Actively Recruiting

Phase Not Applicable
Age: 4Years - 17Years
All Genders
NCT07384585

Feasibility of Light Therapy in the Pediatric Intensive Care Unit (ICU)

Led by Laura Beth Kalvas · Updated on 2026-03-27

30

Participants Needed

1

Research Sites

43 weeks

Total Duration

On this page

Sponsors

L

Laura Beth Kalvas

Lead Sponsor

N

Nationwide Children's Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to understand how easy or difficult it is for critically ill children (4-17 years old) to have light therapy while in the pediatric ICU. Participants will have a light meter at their bedside to measure light levels. Each morning, a light box will be placed at their bedside. Children, family, and staff will be asked to completed feedback surveys regarding the light therapy. Study participation will continue for a maximum of 5 days.

CONDITIONS

Official Title

Feasibility of Light Therapy in the Pediatric Intensive Care Unit (ICU)

Who Can Participate

Age: 4Years - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Anticipated to remain admitted to the study hospital pediatric ICU for additional 48 hours
  • English-speaking parent or legally authorized representative available at the bedside
Not Eligible

You will not qualify if you...

  • Unable to open eyes to receive light therapy (Glasgow Coma Scale eye opening score of 1 or neuromuscular blockade)
  • Contraindications to light therapy such as migraines, retinal disease, diseases with retinal complications, blindness, bipolar disorder, seizure disorder, or traumatic brain injury
  • Suspected or identified neglect or abuse, involvement of Child Protective Services, or ward of state
  • Receiving palliative or end-of-life care
  • Unable to fit light box or cart in patient room

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Nationwide Children's Hospital

Columbus, Ohio, United States, 43205

Actively Recruiting

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Research Team

L

Laura Beth Kalvas, PhD, RN

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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