Efficacy of the ASD Screening and Parent ENgagement (ASPEN) Intervention Program in Low-Resource Communities

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The ASD Screening and Parent ENgagement (ASPEN) program is a culturally adapted, parent-mediated intervention program. The ASPEN program is tailored to address social communication and behavioral difficulties that young children with developmental delays may experience in early childhood. The ASPEN Program includes 12 sessions where parents are provided with psychoeducation about self-care, child development, and evidence-based strategies. Coaching is also provided to train parents on using evidence-based strategies within the home setting. The ASPEN program is delivered by a student clinician and a peer leader. We hypothesize that coaching strategies delivered by the clinician will lead to primary family caregivers learning evidence-based strategies and this will result in improved child outcomes. We hypothesize that education and family support delivered by peer leaders will help primary family caregivers learn social support strategies and this will lead to improved parent outcomes.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 1
Maximum Age: 6
Healthy Volunteers: f
View:

• Child is between 18 months through 6 years of age

• Child has a medical diagnosis or educational classification of Autism or Autism Spectrum Disorder (ASD) or child is at-risk for Autism/ASD as determined by the Modified-Checklist for Autism in Toddlers - Revised/Follow-up Interview (M-CHAT-R/F) and/or Social Communication Questionnaire (SCQ)

• Child resides in a low-resource household as determined by at least one of the following criteria:

• -Child or family has Medicaid as an insurance provider

• -Child's primary caregiver has achieved a high school or lower education

• -Child resides in a household with an annual income of 200% of the Federal Poverty Level

Locations
United States
Texas
University of Texas at Austin
RECRUITING
Austin
Contact Information
Primary
Sandra B Vanegas, PhD
sandra.vanegas@austin.utexas.edu
5122454579
Backup
Sandy Magaña, PhD, MSW
smagana@austin.utexas.edu
5122329216
Time Frame
Start Date: 2020-07-07
Estimated Completion Date: 2025-09-29
Participants
Target number of participants: 320
Treatments
Experimental: Intervention Group
The intervention group will receive a parent manual, a resource packet, and 12 weekly sessions delivered by the clinician and peer leader.
No_intervention: Control Group
The control group will receive a parent manual and a resource packet. Four phone check-ins will be conducted across 12-14 weeks to address questions by the research team.
Authors
Sandra B Vanegas
Related Therapeutic Areas
Sponsors
Collaborators: National Institute on Disability, Independent Living, and Rehabilitation Research
Leads: University of Texas at Austin

This content was sourced from clinicaltrials.gov