The THRIVE Study: Teaching Healthy Regulation in Individuals & Vulnerable Environments
University of California, Irvine · with University of California, Los Angeles, University of Illinois at Chicago · NCT06821035
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 11–14 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 210
- US sites recruiting
- 1
- Study start
- April 17, 2025
- Record last updated
- March 18, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The goal of this 2-arm randomized control trial is to determine the impact of a community health worker delivered coaching intervention, GRIT, on preventing the early initiation of regular use of alcohol and cannabis among adversity-impacted adolescents ages 11-14 who do not regularly use alcohol or cannabis at baseline. The specific aims include:
- Aim 1. Examine the effect of GRIT on preventing the early initiation of regular alcohol and cannabis use over time.
- Aim 2. Examine the role of youth and caregiver self-regulation in mediating the effect of GRIT on adolescent rates of alcohol and cannabis use.
Researchers will compare participants who are randomized to the GRIT intervention to an active control group, receiving a Digital Citizenship Curriculum, to see if those who participate in GRIT experience greater improvements in self-regulation and lower cardiometabolic risks.
Participants will
- Be randomized to either receive the GRIT intervention (experimental group) or the Digital Citizenship Curriculum (active control group)
- Complete 3 in-person visits at baseline, post-intervention, and 12-month post intervention
- Complete HRV assessments using emWave Pro Plus and survey assessments on REDCap during in-person visits.
- Participate in six 60-minute sessions conducted over 8 weeks via Zoom with an assigned community-health worker
- Be invited to complete a booster session at 6-months post-intervention
- Complete online measures at baseline, post-intervention, 6-month, and 12-month post-intervention
Being studied: Garnering Resilience in Traumatized youth and families (GRIT); Digital Citizenship Curriculum (DCC)
Conditions: Adverse Childhood Experiences; Family Functioning
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Youth ages 11-14 years who score in the High-Risk category (i.e., 4 or more ACEs) on the ACEs and Toxic Stress Risk Assessment Algorithm
- Has access to a smartphone and is willing to download applicable apps (95% of all adolescents have access to a smartphone)
- Youth who are able to speak and read in English
- Has a parent/guardian/primary caregiver (18 years or older) who is English- or Spanish-speaking and willing to participate in the intervention.
Exclusion Criteria
- Youth who cannot speak and read in English
- Youth who report any alcohol or cannabis use within the last 14 days
- Youth currently enrolled in another family-based intervention (i.e., family therapy)
- Youth in acute distress who are in immediate need of care (e.g., imminent risk of harm to self or others, active psychosis)
- Youth who report their caregivers' home environment is unsafe to return to, have been deemed unsafe, or require supervised visits by the Department of Children and Family Services (DCFS)
- Youth whose parent/guardian/primary caregiver declines participation will be referred to other programs in their community.
- Due to drug experimentation being common in adolescence, our interest in preventing the early initiation of regular use of alcohol and cannabis use, and youth who regularly use substances requiring a different intervention, we will enroll youth who initially report recent cannabis use but later report no use within the last two weeks and have a confirmatory negative urine drug screening.
Recruiting US locations
The Regents of the University of California, Irvine
Irvine, CA 92697-7600
Site contact: Madison Spiva · 9498247688 · mspiva@uci.edu
Study contacts (from the official record)
- Dawn T. Bounds, Ph.D. · 949-742-7109 · boundsd@hs.uci.edu
- Jenny Fotang · 949-516-1694 · jfotang@hs.uci.edu
Similar studies in California
All healthy volunteers studies in California →- RecruitingHealthy volunteersPhase 1Overnight stay mentioned
A Study to Investigate the Relative Bioavailability and Safety of Different Oral Formulations of Elecoglipron in Healthy Participants
AstraZeneca
- Location
- Glendale, CA + 1 other US site
- Eligibility basics
- Ages 18–55
- RecruitingHealthy volunteersPhase 1Overnight stay mentioned
A Phase I Study to Investigate the Pharmacokinetics and Safety of Capivasertib in Participants With Moderate Hepatic Impairment
AstraZeneca
- Location
- Rialto, CA + 1 other US site
- Eligibility basics
- Ages 18–80
- RecruitingHealthy volunteersPhase 1Overnight stay mentioned
A Study to Learn How the Body Processes the Study Medicine PF-07328948 in People With Reduced Kidney Function
Pfizer
- Location
- Lake Forest, CA + 3 other US sites
- Eligibility basics
- Ages 18–80
- RecruitingHealthy volunteersPhase 1Overnight stay mentioned
Phase 1 Study of SBS-147 in Healthy Adults
Sparian Biosciences, Inc
- Location
- Cypress, CA
- Eligibility basics
- Ages 18–55