Ignite Creation Date:
2024-05-06 @ 8:19 PM
Last Modification Date:
2024-10-26 @ 3:25 PM
Study NCT ID:
NCT06331949
Status:
COMPLETED
Last Update Posted:
2024-03-26
First Post:
2024-03-16
Brief Title:
Video Supported Training on Non-Stress Test Application to Pregnant Women
Sponsor:
Hilal Özbek
Organization:
Tokat Gaziosmanpasa University
Study Overview
Official Title:
The Effect of Video-Assisted Training Given to Pregnant Women on Non-Stress Test Application on Pregnancy Stress and Prenatal Attachment
Status:
COMPLETED
Status Verified Date:
2024-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief 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 mothers 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 babys 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
Detailed Description:
Background NST may negatively affect the stress level and prenatal attachment level in primiparous pregnant women
Purpose This study will be carried out to determine the effect of video-educated midwifery care given to primiparous pregnant women before NST application on pregnancy stress and prenatal attachment levels
Method The data of the research will be collected at Tokat State Hospital after permission During data collection pregnant women who apply to the NST room of the relevant hospital and meet the inclusion criteria for the study will be informed about the researchers and the study Written consent will be obtained from pregnant women who volunteer to participate in the study by filling out the Informed Volunteer Consent Form The training will be held in a suitable room a quiet room where individuals can sit comfortably and see each other in the area where the NST room is located in the hospital Pregnant women will be informed about the purpose of the study the confidentiality of the answers where and how the data will be stored and their questions on the subject will be answered Data collection forms will be given to the participant by the researcher and they will be asked to fill them out The data collection forms will be checked by the researcher to see if they have been filled out completely This process is planned to take approximately 10-15 minutes
Experimental Group In addition to midwifery care training content training videos and brochure-supported training on NST will be provided The NST device will be inserted and to be standard 5 minutes after the procedure begins the volume of the fetal heart sound coming from the device will be increased during the NST recording and the fetal heart sound will be ensured to continue The pregnant woman who will be transferred will rest for about 2 minutes
Control Group No additional applications will be made
Purpose This study will be carried out to determine the effect of video-educated midwifery care given to primiparous pregnant women before NST application on pregnancy stress and prenatal attachment levels
Method The data of the research will be collected at Tokat State Hospital after permission During data collection pregnant women who apply to the NST room of the relevant hospital and meet the inclusion criteria for the study will be informed about the researchers and the study Written consent will be obtained from pregnant women who volunteer to participate in the study by filling out the Informed Volunteer Consent Form The training will be held in a suitable room a quiet room where individuals can sit comfortably and see each other in the area where the NST room is located in the hospital Pregnant women will be informed about the purpose of the study the confidentiality of the answers where and how the data will be stored and their questions on the subject will be answered Data collection forms will be given to the participant by the researcher and they will be asked to fill them out The data collection forms will be checked by the researcher to see if they have been filled out completely This process is planned to take approximately 10-15 minutes
Experimental Group In addition to midwifery care training content training videos and brochure-supported training on NST will be provided The NST device will be inserted and to be standard 5 minutes after the procedure begins the volume of the fetal heart sound coming from the device will be increased during the NST recording and the fetal heart sound will be ensured to continue The pregnant woman who will be transferred will rest for about 2 minutes
Control Group No additional applications will be made
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None