Evaluating an interactive program for infants' gross motor development
The Effects of Playful Pathways, a Play-Based Developmentally Focused Group Program, and How it Affects Caregivers' Health Literacy and Self-Efficacy and Influences Outcomes for Infants
This study is testing an 8-week interactive program for infants aged 0-6 months and their caregivers to see if it helps improve their gross motor skills and overall development.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 10 (estimated) |
| Sex | All |
| Sponsor | Arkansas Colleges of Health Education Academic / other |
| Locations | 1 site (Fort Smith, Arkansas) |
| Trial ID | NCT06139549 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the effects of an 8-week interactive program designed for infants aged 0-6 months and their caregivers. The program focuses on enhancing gross motor development and involves group sessions where caregivers engage with their infants. Researchers will evaluate the infants before and after the program, as well as three months post-program, to identify any developmental delays and gather parent perceptions of the program's effectiveness. The study will include a small sample of 12 infants and their caregivers to explore physical, social, and emotional outcomes.
Who should consider this trial
Good fit: Ideal candidates for this study are infants aged 0-6 months, whether typically developing or with any diagnosis, along with their caregivers.
Not a fit: Patients who are older than 6 months or those who cannot participate in the interactive sessions may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly improve gross motor development in infants and enhance caregiver engagement.
How similar studies have performed: While this approach is relatively novel, similar programs targeting early motor development have shown promise in enhancing developmental outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
All babies typically developing or any diagnosis ages 0 - 6 months; parents/caregivers of babies typically developing or any diagnosis ages 0 - 6 months participating in the intervention. Sample size will be 12 babies ages 0-6 months and their caregivers (1-2 caregivers per baby). Total population 12 infants with up to 30 caregivers. Inclusion criteria: 1. All babies typically developing or any diagnosis ages 0 - 6 months Inclusion criteria for parents/caregivers: 1. At least 18 years of age 2. Able to communicate in and read English 3. Parent/caregiver of baby ages 0 - 6 months who is participating in the program 4. Ability to provide transportation to/from research site(s)
Where this trial is running
Fort Smith, Arkansas
- Arkansas Colleges of Health Education — Fort Smith, Arkansas, United States (Recruiting)
Study contacts
- Principal investigator: Allison N Young, DPT — Arkansas Colleges of Health Education
- Study coordinator: LaVona Traywick, PHD
- Email: lavona.traywick@achehealth.edu
- Phone: 4794016023
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.