Health Information Technology to Improve Bedtime Media Use in Children

Sleep Hygiene, Inadequate Clinical Trial

Official title:

Improving Bedtime Media Use and Sleep Through Health Information Technology

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03177421
• Other study ID #: chsr_bedtime-media-cdss_2017
• Status: Terminated
• Phase: N/A
• Start date: June 13, 2017
• Est. completion date: May 31, 2019

Study information

• Verified date: January 2022
• Source: Indiana University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The objective of this study is to use health information technology to implement and evaluate a counseling recommendation for children who suffer from problematic sleep associated with bedtime media use. Participants will be randomized by clinic to be screened for basic sleep concerns and receive appropriate counseling, or to be screened for sleep concerns and media use, and receive appropriate counseling.

Description:

Children and adolescents are increasingly integrating media and technology into daily life. A large body of research has shown poor sleep-related outcomes related to media exposure, especially in evening or bedtime hours - a trend that holds true from infancy to adolescence. Prior research has demonstrated clinic-based interventions can be effective in reducing general screen time. Yet, little work has been done to leverage existing health information technology to adapt bedtime media use guidelines into sustainable counseling interventions. This study will develop, implement, and evaluate a computerized, evidence-based decision support intervention for reducing inappropriate childhood bedtime media use and improving sleep measures.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 60100
• Est. completion date: May 31, 2019
• Est. primary completion date: May 31, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 2 Years to 18 Years

Eligibility

Inclusion Criteria:

• Attend a participating clinic

• Complete a prescreener form in the clinic

Exclusion Criteria:

• None

Related Conditions & MeSH terms

• Sleep Hygiene, Inadequate

Intervention

Other:
• Problematic bedtime media use counseling
Participants will be screened for bedtime media use and sleep problems, and the clinical decision support system will recommend counseling on the respective problems identified on screening.
• Sleep problem counseling
Participants will be screened for sleep problems, and the clinical decision support system will recommend counseling if problems are identified.

Locations

Country	Name	City	State
United States	Eskenazi Health	Indianapolis	Indiana
United States	Riley Hospital for Children	Indianapolis	Indiana

Sponsors (1)

Lead Sponsor	Collaborator
Indiana University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rate of clinician counseling for problematic bedtime media use and sleep problems		Up to 3 years
Secondary	Change in bedtime media use following clinician counseling		Up to 3 years
Secondary	Change in inadequate sleep quantity following clinician counseling		Up to 3 years
Secondary	Change in daytime sleepiness following clinician counseling		Up to 3 years