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 @ 7:02 PM
Ignite Modification Date:
2025-12-24 @ 7:02 PM
NCT ID:
NCT03892057
Eligibility Criteria:
Inclusion Criteria:
* Hispanics/Latinos recruited from UI Health Pilsen Family Health Center Lower West
* Aged ≥18
* Fluent in English or Spanish with ≥8th grade education
* Elevated sitting blood pressure (≥140/90)
* Ability to read and understand the informed consent
* Ability to access internet from home or in public setting (note, tablet PCs will be made available to all enrolled participants at no charge), and
* Self-reported comfort in with handling of a table computer and website navigation.
Exclusion Criteria:
* Cognitive impairment denoting dementia (assessed using the Short Portable Status Questionnaire-See Appendix E)
* Severely reduced life expectancy (e.g., self-reported diagnosis of metastatic cancer, congestive heart failure, or end-stage kidney disease)
* Self-reported diagnosis of sickle cell disease
* Skin damage or rash in the upper arm region where ambulatory blood pressure monitor is to be placed
* Currently enrolled in psychotherapy, and
* Self-reported history or current diagnosis of bipolar disorder, dissociative disorder, psychosis, or substance abuse; or have severe depression.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT03892057
Study Brief:
Protocol Section:
NCT03892057