Village women trained as mentors to help others take charge of birth control decisions
NCT ID NCT07711717
First seen Jul 17, 2026 · Last updated Jul 24, 2026 · Updated 2 times
Summary
This trial tests whether a community-based program called I-CAN can improve how well women's contraceptive use matches their personal preferences. In rural Uganda, lay women are trained as peer mentors to provide support and information to other women of reproductive age. Villages are randomly assigned to receive the program or not, and researchers compare outcomes like preference-aligned contraceptive use and satisfaction after two years.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a behavioral peer support program called I-CAN, where trained lay women mentor other women on contraceptive decision-making
- What this could lead to
- If effective, this approach could give women in rural communities more control over their reproductive choices without requiring clinic visits.
- What could go wrong
- This is a single trial in one region, and results may not apply elsewhere. The intervention depends on volunteer mentors, which may be hard to sustain long-term.
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 1,560 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2028
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 to 49 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Woman * Ages 18-49 years Exclusion Criteria: * Women who are not able to respond to the survey questions on their own * Not usual resident in study village * Not consenting to the survey
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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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Makerere University School of Public Health
Kampala, Uganda
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