Sleep Disorders Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
For people living with cognitive impairment:
- People who have been diagnosed with Alzheimer's Disease or a related form of dementia, or whose caregiver has reported that they likely have some level of memory or thinking problems
- People who score between 12 and 24 on a standard memory and thinking test called the Montreal Cognitive Assessment (MoCA)
- People who have had one or more sleep problems (such as trouble sleeping) at least three nights per week, as measured by a standard behaviour assessment tool
- People who have an eligible caregiver participating alongside them in the trial
- People who are able to take part in the trial's sessions
For caregivers:
- Adults aged 18 or older who live in the same home as the person with cognitive impairment
- People who regularly help the person they care for with at least one basic daily task (such as bathing or eating) or at least one broader everyday task (such as managing medications or finances), for the past six months
- People who have had trouble falling asleep or staying asleep for the past three months, or who score 5 or higher on a standard sleep quality questionnaire called the Pittsburgh Sleep Quality Index (PSQI)
Who may not be able to join:
- People living with cognitive impairment whose condition is assessed as moderate to severe
- Anyone under 18 years of age
- Women who are pregnant
- People who are currently in prison
- People who are not able to clearly understand English
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Glenna Brewster, PhD, RN, FNP, Emory University
Phone: (404) 712-9164
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Change in insomnia; Change in Sleep Efficiency; Change in in Sleep Onset Latency; Change in Wake After Sleep Onset; Adherence with Study Interventions (feasibility); Satisfaction with intervention components
Can't join this trial?
Data last synced from ClinicalTrials.gov: 20 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.