Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
100 participants
INTERVENTIONAL
2003-01-31
2005-02-28
Brief Summary
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Detailed Description
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One hundred Reiki-naive FM patients will be recruited from a chronic fatigue referral clinic and will participate in an 8-week trial. Patients will be randomized into one of two Reiki groups (direct-contact and distant Reiki) or one of two control groups (sham and placebo). Patients will receive either Reiki or placebo 16 times during the course of the study. Patients will be assessed at study entry, at Weeks 4 and 8, and 12 weeks post-treatment.
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Interventions
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Reiki (distant and direct-contact)
Eligibility Criteria
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Inclusion Criteria
* Willing to undergo randomization and attend treatments regularly
* Willing to stay on a stable medical regimen during the entire 8-week trial and use only acetaminophen for breakthrough pain
* Live within a one-hour drive of the study site
Exclusion Criteria
* Pregnant
* Pending litigation or disability claim related to FM
18 Years
70 Years
ALL
No
Sponsors
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National Center for Complementary and Integrative Health (NCCIH)
NIH
Principal Investigators
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Dedra S. Buchwald
Role: PRINCIPAL_INVESTIGATOR
University of Washington
Locations
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Univ of WA - CFS/FM Research Center
Seattle, Washington, United States
Countries
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Other Identifiers
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