NCT06637735 The Effect of Education on Pregnant Women Perception of Traumatic Childbirth
| NCT ID | NCT06637735 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Sakarya University |
| Condition | Pregnant Women |
| Study Type | INTERVENTIONAL |
| Enrollment | 62 participants |
| Start Date | 2024-07-01 |
| Primary Completion | 2024-12-30 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 62 participants in total. It began in 2024-07-01 with a primary completion date of 2024-12-30.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
During pregnancy, women are exposed to physical, psychological and social changes and may experience anxiety and fears about childbirth. Traumatic birth perception is defined as perceiving birth as a threat to oneself and one\'s baby. This perception can negatively affect women\'s lives in the postpartum period. Midwives are the primary health professionals in preventing traumatic birth perception. In this context, it is envisaged to create an important basis for preventing traumatic birth perception in pregnant women through the training to be given.
Eligibility Criteria
Inclusion Criteria: - Volunteering to participate in the study, * 18 years of age or older, * At least 53 points from the Traumatic Birth Perception Scale * No pregnancy-related risks (such as pre-eclampsia, diabetes, heart disease, placenta previa, oligohydramnios), * The fetus has no health problems (fetal anomaly, intrauterine growth retardation, etc.), * Literate, Exclusion Criteria: - Refused to participate in the research, * Illiterate, * Has a disorder based on a psychiatric/psychological diagnosis, * Pregnant women with communication and language problems will not be included in the study.
Contact & Investigator
Güleser ADA, Master
STUDY CHAIR
sakarya üniversity
Frequently Asked Questions
Who can join the NCT06637735 clinical trial?
This trial is open to female participants only, aged 18 Years or older, up to 40 Years, studying Pregnant Women. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06637735 currently recruiting?
Yes, NCT06637735 is actively recruiting participants. Contact the research team at gada@bartin.edu.tr for enrollment information.
Where is the NCT06637735 trial being conducted?
This trial is being conducted at Türkiye, Turkey (Türkiye).
Who is sponsoring the NCT06637735 clinical trial?
NCT06637735 is sponsored by Sakarya University. The principal investigator is Güleser ADA, Master at sakarya üniversity. The trial plans to enroll 62 participants.