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RECRUITING NA

The Goodnight Screen Media Study

NCT05820555 · View on ClinicalTrials.gov ↗

Study Summary

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 Studied

Interventions

  • BEHAVIORAL Timed evening technology and digital media use (tablet use)
  • BEHAVIORAL no technology and digital media use (screen media use)

Study Locations (1)

Texas

  • Children's Nutrition Research Center — Houston

Trial Details

FieldValue
Enrollment Target 180 participants
Start Date 2023-04-24
Est. Completion 2026-08-31
Phase NA

Sponsor

Baylor College of Medicine

678 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05820555

The ClinicalTrials.gov registry entry for NCT05820555 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 180 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Baylor College of Medicine, which has 678 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Sleep appearing as the primary indexed condition, and to 2 interventions — of which Timed evening technology and digital media use (tablet use) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05820555 reports 1 study location spanning 1 distinct geographic area — top geographies include Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05820555 about?

NCT05820555 is a clinical study titled "The Goodnight Screen Media Study". 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.

What is the current status of trial NCT05820555?

This trial is currently recruiting. It is a NA study. The enrollment target is 180 participants. The study started on 2023-04-24. Estimated completion is 2026-08-31.

What conditions does trial NCT05820555 study?

This clinical trial studies the following conditions: Sleep, Sleep Hygiene. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05820555?

The interventions under investigation include: Timed evening technology and digital media use (tablet use) (BEHAVIORAL), no technology and digital media use (screen media use) (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05820555?

This trial is sponsored by Baylor College of Medicine, which has 678 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05820555 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial