Confirming the Effects of Acupuncture Treatments to Relieve Symptoms of Gulf War Illness

Recruiting N/A Interventional Study
Persian Gulf Syndrome Gulf War Syndrome Multiple Chronic Illnesses Occupational Diseases War-Related Injuries Wounds and Injuries
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
200 (estimated)
Sponsor
University of Utah · Other
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About This Trial
This unblinded Phase II clinical trial will test the effects of individualized acupuncture treatments offered in extant acupuncture practices in the community; practitioners will have had at least 5 years of experience plus additional training provided by the study. Veterans with diagnosed symptoms of Gulf War Illness will be randomized to either six months of biweekly acupuncture treatments (grou…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Deployed to the Gulf Theater of operations (as defined by 38 CFR 3.317, includes Iraq, Kuwait, Saudi Arabia, Bahrain, Qatar, the United Arab Emirates, Oman, the Gulf of Aden, the Gulf of Oman, the Persian Gulf, the Arabian Sea, the Red Sea, and the airspace above all of these …
Contacts

Lisa Conboy

617-718-1917

lisa_conboy@hms.harvard.edu

CONTACT