Actively Recruiting
Developing EEG Biomarkers for OUD Diagnostic, Prognostic, and Predictive Purposes
Led by University of Illinois at Chicago ยท Updated on 2025-07-25
70
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University of Illinois at Chicago
Lead Sponsor
N
National Institute on Drug Abuse (NIDA)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are investigating potential electroencephalography (EEG) biomarkers to help diagnose, monitor, and predict treatment responses in people with Opioid Use Disorder (OUD). This research addresses the urgent need for better tools in managing OUD, a condition that contributes to significant health and societal challenges in the US. The study aims to fill the gap left by the limited effectiveness and side effects of current OUD treatments by exploring brain activity patterns related to addiction. The study will enroll up to 130 participants, including 50 individuals diagnosed with OUD and 20 age-matched healthy controls. Each participant will undergo two EEG sessions: one at the initial visit and another about one week later. During these sessions, EEG recordings will be taken both at rest and while participants complete computer assessments. Additional assessments include questionnaires on demographics, mood, craving, impulsivity, and drug use, along with urine toxicology and hair follicle tests when available. Participants will be carefully screened and provide informed consent before enrollment. The study involves phone screenings, in-person consent, and ongoing communication with investigators. Researchers will analyze EEG brain activity across various frequency bands as the primary outcome. The study also monitors participant safety and allows withdrawal at any time. Total involvement includes the initial visit, follow-up visit approximately one week later, and related assessments during this period.
CONDITIONS
Brief Title
EEG Biomarkers for OUD: Diagnostic, Prognostic, and Predictive Applications
Who Can Participate
Eligibility Criteria
You may qualify if you...
- For OUD subjects: providing informed consent to participate in the study
- Age between 22 and 85 years
- Diagnosed with Opioid Use Disorder for more than 6 months as defined by DSM-5
- Positive urine toxicology screen and experiencing cravings
- Lives in the immediate area with no plans to relocate
- For age-matched controls: providing informed consent to participate in the study
- Age between 22 and 85 years
- Lives in the immediate area with no plans to relocate
You will not qualify if you...
- Recently started on antiepileptic drug therapy
- Ingestion of poppy seeds or herbal teas containing Papaveris fructus
- History of neurological disorders including stroke, brain tumors, or epilepsy
- History of unexplained fainting spells
- History of head injury causing more than momentary loss of consciousness
- History of brain surgery
- Suffering from severe depression
- Active malignancy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 phone screening and 1 in-person consent visit
Duration - Initial visit and 1 week later
Participants undergo EEG testing at rest and during computer assessments to monitor brain activity along with questionnaires and toxicology tests.
2 visits (in-person) approximately 1 week apart
Trial Site Locations
Total: 1 location
1
Clinical & Imaging Research Outcomes Lab
Chicago, Illinois, United States, 60612
Actively Recruiting
Research Team
A
Aksarapak Hengyotmark, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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