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
| Type | Name | Description |
|---|---|---|
| DEVICE | Daytime Bright Light | Daytime 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. |
| DEVICE | Usual Light | Usual 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.