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Mindfulness Based Stress Reduction for Hot Flashes

Primary Purpose

Hot Flashes, Stress

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Mindfulness-based stress reduction
Sponsored by
University of Massachusetts, Worcester
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hot Flashes focused on measuring Hot flashes, vasomotor symptoms, menopause, mindfulness based stress reduction, meditation

Eligibility Criteria

40 Years - 69 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: Average of 5+ hot flashes per day No menses in prior 3 months Ages between 40 and 69 years English speaking Access to a telephone Availability for the entire study period Agree to maintain usual diet Agree to maintain usual exercise habits Consent to the study Exclusion Criteria: Psychiatric illness Illness with less than one year life expectancy Alcohol use ≥ 2 drinks per day Current substance abuse or addiction Use of selective estrogen receptor modulator (SERM) medications within the past 3 months Use of HT within the past 3 months Currently pregnant or breastfeeding Ongoing mindfulness meditation practice

Sites / Locations

  • University of Massachusetts Medical School

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

MBSR

Arm Description

Outcomes

Primary Outcome Measures

Hot flash frequency and intensity

Secondary Outcome Measures

Menopause-related quality of life
Hot Flash-Related Daily Interference Scale
Women's Health Initiative (WHI) Insomnia Rating Scale
5 factor of Mindfulness questionnaire
Health locus of control
Perceived stress
Dietary intake
Compliance with intervention conditions
HADS

Full Information

First Posted
April 20, 2006
Last Updated
October 3, 2012
Sponsor
University of Massachusetts, Worcester
Collaborators
National Center for Complementary and Integrative Health (NCCIH)
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1. Study Identification

Unique Protocol Identification Number
NCT00317304
Brief Title
Mindfulness Based Stress Reduction for Hot Flashes
Official Title
Mindfulness Based Stress Reduction for Hot Flashes
Study Type
Interventional

2. Study Status

Record Verification Date
October 2012
Overall Recruitment Status
Completed
Study Start Date
January 2005 (undefined)
Primary Completion Date
August 2012 (Actual)
Study Completion Date
August 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Massachusetts, Worcester
Collaborators
National Center for Complementary and Integrative Health (NCCIH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Stress appears to be related to hot flash frequency and intensity, and the degree of distress that women experience from their hot flashes appears to be related to their coping resources. This trial is a pilot study to test the effect of participation in a mindfulness-based stress reduction program on hot flash frequency and intensity, as well as menopause-related quality of life.
Detailed Description
The majority of women experience vasomotor symptoms (VMS) such as hot flashes (HF) and night sweats as they transition through menopause, and a substantial minority experience considerable distress and diminished role functioning. Until recently most women found relief through hormone therapy (HT), but concern about the health risks associated with HT has left women with few effective and safe choices for relief from their symptoms other than their own coping strategies. A variety of results from both population and laboratory studies suggest that stress and HF are correlated and that HF are more severe in women with lower coping abilities, but evidence is far from conclusive. Consequently, investigators have called for trials to evaluate the effect of stress reduction interventions on HF. Mindfulness-Based Stress Reduction (MBSR) is a widely available manualized program shown to be an effective adjunctive intervention in reducing medical symptoms and psychological distress for a wide range of stress-related disorders. In a small preliminary study using MBSR we found reductions in HF severity scores and increases in menopause-related quality of life (QOL). This R21 proposal is for a pilot randomized trial of MBSR compared to a wait-list control group for 120 menopausal women experiencing seven or more HF/day of moderate to severe intensity. It aims to: assess feasibility of recruitment, adherence to program intervention, and compliance with assessment instruments in preparation for a larger RCT; and provide preliminary estimates of efficacy of the effects of MBSR in reducing self-reported HF frequency and intensity and improving QOL. In addition, we will use sternal skin conductance as an established objective measure of VMS in a subgroup of 15 women in each arm to test feasibility and obtain information on how objectively measured HF are related to self-reported HF in this setting. Women will be assessed at baseline, at the end of the eight-week MBSR course, and at three months after the end of the course. A secondary aim is to explore whether treatment group differences of HF frequency and intensity and QOL are explained by changes in perceived stress, health-related locus of control and mindfulness. It is anticipated that results from this pilot study will provide data needed to plan a larger more definitive randomized trial on the effect of MBSR on HF frequency and intensity and on the ability to cope with these symptoms.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hot Flashes, Stress
Keywords
Hot flashes, vasomotor symptoms, menopause, mindfulness based stress reduction, meditation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
110 (Actual)

8. Arms, Groups, and Interventions

Arm Title
MBSR
Arm Type
Experimental
Intervention Type
Behavioral
Intervention Name(s)
Mindfulness-based stress reduction
Other Intervention Name(s)
MBSR
Intervention Description
MBSR is an 8-week group-based program of training in mindfulness and its application to the stresses and challenges of everyday life
Primary Outcome Measure Information:
Title
Hot flash frequency and intensity
Time Frame
Baseline, 8 weeks, 24 weeks
Secondary Outcome Measure Information:
Title
Menopause-related quality of life
Time Frame
Baseline, 8 weeks, 24 weeks
Title
Hot Flash-Related Daily Interference Scale
Time Frame
Baseline, 8 weeks, 24 weeks
Title
Women's Health Initiative (WHI) Insomnia Rating Scale
Time Frame
Baseline, 8 weeks, 24 weeks
Title
5 factor of Mindfulness questionnaire
Time Frame
Baseline, 8 weeks, 24 weeks
Title
Health locus of control
Time Frame
Baseline, 8 weeks, 24 weeks
Title
Perceived stress
Time Frame
Baseline, 8 weeks, 24 weeks
Title
Dietary intake
Time Frame
Baseline, 8 weeks, 24 weeks
Title
Compliance with intervention conditions
Time Frame
Baseline, 8 weeks, 24 weeks
Title
HADS
Time Frame
Baseline, 8 weeks, 24 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
69 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Average of 5+ hot flashes per day No menses in prior 3 months Ages between 40 and 69 years English speaking Access to a telephone Availability for the entire study period Agree to maintain usual diet Agree to maintain usual exercise habits Consent to the study Exclusion Criteria: Psychiatric illness Illness with less than one year life expectancy Alcohol use ≥ 2 drinks per day Current substance abuse or addiction Use of selective estrogen receptor modulator (SERM) medications within the past 3 months Use of HT within the past 3 months Currently pregnant or breastfeeding Ongoing mindfulness meditation practice
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
James Carmody, PhD
Organizational Affiliation
University of Massachusetts, Worcester
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Massachusetts Medical School
City
Worcester
State/Province
Massachusetts
ZIP/Postal Code
01655
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
21372745
Citation
Carmody JF, Crawford S, Salmoirago-Blotcher E, Leung K, Churchill L, Olendzki N. Mindfulness training for coping with hot flashes: results of a randomized trial. Menopause. 2011 Jun;18(6):611-20. doi: 10.1097/gme.0b013e318204a05c.
Results Reference
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Mindfulness Based Stress Reduction for Hot Flashes

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