PICU-related Sleep and Circadian Dysregulation Pilot Study
Start Date
12/6/2024
Completion Date
1/1/2027
Summary
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.
Detailed Description
Several of the identified sleep disruptors in a pediatric intensive care environment may not be modifiable, including restricting feeding to daytime hours and providing normal daytime light exposure. This study aims to measure the feasibility of measuring sleep and circadian patterns in a PICU during routine care and during 2 focused sleep promotion interventions: timed daytime light exposure (DLE) and daytime feeding restriction (DFR). The overall objective of this study is to test the hypothesis that, with multi-disciplinary efforts, providing chronotherapeutic care will be feasible and that reliably measuring sleep patterns and the CR of critically ill children with timed salivary melatonin assays and actigraphy is possible.
Eligibility Criteria
Age Range: 3 years to 6 years
Interventions
Daytime light exposure
Daytime restricted feeding
Conditions
Locations
John R. Oishei Children's Hospital
Buffalo, New York 14203
United States