Actively Recruiting
PICU-related Sleep and Circadian Dysregulation Pilot Study
Led by State University of New York at Buffalo · Updated on 2026-03-23
30
Participants Needed
1
Research Sites
108 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
A single center pilot trial investigating the feasibility of using actigraphy and salivary melatonin levels to measure the sleep and circadian rhythm of critically ill children aged 3 to 6 years old. This study will also measure the feasibility of providing daytime light exposure as well as restricting all provided nutrition to during daytime hours.
CONDITIONS
Official Title
PICU-related Sleep and Circadian Dysregulation Pilot Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Child age 3 to 6 years old on the day of PICU admission
- English-speaking parent at the bedside
- Child expected to remain in the PICU over 24 to 48 hours
You will not qualify if you...
- Child is in end-of-life care
- The child is receiving neuromuscular blockade for any reason
- Caregiver or parent not at the bedside
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
John R. Oishei Children's Hospital
Buffalo, New York, United States, 14203
Actively Recruiting
Research Team
A
Amanda B Hassinger, MD
CONTACT
H
Haiping Qiao, MS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
SEQUENTIAL
Primary Purpose
PREVENTION
Number of Arms
3
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