Actively Recruiting

Phase Not Applicable
Age: 48Months - 59Months
All Genders
Healthy Volunteers
NCT05820555

The Goodnight Screen Media Study

Led by Baylor College of Medicine · Updated on 2025-05-09

180

Participants Needed

1

Research Sites

175 weeks

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

To test the timing of evening tablet use on children's circadian phase and sleep (i.e., sleep onset and sleep duration) compared to no screen media use. To explore the effect of evening tablet use on children's inhibitory control and executive function.

CONDITIONS

Official Title

The Goodnight Screen Media Study

Who Can Participate

Age: 48Months - 59Months
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Preschool-aged children between 4.0 and under 5.0 years old and their parent
  • Living in the Greater Houston area
  • Parent must be biological or legal guardian living with the child at least 50% of the time and primarily caring for the child
  • Parent is comfortable participating and answering questionnaires in English
  • Child's primary mobile device must be Android OS 5.0+ used only by the child or shared, or Apple iOS 14.0+ used only by the child
  • Parent and child must be fluent in English
Not Eligible

You will not qualify if you...

  • Child has chronic medical conditions or takes medications affecting sleep or circadian rhythms (e.g., melatonin, steroids), or diagnosed cognitive or learning impairments affecting executive function (e.g., ADHD)
  • Child has blindness or significant vision problems impacting screen media use and sleep

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

Children's Nutrition Research Center

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

J

Jennifer Coon

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

3

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