RECRUITING

Telehealth-Enabled Versus In-Person Parent-Mediated Behavioral Treatment for Challenging Behaviors in Children With ASD

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Randomized Controlled Trial of Telehealth-Enabled Versus In-Person Parent-Mediated Behavioral Treatment for Challenging Behaviors in Children With Autism Spectrum Disorder

Quick Facts

Study Start:2024-01-05
Study Completion:2026-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05268796

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:2 Years to 7 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. 1. Child is aged 2 years 0 months to 7 years 11 months inclusive
  2. 2. Child has a documented diagnosis of ASD
  3. 3. Child exhibits at least one form of daily or hourly self-injurious behavior and/or aggressive behavior on the Behavior Problems Inventory - Short Form (BPI-S)71,72
  4. 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, McKinley, San Miguel, Eddy, Chaves, or Dona Ana.
  5. 5. Caregiver is comfortable speaking and reading in English
  6. 6. The child's caregiver is at least 21 years old
  7. 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. 8. 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. 9. Family lives in an area with consistent cell phone coverage
  1. 1. Caregiver is currently receiving ABA services or direct parent coaching to manage their child's challenging behaviors
  2. 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. 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. 4. Activity restrictions that limit caregiver's ability to respond to their child's challenging behaviors
  5. 5. Child has an underlying medical condition that is better treated with medical intervention
  6. 6. Child only exhibits pica at a daily or hourly frequency on the BPI-S
  7. 7. The caregiver has another child already participating in the study

Contacts and Locations

Study Contact

Scott Hall, PhD
CONTACT
650-498-4799
hallss@stanford.edu

Study Locations (Sites)

Stanford University
Stanford, California, 94305
United States
Behavior Change Institute
Alamogordo, New Mexico, 88310
United States

Collaborators and Investigators

Sponsor: Stanford University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-01-05
Study Completion Date2026-06

Study Record Updates

Study Start Date2024-01-05
Study Completion Date2026-06

Terms related to this study

Additional Relevant MeSH Terms

  • Autism Spectrum Disorder