Video Supported Training on Non-Stress Test Application to Pregnant Women (NCT06331949) | Clinical Trial Compass
CompletedNot Applicable
Video Supported Training on Non-Stress Test Application to Pregnant Women
Turkey (Türkiye)74 participantsStarted 2024-04-01
Plain-language summary
Women go through many practices during their pregnancy. These practices, along with ignorance, create stress in the mother. However, performing the procedures for the first time may increase the mother's stress level. Stress during pregnancy also affects prenatal attachment. Non-Stress Test (NST) Application is a test applied to pregnant women starting from the 28th week of pregnancy and provides information about the baby's well-being and uterine contractions. There is a gap in the literature regarding education for pregnant women undergoing NST regarding stress levels and prenatal attachment. With this study, stress levels and prenatal attachment levels in pregnant women will be determined during NST, which is frequently applied during pregnancy. Additionally, the effects of midwifery care in this process will be realized. In this way, solutions will be produced for problems that may arise. A better quality of midwifery care will be provided
Who can participate
Age range
18 Years – 49 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:
* Primiparous pregnant woman
* Able to read and write
* Pregnant women who are 32 weeks or more pregnant
* No detection problems
* The baby has no health problems
* Having no psychological or physiological health problems
* Pregnant women who accept the research
Exclusion Criteria:
* Under 32 weeks
* Those who did not accept the research
* If the pregnant woman feels uncomfortable during the research,
* Pregnant women who want to leave any part of the research
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.
1This trial looked at how video-based training affects anxiety and emotional bonding in first-time pregnant women — could something like this kind of educational support be helpful for me during my pregnancy, and is it available at this clinic?
2Since the trial measured anxiety using the State-Trait Anxiety Scale, do you think my current anxiety levels around pregnancy monitoring are something we should be tracking or addressing more formally?
3The study focused on non-stress test education for first-time pregnant mothers — how much information will I receive before my own non-stress tests, and do you think better preparation would help reduce my worry about the procedure?
4Now that this trial is completed, has any of its findings about prenatal attachment or anxiety reduction changed how your practice explains fetal monitoring procedures to first-time moms?
5Since this was a non-drug, educational type of study with no assigned phase, what are the limitations of what it can tell us, and are there other evidence-based resources you'd recommend to help me feel more prepared and less anxious during pregnancy monitoring?
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.