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Enrolling by invitationNCT06957548URBACAM-DUpdated Nov 26, 2025

Cardiometabolic Disease Risk Factors in Cameroon

An observational study in Cardiac Disease and Metabolic Disease, sponsored by Johns Hopkins University. Enrolling by invitation at 1 site in Cameroon. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-11-26.

Sponsored by Johns Hopkins University · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
200
Ages
18 Years and older
Sex
All
01

Study summary

Cardiometabolic diseases (CMDs) are a major public health concern in sub-Saharan Africa, including Cameroon. Studies have shown a significant increase in the prevalence of hypertension, diabetes, and obesity in recent years. However, access to timely diagnosis and treatment remains limited, particularly in rural areas. Community-based screening programs have been shown to be effective in identifying individuals with undiagnosed CMD risk factors and promoting early intervention. By leveraging the strengths of community-based approaches, the URBACAM-D study aims to address the growing burden of CMDs in urban Cameroon.

02

Conditions studied

  • Cardiac Disease
  • Metabolic Disease
03

In context

Heart Diseases

2,135 studies on the registry are indexed under Heart Diseases; 252 are open to participants now.

This study's planned enrollment of 200 is below the median of 350 across 592 observational studies indexed under Heart Diseases.

Browse Heart Diseases studies →

Lead sponsor

Johns Hopkins University is the lead sponsor of 1,815 studies on the registry; 315 are open to participants now.

Of its 208 completed or terminated interventional studies of FDA-regulated products, 144 (69%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Urban Cameroon. Newbell, Douala, cameroon.

Eligibility criteria

Inclusion Criteria:

  • Screening is open to any adult over the age of 18 years
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Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
200 participants (estimated)
Patient registry
No

Interventions

  • Diagnostic testCardiometabolic disease

    Cardiometabolic disease screening

06

What researchers measure

Primary outcomes

  1. Prevalence of Cardiometabolic disease risk factors in Urban Cameroon

    To determine the prevalence of undiagnosed and uncontrolled cardiometabolic disease (CMD) risk factors among urban Cameroonians.

    Time frame: 1 year

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Study locations

1 site
  • Newbell Protestant Hospital
    Douala, Littoral Region, Cameroon
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Jul 2025 to primary completion in Oct 2025, 3 months.

How these figures are worked out, and which studies are left out of them.

Registered
Apr 25, 2025
First posted
May 4, 2025
StartActual
Jul 9, 2025
Primary completionActual
Oct 12, 2025
CompletionEst.
Feb 12, 2027
Last update
Nov 26, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Nov 26, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06957548
Responsible party
Sponsor
First posted
May 4, 2025
Start date
Jul 9, 2025
Primary completion
Oct 12, 2025
Completion
Feb 12, 2027 (estimated)
Last update
Nov 26, 2025

Study contacts

Dimitri Tito, DO
principal investigator · Johns Hopkins University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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