Actively Recruiting

Phase 1
Phase 2
Age: 13Years - 17Years
All Genders
NCT06831123

Pathways 2 Success

Led by University of Minnesota · Updated on 2026-04-13

120

Participants Needed

1

Research Sites

102 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study involves a 3-arm randomized controlled trial designed to investigate the feasibility and acceptability of three preventive interventions designed to reduce risk for escalations in adolescent conduct problems. High school students identified to be at risk for conduct problems will be randomly assigned to one of three intervention options, including a mindfulness-based program, a mindfulness-based program augmented by a new mobile app, and a life skills program. Assessments related to intervention outcomes will be completed by adolescents, parents/guardians, and teachers at baseline, 2 weeks post-intervention, and at a 3-month follow-up.

CONDITIONS

Official Title

Pathways 2 Success

Who Can Participate

Age: 13Years - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • A 9th or 10th grade student in a partner school district
  • Referred due to elevated social/emotional risk on a screening tool or concerns about conduct problems at school
  • Adolescents and their parents must be fluent in English
Not Eligible

You will not qualify if you...

  • Currently receiving special education services due to behavioral or emotional disturbance
  • Diagnosed with autism spectrum disorder, pervasive developmental disorders, developmental/intellectual disability, or serious psychiatric disorders requiring specialized mental health treatment such as psychosis, bipolar disorder, or substance use disorder

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Minnesota

Minneapolis, Minnesota, United States, 55414

Actively Recruiting

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Research Team

N

Nicole Morrell

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

3

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