Hypertension Clinical Trial
— CATCHOfficial title:
Implementing and Scaling Up a Team-based Care Strategy for Hypertension Control in Colombia and Jamaica
The CATCH cluster randomized trial will test the implementation and effectiveness outcomes of implementing and scaling up a team-based care strategy for blood pressure control in Colombia and Jamaica.
Status | Recruiting |
Enrollment | 1280 |
Est. completion date | August 31, 2026 |
Est. primary completion date | August 31, 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion criteria for clinics: - Serving >300 hypertensive patients during the previous year - Clinic visits and BP medications are free of charge to patients - Not sharing physicians, nurses, pharmacists, or community health workers (CHWs) with other clinics Inclusion criteria for participants: - Men or women aged = 21 years who receive primary care from participating clinics - Average untreated BP =140/90 mm Hg among individuals without a history of clinical cardiovascular disease (CVD), chronic kidney disease (CKD), or diabetes; average untreated BP =130/80 mm Hg among individuals aged =65 years or those with clinical CVD, CKD, or diabetes; or average treated BP =130/80 mm Hg from six BP readings at two screening visits - Not pregnant or planning to become pregnant in the next 18 months - Able and willing to give informed consent - No plans to change primary care clinic in the next 18 months - Not an immediate family member of staff at the primary care clinic |
Country | Name | City | State |
---|---|---|---|
Colombia | 20 primary care clinics in Colombia | Santander | |
Jamaica | 20 primary care clinics in Jamaica | Kingston |
Lead Sponsor | Collaborator |
---|---|
Tulane University | National Institutes of Health (NIH), Universidad de Santander, Colombia, University of the West Indies, Jamaica |
Colombia, Jamaica,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Acceptability | Measured by validated survey | 18 months | |
Other | Adoption | Defined as % of clinics adopting intervention components | Baseline | |
Other | Appropriateness | Measured by validated survey | 18 months | |
Other | Feasibility (suitability) | Measured by validated survey | Baseline | |
Other | Fidelity | % of each intervention component delivered per protocol | 18 months | |
Other | Implementation Costs | Defined as all costs associated with implementation and assessed from administrative data | 18 months | |
Other | Penetrance | Defined as % of providers using the intervention approach | 18 months | |
Other | Sustainability | % of clinics maintaining intervention | 18 months | |
Primary | Net difference in mean change of systolic blood pressure | Differences in mean change of systolic BP from baseline to 18 months between intervention and control groups | 18 months | |
Secondary | Difference in blood pressure control (<130/80 mm Hg) | Difference in the proportion of patients with systolic BP <130 mm Hg and diastolic BP <80 mm Hg between intervention and control groups at 18 months | 18 months | |
Secondary | Net difference in mean change of diastolic blood pressure | Differences in mean change of diastolic BP from baseline to 18 months between intervention and control groups | 18 months | |
Secondary | Side effects | Differences in medication side effects between intervention and control groups will be assessed by survey. A list of common side effects associated with high blood pressure will be asked of participants to collect presence and frequency of side effects. | 18 months | |
Secondary | Health-related quality of life | Differences in health-related quality of life (measured by EQ-SD and SF-12) between intervention and control groups | 18 months | |
Secondary | Cost-effectiveness | Incremental direct costs per additional percentage of hypertension control | 18 months |
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