Pregnancy prep goes digital: app study aims to boost Women's health Know-How
NCT ID NCT07279857
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a mobile app with weekly lessons and counseling can help women aged 18-49 who plan to get pregnant within two years. About 110 women will either use the app or receive a standard booklet. Researchers will measure changes in knowledge, attitudes, and confidence about preconception health over 12 weeks.
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 110 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
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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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. Women aged 18 to 49 years. 2. In the preconception period and planning to conceive within the next two years. 3. Never been pregnant. 4. Able to read and understand Turkish. 5. Having a smartphone and internet access. 6. Willing to participate and provide informed consent. Exclusion Criteria: 1. Currently pregnant. 2. Having a diagnosed psychiatric disorder that may interfere with participation. 3. Previous participation in structured preconception counseling or training. 4. Being a health professional or a student in a health-related field. 5. Inability to use a mobile application due to cognitive, visual, or physical limitations. 6. Participation in another ongoing research study.
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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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Bayrampaşa İlçe Sağlık Müdürlüğü Aile Sağlığı Merkezleri
Istanbul, Turkey (Türkiye)