Adult Disease Risk Prediction Using Wearables, Hearing, and Health Data

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorNational Health Research Institutes, Taiwan

About this trial

This prospective cohort study aims to develop and validate a personalized disease risk prediction model for adults by integrating multiple sources of health data. The study will recruit community-dwelling adults aged 18 years and older in Taiwan. After providing informed consent, participants will complete a structured questionnaire, undergo pure tone hearing testing, and wear a smartwatch for 2 weeks to collect continuous physiological data, including heart rate and physical activity. With participant authorization, the study will also collect data from personal health records and national health insurance databases to allow longer-term follow-up of health outcomes.

The main goals of the study are to examine the relationships among hearing, lifestyle factors, and wearable device data; to identify combinations of risk factors associated with progression from health to subclinical or chronic disease states; and to develop analytical methods for integrating heterogeneous health data from questionnaires, physiological monitoring, hearing tests, and medical databases. Machine learning methods will be used to identify important predictors and build risk prediction models.

The study hypothesis is that combining hearing measures, lifestyle information, wearable physiological data, and longitudinal medical record data will improve the ability to identify individuals at higher risk of future disease compared with using a single source of information alone. The long-term objective is to support early risk identification, personalized health management, and prevention strategies in community adults.

Eligibility criteria

Qualifiers

Adults aged 18 years and older

Living in the community in Taiwan

Able to understand the study procedures and provide written informed consent

Able and willing to complete the study questionnaire, hearing assessment, and wearable device monitoring procedures

Disqualifiers

Diagnosis of dementia

Too frail or has other health conditions that make participation in the study procedures not feasible

Bilateral deafness without use of any hearing assistive device

Does not have a smartphone or is unable to use a smartphone application required for the study procedures

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

1,500 Participants
are grouped into 1 trial group