NCT06555172

Brief Summary

This feasibility clinical trial aims to assess the feasibility of implementing a 1-month app-based meditation program with officers in the juvenile legal system and other professionals working directly with legal-involved youth.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P25-P50 for not_applicable anxiety

Timeline
Completed

Started Nov 2024

Typical duration for not_applicable anxiety

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 12, 2024

Completed
3 days until next milestone

First Posted

Study publicly available on registry

August 15, 2024

Completed
3 months until next milestone

Study Start

First participant enrolled

November 21, 2024

Completed
1.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2026

Completed
Last Updated

February 10, 2025

Status Verified

February 1, 2025

Enrollment Period

1.4 years

First QC Date

August 12, 2024

Last Update Submit

February 6, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • App adherence

    Days of objective app usage

    1 month

Secondary Outcomes (6)

  • Acceptability

    1 month

  • Appropriateness

    1 Month

  • Feasibility of App Implementation

    1 month

  • Usability

    1 month

  • Satisfaction with intervention

    1 month

  • +1 more secondary outcomes

Other Outcomes (13)

  • Anxiety

    baseline, 1 month, 6 months

  • Depression

    baseline, 1 month, 6 months

  • Workplace burnout

    baseline, 1 month, 6 months

  • +10 more other outcomes

Study Arms (2)

Action In Mindfulness (AIM)+

EXPERIMENTAL

Participants randomized to the intervention arm will receive the AIM+ mindfulness meditation app.

Behavioral: Action In Mindfulness (AIM)+

Resource+

ACTIVE COMPARATOR

Participants randomized to the active control arm will receive the Resource+ informational resource app.

Behavioral: Resource+

Interventions

AIM+ is a smartphone-based app that teaches mindfulness meditation to professionals working with legal-involved youth over a 30-day "path." Each day of the path consists of a brief (approximately 5- to 10-minute) audio-guided meditation practice, with brief videos interspersed to illustrate key concepts and promote engagement. In addition to the 30 daily path files, users have access to a menu of "to go" audio-guided meditation practices that they can use as relevant to their workday (e.g., for professionals to listen to before attending a meeting). AIM+ also includes a menu of audio-guided meditation practices that officers can share with the youth on their caseloads (e.g., for youth to listen to before attending court).

Action In Mindfulness (AIM)+
Resource+BEHAVIORAL

Resource+ is a smartphone-based app that is matched to AIM+ for time and structure, but it includes information on community resources that professionals can provide to the youth with whom they work in place of the meditation content featured in AIM+.

Resource+

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Currently working with youth in the juvenile legal system or related juvenile services and programming
  • English speaking
  • Able to understand and provide consent
  • At least 18 years old
  • Have an Android or Apple smartphone

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Illinois Chicago

Chicago, Illinois, 60612, United States

RECRUITING

Related Publications (1)

  • Kendall AD, Pela E, Amonica D, Jaworski E, Floyd B; AIM+ Community Advisory Board. Feasibility Testing a Meditation App for Professionals Working With Youth in the Legal System: Protocol for a Hybrid Type 2 Effectiveness-Implementation Pilot Randomized Controlled Trial. JMIR Res Protoc. 2025 Apr 24;14:e71867. doi: 10.2196/71867.

MeSH Terms

Conditions

Anxiety DisordersDepressionBurnout, ProfessionalEmotional Regulation

Interventions

MindfulnessHealth Resources

Condition Hierarchy (Ancestors)

Mental DisordersBehavioral SymptomsBehaviorOccupational StressOccupational DiseasesBurnout, PsychologicalStress, PsychologicalSelf-ControlSocial Behavior

Intervention Hierarchy (Ancestors)

Cognitive Behavioral TherapyBehavior TherapyPsychotherapyBehavioral Disciplines and ActivitiesHealth PlanningHealth Care Economics and OrganizationsDelivery of Health CareHealth Care Quality, Access, and Evaluation

Central Study Contacts

Ashley D Kendall, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: Participants will be individually randomized at a 1:1 ratio to 1 of 2 smartphone app conditions: (1) AIM+, a 30-day mindfulness meditation app, or (2) Resource+, a 30-day informational app that is matched to AIM+ for time and structure but provides information on local resources relevant to youth.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

August 12, 2024

First Posted

August 15, 2024

Study Start

November 21, 2024

Primary Completion

April 1, 2026

Study Completion

April 1, 2026

Last Updated

February 10, 2025

Record last verified: 2025-02

Data Sharing

IPD Sharing
Will share

De-identified data may be placed in one or more electronic databases which could be used for other research studies

Shared Documents
STUDY PROTOCOL
Time Frame
Data sharing will generally coincide with publication of the study's main findings and is intended to take place within 1 year after acceptance of the primary manuscripts.
Access Criteria
To be determined

Locations