Multicomponent Intervention to Improve Hypertension Control in Central America
Primary Purpose
Arterial Hypertension
Status
Completed
Phase
Phase 3
Locations
Guatemala
Study Type
Interventional
Intervention
Multicomponent intervention
Sponsored by

About this trial
This is an interventional treatment trial for Arterial Hypertension
Eligibility Criteria
Inclusion Criteria:
- All patients aged ≥40 years with BP >140/90 mmHg at the time of enrollment
- Patients who receive care at government health facilities
Exclusion Criteria:
- Pregnant women
Sites / Locations
- Insitute of Nutrition of Central America and Panama
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Intervention group
Control group
Arm Description
Patients will receive a multicomponent intervention.
Patients will receive the usual care.
Outcomes
Primary Outcome Measures
Proportion of controlled blood pressure
Difference in the proportion of patients with controlled blood pressure (<140/90 mmHg) between the intervention and control groups
Secondary Outcome Measures
Change in systolic blood pressure
Net change in systolic blood pressure from baseline to 18 months
Change in diastolic blood pressure
Net change in diastolic blood pressure from baseline to 18 months
Full Information
NCT ID
NCT03504124
First Posted
April 12, 2018
Last Updated
July 27, 2022
Sponsor
Institute of Nutrition of Central America and Panama
Collaborators
Tulane University School of Public Health and Tropical Medicine, Institute for Clinical Effectiveness and Health Policy, Colorado School of Public Health, National Heart, Lung, and Blood Institute (NHLBI)
1. Study Identification
Unique Protocol Identification Number
NCT03504124
Brief Title
Multicomponent Intervention to Improve Hypertension Control in Central America
Official Title
Implementing a Multicomponent Intervention to Improve Hypertension Control in Central America
Study Type
Interventional
2. Study Status
Record Verification Date
July 2022
Overall Recruitment Status
Completed
Study Start Date
July 17, 2019 (Actual)
Primary Completion Date
April 23, 2022 (Actual)
Study Completion Date
April 23, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Institute of Nutrition of Central America and Panama
Collaborators
Tulane University School of Public Health and Tropical Medicine, Institute for Clinical Effectiveness and Health Policy, Colorado School of Public Health, National Heart, Lung, and Blood Institute (NHLBI)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The investigators propose to assess the needs, barriers, and knowledge gaps of hypertension control programs in the national health care systems of the Central America 4 region LMIC (CA-4: Guatemala, Honduras, El Salvador, and Nicaragua); to conduct a cluster randomized trial to test the effect of a multilevel and multicomponent intervention program leveraging an existing subnational primary healthcare system in Guatemala, on blood pressure (BP) control among hypertensive patients; and to evaluate the adaptability, feasibility, fidelity, and sustainability of implementing the program in the primary health care systems of the CA-4 region. The comprehensive intervention, which includes protocol-based treatment using a standard BP management algorithm, team-based collaborative care, BP audit and feedback, home BP monitoring, and health coaching on antihypertensive medication adherence and lifestyle modification, will last for 18 months. This implementation research study presents high public health impact because it will generate urgently needed data on effective, practical, and sustainable intervention strategies aimed at reducing BP related disease burden in Central America and other low- and middle-income countries.
Detailed Description
Despite advances in hypertension prevention and treatment research, its prevalence is high and increasing, while the proportions of hypertensive patients who are aware, treated, and controlled are low, especially in low- and middle-income countries (LMIC). The investigators propose to: assess the needs, barriers, and knowledge gaps of hypertension control programs in the national health care systems of the Central America 4 region LMIC (CA-4: Guatemala, Honduras, El Salvador, and Nicaragua); conduct a cluster randomized trial to test the effect of a multilevel and multicomponent intervention program on blood pressure (BP) control among Guatemalan hypertensive patients; and evaluate the adaptability, feasibility, fidelity, and sustainability of implementing the program in the primary health care systems of the CA-4 region. The investigators will conduct formative research to assess the needs of system-wide intervention programs, barriers and facilitators of BP control strategies, and knowledge gaps about implementation for improving hypertension control in the CA-4 health care systems. The proposed trial will recruit 1,770 study participants from 32 primary care districts (55 patients aged ≥22 years with uncontrolled hypertension/district) within a subnational primary care network managed by the Guatemalan Ministry of Health. Sixteen health districts will be assigned to an 18-month multicomponent intervention, which includes protocol-based treatment using: a standard blood pressure (BP) management algorithm, team-based collaborative care, BP audit and feedback, home BP monitoring, and health coaching on antihypertensive medication adherence and lifestyle modification, and 16 to usual care. BP and other indicators will be measured at baseline and at months 6, 12, and 18. The primary clinical outcome is the difference in the proportion of patients with controlled BP (<140/90 mmHg) between the intervention and control groups at 18 months. The secondary outcome is net change in systolic and diastolic BP from baseline to 18 months. Fidelity of the intervention measured monthly by intensification of treatment by provider-teams (titration or addition of new medications) and adherence to medications in patients will be the primary implementation outcome. Other implementation outcomes will be measured every 6 months. The RE-AIM framework will guide the development, implementation, and assessment of the intervention, which will translate and adapt the Hypertension Control Program in Argentina that has been proven effective and feasible. This project have assembled a multidisciplinary investigative team, which will collaborate with the public primary care network in Guatemala to conduct this implementation research project. The intervention and study outcomes are patient-centered, and patients, MOH provider-teams, and other stakeholders will be engaged at every step of the proposed study. The investigators will disseminate the study findings and promote scale-up of the proven effective intervention program, which will generate urgently needed data on effective, adoptable, and sustainable intervention strategies aimed at reducing BP-related disease burden in CA-4 and other low-income settings.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Arterial Hypertension
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
A cluster randomized trial including 32 rural health districts managed by the Ministry of Health (MOH) of Guatemala. Sixteen health districts will be assigned to a multicomponent intervention and 16 to usual care. Each health district will recruit 55 patients aged ≥40 years with uncontrolled hypertension.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1854 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Intervention group
Arm Type
Experimental
Arm Description
Patients will receive a multicomponent intervention.
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Patients will receive the usual care.
Intervention Type
Other
Intervention Name(s)
Multicomponent intervention
Intervention Description
An 18-month multicomponent intervention, which includes protocol-based treatment using: a standard blood pressure (BP) management algorithm, team-based collaborative care, BP audit and feedback, home BP monitoring, and health coaching on antihypertensive medication adherence and lifestyle modification.
Primary Outcome Measure Information:
Title
Proportion of controlled blood pressure
Description
Difference in the proportion of patients with controlled blood pressure (<140/90 mmHg) between the intervention and control groups
Time Frame
18 months
Secondary Outcome Measure Information:
Title
Change in systolic blood pressure
Description
Net change in systolic blood pressure from baseline to 18 months
Time Frame
18 months
Title
Change in diastolic blood pressure
Description
Net change in diastolic blood pressure from baseline to 18 months
Time Frame
18 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
All patients aged ≥40 years with BP >140/90 mmHg at the time of enrollment
Patients who receive care at government health facilities
Exclusion Criteria:
Pregnant women
Facility Information:
Facility Name
Insitute of Nutrition of Central America and Panama
City
Guatemala
ZIP/Postal Code
01011
Country
Guatemala
12. IPD Sharing Statement
Citations:
PubMed Identifier
32517806
Citation
Paniagua-Avila A, Fort MP, Glasgow RE, Gulayin P, Hernandez-Galdamez D, Mansilla K, Palacios E, Peralta AL, Roche D, Rubinstein A, He J, Ramirez-Zea M, Irazola V. Evaluating a multicomponent program to improve hypertension control in Guatemala: study protocol for an effectiveness-implementation cluster randomized trial. Trials. 2020 Jun 9;21(1):509. doi: 10.1186/s13063-020-04345-8.
Results Reference
derived
Learn more about this trial
Multicomponent Intervention to Improve Hypertension Control in Central America
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