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Withings Devices Follow-up Study - Hypertension

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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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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