Rested & Ready to Learn
Prevention Strategies to Enhance Young Children's Sleep Development - Part 2
2 other identifiers
interventional
98
1 country
1
Brief Summary
The goal of this pilot randomized controlled trial is to test the feasibility, acceptability, and preliminary signal of effect of a combined school- and home-based sleep promotion program for young children prior to the kindergarten transition.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Feb 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 12, 2025
CompletedFirst Submitted
Initial submission to the registry
March 11, 2025
CompletedFirst Posted
Study publicly available on registry
March 18, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 21, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 30, 2026
CompletedApril 1, 2026
January 1, 2026
11 months
March 11, 2025
March 30, 2026
Conditions
Outcome Measures
Primary Outcomes (9)
Trial-related feasibility - recruitment capability
Recruitment capability will be measured by the proportion of eligible children who enroll at baseline
Through recruitment period, up to 6 weeks
Trial-related feasibility - retention
Retention will be measured by the proportion of enrolled children who remain in the study through the length of the intervention. Reasons for dropout will also be assessed
Weekly through study completion (weeks 1-5)
Intervention-related feasibility - intervention fidelity
Intervention fidelity, the delivery of the intervention as originally planned, will be assessed via teacher report. Intervention fidelity will be assessed with a study-specific questionnaire to assess if all classroom components were delivered as planned.
Weekly through study completion (weeks 1-4)
Intervention-related feasibility - rate of attendance
Children's attendance at school during intervention sessions will be provided by class records.
Weekly through study completion (weeks 1-4)
Intervention-related feasibility - participant adherence to intervention (home)
Adherence to the home-based component will rely on link usage data to assess parent engagement with the online materials. Investigators will extract information related to the number of parents who click links from weekly material and number of parents who do not open links.
Weekly through study completion (weeks 1-4)
Intervention-related feasibility - participant adherence to intervention (school)
School-based adherence will be assessed by a teacher-completed survey which will indicate whether or not they implemented the intervention each week
Weekly through study completion (weeks 1-4)
Intervention-related feasibility - data collection completion rates
Data collection completion rates will be calculated to understand the feasibility of data collection protocols
Weekly through study completion (weeks 1-4)
Intervention-related feasibility - data collection feasibility
Feasibility of data collection procedures will be assessed with qualitative feedback from parents during semi-structured interviews following the study.
Post-intervention (week 5-9)
Acceptability
Acceptability of the intervention conditions is defined as participants' perception that the intervention is satisfactory and will be assessed with short weekly questionnaires for parents and teachers. Overall acceptability will be assessed with an exit-survey consisting of Likert-scale items and open-ended responses to understand likes/dislikes, content, logistics, and feedback for future iterations. Likert-style questions will have response options ranging from 1-5 with greater scores representing higher acceptability.
Weekly through study completion (weeks 1-4), post-intervention (week 5-9)
Secondary Outcomes (7)
Child sleep - device-based duration
Baseline (week 0), post-intervention (week 5), follow up (week 17)
Child sleep - device-based timing
Baseline (week 0), post-intervention (week 5), follow up (week 17)
Child sleep - Bedtime Routines Questionnaire
Baseline (week 0), post-intervention (week 5), follow up (week 17)
Child behavior
Baseline (week 0), post-intervention (week 5), follow up (week 17)
Child inhibition
Baseline (week 0) and post-intervention (week 5)
- +2 more secondary outcomes
Study Arms (2)
Rested & Ready to Learn
EXPERIMENTALThe Rested \& Ready to Learn sleep promotion program includes text messaging to parents, home activities for parents and children to complete together, and brief classroom lessons.
Control
NO INTERVENTIONThe control group will not receive any intervention. They will be placed on a waitlist and will receive the Rested \& Ready to Learn intervention once all assessments are complete.
Interventions
The intervention targets improving young children's sleep by providing parents with sleep education and activities to do at home with their child. Classroom teachers will also deliver a brief lesson aligned with intervention topics to reinforce key messaging in the classroom. The sleep intervention will focus on the benefits of sleep (physical health, social-emotional health, classroom participation/learning), creating and sticking to a bedtime routine, screen use before bed, and developmentally appropriate sleep behavior.
Eligibility Criteria
You may qualify if:
- Child between the ages of 4-6 years
- Currently enrolled in a participating school's 4-year-old kindergarten (4K) classroom
- Parent/guardian willing to complete questionnaires in English
- Parent/guardian must have access to a mobile phone with texting capability
You may not qualify if:
- \- Parent or child has a medical condition that impairs their ability to participate
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of South Carolina
Columbia, South Carolina, 29208, United States
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
March 11, 2025
First Posted
March 18, 2025
Study Start
February 12, 2025
Primary Completion
January 21, 2026
Study Completion
March 30, 2026
Last Updated
April 1, 2026
Record last verified: 2026-01