Can a simple risk calculator help catch prostate cancer earlier in nigerian men?
NCT ID NCT07733440
First seen Jul 29, 2026 · Last updated Jul 30, 2026 · Updated 1 time
Summary
This pilot trial tests whether a risk calculator designed for Nigerian men can help primary care providers better identify those with clinically significant prostate cancer. Researchers will train healthcare workers at community hospitals and then support them in using the tool for at least six months. The main goal is to see if the calculator is feasible and acceptable in everyday practice, not yet to measure its impact on cancer outcomes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Training and supported risk assessment using a prostate cancer risk calculator
- What this could lead to
- If successful, this approach could improve early detection of prostate cancer in Nigerian men, potentially saving lives through earlier treatment.
- What could go wrong
- This is a small pilot study focused on feasibility, not on directly measuring cancer outcomes. The risk calculator may not work as well in real-world settings or may not be adopted by providers.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 89 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Mar 2029
An estimate. Start dates often move.
- Expected to finish
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Aug 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Male participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Training - Eligible primary care providers (for the training surveys) will be healthcare practitioners at community-level hospitals. 2. Supported Risk Assessment (i) Eligible key informants will be eligible primary care providers who were trained and implemented the supported risk assessment and the targeted population of patient participants who received the supported risk assessment. (ii) Eligible patient participants (for the collection of observation data) will be the target population of adult males 40 - 79 years accessing provider services. Exclusion Criteria: \-
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Ahmadu Bello University Teaching Hospital
Zaria, Kaduna State, Nigeria
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Other studies related to the condition(s) this trial covers.
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