RECRUITING

The Goodnight Screen Media Study

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Experimental Effects of Children's Evening Media Use on Circadian Phase, Sleep and Executive Functioning

Quick Facts

Study Start:2023-04-24
Study Completion:2026-08-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05820555

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:48 Months to 59 Months
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. * preschool-aged children (4.0 to \<5.0 years old) and their parent
  2. * living in the Greater Houston area.
  3. * parent must be a biological parent or legal guardian who lives with the child ≥50% of the time and has a primary role of caring for the child
  4. * parent is comfortable participating in the study and responding to questionnaires in English.
  5. * The child does not have to have access to mobile device, but if they do, the primary device they use has to be an Android OS ≥5.0 either used only by the study child or shared with others, or an Apple iOS ≥14.0 that only the child uses.
  6. * Parent and child must be fluent in English.
  1. * The child has a chronic medical condition or takes a medication affecting sleep, or circadian rhythms (e.g., melatonin supplementation, diagnosed sleep disorder, steroid use, etc.) or a diagnosed cognitive or learning impairment affecting EF (e.g., attention deficit hyperactivity disorder).
  2. * Child with blindness or significant vision problems that impacts both screen media use and sleep.

Contacts and Locations

Study Contact

Jennifer Coon
CONTACT
713-798-7143
coon@bcm.edu

Study Locations (Sites)

Children's Nutrition Research Center
Houston, Texas, 77030
United States

Collaborators and Investigators

Sponsor: Baylor College of Medicine

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-04-24
Study Completion Date2026-08-31

Study Record Updates

Study Start Date2023-04-24
Study Completion Date2026-08-31

Terms related to this study

Keywords Provided by Researchers

  • circadian phase
  • sleep
  • evening screen media use

Additional Relevant MeSH Terms

  • Sleep
  • Sleep Hygiene