Actively Recruiting
Experimental Effects of Light And Content From Evening Screen Media Use On Children's Sleep, Executive Functioning, And Emotion Regulation
Led by Baylor College of Medicine · Updated on 2026-06-03
220
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
B
Baylor College of Medicine
Lead Sponsor
E
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are investigating how evening exposure to light from tablet devices and the type of media content shown affect children's sleep, internal body clocks, emotion control, and thinking skills. The study focuses on children aged 8 to 11 years at early stages of puberty (Tanner stage 1 or 2). This randomized controlled trial aims to separate the effects of screen brightness and exciting versus calming content on these outcomes. The study includes 200 children randomly assigned to one of four groups combining bright or dim tablet screen light with either exciting or calming content. Each child will participate in two weekend protocols at home, one with screen use for one hour before bed under their assigned condition, and one with quiet, non-screen activities serving as a control. The order of these weekends is randomized to reduce order effects. Researchers will control bedroom lighting and measure melatonin levels to assess shifts in circadian timing. Sleep will be monitored using wrist activity trackers, heart rate sensors, and subjective sleepiness ratings. During the study, children will maintain a consistent sleep schedule set by their parents. Research staff will visit homes to collect saliva samples for melatonin measurement and conduct tests on emotion regulation and executive function the afternoon after each weekend. The study will track sleep duration, quality, heart rate, arousal, and cognitive performance to understand how evening screen exposure impacts children's sleep and next-day functioning. The total study participation lasts about two weeks with assessments on specific nights and days.
CONDITIONS
Brief Title
SCREENS: Sleep, Circadian Rhythms, and Electronics in the EveNing Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Children between 8.0 and 11.9 years old
- Tanner stage 1 or 2
- Live with their parent(s) or legal guardian at least 50% of the time who primarily cares for the child
- Habitual sleep duration between 8.5 to 11 hours per night
- Child sleeps alone most nights
- Parent and child can communicate, read, and write in English
- If child uses a mobile device, primary device must be Android OS ≥5.0 used only by child or shared, Amazon Fire OS ≥5.0 used only by child, or Apple iOS ≥14.0 used only by child
- Agreement to install usage tracking app or share screenshots from child's device
- Families live in the greater Houston area
You will not qualify if you...
- Child is blind or colorblind
- Significant vision problems
- Developmental or cognitive delays
- Diagnosis of a sleep or psychiatric disorder
- Cognitive or learning impairments affecting executive function (e.g., ADHD)
- Medical conditions impacting sleep
- Taking medications that affect sleep
- Travel across more than 2 time zones in the month before the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Parents and children complete eligibility assessments and consent procedures.
Duration - 1 week
Participants maintain their typical sleep schedule and media use to establish baseline measurements.
Actigraphy and ambient light exposure are monitored at home.
Duration - 2 weekends (3 days each, one week apart)
Participants complete two weekend at-home protocols one week apart, with research staff facilitating assessments and experimental conditions to measure effects of screen media exposure on sleep and circadian rhythms.
Research staff conduct 2 in-home visits per weekend including evening circadian phase assessments and daytime executive function and emotion regulation testing.
Trial Site Locations
Total: 1 location
1
Children's Nutrition Research Center
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
I
Insia Raza, MPH
H
Hafza Dadabhoy
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
4
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