Mindfulness program for youth with anxiety and depression
Official title: Examining the Effectiveness of a Mindfulness-based Intervention for Underserved Adolescents With and Without Caregiver Involvement
Run by University of California, Los Angeles · NCT05353751 · Data updated 2026-05-14
This study is no longer in our active list. It may have stopped recruiting or finished. The details below are as of 2026-05-14 and are kept for reference. Check ClinicalTrials.gov for its current status, or see similar studies below.
This study is testing a 9-week mindfulness program for teens with anxiety or depression to see if doing it together with a parent or caregiver helps improve their mental health.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 12 Years to 17 Years |
| Sex | All |
| Enrollment | 30 (estimated) |
| Sponsor | University of California, Los Angeles Academic / other |
| Locations | 1 site (Imperial, California) |
| Trial ID | NCT05353751 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adolescents aged 12-17 with a current diagnosis of anxiety or depression, along with one of their parents or caregivers.
✕Probably not a fit
Patients with current substance use disorders, suicidality, or certain severe mental health conditions may not benefit from this program.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This pilot intervention explores the effects of a digitally-based mindfulness program called the Kind Minds Program, designed for adolescents aged 12 to 17 with anxiety or depression. The program lasts for 9 weeks and involves both the adolescent and their parent or caregiver participating together. The study aims to assess whether simultaneous participation enhances the mental health benefits for the adolescent. A total of 30 parent-child pairs will be enrolled to evaluate the effectiveness of this combined approach.
Why it matters
Potential benefit: If successful, this program could significantly reduce anxiety and depression symptoms in adolescents while also benefiting their parents or caregivers.
How similar studies have gone: Previous studies have shown that mindfulness interventions can effectively reduce anxiety and depression symptoms, but this specific combined approach is novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Participants will include: 1. one adolescent (aged 12-17 years) with a current diagnosis of an anxiety or depressive disorder) 2. one of their parents/caregivers. 3. Both adolescent and caregiver must speak English to the degree necessary to participate in the intervention program, which is only available in English. 4. Parent and youth must have a smart phone and be willing to download the online mindfulness program. Exclusion Criteria: * Exclusion criteria apply to both caregiver and adolescent and include: 1. current alcohol or substance use disorder or suicidality 2. lifetime diagnosis of bipolar disorder, schizophrenia, autism, conduct disorder, or developmental delay diagnosed by an independent evaluator; 3. English reading level below 4th grade 4. non English speaking 5. currently receiving mindfulness-based mental health services or taking medication to treat anxiety or depression.
Where it's running
-
Imperial High School
Imperial, California, United States Recruiting
Study contacts
- Principal investigator: Denise A Chavira, PhD — University of California, Los Angeles
- Study coordinator: Denise A Chavira, PhD
- Email: dchavira@psych.ucla.edu
- Phone: 3108258466
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Smartphone-supported single-session psychotherapy for postpartum depression
A single online therapy session plus four weeks of app-based support is being tested to see if it reduces depressive symptoms in postpartum women compared with a waitlist.
-
Mindful Smartphone Use: A Mindfulness-Based Program for Teens with Sleep and Mood Challenges
This study tests Mindwire, a mindfulness-based program, to see if it helps teens with problematic phone use who also have depression or anxiety.
-
Tele-based wellbeing centres for women's mental health in Bangladesh
A randomized trial tests whether tele-counselling for depression and anxiety in Bangladeshi women is as effective as in-person counselling.
-
Remote monitoring for adults with depression using ThIA Suivi
This study tests whether adding the ThIA Suivi remote monitoring tool to usual psychiatric care helps adults with depression feel more improved after 3 months compared with standard care alone.
-
HBOT to see if it helps cognition and well‑being in first responders with prior brain injury
This study tests whether 40 hyperbaric oxygen therapy sessions can improve thinking skills and post-concussion symptoms in current or former first responders with a history of brain injury.
-
Focused ultrasound for mood and anxiety disorders
This study tests whether repeated low-intensity focused ultrasound using the ATTN201 device can help people with subsyndromal to moderate depression, anxiety, or OCD.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.