Eligibility Module

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: 2025-12-24 @ 5:08 PM
Ignite Modification Date: 2025-12-24 @ 5:08 PM
NCT ID: NCT05208450
Eligibility Criteria: UH3 IMPLEMENTATION PHASE (Years 4 - 7): INTERVENTION Inclusion Criteria: Patients are eligible if he/she: 1. identifies as Black (through EHR code or self-report) 2. is 18+ years of age 3. has a diagnosis of HTN (identified by ICD-10 codes for HTN) 4. prescribed an antihypertensive medication(s) 5. has a clinic BP \> 130/80 mmHg Exclusion Criteria: Patients will be ineligible for the study if they: 1. are deemed unable to comply with the study protocol (either self-selected or by indicating during screening that s/he could not complete all requested tasks) 2. participate in other hypertension-related clinical trials 3. have significant psychiatric comorbidity or reports of substance abuse (as documented in the EHR) 4. plan to discontinue care at the site within the next 12 months; or 5. are pregnant or planning to become pregnant in the next 12 months IMPLEMENTATION EVALUATION 1. NYULH Primary care provider (MD/DO, NP), Clinical Director, Site Administrator, Medical Assistant, or administrative staff employed at the participating practices and interacts with at least five patients with a diagnosis of hypertension; or 2. NYULH Nurse case manager within centralized service; or 3. Staff and leadership of community- and faith-based organizations serving the Black community; or 4. NYULH Organizational leadership; or 5. NYULH Project Staff: Community Health Workers/CHW Supervisor/Practice Facilitators; and 6. Able and willing to provide consent Exclusion Criteria: 1\. Refusal to participate
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT05208450
Study Brief:
Protocol Section: NCT05208450