NCT06824480 The Effect of Postpartum Debriefing on the Psychological Outcomes
| NCT ID | NCT06824480 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Mersin University |
| Condition | Well-Being, Psychological |
| Study Type | INTERVENTIONAL |
| Enrollment | 72 participants |
| Start Date | 2024-02-01 |
| Primary Completion | 2025-02-07 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
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 72 participants in total. It began in 2024-02-01 with a primary completion date of 2025-02-07.
⚠ 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
This study was planned to determine the effect of re-signification of birth in the early postpartum period on postpartum fear of childbirth, postpartum depression and birth trauma.
Eligibility Criteria
Inclusion Criteria: Women who volunteer to participate in the study, Whose mother tongue is Turkish, Who are between the ages of 18-45, Who are at least primary school graduates, Who are 37-42 weeks pregnant, Who are nulliparous, Who have a healthy pregnancy, Who do not have a psychological condition or psychiatric disorder, Who are monitored and cared for in the first 24 hours after birth at the Tarsus State Hospital Maternity Department, Who approve of the reinterpretation of birth application to be carried out by the researcher will be included in the sample. Exclusion Criteria: Those who did not volunteer to participate in the study, Those who gave birth before the 37th week of pregnancy, Those who were multiparous, Those who had abnormal medical conditions during pregnancy (placental disorder, preeclampsia, premature birth threat, etc.), Those whose native language is not Turkish, Those who have visual, speech and hearing impairments, Those who had an emergency cesarean section, Those who stayed in the hospital for less than 12 hours after birth, Those who received a psychiatric diagnosis during the postpartum period (except those diagnosed with postpartum depression and post-traumatic stress disorder related to birth), Those who could not be reached by phone during the follow-up of the study, Women who developed complications in the first 24 hours after birth and required intensive care, Those whose babies required neonatal intensive care during the postpartum period, Those who experienced another life event that traumatized the woman during the postpartum period (harassment, rape, earthquake, accident, loss of a loved one) etc.) Those who want to withdraw from the study at any stage of the study will not be included in the sample.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT06824480 clinical trial?
This trial is open to female participants only, aged 18 Years or older, up to 45 Years, studying Well-Being, Psychological. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06824480 currently recruiting?
Yes, NCT06824480 is actively recruiting participants. Contact the research team at gozdegokce@gmail.com for enrollment information.
Where is the NCT06824480 trial being conducted?
This trial is being conducted at Mersin, Turkey (Türkiye), Mersin, Turkey (Türkiye).
Who is sponsoring the NCT06824480 clinical trial?
NCT06824480 is sponsored by Mersin University. The trial plans to enroll 72 participants.