Sleep + Cognitive Training for Cognitive Impairment
(SLEEP-COG Trial)
Trial Summary
Will I have to stop taking my current medications?
The trial protocol does not specify whether you need to stop taking your current medications. However, if you are currently prescribed anti-dementia medication, you would not be eligible to participate.
What data supports the effectiveness of the treatment SLEEP + COG for cognitive impairment?
Research suggests that sleep disturbances are linked to cognitive decline, and addressing sleep issues may help improve cognitive performance. Non-drug approaches to improve sleep have been found feasible for people with mild cognitive impairment, indicating potential benefits of the SLEEP + COG treatment.12345
Is the Sleep + Cognitive Training treatment generally safe for humans?
The research articles do not provide specific safety data for the Sleep + Cognitive Training treatment, but they do discuss the effects of sleep deprivation and medications like donepezil on cognitive performance and brain activity. Donepezil, used in some studies, is generally safe but may have varying effects depending on individual susceptibility to sleep deprivation.678910
How does the Sleep + Cognitive Training treatment differ from other treatments for cognitive impairment?
The Sleep + Cognitive Training treatment is unique because it combines sleep, which enhances memory and cognitive functions, with cognitive exercises to improve working memory in older adults. This approach leverages the natural benefits of sleep on brain plasticity and memory consolidation, which are not typically addressed in standard cognitive impairment treatments.911121314
What is the purpose of this trial?
Up to 25% of intensive care unit (ICU) survivors experience cognitive impairment comparable in severity to mild Alzheimer's disease and related dementias after hospital discharge. Older ICU survivors (ages 60 and older) are at highest risk for delirium and subsequent cognitive impairment, which contribute to higher risk for cognitive decline related to Alzheimer's disease and related dementias. Sleep and activity are essential for recovery from critical illness, yet ICU survivors experience both sleep deficiency and profound inactivity. About 75-80% of ICU patients experience circadian dysrhythmia, which contributes to cognitive decline and increases likelihood of developing Alzheimer's disease and related dementias. The scientific premises of the proposed study are: 1) a combined sleep promotion and cognitive training intervention will have synergistic effects to mitigate the risk of cognitive impairment and development of Alzheimer's disease and related dementias in older ICU survivors; and 2) chronotherapeutic timing of interventions (i.e., adjusting timing of interventions according to circadian rhythm) may improve intervention efficacy.
Research Team
Maya N Elias, PhD, MA, RN
Principal Investigator
University of Washington
Eligibility Criteria
This trial is for older ICU survivors aged 60 and above who were functionally independent before hospitalization, stayed in the ICU for over 24 hours, are recovering or have been discharged from the ICU, and speak English or Spanish.Inclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive a combination of SLEEP and COG interventions, or individual SLEEP or COG interventions, for up to 7 days/nights
Follow-up
Participants are monitored for cognitive function and risk of Alzheimer's disease and related dementias
Treatment Details
Interventions
- SLEEP + COG
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Washington
Lead Sponsor
National Institute on Aging (NIA)
Collaborator