Menopausal Treatment Using Relaxation Exercises (MaTURE)

Completed · Not applicable

Conditions studied: Hot Flushes, Hot Flashes

In brief

Hot flashes occur in as many as two thirds of U.S. women during menopause and are severe enough to require treatment in 20%. Although postmenopausal hormone therapy is effective in suppressing hot flashes, it is associated with increased risk for a variety of serious adverse effects. There is an urgent need for alternative treatments that are effective, safe, and easy to use. In this study, the investigators will compare two different types of behavioral relaxation therapies, paced respiration and music therapy, for treatment of menopausal hot flashes. Effects on frequency of hot flashes, other symptom and quality-of-life outcomes associated with hot flashes, and physiologic measures of sympathetic/parasympathetic activity will be examined.

Key facts

Study ID

NCT01466998

Run by

University of California, San Francisco

People needed

123

Starts

2012-01-01

Expected to finish

2014-04-01

Last updated by the study team

2014-05-06

Who can join

Age: 40 and older, up to 59. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Women aged 40 through 59 years at the time of screening.
• Perinenopausal or postmenopausal.
• Adequate adherence to study procedures during a 1-week run-in.
• At least 4 hot flashes per 24 hours recorded by a hot flash monitor and diary.
• Capable of understanding study procedures and giving informed consent.
• Willing to refrain from using other treatments for hot flashes during the study period.

You may not qualify if…

• Pregnant or breastfeeding in the past year.
• Current or recent use of medications known to affect hot flashes.
• Resting blood pressure less than 100/60.
• Spontaneous resting breathing rate less than 10 breaths/minute.
• Chronic medical therapy for pulmonary disease.
• Known sensitivity to adhesives.
• Cardiac pacemaker or implanted defibrillator.
• No access to a telephone.
• Plans to move out of the area or travel by airplane in ways that would interfere with the study.
• Inability to sign an informed consent, participate in interviews, or understand and complete questionnaires in English.
• Report conditions that, in the judgment of the investigators, render potential participants unlikely to follow the protocol.
• Participation in another research study involving investigational drugs or devices.

Where it is running

• University of California, San Francisco — San Francisco, California, United States

Full record on ClinicalTrials.gov

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