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Persian Gulf SyndromePhase 3NCT00007748

Exercise and Behavioral Therapy Trial (EBT).

A Phase 3 study testing Aerobic exercise and Cognitive behavioral therapy in people with Persian Gulf Syndrome, run by US Department of Veterans Affairs at 29 sites in 2 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Persian Gulf Syndrome
What is being tested?
Aerobic exercise and Cognitive behavioral therapy
How many people
1,064 participants
Where
29 sitesin 2 countries
Study dates
Mar 1999to Aug 2001
Phase
Phase 3
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

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).

Trial locations and contacts

29 sites in 2 countries.

29 sites in 2 countries

United States28 sites
  • Vamc - Albuquerque

    Albuquerque, New Mexico, 87108

  • Uniformed Services University

    Bethesda, Maryland, 20814-4799

  • Birmingham Vamc Birmingham Vamc

    Birmingham, Alabama, 35233

  • Birmingham Vamc

    Birmingham, Alabama, 35233

  • Boston Vamc

    Boston, Massachusetts, 02114

  • Boston Medical Center

    Boston, Massachusetts, 02118

  • Boston Vamc

    Boston, Massachusetts, 02130

  • New York Harbor VA Healthcare System, Brooklyn Campus

    Brooklyn, New York, 11209

  • White River Junction Vamc

    Burlington, Vermont

  • Vamc - Dayton

    Dayton, Ohio, 45428

  • VA New Jersey Health Care System, East Orange

    East Orange, New Jersey, 07018

  • Fargo Vamc

    Fargo, North Dakota, 58102

  • Houston Vamc

    Houston, Texas, 77030

  • Philadelphia Vamc

    Philadelphia, Pennsylvania, 19104

  • Portland Vamc

    Portland, Oregon, 97207

  • Richmond Vamc

    Richmond, Virginia, 23249

  • Audie L. Murphy Memorial Veterans Hospital, San Antonio

    San Antonio, Texas, 78284

  • Naval Health Research Center, San Diego

    San Diego, California, 92106-6000

  • Naval Health Research Center, San Diego

    San Diego, California, 92152

  • Naval Health Research Center, San Diego

    San Diego, California, 92186-5122

  • San Francisco Vamc

    San Francisco, California, 94121

  • VA Puget Sound Healthcare System, Seattle Division

    Seattle, Washington, 98108-1597

  • VA Puget Sound Healthcare System, Seattle Division

    Seattle, Washington, 98108

  • John Cochran VAMC, Saint Louis

    St Louis, Missouri, 63106

  • Georgetown University Medical Center

    Washington D.C., District of Columbia, 20007

  • Walter Reed Army Medical Center

    Washington D.C., District of Columbia, 20307-5001

  • VA CT Healthcare System, West Haven

    West Haven, Connecticut, 06516

  • White River Junction Vamc

    White River Jct., Vermont, 05009

Other trials in United States

Puerto Rico1 site
  • San Juan Vamc

    San Juan, 00921-3201

Other trials in Puerto Rico

About this study

Official title: CSP#470 - A Randomized, Multi-Center, Controlled Trial of Multi-Modal Therapy in Veterans With Gulf War Illnesses

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.

Read the 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:

  1. Both aerobic exercise and CBT will lead to improvements in the cardinal symptoms of GWVI: pain, fatigue and cognitive difficulties.
  2. Both aerobic exercise and CBT will lead to decreased levels of distress in persons with GWVI.
  3. 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.

Being tested
Aerobic exercise, Cognitive behavioral therapy
Keywords
aerobic exercise, cognitive behavioral therapy, CBT, Gulf War Illnesses, GWI
Medical subject headings
Persian Gulf Syndrome

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 Jan 2001 (estimated)
  2. Study startMar 1999
  3. Study completionAug 2001

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Factorial
Masking
None (open label)
Enrolment
1,064 participants
IDs, dates and publications
ClinicalTrials.gov ID
NCT00007748
Sponsor's protocol ID
470
Status last verified
Jun 2015
First submitted
29 Dec 2000
Last updated
26 Jun 2015
Results posted
No

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Aerobic exercise and Cognitive behavioral therapy in people with Persian Gulf Syndrome, run by US Department of Veterans Affairs at 29 sites in 2 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 26 Jun 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 29 sites in United States, Puerto Rico. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Jun 2015.

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