View Clinical Trial (Medical Research Study)
Effect of Yoga on Objective and Subjective Menopausal Hot Flashes - NCT01073397-27157(Clinical Trial 563089)
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| City: |
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Winston-Salem |
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State:
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NC |
| Zip Code: |
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27157 |
| Conditions: |
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Vasomotor Symptoms |
| Purpose: |
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The purpose of this research study is to compare yoga and health and wellness classes for
helping perimenopausal or newly postmenopausal women who are experiencing hot flashes. The
investigators want to learn about the effects of yoga and health and wellness classes on
symptoms and other quality of life issues. The results of this study may provide important
knowledge to women and clinicians who counsel women with menopausal hot flashes.
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| Study summary: |
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Hot flashes and/or night sweats are the most common and troubling symptoms associated with
menopause. It is estimated that 64% to 87% of women report experiencing hot flashes for an
average of about 4 years. For many women, these symptoms are frequent and severe enough to
become debilitating and interfere with daily activities. They often occur at night,
disturbing sleep and leading to daytime irritability, fatigue and depressed mood. About
30-40% of menopausal women seek medical help for hot flashes. Relief from hot flashes has
been shown to be the primary reason that women initiate hormone therapy (HT).
HT is currently the gold standard for treatment of vasomotor symptoms. A Cochrane Database
systematic review showed a 75% reduction in hot flash frequency with hormone therapy
compared to placebo.1 However, recent findings from the Women's Health Initiative (WHI)
trial indicate that benefits of HT are outweighed by risks, such as coronary heart disease,
stroke, pulmonary embolism, breast cancer, and probable dementia. The wide publicity of the
WHI results has heightened women's concerns about taking HT and many women have sought
alternative treatments for hot flashes. These alternatives include other pharmaceutical
agents, herbal or dietary remedies, and behavioral therapies. Unfortunately, many of these
agents have a high incidence of side effects or have not been shown to be effective. A
recent NIH conference has called for more research on alternative treatments for hot
flashes.
Behavioral interventions involving relaxation and slow deep, abdominal breathing have been
found to be useful for reducing mild- to moderate-intensity hot flashes. Although the
physiological mechanisms for the effectiveness of these interventions are not completely
understood, there is some suggestion that they may help reduce sympathetic activity which is
related to the narrowing of the thermoneutral zone. It is currently thought that hot
flashes are linked to a disruption in thermoregulation and that elevated levels of brain
norepinephrine may be the primary mechanism for altered thermoregulation. Breathing
techniques form the most integral core of any yoga practice which involves the combination
of physical postures (asanas), breathing (pranayama), and deep relaxation (savasana).
Despite suggestions that yoga may be beneficial for the relief of hot flashes, these
potential benefits have not been well-studied.
To date, treatment efficacy for hot flashes has been limited to self-reported, subjective
symptoms. While subjective hot flashes are important from a woman's perspective in her
decision-making with respect to treatment, research has shown that they can be influenced by
mood and reporting biases. Objective measures are not subject to these biases and have the
advantage of providing insight as to whether an intervention has a physiological effect.
However, until recently, reliable objective measures that could be used in an ambulatory
setting were not available. NCCAM has recently funded the development of new technologies
to monitor objective hot flashes in an ambulatory setting, as measured by skin conductance.
This technology greatly enhances our ability to fully evaluate the impact of treatment on
both subjective and objective hot flashes.
The primary goal of this R21 pilot grant is to obtain preliminary data on the efficacy of
Integral Yoga for reducing self-reported menopausal hot flashes. Secondary aims are to
determine the impact of yoga on objective hot flashes and other outcomes and study
feasibility. Our primary hypothesis will be a greater reduction in subjective hot flash
frequency and severity in the yoga group than in two control groups. Secondary outcomes
will include a greater reduction in objective hot flash frequency; a greater decrease in hot
flash interference; and greater improvement in sleep, other symptoms, mood, perceived
stress, and overall quality of life in the yoga group. |
| Criteria: |
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Inclusion Criteria:
- At least 2 months since last menses
- Age 45-58 years
- Moderate to severe vasomotor symptoms for at least 4 weeks (at least 4/day on
average)
- Self-reported general good health
- Adequate English to understand informed consent form, questionnaires, and converse
with study staff
- Agree not to use pharmaceutical agents for treating hot flashes during the study
Exclusion Criteria:
- Hormone therapy use within 12 weeks prior to study screening, including systemic
estrogen, progestin or androgen therapy
- Selective estrogen receptor modulator (Evista® and Novaldex®) or aromatase inhibitor
use within 6 months
- Cancer at any time
- Untreated thyroid disease
- Initiation of herbal or nutritional supplements for hot flashes within the past 4
weeks
- Significant psychiatric disorder, including regular use of antidepressants or
anxiolytics
- Regular use of clonidine or Bellergal® within the past 12 weeks
- Any past use of yoga for hot flashes
- Yoga or Acupuncture for any reason within the past 3 months |
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| Study is available at: |
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Wake Forest University Health Sciences Winston-Salem, NC 27157 United States
Primary Contact: Emily Smith, BS Email: emsmith@wfubmc.edu Phone: 336-716-5619 |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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March 23, 2011 |
Modifications to
this listing: |
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above to view all information about this clinical trial. |
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