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
NA
12 participants
INTERVENTIONAL
2005-09-30
2005-12-31
Brief Summary
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Detailed Description
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The main efficacy outcomes are change in number of hot flashes per week and change in severity of hot flashes from baseline to post-training reported on a 7-day diary. We will also measure changes in sleep and quality of life.
Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Interventions
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Yoga
Eligibility Criteria
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Inclusion Criteria
2. Successful completion of a Hot Flash Diary.
3. Able and willing to attend yoga training sessions, maintain yoga logs, and practice yoga at home.
Exclusion Criteria
2. Use of other treatments for hot flashes (estrogens, progestins, clonidine, selective serotonin reuptake inhibitors,relaxation techniques or acupuncture) within 4 weeks of enrollment in the trial and do not agree to refrain from using these therapies for the duration of the trial.
3. Use of raloxifene or tamoxifen within three months of enrollment.
4. Any condition that, in the investigator's opinion, would preclude the participant from being able to understand and follow the yoga training or from completing the trial, including severe illness, plans to move, substance abuse, significant psychiatric problems, or dementia.
\-
40 Years
65 Years
FEMALE
Yes
Sponsors
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University of California, San Francisco
OTHER
Principal Investigators
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Deborah Grady, MD, MPH
Role: PRINCIPAL_INVESTIGATOR
University of California, San Francisco
Locations
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UCSF Women's Health Clinical Research Center
San Francisco, California, United States
Countries
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Other Identifiers
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H5287-26599
Identifier Type: -
Identifier Source: org_study_id
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