Clinical trial Recruiting at 1 site Interventional Ages 13 to 18

Telehealth mindfulness program for adolescents with autism and their caregivers

Official title: Telehealth Mindfulness-based Intervention for Adolescents With Autism Spectrum Disorder and Their Caregivers

Run by Southwest Autism Research & Resource Center · NCT07501286 · Data updated 2026-11-12

This study tests whether an 8-week telehealth group mindfulness program plus daily app use can reduce depression and anxiety in autistic adolescents compared with using a mindfulness app alone.

More Autism Spectrum Disorder trials

Quick facts

Study typeInterventional
Ages13 Years to 18 Years
SexAll
Enrollment160 (estimated)
SponsorSouthwest Autism Research & Resource Center
Academic / other
Locations1 site (Phoenix, Arizona)
StatusRecruiting
StartedMarch 24, 2026
Main results expectedNovember 2027
Study endsFebruary 2028
Registry record updatedMarch 30, 2026
Trial IDNCT07501286 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adolescents aged 13–18 with a confirmed ASD diagnosis, who are verbally communicative, have IQ ≥70, speak English, and have a caregiver able to participate are the ideal candidates.

Probably not a fit

Non-verbal adolescents, those with intellectual disability (IQ <70), or individuals with physical or co-occurring conditions that prevent participation are unlikely to benefit from this specific intervention as tested.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized interventional trial compares an 8-week MINDful TIME program—weekly 90-minute Zoom group sessions attended by the adolescent together with a parent or caregiver plus daily app practice—against an active control of daily use of a mindfulness meditation mobile app. Participants complete virtual intake, baseline, weekly electronic meditation diaries, and follow-up visits conducted remotely. Eligibility is limited to English-speaking, verbally communicative adolescents aged 13–18 with a confirmed ASD diagnosis and IQ ≥70, and caregivers must be available to join sessions. The trial is run through the Southwest Autism Research & Resource Center with data collected entirely via telehealth visits and electronic measures.

Why it matters

Potential benefit: If successful, the intervention could reduce anxiety and depression symptoms in autistic adolescents and improve coping skills while also providing structured caregiver support.

How similar studies have gone: Small pilot studies and feasibility trials of mindfulness approaches in autistic youth have shown promise for reducing anxiety and improving mood, but larger randomized comparisons remain limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adolescents must be ages 13 to 18 years
* Formal clinical or educational ASD diagnosis confirmed by the study team (i.e., review of formal diagnostic report from the diagnosing practitioner or Multidisciplinary Evaluation Team report (MET) shared with the research team by the family) )
* Must be willing to be randomized to a treatment or delayed treatment control group
* Must be able to attend at least 7 of the 8 group meetings
* 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

Exclusion Criteria:

* Non-verbal participants will be excluded to ensure test compliance and increase sample homogeneity.
* Participants with IQ scores \<70 will be excluded because the intervention was developed for individuals without intellectual disability.
* 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)
* Participants who report active suicidal ideation

Where it's running

  • Southwest Autism Research & Resource Center
    Phoenix, Arizona, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.