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Study identifier: NCT06411561 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Critical Illness · Delirium · Cognitive Impairment  ·  Sponsor: University of Washington

PhaseNA
Planned participants100
Who can joinAll sexes, 60 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Maya N Elias, PhD, MA, RN  ·  206-543-8564  ·  mnelias@uw.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of WashingtonSeattle, Washington, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06411561