Mindfulness eases anxiety in teens with autism
NCT ID NCT06577623
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This study tested an in-person mindfulness program for adolescents with autism and their caregivers. The goal was to help reduce stress, anxiety, and depression. 28 teens and their caregivers took part in group sessions. The program aimed to improve mental health and well-being.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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28 people
The number who actually took part.
- Started
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Aug 2024
- Finished
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Jan 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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13 to 18 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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 the formal diagnostic or educational report) * Must be able to attend at least 7 of the 8 in-person 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 disabilities. * 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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Southwest Autism Research and Resource Center
Phoenix, Arizona, 85006, United States
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