NCT06882005

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
98

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Feb 2025

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 12, 2025

Completed
27 days until next milestone

First Submitted

Initial submission to the registry

March 11, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

March 18, 2025

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 21, 2026

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 30, 2026

Completed
Last Updated

April 1, 2026

Status Verified

January 1, 2026

Enrollment Period

11 months

First QC Date

March 11, 2025

Last Update Submit

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

EXPERIMENTAL

The 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.

Behavioral: Rested & Ready to Learn

Control

NO INTERVENTION

The 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.

Rested & Ready to Learn

Eligibility Criteria

Age4 Years - 6 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

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

Location

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

Locations