RecruitingNot ApplicableNCT06411561

A Multi-Modal Combination Intervention to Promote Cognitive Function in Older Intensive Care Unit Survivors


Sponsor

University of Washington

Enrollment

100 participants

Start Date

Dec 26, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 60 Years

Plain Language Summary

Simplified for easier understanding

This study tests a program combining multiple strategies — such as mental exercises and lifestyle coaching — to help older adults maintain or improve their thinking and memory after surviving a serious illness in the intensive care unit (ICU). Many ICU survivors experience cognitive decline after discharge, and this trial aims to prevent that. **You may be eligible if...** - You are 60 years or older - You were admitted to the ICU for more than 24 hours at the University of Washington or Harborview Medical Center - You have moved from intensive care to regular hospital care or are being discharged - You speak English or Spanish fluently - You were fully independent in daily activities before your hospitalization **You may NOT be eligible if...** - You have a history of Alzheimer's disease or dementia, or take anti-dementia medications - You have a history of bipolar disorder or schizophrenia - You experienced a stroke or traumatic brain injury during this hospital stay - You have severe vision, hearing, or physical impairments Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALSLEEP + COG

Combination of SLEEP and COG interventions

BEHAVIORALCOG

Daily 30-minute session of computerized cognitive training

BEHAVIORALSLEEP

Nighttime use of both ear plugs and eye masks

BEHAVIORALAC

Educational modules on cognitive and sleep health


Locations(1)

University of Washington

Seattle, Washington, United States

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NCT06411561


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