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Behavioral Intervention
Meditation App for Stress Management
N/A
Waitlist Available
Research Sponsored by University of Illinois at Chicago
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
At least 18 years old
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 and 6 month
Awards & highlights
No Placebo-Only Group
Summary
This trial aims to see if a 1-month meditation program using a mobile app can be successfully used by officers and professionals working with young people in the legal system.
Who is the study for?
This trial is for officers and professionals working with youth in the juvenile legal system. It's designed to see if using a meditation app can help them manage emotions, depression, burnout, and anxiety over one month.
What is being tested?
The trial is testing two app-based meditation programs: Resource+ and Action In Mindfulness (AIM)+. Participants will use these apps regularly to explore their effectiveness in improving mental well-being.
What are the potential side effects?
Since this trial involves meditation apps, there are no direct medical side effects expected. However, participants may experience increased awareness of personal stress or emotional discomfort initially.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 18 years old or older.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 and 6 month
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 and 6 month
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
App adherence
Secondary study objectives
Acceptability
Appropriateness
Feasibility of App Implementation
+3 moreOther study objectives
Alcohol use
Anger
Anxiety
+8 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Action In Mindfulness (AIM)+Experimental Treatment1 Intervention
Participants randomized to the intervention arm will receive the AIM+ mindfulness meditation app.
Group II: Resource+Active Control1 Intervention
Participants randomized to the active control arm will receive the Resource+ informational resource app.
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Who is running the clinical trial?
University of Illinois at ChicagoLead Sponsor
638 Previous Clinical Trials
1,569,079 Total Patients Enrolled
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7,445 Patients Enrolled for Depression
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