Improving hypertension care in Ghana and Baltimore
Official title: Addressing Hypertension Care in Africa (ADHINCRA) Program
Run by Johns Hopkins University · NCT06986590 · Data updated 2026-11-12
This program tests whether a package of patient-, provider-, and health-system interventions can improve blood pressure control for adults ages 18–70 with hypertension who receive care at participating clinics and own a smartphone.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 70 Years |
| Sex | All |
| Enrollment | 800 (estimated) |
| Sponsor | Johns Hopkins University Academic / other |
| Locations | 17 sites (Baltimore, Maryland and 16 other locations) |
| Status | Recruiting |
| Started | January 9, 2026 |
| Main results expected | March 2028 |
| Study ends | September 2028 |
| Registry record updated | January 14, 2026 |
| Trial ID | NCT06986590 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18–70 with diagnosed hypertension (systolic BP ≥140 mmHg) who are treatment-naive or on a single antihypertensive, receive primary care at a participating site, can consent in a study language, and own a smartphone are ideal candidates.
✕Probably not a fit
Patients with severely elevated BP (≥180/110 mmHg), diabetes, prior stroke or coronary or kidney disease, end-stage renal disease on dialysis, pregnancy, cognitive impairment, or those without a smartphone are unlikely to qualify or benefit from this program.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The ADHINCRA Program implements a bundle of multilevel, evidence-based interventions that address patient-, provider-, and health-system factors contributing to uncontrolled hypertension. The program is being delivered at primary care sites in the Ashanti Region of Ghana and at Johns Hopkins in Baltimore, with smartphone-supported components and clinic-based workflow changes. Eligible participants are adults 18–70 with systolic BP ≥140 mmHg who are treatment-naive or on monotherapy, while people with severe hypertension, diabetes, established cardiovascular or kidney disease, pregnancy, or cognitive impairment are excluded. The aim is to increase hypertension control rates and produce a rigorous, scalable model for wider adoption to reduce future cardiovascular, stroke, and kidney disease risk.
Why it matters
Potential benefit: If successful, the program could improve blood pressure control and lower the risk of heart attack, stroke, and kidney disease by providing a scalable care model.
How similar studies have gone: Similar multilevel and digital-support interventions in low- and middle-income settings have improved blood pressure control in other programs, although effectiveness and scalability have varied by context.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Aged 18 -70 years. * Diagnosis of hypertension and elevated systolic blood pressure measure (≥140 mmHg) on the most recent clinic visit without a diabetes diagnosis. * Hypertension treatment naive or on monotherapy. * Receives primary care at one of the participating sites. * Willing and able to provide informed consent in English, Twi, Dagbani, Ewe, Hausa, or Yoruba. * Owns a smartphone (Android or iOS). Exclusion Criteria: * Age \<18 years or \>70 years. * Severely elevated BP (≥180/110mmHg). * Diagnosis of stroke, coronary artery disease, or kidney disease. * Diagnosis of end-stage renal disease (ESRD) treated with dialysis. * Serious medical condition which either limits life expectancy or requires active management (e.g., cancer). * Cognitive impairment or other conditions preventing study participation * Pregnant or currently nursing a child * Unwilling to provide informed consent
Where it's running
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Manhyia Government Hospital
Kumasi, Ashanti Region, Ghana Recruiting -
St. John of God Catholic Hospital
Duayaw Nkwanta, Bono, Ghana Recruiting -
Northern Regional Hospital
Tamale, Northern Region, Ghana Recruiting -
Akure South Hospital
Akure, Ondo State, Nigeria Recruiting -
Johns Hopkins University
Baltimore, Maryland, United States Active not recruiting -
Dominase SDA Hospital
Bekwai, Ashanti Region, Ghana Not yet recruiting
Show 11 more locations
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Kumasi South Hospital
Kumasi, Ashanti Region, Ghana Not yet recruiting -
Tafo Government Hospital
Tafo, Ashanti Region, Ghana Not yet recruiting -
Berekum Holy Family Hospital
Berekum, Bono, Ghana Not yet recruiting -
Tamale Teaching Hospital
Tamale, Northern Region, Ghana Not yet recruiting -
Ho Municipal Hospital
Ho, Volta Region, Ghana Not yet recruiting -
South Tongu District Hospital
Sogakope, Volta Region, Ghana Not yet recruiting -
Akoko North East
Ondo, Ondo State, Nigeria Not yet recruiting -
Akoko North West
Ondo, Ondo State, Nigeria Not yet recruiting -
Akoko South East
Ondo, Ondo State, Nigeria Not yet recruiting -
Akoko South West
Ondo, Ondo State, Nigeria Not yet recruiting -
Owo General Hospital
Owo, Ondo State, Nigeria Not yet recruiting
Study contacts
- Principal investigator: Yvonne Commodore-Mensah, PhD, MHS, RN — Johns Hopkins University
- Study coordinator: Yvonne Commodore-Mensah, PhD, MHS, RN
- Email: ycommod1@jhmi.edu
- Phone: 410-614-1519
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.