Exercise and Behavioral Therapy Trial (EBT).
Primary Purpose
Persian Gulf Syndrome
Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Aerobic exercise
Cognitive behavioral therapy
Sponsored by
About this trial
This is an interventional treatment trial for Persian Gulf Syndrome focused on measuring aerobic exercise, cognitive behavioral therapy, CBT, Gulf War Illnesses, GWI
Eligibility Criteria
Gulf War era veterans deployed to the South West Asia theater of operations between August 1990 and August 1991 who have two of the following three symptoms that began after 1990 lasting more than 6 months and continuing to present - fatigue that limits usual activities (work, recreation or social), musculoskeletal pain involving more than one region of the body or neurocognitive dysfunction (self-reported difficulties in memory, concentration, or attention).
Sites / Locations
- Birmingham Vamc Birmingham Vamc
- Birmingham Vamc
- Naval Health Research Center, San Diego
- Naval Health Research Center, San Diego
- Naval Health Research Center, San Diego
- San Francisco Vamc
- VA CT Healthcare System, West Haven
- Georgetown University Medical Center
- Walter Reed Army Medical Center
- Uniformed Services University
- Boston Vamc
- Boston Medical Center
- Boston Vamc
- John Cochran VAMC, Saint Louis
- VA New Jersey Health Care System, East Orange
- Vamc - Albuquerque
- New York Harbor VA Healthcare System, Brooklyn Campus
- Fargo Vamc
- Vamc - Dayton
- Portland Vamc
- Philadelphia Vamc
- Houston Vamc
- Audie L. Murphy Memorial Veterans Hospital, San Antonio
- White River Junction Vamc
- White River Junction Vamc
- Richmond Vamc
- VA Puget Sound Healthcare System, Seattle Division
- VA Puget Sound Healthcare System, Seattle Division
- San Juan Vamc
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT00007748
First Posted
December 29, 2000
Last Updated
June 25, 2015
Sponsor
US Department of Veterans Affairs
Collaborators
United States Department of Defense
1. Study Identification
Unique Protocol Identification Number
NCT00007748
Brief Title
Exercise and Behavioral Therapy Trial (EBT).
Official Title
CSP#470 - A Randomized, Multi-Center, Controlled Trial of Multi-Modal Therapy in Veterans With Gulf War Illnesses
Study Type
Interventional
2. Study Status
Record Verification Date
June 2015
Overall Recruitment Status
Completed
Study Start Date
March 1999 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
August 2001 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
US Department of Veterans Affairs
Collaborators
United States Department of Defense
4. Oversight
5. Study Description
Brief Summary
This trial is a study of Gulf War era veterans who have unexplained chronic medical symptoms such as pain, fatigue, and/or cognitive difficulties. The treatments to be studied, cognitive behavior therapy (CBT) and aerobic exercise, have been shown to be effective in alleviating symptoms in individuals with other similar types of illnesses, such as chronic fatigue syndrome and fibromyalgia. This is a Phase 3, 2X2 factorial designed study. All study participants are assigned to one of four treatment groups - CBT and aerobic exercise, aerobic exercise alone, CBT alone or usual and customary care. This study durations is 28 months; 1092 participants were enrolled and will be followed in clinic at 3, 6 and 12 months after enrollment.
Detailed Description
Primary Hypothesis:
The primary hypothesis is that both aerobic exercise and cognitive behavioral therapy (CBT) will significantly improve physical function (as measured by the Physical Component Summary Scale of the SF-36V) in veterans with Gulf War Veterans' Illnesses (GWVI), and the combination of cognitive behavioral therapy and aerobic exercise will be more beneficial than either therapy alone.
Secondary Hypotheses:
Both aerobic exercise and CBT will lead to improvements in the cardinal symptoms of GWVI: pain, fatigue and cognitive difficulties.
Both aerobic exercise and CBT will lead to decreased levels of distress in persons with GWVI.
Both aerobic exercise and CBT will lead to improvements in emotional functioning in persons with GWVI.
Primary Outcomes: Improvement on the Physical Component Summary Scale of the SF-36V of more than 7 units at one year relative to baseline.
Interventions: Twelve one-hour weekly sessions of Cognitive behavioral therapy, aerobic exercise, the combination of the two therapies (12 one-hour sessions of CBT and 12 one-hour sessions of aerobic exercise) and a control group that receives usual and customary care.
Study Abstract: This trial was a study of Gulf War era veterans who have unexplained chronic medical symptoms such as pain, fatigue, and/or cognitive difficulties. All Gulf War veterans who were deployed to the South West Asia theater of operations between August 1990 and August 1991 were eligible for the study if they had at least two of the following three symptoms that began after August of 1990, lasting for more than six months and occurring up to present: 1. fatigue that limits usual activities (work, recreation, or social), 2. musculoskeletal pain involving two or more regions of the body, and neuro-cognitive dysfunction (self-reported difficulties in memory, concentration, or attention). Veterans who met enrollment criteria were randomized to one of four treatment arms: 1. CBT plus aerobic exercise, 2. aerobic exercise alone, 3. CBT alone, and 4. usual and customary care. Treatment was given for three months in group format. The CBT and exercise groups met for one hour, once a week for 12 weeks for a total of 12 hourly sessions. The interventions were standardized and all investigators were trained in the use of these methods prior to start up of the trial. The target sample size was 1064 veterans with GWVI to be accrued from 20 Medical Centers (18 VA and 2 DOD). All veterans were followed for one year and outcomes measured at 3 months (immediately following the end of treatment), 6 months and 12 months after enrollment.
The study was kicked-off in April 1999 and enrollment ended on September 5, 2000, during which 1092 veterans were randomized. Patient follow-up concluded on September 30, 2001 and the final DSMB meeting was held on November 28, 2001. The major finding was that there were no significant differences in the proportion of veterans who reported an improvement in physical function at one year among the treatment groups (11.5% for usual care, 11.7% for exercise, 18.4% for CBT and 18.5% for CBT + exercise). However, statistically significant improvements in fatigue, cognitive symptoms, distress, and mental health functioning were observed with exercise alone and with exercise plus CBT compared to usual care. CBT alone had a statistically significant effect on cognitive symptoms and in mental health functioning. Except for affective pain, which improved with CBT alone or with exercise, neither treatment had a significant effect on the other three measures of pain. In summary, neither exercise nor CBT had a significant impact on physical function for veterans with GWVI but both treatments, especially exercise, resulted in improvement in fatigue, cognitive symptoms, distress and mental health functioning.
Results embargoed until publication.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Persian Gulf Syndrome
Keywords
aerobic exercise, cognitive behavioral therapy, CBT, Gulf War Illnesses, GWI
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1064 (false)
8. Arms, Groups, and Interventions
Intervention Type
Behavioral
Intervention Name(s)
Aerobic exercise
Intervention Type
Behavioral
Intervention Name(s)
Cognitive behavioral therapy
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Gulf War era veterans deployed to the South West Asia theater of operations between August 1990 and August 1991 who have two of the following three symptoms that began after 1990 lasting more than 6 months and continuing to present - fatigue that limits usual activities (work, recreation or social), musculoskeletal pain involving more than one region of the body or neurocognitive dysfunction (self-reported difficulties in memory, concentration, or attention).
Facility Information:
Facility Name
Birmingham Vamc Birmingham Vamc
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35233
Country
United States
Facility Name
Birmingham Vamc
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35233
Country
United States
Facility Name
Naval Health Research Center, San Diego
City
San Diego
State/Province
California
ZIP/Postal Code
92106-6000
Country
United States
Facility Name
Naval Health Research Center, San Diego
City
San Diego
State/Province
California
ZIP/Postal Code
92152
Country
United States
Facility Name
Naval Health Research Center, San Diego
City
San Diego
State/Province
California
ZIP/Postal Code
92186-5122
Country
United States
Facility Name
San Francisco Vamc
City
San Francisco
State/Province
California
ZIP/Postal Code
94121
Country
United States
Facility Name
VA CT Healthcare System, West Haven
City
West Haven
State/Province
Connecticut
ZIP/Postal Code
06516
Country
United States
Facility Name
Georgetown University Medical Center
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20007
Country
United States
Facility Name
Walter Reed Army Medical Center
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20307-5001
Country
United States
Facility Name
Uniformed Services University
City
Bethesda
State/Province
Maryland
ZIP/Postal Code
20814-4799
Country
United States
Facility Name
Boston Vamc
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States
Facility Name
Boston Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02118
Country
United States
Facility Name
Boston Vamc
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02130
Country
United States
Facility Name
John Cochran VAMC, Saint Louis
City
St. Louis
State/Province
Missouri
ZIP/Postal Code
63106
Country
United States
Facility Name
VA New Jersey Health Care System, East Orange
City
East Orange
State/Province
New Jersey
ZIP/Postal Code
07018
Country
United States
Facility Name
Vamc - Albuquerque
City
Albuquerque
State/Province
New Mexico
ZIP/Postal Code
87108
Country
United States
Facility Name
New York Harbor VA Healthcare System, Brooklyn Campus
City
Brooklyn
State/Province
New York
ZIP/Postal Code
11209
Country
United States
Facility Name
Fargo Vamc
City
Fargo
State/Province
North Dakota
ZIP/Postal Code
58102
Country
United States
Facility Name
Vamc - Dayton
City
Dayton
State/Province
Ohio
ZIP/Postal Code
45428
Country
United States
Facility Name
Portland Vamc
City
Portland
State/Province
Oregon
ZIP/Postal Code
97207
Country
United States
Facility Name
Philadelphia Vamc
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
Houston Vamc
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
Audie L. Murphy Memorial Veterans Hospital, San Antonio
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78284
Country
United States
Facility Name
White River Junction Vamc
City
Burlington
State/Province
Vermont
Country
United States
Facility Name
White River Junction Vamc
City
White River Jct.
State/Province
Vermont
ZIP/Postal Code
05009
Country
United States
Facility Name
Richmond Vamc
City
Richmond
State/Province
Virginia
ZIP/Postal Code
23249
Country
United States
Facility Name
VA Puget Sound Healthcare System, Seattle Division
City
Seattle
State/Province
Washington
ZIP/Postal Code
98108-1597
Country
United States
Facility Name
VA Puget Sound Healthcare System, Seattle Division
City
Seattle
State/Province
Washington
ZIP/Postal Code
98108
Country
United States
Facility Name
San Juan Vamc
City
San Juan
ZIP/Postal Code
00921-3201
Country
Puerto Rico
12. IPD Sharing Statement
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Exercise and Behavioral Therapy Trial (EBT).
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