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The Longitudinal Study of Stimulant Use Disorder — STIM-RAD  

Healthy Clinical Trial

Official title:
Observational Longitudinal Study of Individuals With Stimulant Use Disorder: Research and Development of a Biosignature

Clinical Trial Summary

This research is a 5-year observational, longitudinal registry study with no treatment or medication provided as part of participation. Individuals with current or lifetime stimulant use disorder, in addition to healthy control individuals, may be eligible to participate in this study. A variety of assessments and tasks including Magnetic Resonance Imaging (MRI), Electroencephalography (EEG), blood draws, urine drug screens, and both self-report and clinician-rated assessments will be used to assess biomarkers in this population. This study has a visit schedule of four in-person visits and eight remote visits per year.

Clinical Trial Description

This project is a five-year observational study that will use a variety of assessments and tasks to phenotype participants with lifetime or current Stimulant Use Disorder as well as healthy control individuals. The data collection will include collecting urine samples for diagnostic tracking, socio-demographic and lifestyle factors, clinical and behavioral assessments, blood-based biomarkers, genomics, cell-based assays, EEG, and MRI to establish phenotypic biosignature subtypes over the longitudinal timeline. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06073340
Study type Observational
Source University of Texas Southwestern Medical Center
Contact Manish Jha, M.B.B.S
Phone (214) 648-0156
Email Manish.Jha@UTSouthwestern.edu
Status Recruiting
Phase
Start date November 16, 2023
Completion date November 16, 2033
View Details
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