Clinical trial Recruiting at 3 sites Interventional Ages 12 to 17

Mindfulness program for reducing negative emotions in at-risk youth

Official title: Targeting Negative Affect Through Mindfulness Training in Youth at Risk for Internalizing Problems (R33)

Run by Vanderbilt University · NCT06526052 · Data updated 2026-11-12

This study is testing if an online mindfulness program can help teenagers aged 12 to 17 who struggle with negative emotions feel better and reduce their anxiety and mood problems.

Quick facts

Study typeInterventional
Ages12 Years to 17 Years
SexAll
Enrollment360 (estimated)
SponsorVanderbilt University
Academic / other
Locations3 sites (Los Angeles, California and 2 other locations)
StatusRecruiting
StartedApril 1, 2024
Main results expectedApril 2027
Study endsApril 2027
Registry record updatedNovember 3, 2026
Trial IDNCT06526052 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adolescents aged 12 to 17 who exhibit high levels of trait negative affect and can provide parental consent.

Probably not a fit

Patients currently diagnosed with significant anxiety or depressive disorders, or those with serious suicidal ideation, will 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 clinical trial aims to evaluate the effectiveness of an online mindfulness program in reducing mood and anxiety symptoms among adolescents aged 12 to 17 who exhibit high levels of negative affect. Participants will be randomly assigned to either the mindfulness intervention, an active supportive comparison condition, or a no-intervention control group. The study will assess changes in momentary negative affect and internalizing problems before, immediately after, and six months following the intervention. The goal is to determine if the mindfulness program can effectively lower negative emotions and prevent the onset of anxiety and depression in at-risk youth.

Why it matters

Potential benefit: If successful, this program could significantly reduce mood and anxiety symptoms in adolescents, improving their overall mental health.

How similar studies have gone: Previous studies have shown that mindfulness interventions can effectively reduce negative affect and internalizing symptoms in children and adolescents.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Ages 12, 13, 14, 15, 16, 17
* Parental Consent
* Participant Assent
* Live in Illinois, California, or Tennessee

Exclusion Criteria:

* current diagnosis of an anxiety or depressive disorder with significant clinical impairment
* current alcohol or substance use disorder
* current serious suicidal ideation or behavior
* lifetime diagnosis of bipolar disorder, schizophrenia, autism, conduct disorder, or developmental delay
* reading level below 4th grade
* not English speaking at a level that would allow them to participate in the intervention and assessments

Where it's running

  • University of California, Los Angeles
    Los Angeles, California, United States
    Recruiting
  • Northwestern University
    Evanston, Illinois, United States
    Recruiting
  • Vanderbilt University
    Nashville, Tennessee, United States
    Recruiting

Study contacts

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.