Impact of a Web-Based Mind-Body Awareness Program on Women Undergoing Infertility Treatment (NCT06585137) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Impact of a Web-Based Mind-Body Awareness Program on Women Undergoing Infertility Treatment
Turkey (Türkiye)78 participantsStarted 2026-07-10
Plain-language summary
The goal of this two-group parallel randomized controlled study is to determine the effect of a web-based mind-body-based awareness program based on Meleis Transition Theory on fertility awareness and readiness levels in women receiving infertility treatment.
Who can participate
Age range
23 Years – 45 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:
* Volunteering to participate in research
* Being diagnosed with primary infertility
* Starting the infertility treatment process
* Having attempted IVF at most twice before
* Being able to speak and understand Turkish
* Being at least a primary school graduate
* Not taking part in any psychological or social support group.
* Not having completed or currently participating in any mind/body program for fertility.
Exclusion Criteria:
* Women applying for frozen embryo transfer without ovarian stimulation
* Being diagnosed with secondary infertility
* Having a diagnosis of a chronic disease
* Having communication problems (vision, hearing)
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
Fertility Awareness Scale
Timeframe: A pre-test will be administered before the study begins. Then, a post-test will be administered three times, 1 day after the OPU procedure, then at 3 months and 6 months.
2
Fertility Preparedness Scale for Women Receiving Fertility Treatment
Timeframe: A pre-test will be administered before the study begins. Then, a post-test will be administered three times, 1 day after the OPU procedure, then at 3 months and 6 months.