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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT03082040 |
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Date of registration:
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06/03/2017 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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A Home-based Breathing Training on Menopausal Symptoms
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Scientific title:
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Effects of a Home-based Breathing Training on Menopausal Symptoms Among Community Menopausal Women |
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Date of first enrolment:
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October 26, 2016 |
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Target sample size:
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57 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03082040 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Crossover Assignment. Primary purpose: Treatment. Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor).
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Phase:
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N/A
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Countries of recruitment
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Taiwan
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Contacts
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Name:
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Yuh-Kae Shyu, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Fu Jen Catholic University |
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Key inclusion & exclusion criteria
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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., ß-blockers,
etc.
Age minimum:
45 Years
Age maximum:
64 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Menopause
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Menopause Related Conditions
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Intervention(s)
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Behavioral: home-based breathing training
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Primary Outcome(s)
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Menopausal symptoms
[Time Frame: Posttest (4 weeks from baseline)]
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Menopausal symptoms
[Time Frame: Baseline]
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Secondary Outcome(s)
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Autonomic functions (Blood pressure)
[Time Frame: Posttest (4 weeks from baseline)]
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Autonomic functions (heart rate)
[Time Frame: Baseline]
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Autonomic functions (Blood pressure)
[Time Frame: Baseline]
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Autonomic functions (heart rate variability)
[Time Frame: Baseline]
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Autonomic functions (heart rate variability)
[Time Frame: Posttest (4 weeks from baseline)]
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Autonomic functions (heart rate)
[Time Frame: Posttest (4 weeks from baseline)]
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Secondary ID(s)
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MOST105-2314-B-030-006
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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