Impact of Bedtime Routines on Sleep and Development in Toddlers

Sponsor
Saint Joseph's University, Philadelphia (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT04592172
Collaborator
Temple University (Other), Simms/Mann Family Foundation (Other), CuddleBright Cares (Other), Johnson & Johnson Consumer Inc. (J&JCI) (Industry)
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Study Details

Study Description

Brief Summary

Investigators will recruit up to 100 families (children aged 12.0 to 14.9 months and their primary caregivers) at their scheduled 12-month well child care infant visit at Temple Pediatric Care. The purpose of this randomized controlled trial is to examine the impact of implementation of a bedtime routine program, Connect, Calm, & Comfort: 3 Cs for Bedtime ZZZs, to promote better sleep and improve developmental outcomes in toddlers from primarily low-income families.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Bedtime Routine Education
N/A

Detailed Description

A bedtime routine is a key factor in the promotion of not only healthy sleep, but also potentially of broad development and wellbeing in early childhood. A bedtime routine, in and of itself, embodies the characteristics of nurturing care and early child stimulation especially for at-risk children. It is consistent with the Lancet Early Childhood Series Steering Committee emphasizing the need for nurturing care, which includes adequate health, nutrition, security and safety, responsive caregiving, and early learning opportunities, to help young children (ages 0-5 years) reach their full developmental potential, and to build a strong foundation for subsequent development, health, and wellbeing. Common, adaptive components of a bedtime routine can contribute to an array of positive developmental outcomes beyond improved sleep, inclusive of language development, literacy, child emotional and behavioral regulation, parent-child attachment, and family functioning, among other outcomes. Although studies have been conducted on the relationship between bedtime routines and sleep, there have been few studies looking at bedtime routines and other developmental outcomes.

Study Design

Study Type:
Interventional
Actual Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
100 caregiver-infant dyads (infants ages 12.0 to 14.9 months) will be recruited from Temple Pediatric Care Outpatient Pediatric office with follow-up visits at approximately 15 and 24 months of age.100 caregiver-infant dyads (infants ages 12.0 to 14.9 months) will be recruited from Temple Pediatric Care Outpatient Pediatric office with follow-up visits at approximately 15 and 24 months of age.
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Impact of Bedtime Routines on Sleep and Development in Toddlers
Actual Study Start Date :
Nov 20, 2020
Anticipated Primary Completion Date :
Nov 1, 2022
Anticipated Study Completion Date :
Nov 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Bedtime Routine Education

50 families will be randomly assigned to receive the bedtime routine intervention, 3 Cs for Bedtime ZZZs delivered by research assistants at the 12-month and 15-month well-child visits, in additional to receiving usual clinical care. The intervention will take approximately 30-45 minutes to implement at each study visit. Research assistants will be trained and supervised by board-certified Behavioral Sleep Medicine providers. This intervention focuses on developing an individualized bedtime routine, including such activities as a bath, teeth-brushing, reading stories, singing songs, and cuddling, based on parent's preferences. Families will receive appropriate materials for their bedtime routine, including a CuddleBright kit, bedtime books, toothbrush/toothpaste, and the created bedtime chart to take home.

Behavioral: Bedtime Routine Education
The intervention aims to promote healthy sleep and improved developmental outcomes in infants. Individualized bedtime routine education, including such activities as a bath, teeth-brushing, reading stories, singing songs, and cuddling will be implemented by research assistants at the 12-month well-child visit. Reinforcement of the bedtime routine education will be implemented at the 15-month visit. Each individualized bedtime routine will incorporate 3-5 steps and a bedtime routine chart depicting those steps will be created and provided to the families. Families will receive materials for their bedtime routines, including a CuddleBright kit, 1-2 additional bedtime books, toothbrush/toothpaste , and the created bedtime chart. On top of that, families will also receive a children's book provided by Reach Out and Read through the study period.

No Intervention: Control group

50 families will be randomly assigned to control group (usual care).

Outcome Measures

Primary Outcome Measures

  1. Change in sleep outcomes [15-month and 24-month visits]

    Caregivers will report on their toddlers sleep in the previous 2 weeks at baseline (12 months of age) and at 15-months and 24-months, using the well-validated and widely used Brief Infant Sleep Questionnaire-Revised (Short Form) (BISQ-R). The BISQ-R contains items related to the child sleep environment (e.g., sleep space, location, and arrangement) and patterns (e.g., bedtime, sleep onset latency, night awakening frequency and duration, wake time). Items also assess caregiver-perceived child sleep problems (e.g., overall sleep problem severity, bedtime resistance severity). The BISQ-R has 3 subscales, Infant Sleep, Parent Behavior, and Parent Perception. Scores range from 0-100, with higher scores denoting better sleep.

Secondary Outcome Measures

  1. Developmental outcomes [15-month and 24-month visits]

    The Ages & Stages Questionnaires (ASQ) is an age-specific, reliable and well-validated measure to predict developmental outcomes. Caregivers will report on their infant/child's communication and personal-social skills. Each domain consists of 6 questions and each question is scored with 10 points for "yes," 5 for "sometimes," and 0 for "no," yielding scores ranging from 0 to 60 for each domain. Lower scores denote potential developmental concerns.

  2. Socio-emotional outcomes [15-month and 24-month visits]

    The Brief Infant-Toddler Social and Emotional Assessment (BITSEA) is a screener derived from the longer ITSEA. It is a parent questionnaire that assesses the social-emotional development of children ranging in age from 12 to 36 months. Caregivers will rate each statement that best describes the child's behavior in the past month, with scores ranging from 0 to 84. Higher scores denote possible social-emotional/ behavioral concerns.

  3. Parent stress [15-month and 24-month visits]

    The Parenting Stress Index (PSI) Short form is a 36-items reliable measure to assess total parenting stress with high internal consistency. It consists of three subscales: parental distress, parent-child dysfunctional interaction, and difficult child. Statements on this measure are rated on a 5-point Likert scale from strongly agree to strongly disagree, with scores ranging from 36 to 180. Higher scores denote higher level of stress in parent-child relationship.

  4. Treatment acceptability [15-month and 24-month visits]

    Caregivers randomized to the bedtime routine education arm will complete the treatment acceptability/bedtime routine evaluation form. Caregivers will rate 7 statements related to the perceived helpfulness/efficacy and acceptability of the intervention using a 5-point Likert scale from strongly disagree to strongly agree, with total scores ranging from 0 to 35. Higher scores indicate higher perceived helpfulness and acceptability of the intervention.

Eligibility Criteria

Criteria

Ages Eligible for Study:
12 Months to 15 Months
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Presenting to a well child visit

  • Child between 12.0 to 14.9 months of age

  • English-speaking

  • Caregiver is legal guardian of infant

  • Caregiver is primary caregiver of infant

Exclusion Criteria:
  • Non-English speaking

  • Absence of primary caregiver at both the 12-month and 15-month well-child visit

Contacts and Locations

Locations

Site City State Country Postal Code
1 Temple Pediatrics Philadelphia Pennsylvania United States 19140

Sponsors and Collaborators

  • Saint Joseph's University, Philadelphia
  • Temple University
  • Simms/Mann Family Foundation
  • CuddleBright Cares
  • Johnson & Johnson Consumer Inc. (J&JCI)

Investigators

  • Principal Investigator: Megan Heere, MD, Temple University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Saint Joseph's University, Philadelphia
ClinicalTrials.gov Identifier:
NCT04592172
Other Study ID Numbers:
  • 2020-02
First Posted:
Oct 19, 2020
Last Update Posted:
May 10, 2022
Last Verified:
May 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 10, 2022