By InvitationNot Applicable

Smart Devices-based Longitudinal Assessment of Patterns of Insomnia

France17,000 participantsStarted 2025-02-18

Plain-language summary

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

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 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 Criteria: * 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.

What they're measuring

insomnia presence/absence using a Questionnaire

Timeframe: From enrollment and for 26 weeks

Severity of Insomnia using a Questionnaire

Timeframe: : From enrollment and for 26 weeks

Trial details

NCT IDNCT07430878

SponsorWithings

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2027-05

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