A before-after comparison study of a novel self-care application to develop an individualized lifestyle intervention to prevent and manage menopausal symptoms
Not Applicable
Recruiting
- Conditions
- Menopausal symptoms
- Registration Number
- JPRN-UMIN000052302
- Lead Sponsor
- Kyoto University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 120
Inclusion Criteria
Not provided
Exclusion Criteria
Those with the following comorbidities: coronary artery disease, pheochromocytoma, neurasthenia, psychiatric disorders, uncontrolled thyroid dysfunction, uncontrolled hypertension or any other comorbidity that the doctor considers unsuitable for study participation Those who have started using new drugs (e.g. hormone replacement therapy or antidepressants) within 30 days Those who are pregnant or lactating
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity of menopausal symptoms: Modified version of the menopausal symptoms rating chart for Japanese women (26 weeks after the start of the intervention)
- Secondary Outcome Measures
Name Time Method