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PICU-related Sleep and Circadian Dysregulation Pilot Study

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 nut

Condition(s)Circadian Dysrhythmia, Sleep Disturbance, Critical Illness, Children, Only
StatusRecruiting
PhaseNA
Study typeInterventional
SummaryA 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.
Who can participateInclusion Criteria: 1. Child age 3 to 6 years old on the day of PICU admission 2. English-speaking parent at the bedside 3. Child expected to remain in the PICU over 24 to 48 hours Exclusion Criteria: 1. Child is in end-of-life care 2. The child is receiving neuromuscular blockade for any reason 3. Caregiver or parent not at the bedside
Ages3 Years to 6 Years
SexAll
Lead sponsorState University of New York at Buffalo
LocationsBuffalo, New York, United States
Start date2024-12-06
NCT IDNCT06505447
Official listinghttps://clinicaltrials.gov/study/NCT06505447

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