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Circadian Rhythm Monitoring Study

StatusNot Yet Recruiting
PhaseNot applicable
SponsorResMed
Started
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Record History

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  1. Primary endpoint(s) modified
    • Start date: Feb 2026 to Jul 2026
    • Primary completion pushed from May 2026 to Oct 2026
    • Study completion pushed from Jun 2026 to Dec 2026
    v2
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
ResMed
18 trials monitored
See 2 trials at risk
This will be a single-center, prospective observational study designed to evaluate the feasibility and accuracy of a new wearable device for non-invasive continuous monitoring of physiological signals to derive circadian rhythm. Melatonin sampling will be included for comparison against wearable-derived measures
Trial Details
NCT Number NCT07336654
Lead Sponsor ResMed
Conditions
(from sponsor)		 Circadian Rhythm
Enrollment 30 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov