Smart Devices-based Longitudinal Assessment of Patterns of Insomnia

Enrolling by invitation · Not applicable

Conditions studied: Insomnia

In brief

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

Key facts

Study ID

NCT07430878

Run by

Withings

People needed

17000

Starts

2025-02-18

Expected to finish

2027-05-17

Last updated by the study team

2026-03-18

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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.

You may not qualify if…

• 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.

Where it is running

• Withings — Issy-les-Moulineaux, France

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.