Testing the Effectiveness and Implementation of a Meditation App for Youth in the Legal System
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Bodhi AIM (intervention group), HIB (control group).
- Who it may be relevant to
- Registry conditions: Behavioral Health. Basic parameters: 13 years — 20 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Effectiveness and Implementation of a Meditation App Addressing Substance Use, Sexual Health, and Emotion Regulation Among Legal-Involved Youth
Overview
The goals of this hybrid type 2 randomized controlled trial (RCT) are to evaluate the effectiveness and individual-level implementation of a 1-month app-based meditation program with youth on probation in Cook County, IL. The primary questions it is designed to answer are: 1. Is the meditation app associated with improvements in behavioral health outcomes including cannabis use problems? 2. Do improvements in emotion regulation appear to mediate the effects of the meditation app on these behavioral health outcomes? 3. Will youth adequately adhere to the meditation app?
Detailed description
This remote study will enroll 300 youth on probation in Cook County, IL, which encompasses Chicago and its surrounding suburbs. Youth will be individually randomized to use either the meditation app or an active control app matched for time/structure daily for 30 days. Health outcomes will be self-reported at baseline, 1 month, and 6 months, and in real time via 1-week "bursts" of ecological momentary assessment (EMA) at baseline and 1 month (i.e., approximately overlapping with the last week of app use). Objective adherence to both apps will be captured automatically via in-app analytics.
Interventions
- Behavioral Bodhi AIM (intervention group)
AIM (Action In Mindfulness) is a smartphone app that teaches users to establish a daily meditation practice via a 30-day "path," with each day consisting of a brief audio- or video-guided file. In addition to the 30 daily path files, users have access to a menu of "to go" audio-guided meditation practices that they may access any time to prepare for particular situations. - Behavioral HIB (control group)
HIB (Health In Balance) is a smartphone app that is matched to AIM for time and structure, but includes health promotion content (e.g., educational information on substance use) in place of the meditation content featured in AIM. Like AIM, HIB includes a 30-day "path" of audio and video files, along with a menu of "to go" audio files that users may access any time to review key intervention concepts.
Primary outcome measures
- Cannabis use problems [Time frame: baseline, 1 month, 6 months]
- App adherence [Time frame: 1 month]
Secondary outcome measures (9)
- Sexual behaviors [Time frame: baseline, 1 month, 6 months]
- Negative mood regulation [Time frame: baseline, 1 month, 6 months]
- Anxiety [Time frame: baseline, 1 month, 6 months]
- Depression [Time frame: baseline, 1 month, 6 months]
- Self-efficacy [Time frame: baseline, 1 month, 6 months]
- Alcohol use problems [Time frame: baseline, 1 month, 6 months]
- Real-time mood states [Time frame: baseline, 1 month]
- Real-time cannabis use [Time frame: baseline, 1 month]
- Real-time alcohol use [Time frame: baseline, 1 month]
Eligibility criteria
Inclusion criteria
- 13-20 years old
- In probation programming (i.e., in legal programming but not detained) in Cook County
- Have access to an Apple/Android smartphone
- Understand and provide assent/consent
- Have legal guardian permission (if under 18 years old)
- English-speaking, due to norming of instruments
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Prevention
Study locations
United States · 1 center
- University of Illinois at Chicago — Chicago
Identifiers
NCT: NCT06997120 · 2025-0066 · R01DA061795