Lead Sponsor Collaborator
North Texas Veterans Healthcare System

Country where clinical trial is conducted

United States, 

References & Publications (1)

Shivakumar G, Anderson EH, Surís AM, North CS. Exercise for PTSD in Women Veterans: A Proof-of-Concept Study. Mil Med. 2017 Nov;182(11):e1809-e1814. doi: 10.7205/MILMED-D-16-00440. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Clinician Administered Posttraumatic Stress Disorder Scale (CAPS) Changes from baseline to week 12.
Secondary PTSD Checklist Changes from baseline to week 12.
Secondary Inventory of Depressive Symptomatology (Self-Report) (IDS-SR) Changes from baseline to week 12.
Secondary Pain Scale Changes from baseline to week 12.
Secondary Quality of Life Enjoyment and Satisfaction Questionnaire (Q-LES-Q) Changes from baseline to week 12.
Secondary Safety (Monitoring for common side effects associated with aerobic exercise and adverse events). 12 Weeks
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