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A Home-based Breathing Training on Menopausal Symptoms

Effects of a Home-based Breathing Training on Menopausal Symptoms Among Community Menopausal Women

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03082040
Enrollment
57
Registered
2017-03-17
Start date
2016-10-26
Completion date
2017-12-20
Last updated
2020-06-05

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

Conditions

Menopause, Menopause Related Conditions

Brief summary

This is a prospective, triple-blinded and randomized controlled trial examining the effects of a home-based breathing training assisted with biofeedback on menopausal symptoms and autonomic functions among community menopausal women. We also examines whether the changes in autonomic functions would be mediators between slow breathing and menopausal symptoms. This study will include menopausal women, aged from 45 to 64, who experienced menopausal symptoms. Participants will be randomly assigned to either an intervention group (n = 80) or a waiting-list control group (n = 80). The intervention group will undergo the home-based breathing training 20 minutes twice daily and participants in the control condition will participate the same breathing training after a four-week waiting list period. The primary outcome measures are menopausal symptoms measured by symptom diaries of menopausal symptoms and the Greene Climacteric Scale (GCS). Secondary outcome measures are autonomic functions expressed by blood pressure (BP), heart rate (HR) and heart rate variability (HRV). Measurements will be taken at baseline, week 4, and week 8.

Detailed description

Ditto

Interventions

BEHAVIORALhome-based breathing training

The intervention group will undergo a home-based breathing training 20 minutes twice daily for four weeks. Participants in the control condition will participate the same breathing training after a four-week waiting list period.

Sponsors

Ministry of Science and Technology, Taiwan
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
45 Years to 64 Years
Healthy volunteers
Yes

Inclusion criteria

* aged from 45 to 64, reporting cessation of menstrual cycles with natural causes ≧ 12 consecutive months * the Greene Climacteric Scale (GCS) Chinese version scores ≧ 1

Exclusion criteria

* clinically diagnosed with history of cardiac arrhythmia, coronary heart disease, heart failure, kidney disease, hypertension, chronic low blood pressure, diabetic neuropathy, psychosis or mental deficiency * received hormone replacement therapy prescribed by gynecological physicians * took cardiac medications which may affect the autonomic functions, ex., β-blockers, etc.

Design outcomes

Primary

MeasureTime frameDescription
Menopausal symptomsBaselineAssessments using the Greene Climacteric Scale (GCS) for self-reported menopausal symptoms

Secondary

MeasureTime frameDescription
Autonomic functions (Blood pressure)BaselineAssessments using A&D sphygmomanometer (Model 767Plus, A&D Co., LTD., Japan) for systolic blood pressure and diastolic blood pressure
Autonomic functions (heart rate)BaselineAssessments using EKG sensors to detect heartbeat signals, and then be analyzed by the BioGraph Infiniti software.
Autonomic functions (heart rate variability)BaselineA 3-lead EKG and Cardiopro Software were used to assess and analyze the heart rate variability in time domain, including SDNN (standard deviation of all NN intervals), rMSSD (the root mean square successive difference of normal-to-normal intervals) and pNN50 (NN50 count divided by the total number of all NN intervals).

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026