Clinical Trials Logo

Clinical Trial Summary

150 males and 150 females ages 14-17 years-old will be enrolled in an observational, longitudinal study. There are three planned in-person visits: a baseline assessment, an 18-month follow-up, and a 36-month follow-up. The in-person visits will include assessment of substance use and other individual differences (e.g., reward function, psychiatric history), neuromelanin-sensitive MRI, as well as functional brain activation collected while the participant is at rest (resting-state fMRI) and while the participant completes a Monetary Incentive Delay task. Subjects will also be asked to complete past 90-day substance use assessments remotely every 90 days for 36 months.


Clinical Trial Description

Substance use disorders affect several million people in the United States every year, create significant economic burden, and cause tremendous suffering at the person, family, and societal levels. This proposal aims to investigate the dynamic interplay between pediatric substance use (a risk factor for substance use disorders) and rate of neuromelanin accumulation (a proxy for dopamine function) for the first time. Thus, this research seeks to identify a brain mechanism (dopamine function) that could be targeted in youth by future treatments in order to prevent onset of substance use disorders. The goals of this study require a prospective imaging design that relies on the naturally-occurring adolescent substance use (e.g., differences in timing and amount of substance use is treated as quasi-experimental). Importantly, we will begin data collection in a cohort on the cusp of entering a high-risk period of substance use initiation and conclude data collection after 36-months to capture substance use escalation. An intermediate 18-month follow-up NM-MRI scan is needed to help clarify the magnitude of early changes in NM accumulation. Thus, this is a longitudinal, observational study. Of note, the use of the Monetary Incentive Delay fMRI task at baseline, 18-month, and 36-month follow-ups fulfills the NIH criteria of a basic experimental studies involving humans (BESH). Thus, this study as a whole qualifies as a clinical trial based on the determination: 1. The study involves humans 2. The participants are prospectively assigned to an intervention, which in this case means that the subject will be assigned to complete the Monetary Incentive Delay fMRI task while lying in the MRI scanner. 3. The study is designed to evaluate the effect of the intervention on participants, which in this case means that we will evaluate the effect of the Monetary Incentive Delay task on brain activation in participants. 4. The effect being evaluated is a health-related biomedical or behavioral outcome, which in this case means fMRI brain activation between win and loss conditions, as well as between phases of anticipation and consummation/outcome. In brief, use of this fMRI task is a single arm, non-masked, non-randomized, basic science intervention. This does not match any of the NIH-defined clinical trials phases (n/a). The fMRI data (brain activation) is the primary outcome measure of the BESH intervention, but is a tertiary outcome in the context of this longitudinal study. The task is utilized for its short-lived, reversible, and benign effects (e.g., brief changes in brain activation). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06369623
Study type Interventional
Source Stony Brook University
Contact Greg Perlman, PhD
Phone 1-631-638-1922
Email greg.perlman@stonybrookmedicine.edu
Status Recruiting
Phase N/A
Start date April 6, 2024
Completion date November 30, 2028

See also
  Status Clinical Trial Phase
Recruiting NCT05525962 - Vulnerability/Resilience Factors Influencing the Developmental Trajectories and Adaptive Methods of Children and Adolescents in Child Welfare System.
Completed NCT01821950 - Evaluation of Yoga for Substance Use Risk Factors in a School Setting N/A
Completed NCT01955265 - Promoting Adolescent Development Through Sports in Hong Kong N/A
Active, not recruiting NCT03209102 - Emotional Regulation and Impulsivity Among Adolescents With Borderline Personality Disorder Phase 2
Completed NCT06159738 - Parental Cognitions and Children's Wellbeing
Completed NCT05095883 - Correlation Between Body Weight and Foot Progression Angle in Adolescents
Completed NCT03085160 - Project EAT: Eating and Attitudes in Teens N/A
Withdrawn NCT05073562 - Nutrition Intervention to Address Anemia Among Adolescent Girls in Liberia N/A
Completed NCT04162977 - Adapting Personality-Targeted Interventions for Reducing Substance Misuse and Related Outcomes in Youth in Youth Protection Services N/A
Completed NCT05500131 - The Association Between Restricted Ankle Joint Dorsiflexion and Dynamic Knee Valgus
Completed NCT03647553 - The Nash-wo-Numa (Childhood Growth & Development) Study
Completed NCT03086161 - Mood and Excess Weight Gain in Adolescent Pregnancy N/A
Completed NCT04640389 - Rural-urban Disparities in the Nutritional Status of Younger Adolescents in Tanzania.
Completed NCT03574129 - Adolescent Transition To Adult Care for HIV-infected Adolescents in Kenya N/A
Recruiting NCT04128644 - Thoughts and Health - Preventing Depression in Adolescents N/A
Not yet recruiting NCT03704649 - Evaluating a Participatory Nutrition Education Model on Nutrition Literacy of Adolescent Girls in Rural Ghana. N/A
Active, not recruiting NCT04992299 - Mindfulness-Based Intervention for Depression and Insulin Resistance in Adolescents N/A
Completed NCT03527641 - United for Health: Type 2 Diabetes Prevention in Latino Teens N/A
Not yet recruiting NCT06299267 - The Effect of Dual Task on Manual Skill Performance in Children and Adolescents N/A
Completed NCT03493243 - Teenagers After London Terrorist Attack