Sexually Transmitted Infections in Migrant Women (NCT07471412) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Sexually Transmitted Infections in Migrant Women
100 participantsStarted 2026-03-01
Plain-language summary
The main objective of this study is to evaluate the effect of structured sexual health education for immigrant women on their levels of sexual health self-efficacy and reproductive autonomy using a randomized controlled design.
Who can participate
Age range
18 Years – 65 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* To be eligible, applicants must:
* Be 18 years of age or older,
* Have immigrant status and reside in Turkey,
* Be one of the women who applied to or benefited from the services of the
Exclusion Criteria:
* Being under 18 years of age,
* Refusal to give informed consent for participation in the study,
* Having a serious cognitive impairment or psychiatric condition that may prevent regular participation in the training and data collection process,
* Having a severe language barrier that prevents communication during the study process and that cannot be overcome with translation or written materials,
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
The primary endpoint will be the difference in mean knowledge scores between baseline (pre-intervention) and post-intervention assessments.
Timeframe: Pre-intervention (week 0), post-intervention (week 8), and 3-month follow-up.