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Enhancing Sleep Quality for Nursing Home Residents With Dementia - R33 Phase
Enhancing Sleep Quality for Nursing Home Residents With Dementia: Pragmatic Trial of an Evidence-Based Frontline Huddling Program
Who can join
Ages 50 and older · All sexes
Full eligibility criteria
Inclusion Criteria: * Nursing home residents aged \>=50 years with an Alzheimer disease or related dementia (ADRD) diagnosis, identified by nursing home staff participating in frontline LOCK sleep huddles as having sleep problems Exclusion Criteria: * Residents with a high risk of OSA who are not being treated for OSA because actigraph measurements are inaccurate in that population. * Residents who have a persistent bilateral resting tremor or paralysis in both arms (a subset of persons with Parkinson's disease and related significant tremor-causing diagnoses), due to actigraph measurement inaccuracies
About the study
This study seeks to improve clinical outcomes for an important, growing, and vulnerable population-nursing home residents with Alzheimer's disease or related dementias-by testing an evidence-based intervention to improve these residents' sleep. It will also examine the implementation and sustainment of this intervention.
What is being tested
- LOCK Sleep Program (behavioral)
- No intervention (control period/baseline data collection) (other)
Sponsor: University of Alabama, Tuscaloosa · Participants: 456 · Started: Sep 7, 2023
Contact the study team
- Lynn Snow, PhD · Phone: 205-201-0312
- Brian Cox, MS · Phone: 205-348-7518
Official record on ClinicalTrials.gov — NCT05820919
Locations in the U.S.
| Colorado | Vivage/Beecan Corporation, Lakewood |
| Tennessee | National HealthCare Corporation, Murfreesboro |
| Texas | Caraday Healthcare, LLC, San Marcos |
Conditions
From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.