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Behavioral Intervention

Practice Facilitation for High Blood Pressure (CIRCL-Chicago Trial)

N/A
Waitlist Available
Research Sponsored by Northwestern University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 years
Awards & highlights
No Placebo-Only Group

Summary

This trial aims to adapt a proven set of methods to manage high blood pressure for use in the South Side of Chicago. It focuses on minority residents who have high rates of hypertension. Community health workers and church facilitators will help manage blood pressure with support from local clinics and shared data.

Who is the study for?
This trial is for adults aged 18-89 living in Chicago's South and West Sides, who are patients within participating clinics or churches. It aims to help those affected by high blood pressure and cardiovascular disease, especially minority populations.
What is being tested?
The study tests a community-centered health intervention adapted from Kaiser Permanente's model. It includes simplified treatment regimens and support from local health workers, with the goal of improving blood pressure control through faith-based organizations.
What are the potential side effects?
Since this trial focuses on implementing a healthcare strategy rather than testing new medications, it does not have direct medical side effects. However, there may be indirect impacts related to changes in healthcare delivery.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and 2 years for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Blood pressure
Secondary study objectives
Acceptability of Intervention Measure
Feasibility of implementation

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Practice FacilitationExperimental Treatment1 Intervention
Practice Facilitation to support implementation of the Kaiser Blood Pressure Control Bundle
Group II: Non-Practice FacilitationActive Control1 Intervention
implementation of the Kaiser Blood Pressure Control Bundle without Practice Facilitation

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for high blood pressure include ACE inhibitors, which block the conversion of angiotensin I to angiotensin II, a potent vasoconstrictor, thereby relaxing blood vessels. ARBs (Angiotensin II Receptor Blockers) prevent angiotensin II from binding to its receptors, also leading to vasodilation. Calcium channel blockers inhibit calcium ions from entering vascular smooth muscle cells, causing relaxation and reduced vascular resistance. Diuretics help the kidneys remove excess sodium and water from the body, decreasing blood volume and pressure. Beta-blockers reduce heart rate and the force of contraction, lowering blood pressure. These mechanisms are essential for managing high blood pressure to prevent complications like stroke and heart disease.
Cerebrovascular protection and antihypertensive therapy.

Find a Location

Who is running the clinical trial?

Northwestern UniversityLead Sponsor
1,640 Previous Clinical Trials
951,812 Total Patients Enrolled
University of UtahOTHER
1,137 Previous Clinical Trials
1,785,790 Total Patients Enrolled
Pastors 4 PCORUNKNOWN
~3840 spots leftby Apr 2026