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临床试验/NCT07382609
NCT07382609已完成不适用

The Effect of Creating a Birth Story in the Labor Room on Fear of Childbirth and Birth Comfort in Primiparous Pregnant Women

Inonu University1 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2024年3月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
58
试验地点
1
主要终点
Prenatal Self Evaluation Questionnaire score

研究概览

简要总结

The aim of this study is to reduce the fears of women who will give birth and increase their comfort. In the literature review conducted for this purpose, no study has yet been found that examines the effect of creating a birth story in the labor room on the fear of birth and birth comfort in primiparous pregnant women. In order to fill this gap in the literature, pregnant women in the labor room will be asked to create their birth stories and the effect of this on fear of birth and birth comfort will be examined.

The hypotheses of the study are as follows:

H1a: Creating a birth story in the labor room affects fear of birth H1b: Creating a birth story in the labor room affects birth comfort.

详细描述

The aim of this study is to examine the effect of creating a birth story in the labor room on the fear of childbirth and the comfort of pregnant women. Data will be collected from primiparous pregnant women who are admitted to the labor room in the maternity ward of Gölbaşı State Hospital and are in the latent phase. Women will be informed about the study and will be asked whether they will participate in the study. Informed consent forms will be distributed to women who agree to participate in the study. Data collection tools will be applied to women who agree to participate in the study by the researcher through face-to-face interviews. Data collection will be completed with the end of the latent phase (≥ 4-6 cm). No intervention will be applied to women in the control group, however, the Personal Information Form, Prenatal Self-Assessment Scale-Fear of Childbirth Subscale and Childbirth Comfort Scale will be applied simultaneously with the experimental group. Pre-test data collection questionnaires will be applied to pregnant women in the experimental group at the beginning of the latent phase and pregnant women will be asked to create their own birth stories. A transparent wall board will be attached to the wall of the labor room and pregnant women will be given appropriate pens and asked to write their feelings and thoughts on this board and in this way, birth stories will be created. If pregnant women wish, their photographs will be taken and attached to this board. After the birth story is created, the post-test data collection tools will be applied to the pregnant woman again and the data collection process will be completed.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Supportive Care
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • All primiparous pregnant women who are literate,
  • Over the age of 18,
  • Not experiencing a risky pregnancy,
  • Not becoming pregnant with assisted reproductive techniques,
  • Planned to have a vaginal birth,
  • In the latent phase of labor,
  • Do not have any psychiatric disorders,
  • Do not have any health problems in themselves or their babies,
  • Do not have a history of ex fetus will be included in the study.

排除标准

  • Pregnant women with an indication for caesarean section during the latent phase of labour will not be included in the study.

研究组 & 干预措施

No Intervention:

No Intervention

GROUP WITHOUT BIRTH STORY

Experimental

Experimental

Birth story creating group

干预措施: BIRTH STORY EXPERIMENTAL GROUP (Behavioral)

结局指标

主要结局

Prenatal Self Evaluation Questionnaire score

时间窗: Baseline (latent phase of labor) and prior to active labor (at 4 cm cervical dilatation)]

The scale developed by Lederman determines women's adaptation to pregnancy and motherhood. This scale is a 4-point Likert-type scale with 7 sub-dimensions and 79 items. The scores that can be obtained from the scale are between 10 and 40.

次要结局

  • Childbirth Comfort Questionnaire- CCQ score(Immediately prior to active labor (at 4 cm cervical dilatation))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Esra Tan

Master's Degree Student in Midwifery, Clinical Midwife

Inonu University

研究点 (1)

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