A Randomized Controlled Trial Testing the Effect of the Youth Mindful Awareness Program on Negative Affect (YMAP2).

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age12-17
SponsorVanderbilt University

About this trial

The goal of this randomized clinical trial is to compare the effects of an online mindfulness program to an active supportive comparison condition and a no-intervention control group on reducing and preventing mood and anxiety symptoms in at-risk youth. Youth who are high on trait negative affect will be randomized to one of the three conditions. The primary outcomes of interest are reductions in momentary negative affect and internalizing problems in adolescents ages 12 to 17 years old. All participants will be evaluated prior to being randomized, after the 9-session intervention period, and at a 6-month follow-up.

The first hypothesis is that the mindfulness intervention will predict decreases in stressor-reactive momentary negative affect and internalizing symptoms. The second hypothesis is that changes in momentary negative affect will partially account for the effects of the mindfulness intervention on internalizing symptoms.

Eligibility criteria

Qualifiers

Ages 12, 13, 14, 15, 16, 17

Parental Consent

Participant Assent

Live in Illinois, California, or Tennessee

Disqualifiers

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

Trial design

Treatments tested in this trial

  • Mindfulness Program
  • Active Comparator

Treatment groups

360 Participants
are divided into 3 treatment groups

Sponsors and collaborators

Vanderbilt University

Lead sponsor

National Institute of Mental Health (NIMH)

Collaborator