Withings Devices Follow-up Study - Hypertension

Withings

Status: Invitation-only

Conditions: Hypertension

Treatments: Other: Questionnaire

Study type: Observational

Funder types: Industry

Identifiers

NCT06692413

WIQUEST-HTA

Details and patient eligibility

About

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

Enrollment: 1,000 estimated patients

Sex: All

Ages: 21+ years old

Volunteers: Accepts Healthy Volunteers

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.

Trial design

1,000 participants in 1 patient group

Withings device users

Description:

Active Withings device users having at least 2 years of device data

Treatment:

Other: Questionnaire