Smart Devices-based Longitudinal Assessment of Patterns of Insomnia

NCT07430878 · tracked via the Priya Life Science France tracker

Sponsor

Withings

Phase

Not applicable

Started

2025-02-18

Last updated

2026-03-18

Condition(s) studied

Insomnia

Investigational drug(s) / intervention(s)

Use of the Withings sleep-related devicesQuestionnaires

Use of the Withings sleep-related devices: The participants are asking to use their Withings sleep-related device(s) as much as possible

Questionnaires: The participant are asking to answer several questionnaires regarding their quality of sleep via Withings mobile application

Study 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

Eligibility

Sex

ALL

Min age

18 Years

Max age

—

Healthy volunteers

Accepted

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.

Primary outcome measure(s)

insomnia presence/absence using a Questionnaire — From enrollment and for 26 weeks
Severity of Insomnia using a Questionnaire — : From enrollment and for 26 weeks

Trial sites (1)

Facility	City	Region	Status
Withings	Issy-les-Moulineaux	France

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07430878 on ClinicalTrials.gov ↗ ← All trials in France