RECRUITING

In-Person Mindfulness-based Intervention for Adolescents with Autism Spectrum Disorder and Their Caregivers

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

Adolescents with ASD often have co-occurring mental health symptoms like stress, anxiety, and depression. The investigators are conducting this research study to develop interventions for adolescents with ASD that will improve co-occurring mental health symptoms.

Official Title

In-Person Mindfulness-based Intervention for Adolescents with Autism Spectrum Disorder and Their Caregivers

Quick Facts

Study Start:2024-08-14
Study Completion:2026-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06577623

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:13 Years to 18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adolescents must be ages 13 to 18 years
  2. * Formal clinical or educational ASD diagnosis confirmed by the study team (i.e., review of the formal diagnostic or educational report)
  3. * Must be able to attend at least 7 of the 8 in-person group meetings
  4. * English speaking: Adolescents and their parent/caregivers must be English-speaking because the screening and behavioral measures are in English, as well as the intervention content
  1. * Non-verbal participants will be excluded to ensure test compliance and increase sample homogeneity.
  2. * Participants with IQ scores \<70 will be excluded because the intervention was developed for individuals without intellectual disabilities.
  3. * Participants with a physical disability or co-occurring condition that may prevent participation in the weekly group meetings (e.g., selective mutism; aggressive behavior; inability to participate in a 90-minute video conference meeting each week)
  4. * Participants who report active suicidal ideation

Contacts and Locations

Study Contact

Nicole Matthews, Ph.D.
CONTACT
480-582-9499
nmatthews@autismcenter.org

Principal Investigator

Nicole Matthews, Ph.D.
PRINCIPAL_INVESTIGATOR
Southwest Autism Research & Resource Center

Study Locations (Sites)

Southwest Autism Research and Resource Center
Phoenix, Arizona, 85006
United States

Collaborators and Investigators

Sponsor: Southwest Autism Research & Resource Center

  • Nicole Matthews, Ph.D., PRINCIPAL_INVESTIGATOR, Southwest Autism Research & Resource Center

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 Date2024-08-14
Study Completion Date2026-12

Study Record Updates

Study Start Date2024-08-14
Study Completion Date2026-12

Terms related to this study

Additional Relevant MeSH Terms

  • Autism Spectrum Disorder
  • Autism