The Effect of Electro-fetal monıtorısıon Sound on Anxiety, paın and Postpartum
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 80
- 试验地点
- 1
- 主要终点
- VİSUAL ANALOG SCALE
研究概览
简要总结
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.
详细描述
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 baby's 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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- Single (Participant)
盲法说明
Which of the participants is the control or intervention group will be selected by randomization.
入排标准
- 年龄范围
- 18 Years 至 35 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Who are december the age range of 18- 35,
- •The least literate,
- •Which is the primiparous,
- •who is at the 38-42 week of gestation
- •With a single pregnancy in the vertex position,
- •Who does not have a systemic disease that will interfere with normal delivery (gestational diabetes, preeclampsia, etc.),
- •Who is in the active phase of labor * Pregnant women who have agreed to participate in the study and received informed consent will be included in the study
排除标准
- •37. week
- •not between the weeks dec
- •It is a multipart,
- •Anyone who has any problems with communication,
- •Who has ceased to be involved in the study,
- •An unexpected complication develops (cesarean section of the pregnant woman, development of fetal distress in the fetus, etc.).
- •Oxytocin induction is applied Pregnant women who have been given pain medication (Aldolan, diazem) are
研究组 & 干预措施
Control
Control group pregnant women will be selected using randomization. their babies' fetal voice will not be listened.
Intervention
Pregnant women in the intervention group will be selected using randomization. the fetal voice of their babies will be listened to for about 3-5 minutes with a Non-stress Tester.
干预措施: Non-stress test (Device)
结局指标
主要结局
VİSUAL ANALOG SCALE
时间窗: immediately Before application
Visual analog scale: The scoring system is between 0 and 10. 0 is considered as no pain, while 10 is considered as unbearable pain.
STATUS AND CONTINUOUS ANXIETY SCALE
时间窗: immediately Before application
The state anxiety scale consists of 20 statements. The state anxiety scale requires the individual to answer the feelings or behaviors experienced in the current situation by marking one of the options such as (1) Not at all, (2) A little, (3) A lot and (4) Completely according to the degree of severity.
次要结局
未报告次要终点
研究者
YASEMİN AYDIN KARTAL
Assoc. Prof.
Saglik Bilimleri Universitesi