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Withings Devices Follow-up Study - Hypertension

Reason given: The PI couldn't participate to the study finally

Key facts

Where
New Haven, United StatesSee the site

Where in United States

  • Yale University Medical School, Department of NeurologyNew Haven, United StatesNo longer taking part

Trial details

Who runs it
Withings
Trial code
NCT06692413
Record updated
19 February 2026
Original description
The primary objective is to evaluate the accuracy to predict uncontrolled hypertension with Withings device data.Read full original descriptionShow less

The primary objective is to evaluate the accuracy to predict uncontrolled hypertension with Withings device data.

Inclusion: 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: 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.

ClinicalTrials.gov NCT06692413