跳至主要内容
临床试验/NCT06331949
NCT06331949已完成不适用

The Effect of Video-Assisted Training Given to Pregnant Women on Non-Stress Test Application on Pregnancy Stress and Prenatal Attachment

Hilal Özbek2 个研究点 分布在 2 个国家目标入组 74 人开始时间: 2024年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
74
试验地点
2
主要终点
State-Trait Anxiety Scale

研究概览

简要总结

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 mother's 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 baby's 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

详细描述

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

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)

入排标准

年龄范围
18 Years 至 49 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Primiparous pregnant woman
  • Able to read and write
  • Pregnant women who are 32 weeks or more pregnant
  • No detection problems
  • The baby has no health problems
  • Having no psychological or physiological health problems
  • Pregnant women who accept the research

排除标准

  • Under 32 weeks
  • Those who did not accept the research
  • If the pregnant woman feels uncomfortable during the research,
  • Pregnant women who want to leave any part of the research

研究组 & 干预措施

Control Group

No Intervention

No additional applications will be made

Experimental Group

Experimental

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.

干预措施: video assisted training (Other)

结局指标

主要结局

State-Trait Anxiety Scale

时间窗: Baseline]

It requires the person to mark one of four options, such as 1 (Not at all), 2 (Somewhat), 3 (A lot), 4 (Completely), depending on the intensity of his/her feelings about himself/herself at a certain time and under certain conditions.

Prenatal Attachment Inventory (PAI)

时间窗: Baseline]

PAI is used to explain the thoughts, feelings, and situations experienced by the woman during pregnancy and to determine the level of attachment to the baby in the prenatal period. The increase in the score received by the pregnant woman indicates that her attachment level also increases.

次要结局

  • State-Trait Anxiety Scale(after training is completed)
  • Prenatal Attachment Inventory (PAI)(after training is completed)

研究者

发起方
Hilal Özbek
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Hilal Özbek

Assist. Prof. Dr.

Tokat Gaziosmanpasa University

研究点 (2)

Loading locations...

相似试验