A study for a Predictive Data Model for Symptoms of Premenstrual Syndrome using a Wearable Device
- Conditions
- /A
- Registration Number
- JPRN-UMIN000051467
- Lead Sponsor
- TechDoctor,Inc.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 150
Not provided
1.Those who have difficulty in health management due to perioperative period, infection, or disease under treatment 2.Patients who were taking hormonal drugs such as pills, antipsychotic drugs within 2 months from the start of the study, those who were diagnosed with other mental disorders, and those who were diagnosed with gynecological disorders 3.Those who have not had menstruation for 3 months or more (secondary amenorrhea), those who are menopausal,those who are pregnant,or those who are breastfeeding 4.Those who are judged by the research director to be difficult to use the sensing device 5.Implanting a device that can affect heart rate, such as a pacemaker depressed person 6.Persons using drugs that can affect heart rate 7.Subjects who may develop skin rashes due to continuous use of the sensing device 8.Others who are judged by the principal investigator to be inappropriate to participate in this research
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method