Persian Gulf Syndrome Clinical Trial
Official title:
Acupuncture in the Treatment of Gulf War Illness
Verified date | May 2015 |
Source | New England School of Acupuncture |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Federal Government |
Study type | Interventional |
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).
Status | Completed |
Enrollment | 104 |
Est. completion date | January 2013 |
Est. primary completion date | January 2013 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 39 Years and older |
Eligibility |
Inclusion 1. 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 locations" between August 1990 and the present date, 2. they have at least 2 of the following symptoms from the 3 CDC clusters of symptom that have lasted for more than 6 months. Each symptom cluster must be characterized as "mild-moderate" or "severe" with at least one symptom in each cluster required to be severe. The clusters are: A-Fatigability - fatigue 24 hours or more after exertion B-Mood and Cognition - feeling depressed or - feeling irritable or - difficulty thinking or concentrating or - feeling worried, tense, anxious or - problems finding words or - problems getting to sleep C-Musculoskeletal - joint pain or muscle pain Exclusion: - Currently enrolled in another clinical trial - Have another disease that likely could account for the symptoms, as determined by our Medical Monitor - Severe psychiatric illness (in the last 2 years psychiatric hospitalization, suicidal attempt, alcohol or substance abuse, use of antipsychotic medication) as measured by the Primary Care Evaluation of Mental Disorder (Prime MD). - Unable to complete the protocol on based on the evaluation of the Medical Monitor |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Investigator, Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | New England School of Acupuncture | Newton | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
New England School of Acupuncture | United States Department of Defense |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | SF-36P | Ten items addressing physical functioning which are part of a short-form health survey with 36 questions. Scores range between 0 and 100 with higher scores indicating better function. | 2 months | No |
Primary | SF-36P | Ten items addressing physical functioning which are part of a short-form health survey with 36 questions. Scores range between 0 and 100 with higher scores indicating better function. | 6 months | No |
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