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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01052454
Other study ID # AT002910
Secondary ID
Status Completed
Phase Phase 0
First received January 18, 2010
Last updated January 19, 2010
Start date September 2005

Study information

Verified date January 2010
Source University of Massachusetts, Worcester
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This is a study to determine if participation in a mindfulness-based stress reduction program is feasible for women experiencing five or more hot flashes/day, and whether it affects either the frequency and/or intensity of their hot flashes, or the degree of bother they experience from them


Recruitment information / eligibility

Status Completed
Enrollment 110
Est. completion date
Est. primary completion date May 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Women experiencing 5 or more hot flashes/day

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Mindfulness-based stress reduction
Participants in the MBSR arm attend eight weekly classes.

Locations

Country Name City State
United States UMass Medical School Worcester Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
University of Massachusetts, Worcester

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Hot Flash intensity/bother
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