The Effect of Fetal Heartbeat Monitoring on Prenatal Attachment and Partner Adjustment

Pregnancy Related Clinical Trial

Official title: Evaluation of Prenatal Attachment Levels and Spousal Adjustment in Nulliparous Couples Performing Fetal Heartbeat Monitoring

Status Not yet recruiting

Clinical Trial Summary

The aim of this interventional study is to obtain information about determining the effect of the following drugs. To evaluate prenatal attachment levels and spousal adjustment in nulliparous couples with fetal heart rate monitoring. The main questions it aims to answer are: - Does fetal heart rate monitoring affect the attachment of pregnant women? - Does fetal heart rate monitoring affect fathers' attachment? - Does fetal heart rate monitoring affect pregnant women's adjustment to motherhood?

Clinical Trial Description

Data will be collected from women who meet the inclusion criteria and agree to participate in the study. Data collection tools will be collected in 2 stages by the researcher using a questionnaire form by face-to-face interview method in a suitable room in previously determined hospitals. In the first stage (Day 1); couples who meet the inclusion criteria will be informed about the study and written consent will be obtained from those who agree to participate in the study. The pre-test data collection phase will be completed by applying data collection tools. Then, the prospective fathers will be trained by the researchers on how to apply the 1st and 2nd leopold maneuvers using visual materials. Each couple will be provided with a stethoscope to listen to the fetal heartbeat, and they will be given a schedule to listen to the fetal heartbeat together for 5-10 minutes at least once a day for 15 days. During the training, the couples will be able to detect the fetal heartbeat in a healthy way and an appointment will be made for the second phase and the first phase of the study will be completed (approximately 10-15 minutes). In the second phase (Day 15); the researchers will contact the women again and invite them to the ASM. Then, stethoscopes and charts will be received from the couples, data collection tools will be applied again and post-test data will be collected (1-5 minutes) and the data collection phase will be completed. Pre-test data will be collected by applying data collection tools (Personal Information Form, Prenatal Self-Assessment Scale, Prenatal Mother Attachment Scale and Prenatal Father Attachment Scale) to the couples in the intervention group (Nulliparous Couples Monitoring Fetal Heartbeat) in the first interview. Then, the researchers will provide training on listening to the fetal heartbeat in the first stage and in the last session (Day 15), the data collection tools will be applied to the couples again and the post-test data will be collected and thus the data collection process will be completed. No intervention will be applied to the women in the control group, however, in the first interview (Day 1), data collection forms (Personal Information Form, Prenatal Self-Assessment Scale, Prenatal Maternal Attachment Scale and Prenatal Paternal Attachment Scale) will be applied and pre-test data will be collected. Then, the post-test data will be collected by applying the data collection forms to the women again in the last session (Day 15) simultaneously with the application schedule in the experimental group and the data collection process will be completed. ;

Related Conditions & MeSH terms

• Pregnancy Related

• NCT number: NCT06148415
• Study type: Interventional
• Source: Kahramanmaras Sutcu Imam University
• Contact: Esra KARATAS OKYAY, PhD
• Phone: 05432125225
• Email: esrakaratas44@hotmail.com
• Status: Not yet recruiting
• Phase: N/A
• Start date: December 2023
• Completion date: June 2024