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Enrolling by invitationNo phase

Smart Devices-based Longitudinal Assessment of Patterns of Insomnia

This trial has no sites in United States.

It has sites in one country. Choose a country to see its sites.

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

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Trial details

Who runs it
Withings
Trial code
NCT07430878
Record updated
18 March 2026
Original description
The objective of the study is to develop an algorithm to detect insomnia and classify its severity, based on data collected during the use of Withings products and from questionnaires sent to usersRead full original descriptionShow less

The objective of the study is to develop an algorithm to detect insomnia and classify its severity, based on data collected during the use of Withings products and from questionnaires sent to users

Inclusion: is an adult(18 years old or more); is affiliated or eligible to a social security system; has expressed their consent to take part in the study; owns any of the following Withings monitoring devices: ScanWatch, ScanWatch 2 or Sleep Analyzer; has Withings mobile application with version greater or equal to 5.12.

Exclusion: Minors under 18 years old; Subjects having refused to give their consent; Vulnerable subjects according to the country regulation in force:; Individuals deprived of liberty by a court, medical or administrative order,; Individuals legally protected or unable to express their consent to take part in the study,; Individuals unaffiliated to or not beneficiary of a social security system,; Individuals who fit in multiple categories above,; Individuals linguistically or mentally unable to express their consent.

ClinicalTrials.gov NCT07430878