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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05268796
Other study ID # AR210221
Secondary ID
Status Recruiting
Phase Phase 2/Phase 3
First received
Last updated
Start date January 2024
Est. completion date June 2026

Study information

Verified date January 2024
Source Stanford University
Contact Scott Hall, PhD
Phone 650-498-4799
Email hallss@stanford.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the research is to determine whether parent-mediated behavior therapy for challenging behavior commonly displayed by children with autism spectrum disorder (ASD) can be as effective when delivered via telehealth as when delivered in-person.


Recruitment information / eligibility

Status Recruiting
Enrollment 90
Est. completion date June 2026
Est. primary completion date June 2026
Accepts healthy volunteers No
Gender All
Age group 3 Years to 5 Years
Eligibility Inclusion criteria: 1. Child is aged 3 years, 0 months to 5 years, 11 months inclusive 2. Child has a diagnosis of ASD (confirmed by diagnostic report) 3. Child is reported to exhibit at least one form of daily or hourly self-injurious behavior and/or aggressive behavior on the Behavior Problems Inventory -Short Form (BPI-S). 4. Family lives in one of the following counties in New Mexico and Texas: Bernalillo, Santa Fe, Valencia, Sandoval, Torrance, Socorro, Cibola, Los Alamos, El Paso, Hudspeth, Otero, or Dona Ana 5. Caregiver is comfortable speaking and reading in English 6. The child's primary caregiver is at least 21 years old. 7. The same caregiver is consistently available for one hour per week for a 12-week period in their home with their child between 9am and 7pm Monday through Friday to take part in the research 8. The child's primary caregiver is willing to adhere to the study intervention regimen and be willing to have a clinician come into their home for 1 hour per week for 12 weeks. 9. Family lives in an area with consistent cell phone coverage Exclusion criteria: 1. Caregiver is currently receiving ABA services or direct parent coaching to manage their child's challenging behaviors 2. Child engages in behavior that may inflict moderate to severe damage on the individual or on other people (e.g. biting through the skin, eye gouging, fracturing bones, significant damage to property) with minor or major medical intervention required. 3. Child has a sensory or physical impairment that precludes participation (e.g., epilepsy, vision or hearing impairment) or has a diagnosis of another genetic condition (e.g., fragile X syndrome) 4. Activity restrictions that limit caregiver's ability to respond to their child's challenging behaviors 5. Child has an underlying medical condition that is better treated with medical intervention 6. Child only exhibits pica at a daily or hourly frequency 7. Child has a sibling or twin already participating in the study

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Behavior therapy
Caregivers will be coached either in-person or via telehealth to implement function-based behavioral treatment in 1-hour sessions each week with their child over 12 weeks.
Other:
Psychoeducation
Caregivers will complete online education modules in 1-hour sessions each week over 12 weeks.

Locations

Country Name City State
United States Behavior Change Institute Alamogordo New Mexico
United States Stanford University Stanford California

Sponsors (3)

Lead Sponsor Collaborator
Stanford University Behavior Change Institute, United States Department of Defense

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Frequency of challenging behavior In-session observations of challenging behavior 4 week intervals
Primary Parenting Stress Index Severity of parent stress Previous 4 weeks
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