Clinical trial Recruiting at 1 site Phase1; Phase2 Interventional Ages 13 to 17

Preventive interventions for at-risk high school students with conduct problems

Official title: Pathways 2 Success: A Study of School-Based Prevention Programs Supporting Positive Adolescent Development

Run by University of Minnesota · NCT06831123 · Data updated 2026-11-12

This study is testing three different programs to see if they can help high school students who are at risk for behavior problems feel better and make better choices.

Quick facts

PhasePhase1; Phase2
Study typeInterventional
Ages13 Years to 17 Years
SexAll
Enrollment120 (estimated)
SponsorUniversity of Minnesota
Academic / other
Locations1 site (Minneapolis, Minnesota)
StatusRecruiting
StartedMarch 12, 2025
Main results expectedFebruary 28, 2027
Study endsFebruary 28, 2027
Registry record updatedApril 13, 2026
Trial IDNCT06831123 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are 9th or 10th grade students in partner schools who have been identified as at risk for conduct problems.

Probably not a fit

Patients currently receiving special education services for behavioral or emotional disturbances or those with serious psychiatric disorders may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study is a randomized controlled trial that evaluates the feasibility and acceptability of three different preventive interventions aimed at reducing the risk of conduct problems in adolescents. High school students identified as at risk will be assigned to one of three groups: a mindfulness-based program, a mindfulness-based program enhanced with a mobile app, or a life skills program. Assessments will be conducted by adolescents, parents, and teachers at baseline, two weeks after the intervention, and at a three-month follow-up to measure outcomes.

Why it matters

Potential benefit: If successful, this study could provide effective preventive strategies to help at-risk adolescents manage conduct problems and improve their social-emotional well-being.

How similar studies have gone: Other studies have shown promise in using mindfulness and life skills programs for adolescents, suggesting that this approach may be effective.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. A 9th or 10th grade student in a partner school district
2. Referral due to elevated social/emotional risk indicated on a standardized screening tool or a referral from school support staff due to concerns about school-based conduct problems
3. Adolescents and their parents must be fluent in English

Exclusion Criteria:

1. Currently receiving special education services (i.e., an IEP) due to a behavioral or emotional disturbance
2. Existing diagnoses of autism spectrum disorder, pervasive developmental disorders, developmental/intellectual disability, or serious psychiatric disorders requiring specialized mental health treatment (e.g., psychosis, bipolar, substance use disorder, etc.)

Where it's running

  • University of Minnesota
    Minneapolis, Minnesota, United States
    Recruiting

Study contacts

  • Principal investigator: Timothy Piehler — University of Minnesota
  • Study coordinator: Nicole Morrell
  • Email: morre006@umn.edu
  • Phone: 612-624-2600

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.