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A randomized, controlled clinical trial: the effects of mindfulness-based stress reduction program on the reduction of menopausal symptoms among Chinese peri-menopausal and post-menopausal women in the community

A randomized, controlled clinical trial: the effects of mindfulness-based stress reduction program on the reduction of menopausal symptoms among Chinese peri-menopausal and post-menopausal women in the community

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003192
Enrollment
Unknown
Registered
2013-04-10
Start date
2013-09-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

menopausal symptoms

Interventions

Two groups:The program will include daily homework exercises that consist of guided (taped) or unguided awareness exercises directed at increasing moment-by-moment non-judgmental awareness of bodily s
(to be continued):The curriculum will include training in mindfulness through (1) a body scan, the gradual moving of attention through the body from head to feet while lying on a mat on the floor, bri
(2) sitting meditation, in which attention is brought to breathing sensation
(to be continued:and (3) mindful stretching exercises, to cultivate awareness during simple stretching movement. The key themes of MBSR will include the empowerment of participants and a focus on awar
(to be continued):Participants are guided to develop a “decentered” perspective on thoughts and feelings, in which these are viewed as passing events in the mind.
Duration of intervention:
(to be continued):The MBSR program will consist of two-and-a-half-hour weekly sessions for eight weeks with a total of 20 hours.
Description / name of comparative treatments:
(to be continued):The MEC will consist of an eight-week psycho-education intervention that is based on principles used in a health education intervention for middle-aged women to increase their knowle
(to be continued):These sessions will include health education with respect to information about the menopause, self-help and medical treatments, discussion of expectations and beliefs about the menop

Sponsors

Division of Family Medicine and Primary Healthcare, School of Public Health and Primary Care, The Chinese University of Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
40 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) women aged 40-60,1, 6 who are peri-menopausal or early post-menopausal1 (but who are not affected by hysterectomy, oophorectomy or pregnancy). In this study, peri-menopausal status is defined as the period immediately prior to the menopause with change in menstrual pattern and irregular cycle (defined as changes in frequency compared with 12 months ago) and post-menopausal status is defined as absence of periods for at least 12 months; (2) women having a somatic symptom score of six or above on the Greene Climacteric Symptom Score; and (3) women who are willing to maintain the present exercise, dietary pattern, and dose of any soy supplements.

Exclusion criteria

Exclusion criteria: (1) psychiatric and medical comorbidities that are potentially life-threatening (i.e., psychosis, suicidal ideation, terminal medical illness) or conditions expected to severely limit patient participation or adherence (e.g., psychosis, current substance or alcohol abuse, dementia, pregnancy); and (2) medical conditions or medications that may affect menopausal symptoms including hot flushes (such as the presence of thyroid disease or the use of selective estrogen receptor modulator, hormone therapy, or the use of traditional Chinese medicine for the menopause). (3) Women who have previously practiced or are currently practicing meditation will be excluded from the study. Women with breast cancer are eligible as long as they have completed all the treatments for their cancer with partial or total remission for at least six months. The women will be asked to report their initiation of the use of any medications during the study, and women who use any anxiolytics or SSRIs will be asked to keep their present dosage stable and to immediately report any changes during the study period.

Design outcomes

Primary

MeasureTime frame
climacteric symptoms;

Secondary

MeasureTime frame
Stress;Mindfulness;Health related quality of life;

Countries

China

Contacts

Public ContactSamuel Yeung Shan Wong

The Chinese University of Hong Kong

yeungshanwong@cuhk.edu.hk+852 22528774

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026