Fertility boost? gamified lifestyle program aims to empower women during IVF
NCT ID NCT07460661
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether a gamified healthy lifestyle training program can help women going through fertility treatments (like IVF) adopt healthier habits and feel more in control. About 105 women will be split into three groups: one gets the game-like program plus a booklet, one gets only the booklet, and one gets standard care. Researchers will measure changes in lifestyle behaviors and self-efficacy after one and three months.
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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 105 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Mar 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2027
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: * Women aged 18-49 years * Diagnosed with primary infertility * Currently undergoing assisted reproductive treatment (IUI, IVF, or ICSI) * Able to read, understand, and communicate in Turkish * Have access to a digital device (mobile phone, tablet, or computer) and internet connection * Provide voluntary written informed consent Exclusion Criteria: * Diagnosed psychiatric disorder that may interfere with participation * Presence of a severe medical condition (e.g., active cancer or other serious systemic disease) that may affect treatment outcomes * Medical complications requiring hospitalization during the study period * Communication barriers preventing completion of study procedures * Withdrawal of consent at any time during 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.
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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Istanbul Provincial Health Directorate Zeynep Kamil Women and Children Diseases Traning and Research Hospital
Istanbul, Uskudar, 34668, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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- Sperm sorting showdown: can a microchip pick the best sperm for pregnancy?