Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 12:36 AM
Ignite Modification Date:
2025-12-25 @ 12:36 AM
NCT ID:
NCT06569667
Eligibility Criteria:
Inclusion Criteria:
1. ≥18 years of age;
2. fluent in English and/or Spanish;
3. self-reported non-prescription opioid use \<30 days prior to consent;
4. provision of informed consent;
5. planned stay in NYC ≥12 month;
6. self-identified Black and/or Latinx race/ethnicity;
7. positive urine toxicology for opioids per EMR records;
8. diagnosis of OUD per the Diagnostic and Statistical Manual of Mental Disorders-5
9. self-reported interest in initiating buprenorphine in primary care
10. must have a mobile phone data plan.
Exclusion Criteria:
1. inability to comprehend text content written at a 3rd grade reading level;
2. physical or visual disability preventing mobile phone use;
3. self-reported receipt of medications for OUD in past 30 days.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
99 Years
Study:
NCT06569667
Study Brief:
Protocol Section:
NCT06569667