Deworming through doctor visits: a smarter way to fight worms?
NCT ID NCT07507461
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether giving deworming drugs during regular healthcare visits works better than the usual special campaigns. Over 1,200 people in Western Kenya took part, including community members, health workers, and officials. Researchers measured how practical, affordable, and well-covered this integrated approach was compared to the standard method.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could show a more sustainable and cost-effective way to deliver deworming treatment through existing health systems, reducing worm infections in communities.
- What could go wrong
- This is a completed case study, not a controlled trial of a new drug. Results may not apply to other regions or diseases, and the approach depends on local health system strength.
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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1,229 people
The number who actually took part.
- Started
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May 2025
- Finished
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Oct 2025
- 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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14 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.
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. All eligible community members, including school-age children (SAC; 5-14 years) and adults (15 years and above) receiving targeted treatment for SCH. 2. Preschool-age children (PRESAC; 1-4 years), school-age children (SAC; 5-14 years), and adults (15 years and above) receiving targeted treatment for STH. 3. Must be residents of the target counties (Vihiga, Kakamega, Bungoma, and Trans-Nzoia). Exclusion Criteria Residents in wards outside the 122 non-Interruption of Transmission (non-IoT) wards.
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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.
Contacts and locations
Locations
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Community Based, no facility
Kakamega, Kenya
More trials for these conditions
Other studies related to the condition(s) this trial covers.