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Online mindfulness program for autistic teens and their caregivers

Tests a mindfulness program for easing depression and anxiety in autistic teenagers.

Plain-language title generated from the registry record
Registry title: Telehealth Mindfulness-based Intervention for Adolescents With Autism Spectrum Disorder and Their Caregivers

Key facts

Where
Phoenix, United StatesSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 13 and 18 years old?

Source: NCT07501286, who can take part

Where in United States

  • Southwest Autism Research & Resource CenterPhoenix, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Nicole Matthews, Ph.D.
Trial code
NCT07501286
Record updated
30 March 2026
Original description
The goal of this clinical trial is to learn whether a mindfulness-based intervention can reduce depression and anxiety in autistic adolescents. The main question this trial aims to answer is: Do adolescents who complete MINDful TIME show reductions in depression and anxiety compared to an active control group? Researchers will compare adolescents who complete MINDful TIME to adolescents who are instructed to use a mindfulness meditation mobile-app to see if changes in anxiety and depression differ between the two groups.Read full original descriptionShow less

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

The goal of this clinical trial is to learn whether a mindfulness-based intervention can reduce depression and anxiety in autistic adolescents. The main question this trial aims to answer is: Do adolescents who complete MINDful TIME show reductions in depression and anxiety compared to an active control group? Researchers will compare adolescents who complete MINDful TIME to adolescents who are instructed to use a mindfulness meditation mobile-app to see if changes in anxiety and depression differ between the two groups.

Participants will either:

* Attend weekly 90-minute MINDful TIME group meetings through Zoom with their parent or caregiver for a total of 8-weeks and use a mindfulness meditation app daily, or * Use a mindfulness meditation app daily for 8-weeks

All participants will:

* Attend virtual intake, baseline, and follow-up visits to complete data collection * Complete a weekly electronic meditation diary

Inclusion: 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: 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); 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 who report active suicidal ideation.

ClinicalTrials.gov NCT07501286