Clinical trial Recruiting at 1 site Observational

Sleep detection in long-term care residents

Official title: Sleep Detection in Older Adults Living in Long-term Care Facilities: An Inter-rater Reliability Agreement Study

Run by Eastern Switzerland University of Applied Sciences · NCT07819409 · Data updated 2026-11-12

This study tests how well contactless sleep sensors track sleep patterns in older adults living in long-term care facilities.

Quick facts

Study typeObservational
SexAll
Enrollment52 (estimated)
SponsorEastern Switzerland University of Applied Sciences
Academic / other
Locations1 site (Sankt Gallen, St.Gallen)
StatusRecruiting
StartedAugust 28, 2025
Main results expectedFebruary 2027
Study endsAugust 2027
Registry record updatedSeptember 17, 2026
Trial IDNCT07819409 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Older adults living in long-term care facilities who can give informed consent.

Probably not a fit

Residents with certain neurocognitive disorders or specific dementia subtypes may not benefit from the findings.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study compares 24-hour sleep measurements from contactless sleep sensors with traditional methods in residents of long-term care facilities. It aims to understand day-to-day variability and how accurately CSTs reflect sleep, wake times, and restfulness in older adults. The project explores how sleep measurement differences relate to cognitive and functional outcomes, using a real-world long-term care setting. It focuses on test-retest variability to determine smallest detectable differences for intraday changes. The findings could inform feasible, low-burden sleep monitoring in this population.

Why it matters

Potential benefit: If successful, CSTs could provide a practical way to monitor sleep over 24 hours in older adults without overnight lab visits.

How similar studies have gone: Previous work shows CSTs can approximate PSG but variability across days and devices remains a concern; this study adds real-world data in nursing home settings.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Signed informed consent
* Older adults living in the long-term care facilities

Exclusion Criteria:

* Neurocognitive disorders based on Alzheimer's Disease, Parkinson's disease, Lewy body dementia or Mixed dementia according to patient record

Where it's running

  • Easternswiss University of Applied Sciences
    Sankt Gallen, St.Gallen, Switzerland
    Recruiting

Study contacts

  • Principal investigator: Eling D de Bruin, Prof. Dr. — Eastern Swiss University of Applied Sciences, ETH Zruich
  • Study coordinator: Eling D de Bruin, Prof. Dr.
  • Email: eling.debruin@ost.ch
  • Phone: +41 58 257 14 11

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.