NCT06045988 · NOT YET RECRUITING

Automated, Assistive, Non-Contact Sleep Quality Monitor for Individuals With Alzheimer's Disease

This study tests a sensor that tracks sleep without anything worn on the body. It is used with people who have Alzheimer's or related dementia and live in long-term care. Researchers want to know if sharing the sleep data with care staff helps them spot sleep problems sooner and adjust care. It is a device study with no phase, so it is not a drug trial.

You may qualify if

  • Diagnosis of Alzheimer's Disease (AD) or Alzheimer's Disease Related Dementias (ADRD)
  • Residents of long-term care (LTC) facility study site location for a minimum of 30 days.
  • Willingness to consent to study or when a potential participant lacks decision making capacity (determined by LTC facility clinical provider) willingness of a Legally Authorized Representative (LAR) to consent to study participation on potential participant's behalf.

You're excluded if

  • Currently on hospice

The sponsor's own eligibility wording, lightly reformatted. The study team makes the final eligibility decision — worth discussing with your doctor.

Eligibility criteria as of 2026-06-26

View full record on ClinicalTrials.gov

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