RECRUITING

Kind Minds Program for Youth with Anxiety and Depression

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

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

Quick Facts

Study Start:2022-05-31
Study Completion:2025-03-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05353751

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:12 Years to 17 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. * Participants will include:
  2. 1. one adolescent (aged 12-17 years) with a current diagnosis of an anxiety or depressive disorder)
  3. 2. one of their parents/caregivers.
  4. 3. Both adolescent and caregiver must speak English to the degree necessary to participate in the intervention program, which is only available in English.
  5. 4. Parent and youth must have a smart phone and be willing to download the online mindfulness program.
  1. * Exclusion criteria apply to both caregiver and adolescent and include:
  2. 1. current alcohol or substance use disorder or suicidality
  3. 2. lifetime diagnosis of bipolar disorder, schizophrenia, autism, conduct disorder, or developmental delay diagnosed by an independent evaluator;
  4. 3. English reading level below 4th grade
  5. 4. non English speaking
  6. 5. currently receiving mindfulness-based mental health services or taking medication to treat anxiety or depression.

Contacts and Locations

Study Contact

Denise A Chavira, PhD
CONTACT
3108258466
dchavira@psych.ucla.edu
Danielle Smith, PhD
CONTACT
Danielle.Sayre@gmail.com

Principal Investigator

Denise A Chavira, PhD
PRINCIPAL_INVESTIGATOR
University of California, Los Angeles

Study Locations (Sites)

Imperial High School
Imperial, California, 92251
United States

Collaborators and Investigators

Sponsor: University of California, Los Angeles

  • Denise A Chavira, PhD, PRINCIPAL_INVESTIGATOR, University of California, Los Angeles

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-05-31
Study Completion Date2025-03-30

Study Record Updates

Study Start Date2022-05-31
Study Completion Date2025-03-30

Terms related to this study

Keywords Provided by Researchers

  • mindfulness
  • children
  • adolescents
  • anxiety
  • depression

Additional Relevant MeSH Terms

  • Child Anxiety
  • Depression