Clinical Trials Directory

Trials / Completed

CompletedNCT03684460

Daytime Bright Light, Circadian Abnormalities, and Delirium in Medical ICU Patients

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
68 (actual)
Sponsor
Yale University · Academic / Other
Sex
All
Age
50 Years
Healthy volunteers
Not accepted

Summary

To determine if daytime bright light will promote circadian alignment and shorten or prevent delirium.

Detailed description

To determine if daytime bright light will promote circadian alignment and shorten or prevent delirium. The objective is to conduct a randomized controlled trial to determine if a circadian entrainment intervention, daytime bright light, will promote circadian alignment and reduce days of delirium

Conditions

Interventions

TypeNameDescription
DEVICEDaytime Bright LightDaytime Bright Light (DBL) will be delivered by a free-standing apparatus set to deliver 10,000 lux. The device will be placed at the bedside within 36 inches of the patient's head and is expected to provide at least 1,250 lux at the angle of gaze. To remain in the study, the patient must be in the Intensive Care Unit (ICU) through 13:00 on day 2 (e.g., the first day of potential intervention). After day 2, DBL and other study activities will continue if the patient is transferred out of the ICU to the general medical floor.
DEVICEUsual LightUsual care lighting in ICU. To remain in the study usual care patients must also remain in the MICU through 13:00 on day 2.

Timeline

Start date
2019-07-08
Primary completion
2024-03-28
Completion
2024-03-28
First posted
2018-09-25
Last updated
2024-05-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03684460. Inclusion in this directory is not an endorsement.