Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
ACTIVE NOT RECRUITING
NCT06249217
PHASE1/PHASE2

Good Nights Sleep Program to Improve Child and Family Sleep

Sponsor: Auburn University

View on ClinicalTrials.gov

Summary

The purpose of this study is to pilot a randomized clinical trial designed to improve the sleep environments, sleep hygiene practices, and the duration and quality of sleep of children and parents in low-income families. It is hypothesized that child and parent sleep (assessed through subjective reports of sleep, sleep environments, sleep hygiene practices, and objective sleep data via sleep actigraphy collected with Fitbit watches) in the intervention group will improve between Week 2 (intervention session) and Week 4 (post-intervention session) as compared to child and parent sleep in the waitlist-control group.

Official title: Good Nights Sleep Program: Pilot of a Randomized Clinical Trial to Improve Child and Family Sleep

Key Details

Gender

All

Age Range

7 Years - 10 Years

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2024-02-01

Completion Date

2024-10-01

Last Updated

2024-08-23

Healthy Volunteers

Yes

Interventions

BEHAVIORAL

Good Nights Sleep Program

The Good Nights Sleep Program arm adapts established evidence-based motivational practices to change child and family sleep environments and sleep hygiene practices. At Week 0, participants will provide a comprehensive assessment of sleep environment and sleep hygiene practices and will be issued a Fitbit watch to wear for the duration of the study. At Week 2, participants will receive information about the benefits of good sleep, feedback about their sleep environment and sleep hygiene practices based on the Week 0 assessment data to implement at home, and sleep environment modification items based on participant-identified areas of need (e.g., a fan, sound machine, bedding). At Week 4, families in the Good Nights Sleep Program arm will provide post-intervention assessment data and feedback on the intervention and families in the Waitlist-Control arm can elect to receive the intervention if they choose to.

Locations (1)

Room 266, ARTF Building, 570 Devall Drive

Auburn, Alabama, United States