Fibromyalgia (FM) Musculoskeletal Diseases Fibromyalgia
Conditions
Interventions
One hundred FM patients will participate in a 12-week trial.
These patients will be randomized into 3 control groups and 1 "true" acupuncture group. The control groups will consist of a group receivin
Sponsors
National Center for Complementary and Alternative Medicine (NCCAM) (USA)
Eligibility
Inclusion criteria
Inclusion criteria: Male or Female, aged 18 and over with Fibromyalgia
Exclusion criteria
Exclusion criteria: Not provided at time of registration
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome was subjective pain as measured by a 10-cm visual analogue scale ranging from 0 (no pain) to 10 (worst pain ever). Measurements were obtained at baseline; 1, 4, 8, and 12 weeks of treatment; and 3 and 6 months after completion of treatment. Participant blinding and adverse effects were ascertained by self-report. The primary outcomes were evaluated by pooling the 3 sham-control groups and comparing them with the group that received acupuncture to treat fibromyalgia. | — |
Secondary
| Measure | Time frame |
|---|---|
| Not provided at time of registration | — |
Countries
United States of America
Outcome results
None listed