Withings Devices Follow-up Study - Hypertension
- Conditions
- Hypertension
- Registration Number
- NCT06692413
- Lead Sponsor
- Withings
- Brief Summary
The primary objective is to evaluate the accuracy to predict uncontrolled hypertension with Withings device data.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ENROLLING_BY_INVITATION
- Sex
- All
- Target Recruitment
- 1000
Inclusion Criteria
- Male or female who are 21 years of age or older,
- Participant living in the United States,
- Participant with data recorded in WITHINGS database,
- Active WITHINGS device users having at least 2 years of data,
- Subject able to read, understand, and provide written informed consent,
- Subject willing and able to participate in the study procedures as described in the consent form,
- Subject able to communicate effectively with and willing to follow instructions from the study staff.
Exclusion Criteria
- Minors under 21 years old,
- Subject who refused to participate in the study,
- Subject who did not reply to the questionnaire,
- Subject who objected to the processing of his or her data after the start of the study.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Prediction of uncontrolled hypertension 2 years Correlation between uncontrolled hypertension, Withings data, and survey answers
- Secondary Outcome Measures
Name Time Method Correlation between Framingham risk score and EQ-5D-5L answers and Withings data 2 years Correlation between Framingham risk score and EQ-5D-5L answers and Withings data
Number of Questionnaires answers per participant 2 years Number of Questionnaires answers per participant
Trial Locations
- Locations (1)
Yale University Medical School, Department of Neurology
🇺🇸New Haven, Connecticut, United States