Actively Recruiting

Phase Not Applicable
Age: 14Years - 19Years
All Genders
NCT06626425

Well-being Training for Adolescent Depressive Symptoms (TeenWell Study)

Led by University of Wisconsin, Madison · Updated on 2026-01-07

200

Participants Needed

1

Research Sites

107 weeks

Total Duration

On this page

Sponsors

U

University of Wisconsin, Madison

Lead Sponsor

N

National Institute of Mental Health (NIMH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study is being done to see if the Healthy Minds Program app helps adolescents with elevated depressive symptoms. Up to 200 participants will be on study for 20 weeks.

CONDITIONS

Official Title

Well-being Training for Adolescent Depressive Symptoms (TeenWell Study)

Who Can Participate

Age: 14Years - 19Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 14 to 19
  • Currently in high school (9th to 12th grade) or would be in high school if enrolled
  • Proficient in English
  • Able to provide informed consent (if 18 or older) or assent and parent/guardian consent (if under 18)
  • PROMIS Depression Scale T-score of 60 or higher
  • Stable dose of psychotropic medication for 4 or more weeks if applicable
  • Willing and able to complete all study procedures
Not Eligible

You will not qualify if you...

  • Has received a high school diploma or equivalency (HSED or GED)
  • Meditates weekly or more frequently
  • Prior use of the Healthy Minds Program app
  • Prior use of the water tracking app
  • Current active suicidal thoughts with intent at baseline
  • History of psychosis or mania
  • Practices mindfulness-based therapies (e.g., ACT, DBT, MBSR) weekly or more in last 6 months or plans to start during study

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

Center for Healthy Minds, University of Wisconsin Madison

Madison, Wisconsin, United States, 53705

Actively Recruiting

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Research Team

M

Matthew Hirshberg, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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