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A study for a Predictive Data Model for Symptoms of Premenstrual Syndrome using a Wearable Device

A study for a Predictive Data Model for Symptoms of PremenstrualSyndrome using a Wearable Device - A study for a Predictive Data Model for Symptoms of PremenstrualSyndrome using a Wearable Device

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000051467
Enrollment
150
Registered
2023-07-01
Start date
2023-07-18
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

None listed

Interventions

None listed

Sponsors

TechDoctor,Inc.
Lead Sponsor
LOTTE CO., LTD.
Collaborator

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1.Females aged between 18 and 60 at the time of informed consent 2.Those who own a smartphone terminal on which applications can be installed, have no plans to change models during the research period, and agree to the terms of use regarding the sensing devices and applications used in this research. 3.Those who can obtain written consent to participate in this research and to provide information to this research before participating in this research

Exclusion criteria

Exclusion criteria: 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

Design outcomes

Primary

MeasureTime frame
Since this study is a hypothesis-exploratory study, the correlations between objective evaluation indices that can be obtained from the sensing devices and subjective evaluation indices obtained from the questionnaire scores will be comprehensively compared. Objective metrics that can be obtained from sensing devices *Stress related values *Sleep efficiency related value *Momentum-related value *Blood oxygen concentration *Amount of activity *Information that can be obtained from other sensing devices Subjective evaluation *MDQ *Score of research subject questionnaire When there is a request from the person to wear *Blood glucose related values obtained from continuous blood glucose meter data

Countries

Japan

Contacts

Public ContactKazumichi Minato

TechDoctor,Inc. CEO

minato@technology-doctor.com03-5476-8889

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026