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Smart Devices-based Longitudinal Assessment of Patterns of Insomnia

NCT07430878 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 17000

Last updated 2026-03-18

No results posted yet for this 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

Conditions

Interventions

DEVICE

Use of the Withings sleep-related devices

The participants are asking to use their Withings sleep-related device(s) as much as possible

OTHER

Questionnaires

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

Sponsors & Collaborators

  • INSERM Neurodiderot UMR 1141

    collaborator UNKNOWN

  • Université Paris Cité

    collaborator OTHER

  • Reykjavik University

    collaborator OTHER

  • Withings

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-02-18
Primary Completion
2027-05-31
Completion
2027-05-17

Countries

  • France

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07430878 on ClinicalTrials.gov