Enhancing Sleep Quality for Nursing Home Residents With Dementia

This study is testing a program called LOCK to improve sleep for nursing home residents with Alzheimer's disease or related dementias. The LOCK program trains nursing home staff using a team-based approach to help residents sleep better. Researchers will compare residents' sleep during a period with no special intervention to their sleep after the LOCK program is put in place. The study aims to enroll 456 participants. To join, you must be at least 50 years old, have an Alzheimer's disease or related dementia diagnosis, and be identified by staff as having sleep problems. Success will be measured by how much sleep improves, using a device called an actigraph (a wrist-worn device that measures movement to estimate sleep). The current recruitment status is unclear.

Study design
This study is an interventional, stepped-wedge randomized controlled trial involving 456 participants. It compares a period of no intervention to the LOCK sleep program.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Sleep will be measured during a 15-week sleep intervention period.

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NCT05820919

Enhancing Sleep Quality for Nursing Home Residents With Dementia - R33 Phase

Recruiting
NAAges 50+InterventionalTreatment
University of Alabama, Tuscaloosa
~456 participants
Updated 2024-03-12 on ClinicalTrials.gov
What's tested:LOCK Sleep ProgramNo intervention (control period/baseline data collection)

At a glance

Recruiting sites
3 of 3 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Sleep (actigraph measurement)
Measured over 15 week sleep intervention period
Alzheimer Disease
Dementia
Sleep Disorder
Sleep Disturbance
3 sites across 3 states
Colorado1
Tennessee1
Texas1
  • Lynn Snow, PhD · PRINCIPAL_INVESTIGATOR · The University of Alabama

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Eligibility criteria

Inclusion

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

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
  • Sleep (actigraph measurement)15 week sleep intervention period

    Total sleep time (total minutes asleep each nighttime period - 10pm to 7am)