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OpenTrials
Completed

NCT Number: NCT05353751

Kind Minds Program for Youth With Anxiety and Depression

Rates of anxiety and depression in youth are substantial, causing a major unmet need for effective interventions. Participation in mindfulness interventions has been demonstrated to reduce anxiety and depressive symptoms among teenagers. Parents' participation in mindfulness interventions has also been shown to reduce their children's mental health symptoms. However, there is no available evidence regarding potential additional benefits for adolescents' mental health of having both the adolescent and their parent or caregiver learn and practice mindfulness simultaneously.

This pilot intervention study aims to explore potential additive effects of parent/caregiver participation in a digitally-based, kindness-focused, coached mindfulness intervention program for adolescents that lasts 9 weeks. Participating parent/caregiver-child pairs (n = 30) will include one teenager between 12 and 17 years old with a current diagnosis of an anxiety or depressive disorder and one parent/caregiver. All adolescent participants will take part in the mindfulness intervention. Half of the parents/caregivers will be randomized to also take part in the mindfulness program. Outcomes will be compared between families in which only the teen participates in the mindfulness program and families in which the teen and parent/caregiver participate in the intervention.

Adolescents and parents/caregivers will take part in evaluations before, in the middle of, and after the end of the mindfulness program, meaning that participation in the study will take a total of approximately 12 weeks. Pre, mid, and post evaluations will include online questionnaires. Pre and post evaluations will also include clinical interviews via phone or video conference. Evaluations will include measures of mental health diagnoses and symptoms, mood, interpersonal and family functioning, mindfulness, and perceptions of/satisfaction with the program. Participating adolescents and parents/caregivers will also fill out weekly brief questionnaires of anxiety and depressive symptoms. The primary outcome of interest is adolescent mental health, including anxiety and depressive symptoms.

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Key information

Age range

12 year–17 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Imperial High School

Imperial, California, 92251, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants will include:
  • one adolescent (aged 12-17 years) with a current diagnosis of an anxiety or depressive disorder)
  • one of their parents/caregivers.
  • Both adolescent and caregiver must speak English to the degree necessary to participate in the intervention program, which is only available in English.
  • 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:
  • current alcohol or substance use disorder or suicidality
  • lifetime diagnosis of bipolar disorder, schizophrenia, autism, conduct disorder, or developmental delay diagnosed by an independent evaluator;
  • English reading level below 4th grade
  • non English speaking
  • currently receiving mindfulness-based mental health services or taking medication to treat anxiety or depression.

Treatment and study plan

Kind Minds Program

Behavioral

The KMP intervention uses an online mindfulness phone based program. During the 9-week program, Community Health Worker (CHW) Kindness Coaches will meet weekly for 30 minutes via Zoom with either a) the caregiver and adolescent (in separate meetings), or b) the adolescent only to review and complete a new "session" using the online mindfulness program. Participants will be prompted to complete mindfulness activities between sessions by notifications, conducive to their school and work schedules. Weekly content and meditations/activities focus on mindfulness skills of present moment awareness, nonjudgment, compassion, and gratitude.

Primary outcomes

  1. Patient Health Questionnaire-9

    Time frame: 12-14 weeks after baseline assessment

    self report of depressive symptoms

  2. Generalized Anxiety Disorder-7

    Time frame: 12-14 weeks after baseline assessment

    self report of anxiety symptoms

  3. SCARED -Screen for child anxiety and related emotional disorders

    Time frame: 12-14 weeks after baseline assessment

    self report of anxiety symptoms

Secondary outcomes

  1. Kiddie Schedule for Affective Disorders and Schizophrenia interview -anxiety and depressive disorder modules

    Time frame: 12-14 weeks after baseline assessment

    remission on primary anxiety or primary depressive disorder diagnosis

Sponsors and collaborators

Lead sponsor

University of California, Los Angeles

Other

Registry information

Official study title

Examining the Effectiveness of a Mindfulness-based Intervention for Underserved Adolescents With and Without Caregiver Involvement

Acronym: KMP

Important dates

Study start
2022
Primary completion
2025
Study completion
2025
First posted
Apr 29, 2022
Registry last updated
Mar 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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