Hypertension
Conditions
Brief summary
The primary objective is to evaluate the accuracy to predict uncontrolled hypertension with Withings device data.
Interventions
OTHERQuestionnaire
Users who consent to the study will receive a questionnaire every 3 months
Sponsors
Withings
Study design
Observational model
COHORT
Time perspective
OTHER
Eligibility
Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
Yes
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.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Prediction of uncontrolled hypertension | 2 years | Correlation between uncontrolled hypertension, Withings data, and survey answers |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| 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 |
Countries
United States
Contacts
PRINCIPAL_INVESTIGATORde Havenon, MD
Yale University School of Medicine, Dept of Neurology
Outcome results
None listed