Can a special education program boost reproductive health in women with HIV?
NCT ID NCT07423364
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested a reproductive health education program designed for women living with HIV. The program aimed to increase knowledge about reproductive health and encourage healthy behaviors. Sixty women participated, and researchers measured changes in their knowledge and attitudes. The goal was to see if this type of education can empower women with HIV to better manage their reproductive health.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- reproductive health education program
- What this could lead to
- If successful, this program could help women with HIV make more informed reproductive health choices and adopt healthier lifestyles.
- What could go wrong
- This is a small, completed study with 60 participants, so results may not apply to all women with HIV. The program's long-term impact is unknown.
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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60 people
The number who actually took part.
- Started
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Jul 2020
- Finished
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Jun 2022
- 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.
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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.
Sampling Inclusion Criteria * Female individuals * Individuals diagnosed with HIV * Individuals aged 18-49 years * Sexually active individuals Sample Exclusion Criteria * Being pregnant * Being postpartum * Individuals with disabilities * Individuals whose gender identity does not match their biological sex at birth, those receiving hormonal therapy, or other conditions that do not fit the specific biological focus of the study.
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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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Non-Governmental Organizations
Istanbul, Turkey (Türkiye)
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