Acupuncture in the Treatment of Gulf War Illness
Completed · Phase 1/Phase 2
Conditions studied: Persian Gulf Syndrome
In brief
This unblinded Phase II clinical trial tested the effects of individualized acupuncture treatments offered in extant acupuncture practices in the community; practitioners had at least 5 years of experience plus additional training provided by the study. Veterans with diagnosed symptoms of Gulf War Illness were randomized to either six months of biweekly acupuncture treatments (group 1, n=52) or 2 months of waitlist followed by weekly acupuncture treatments (group 2, n=52). Measurements were taken at baseline, 2, 4 and 6 months. The primary outcome is the SF-36 physical component scale score (SF-36P).
Key facts
- Study ID
- NCT01305811
- Run by
- New England School of Acupuncture
- People needed
- 104
- Starts
- 2009-07-01
- Expected to finish
- 2013-01-01
- Last updated by the study team
- 2015-06-15
Who can join
Age: 39 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- New England School of Acupuncture — Newton, Massachusetts, United States
Full record on ClinicalTrials.gov
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