Ignite Creation Date:
2024-05-06 @ 8:09 PM
Last Modification Date:
2024-10-26 @ 3:21 PM
Study NCT ID:
NCT06271889
Status:
RECRUITING
Last Update Posted:
2024-02-22
First Post:
2021-12-02
Brief Title:
The Effect of Electro-fetal monıtorısıon Sound on Anxiety paın and Postpartum Bonding at the First Phase of Delivery
Sponsor:
Saglik Bilimleri Universitesi
Organization:
Saglik Bilimleri Universitesi
Study Overview
Official Title:
The Effect of Electro-fetal monıtorısıon Sound on Anxiety paın and Postpartum
Status:
RECRUITING
Status Verified Date:
2024-02
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:
University of Health Sciences Istanbul Umraniye training and Research Hospital Clinic of Obstetrics and gynecology birth maternity and Child Health Hospital Aydın to the clinic pregnant women pregnant women in active labor act and received acceptance to delivery to the fetal heart sound by existing tripped fetal heart sounds of pregnant women anxiety pain and the birth in order to determine the effect of connecting the end of the level will be conducted The study will guide midwives in reducing the anxiety or pain of pregnant women
Detailed Description:
Application of the Research Informed voluntary consents will be obtained in written and oral form by giving the necessary information about the study to pregnant women before the application The form will be signed Environmental stimuli before the procedure noise heat light touch etc will be brought under control Pregnant women admitted to the maternity hospital will be assigned to the intervention and control group using computer-aided randomization Routine maintenance will be applied to both groups in the study Anamnesis and blood are routinely taken from pregnant women admitted to the maternity unit within the scope of routine care in the institution where the research was conducted and NST is connected by inserting an intravenous catheter STAI and VAS will be filled in before the application to both groups of pregnant women after application the forms will be applied again at the beginning of the active phase cervical opening 4-5 cm and at the end cervical opening 6-7 cm In both groups pulse respiration and oxygen saturation will be evaluated with body temperature at the beginning of the active phase cervical opening 4-5 cm and at the end cervical opening 6-7 cm before and after the application With decemberibel meter the frequency range will be kept within the range of 30 dB-90 dB Participants will be able to adjust the volume of their babys voice at their own level No noninvasive and invasive interventions will be applied to pregnant women in the intervention group during the application If the control group is pregnant only routine care will be performed Both groups of pregnant women will be completed with STAI VAS and the Postpartum Attachment scale before and after the application The researcher should constantly monitor and evaluate the mother and fetus during the application process and when discomfort develops the procedure will be terminated and the clinical specialist physician will be informed
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?:
False
Is an FDA AA801 Violation?:
None