Can a smartphone app beat cervical cancer in rural kenya?
NCT ID NCT05848557
First seen Jun 24, 2026 · Last updated Aug 14, 2026 · Updated 4 times
Summary
This study is testing a mobile app called mSaada that helps community health workers educate women, track screening, and send reminders for cervical cancer screening. The trial involves 6,000 women and health workers across 12 health facilities in western Kenya. The goal is to see if the app increases screening rates, treatment follow-up, and knowledge about cervical cancer.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- mSaada mobile health application
- What this could lead to
- If successful, this could show that a simple mobile app can significantly boost cervical cancer screening rates and follow-up care in low-resource settings.
- What could go wrong
- This is a pilot and early-stage trial focused on feasibility and usability, not yet on clinical outcomes. The app may not work as well in real-world conditions or may not be adopted widely.
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 6,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2024
- Expected to finish
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Jun 2027
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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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
R21 Aim 1 Community health volunteers (CHVs), facility providers and supervisors, Ministry of Health officials Inclusion Criteria: * 18 years or older * be employed by a government clinic * be working in cervical cancer screening Exclusion Criteria: * Does not understand the study purpose and details * Is not willing to provide informed consent Women Inclusion Criteria: \- between 30 and 65 years old Exclusion Criteria: * Does not understand the study purpose and details * Is not willing to provide informed consent Aim 2 Community health volunteers (CHVs) Inclusion Criteria: * 18 years or older * be employed by a government clinic * be working in cervical cancer screening Exclusion Criteria: * Does not understand the study purpose and details * Is not willing to provide informed consent Women Inclusion Criteria: * between 30 and 65 years old * intact cervix and uterus * able to provide informed consent. Exclusion Criteria: * Does not understand the study purpose and details * Is not willing to provide informed consent R33 Women (knowledge and risk perception surveys) We plan to enroll approximately 600 women (50 per health facility) to complete a survey about cervical cancer and HPV knowledge, risk perception and screening awareness, acceptability and self-efficacy.\\ Eligibility criteria for women participants include: * Reside within Siaya County, in one of the study communities * Eligible for cervical cancer screening per the Kenya Ministry of Health guidelines and * Ability to provide informed consent. CHPs in both arms will be asked to complete a survey about their self-efficacy, knowledge of HPV and cervical cancer, and the usability of the mSaada app (CHPs in the intervention arm only). Inclusion: * CHV participants must be employed by government clinics in Siaya County, and * be able to provide informed consent. Exclusion: * Does not understand the study purpose and details * Is not willing to sign an informed consent
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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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Kenya Medical Research Institute
RECRUITINGKisumu, Kisumu County, Kenya
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