Education Program for Caregivers of Children With Gross Motor Delays

Three for the Under Three

The main objective of this project is to determine whether an educational intervention delivered via social media can improve parent understanding of child development and progression in child's developmental goals. A secondary objective is to determine whether this intervention can improve parent-related outcomes, such as well-being, parent-child bonding, attitudes toward parenting, satisfaction with the educational program.

Study Overview

• Status: Completed
• Conditions: Gross Motor Development Delay
• Intervention / Treatment: Behavioral: Parent Educational Program

Detailed Description

Gross motor delays in childhood are common, though they vary in severity and outcome. Early detection and intervention are critical to promote best neurodevelopmental outcomes for these children; equally important is support for parents and/or caregivers of children with identified motor delays. Parent education programs for caregivers of children with gross motor delays have been shown to improve parent knowledge of motor development and decrease parental stress when offered in conjunction with physical therapy treatment, however, there is a lack of peer-reviewed evidence demonstrating the efficacy of educational interventions provided over a social media platform for the population targeted in this study.

Caregivers of children with gross motor delays will be randomized to receive an educational intervention delivered via social media over a 9 week period, or to receive the intervention after a 9 week waiting period.

• Study Type: Interventional
• Enrollment (Actual): 92
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • Georgia
    • Atlanta, Georgia, United States, 30322
      • Children's Healthcare of Atlanta
    • Atlanta, Georgia, United States, 30322
      • Emory University
    • Atlanta, Georgia, United States, 30322
      • Emory Healthcare System

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 14 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Parent or legal guardian of child under 3 years with an identified motor delay
• Access to device with high-speed internet to access Facebook
• English speaking
• Resides in the continental United States

Exclusion Criteria:

• Non-English-speaking

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Parent Educational Program; Caregivers of children with gross motor delays who are randomized to receive an educational intervention delivered through social media.	Behavioral: Parent Educational Program; The intervention is a series of 9 educational modules delivered via social media that will teach participants: 1) principles of infant learning, 2) principles of infant motor learning, and 3) principles of positive parenting.
No Intervention: Control Group; Caregivers of children with gross motor delays who are randomized to the waitlist control group who will receive an educational intervention delivered through social media after a 9 week waiting period.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in Child Development Understanding Score	Parent understanding of child development will be measured using a 24-item questionnaire with true/false and multiple choice questions. Total scores range from 0 to 24 and higher scores indicate better understanding of child development.	Baseline, Week 9 (post-intervention)
Change in Child Development Goals	Progression in specific developmental goals will be measured qualitatively by asking parents what their motor goals are for their child at the baseline assessment and asking what improvement have been made for those goals following completion of the intervention. A score is not calculated for this assessment.	Baseline, Week 9 (post-intervention)
Change in Developmental Assessment of Young Children - Second Edition (DAYC-2) Gross Motor Subdomain Score	Progression in child's developmental goals are measured with administration of the Gross Motor Subdomain of the DAYC-2 instrument. Children are assessed on age appropriate gross motor skills and items receive a score of 1 if the child exhibits the skill or a score of 0 if the skill is not exhibited or is exhibited inconsistently. The number of items varies based on the age of the child. Raw scores are standardized and the standardized scores correspond with a descriptive term, where scores less than 70 = Very Poor, scores of 70-79 = Poor, scores of 80-89 = Below Average, scores of 90-110 = Average, scores of 111-120 = above average, scores of 121-130 = superior, and scores greater than 130 are Very Superior.	Baseline, Week 9 (post-intervention)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in Parenting Stress Index, Fourth Edition Short Form (PSI-4-SF) Score	To assess parental stress, the PSI-4-SF yields scores on the following subscales: 1) Parental Distress, 2) Parent-Child Dysfunctional Interaction, and 3) Difficult Child. The instrument has 36 items which are responded to on a 5-point scale ranging from Strongly Agree to Strongly Disagree. A Total Stress Score is obtained by combining the subscales. The software to score the PSI-4-SF provides a percentile score. Percentile scores between 16 and 84% are considered normal stress, while scores of 85-89% indicate high stress and scores of 90% or higher indicate stress levels that may be clinically significant.	Baseline, Week 9 (post-intervention)
Change in Mother-to-Infant Bonding Scale (MIBS) Score	The Mother-to-Infant Bonding Scale (MIBS) is an 8-item questionnaire in which the mother/caregiver self-reports her feelings towards her baby. Responses are given on a 4-point scale where 0 = not at all and 3 = very much. Total scores range from 0 to 24 and some items are reversed scored so that higher scores indicate worse bonding between mother and infant.	Baseline, Week 9 (post-intervention)
Change in Perceived Maternal Parenting Self-Efficacy (PMP S-E) Score	Attitude towards parenting is measured using the Perceived Maternal Parenting Self-Efficacy (PMP S-E) instrument. The PMP S-E is a 20-item Likert scale survey asking parents to rate personal importance/value of parenting and confidence in parenting choices. Responses are given on a 4-point scale where 1 = strongly disagree and 4 = strongly agree. Total scores range from 20 to 80 and higher scores indicate greater parenting self-efficacy.	Baseline, Week 9 (post-intervention)
Change in Satisfaction with Learning Content	Parent satisfaction with the program will be assessed with weekly surveys asking participants to respond to 15 statements to measure how well they liked the content and delivery method of the educational modules. Responses are given on a 5-point scale where 1 = strongly disagree and 5 = strongly agree. Total scores range from 15 to 75, where higher scores indicate greater satisfaction with the learning content.	Up to Week 9
Satisfaction with the Intervention	Parent satisfaction with the program will be assessed qualitatively through facilitated discussions at the conclusion of the intervention period. This assessment of satisfaction is not measured quantitatively and a score is not calculated.	Week 9 (post-intervention)

Collaborators and Investigators

• Sponsor: Emory University
• Investigators: Principal Investigator: Nathalie Maitre, MD, PhD, Emory University

Study record dates

Study Major Dates

• Study Start (Actual): September 28, 2022
• Primary Completion (Actual): November 2, 2023
• Study Completion (Actual): November 2, 2023

Study Registration Dates

• First Submitted: September 13, 2022
• First Submitted That Met QC Criteria: September 13, 2022
• First Posted (Actual): September 15, 2022

Study Record Updates

• Last Update Posted (Actual): February 20, 2024
• Last Update Submitted That Met QC Criteria: February 19, 2024
• Last Verified: February 1, 2024

More Information

Terms related to this study

• Other Study ID Numbers: Study00004252

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No