Village women trained as mentors to help others take charge of birth control decisions

NCT ID NCT07711717

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

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Status unknown
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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

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

About 1,560 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Oct 2026

An estimate. Start dates often move.

Expected to finish

Dec 2028

An estimate. End dates often move.

Lead sponsor

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

18 to 49 years

Sex

Female participants only

Healthy volunteers

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

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

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How to take part

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Contacts and locations

Locations

  • Makerere University School of Public Health

    Kampala, Uganda

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