Assessing the Effectiveness of Reciprocal Imitation Teaching in Part C Early Intervention Settings (Sprout Study)
Autism Spectrum Disorder
About this trial
This is an interventional treatment trial for Autism Spectrum Disorder focused on measuring ASD, Autism
Eligibility Criteria
Inclusion Criteria:
EI Providers:
- Speak and read English
- Work at a participating Part C practice or agency
- Have an active caseload that includes at least two children with ASD or suspected ASD
- Are willing to invite families to participate in this study
Caregivers and Toddlers (recruited from EI provider caseloads):
- Caregivers speak and read English or Spanish
- Caregivers are at least 18 years of age
- Caregivers are willing and able to participate in intervention sessions and research tele-visits that are video-recorded by research staff
- Child receives services from one of the participating agencies and attends regular sessions with the enrolled provider
- Child is between 18 and 30 months of age at study entry
- Child has a diagnosis of ASD or displays social communication impairments consistent with ASD
Exclusion Criteria:
• Child has no severe visual, auditory, or physical impairments and no serious medical, genetic, or neurological conditions that would impede their ability to engage in RIT.
Sites / Locations
- University of WashingtonRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
RIT Training Group
Daily Routines
Providers in the RIT group (n=30) will receive an 8-hour virtual workshop (2 half-days) on RIT implementation and caregiver coaching. Each provider will invite 2 families in their caseload to participate in the study. Providers will coach families in the use of RIT. One intervention session for each enrolled family will be videotaped and scored for RIT fidelity.
Providers in the Routines Control group (n=30) will receive a 3-hour virtual workshop focused on helping providers coach caregivers on how to increase children's participation and social engagement during everyday home routines (i.e., snack time, bedtime, bath time, and family playtime). Each provider will invite 2 families in their caseload to participate in the study. One intervention session for each enrolled family will be videotaped and scored for RIT fidelity to ensure contamination has not occurred and the control condition providers are not utilizing RIT strategies.