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临床试验/NCT07299136
NCT07299136已完成不适用

Evaluating the Effect of Hugging and Praying on Traumatic Birth Perception, Birth Pain, and Birth Anxiety

NURTEN ÖZÇALKAP1 个研究点 分布在 1 个国家目标入组 164 人开始时间: 2025年4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
发起方
入组人数
164
试验地点
1
主要终点
Information Form

研究概览

简要总结

Pregnant women participating in our study will receive the intervention (hugging, praying, and hugging + praying) from the researcher or a relative as often as they wish during labor and contractions. These sessions will be administered during each stage of labor, taking into account when the pregnant woman is ready to begin the intervention.

详细描述

Pregnant women participating in our study will receive the intervention (hugging, praying, and hugging + praying) from the researcher or a relative as often as they wish during labor and contractions. These sessions will be administered during each stage of labor, taking into account when the pregnant woman is ready to begin the intervention.

For the hugging group, hugging sessions will be performed whenever the pregnant woman wants and during contractions, if she wishes, by a relative (husband, mother, sister, etc.) or midwife. The pregnant woman can be hugged for as long as she wants or for 5-10 minutes. For the prayer group, whenever the pregnant woman wishes, or during contractions if she wishes, a close relative (husband, mother, sister, etc.) or midwife will recite a prayer chosen by the pregnant woman, if she has one; if she does not have a preferred prayer, the first 5 verses of Surah Al-Inshiqaq will be recited:

In the name of Allah, the Most Gracious, the Most Merciful

  1. When the sky is split asunder,
  2. And obeys the command of its Lord,
  3. When the earth is stretched out flat,
  4. And casts forth what is within it,
  5. And obeys the command of its Lord, every person will be confronted with what they have done! To be read together Before starting the first session, the "Information Form," "Visual Analog Scale," Traumatic Birth Perception Scale, and "Oxford Birth Anxiety Scale (Appendix 4)" will be administered. and at the end of the first, second, and fourth stages of birth, the "Visual Analog Scale," "Traumatic Birth Perception Scale," and "Oxford Birth Anxiety Scale" will be administered.

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
None

入排标准

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

入选标准

  • Age ≥18 years
  • No communication barriers
  • Applying to Ağrı Training and Research Hospital for normal delivery within the study dates
  • Volunteering to participate in the study
  • No contraindications for normal vaginal delivery (e.g., cephalopelvic disproportion)
  • Being at term (38-42 weeks)
  • No condition preventing praying and hugging

排除标准

  • Refusal to participate in the study
  • Maternal disease (heart disease, diabetes, etc.)
  • Having a preterm or postterm pregnancy
  • Undergoing an emergency cesarean section during follow-up
  • Having a fetal malformation (anencephaly, Down syndrome, etc.)
  • Not answering the questions in the questionnaire

研究组 & 干预措施

Group 1

Experimental

Hugging

干预措施: Hugging group, (Other)

Group 2

Experimental

Praying

干预措施: Prayer group (Other)

Group 3

Experimental

Hugging and Praying

干预措施: Hugging and Praying group (Other)

Group 4

No Intervention

CONTROL

结局指标

主要结局

Information Form

时间窗: Before starting the first session average 8 months

This form, prepared by the researcher in line with the literature, inquires about the socio-demographic characteristics of the participants.

Visual Analog Scale (VAS)

时间窗: average 8 months

It is a one-dimensional scale that objectively assesses a pregnant woman's perception of pain. It allows some values that cannot be measured numerically to be converted into numerical values. In 1921, Hayes and Peterson argued that emotional levels could be expressed on lines. The VAS was first developed and used by Bond and Pilowsky in 1966. The VAS is a 100 mm (10 cm) ruler used to quantitatively determine pain intensity, with one end representing painlessness (0 = no pain) and the other end representing the most severe pain (10 = severe pain). The patient marks any point between the two points that corresponds to the severity of their pain. The distance between the end of the scale representing painlessness and the point marked by the patient is measured with a ruler and recorded in centimeters. This numerical value indicates the pregnant woman's pain intensity. 0 cm = No pain, 0.53 cm = Mild pain, 3.5-6.5 = Moderate (Ergin, 2013; Aslan, 2006; Mucuk, 2009).

Traumatic Birth Perception Scale

时间窗: average 8 months

TThe Traumatic Birth Perception Scale (TBRS), developed by Yalnız et al. in 2016, is a thirteen-item, unidimensional Likert-type separation scale (Yalnız et al., 2016). Scores range from 0 to 10 for all items not requiring reverse scoring. The minimum scale score is 0 and the maximum is 130. The total scale score ranges from 0 to 26, indicating very low levels of perception of traumatic birth; 27 to 52, indicating low levels; 53 to 78, indicating moderate levels; 79 to 104, indicating high levels; and 105 to 130, indicating very high levels of perception of traumatic birth. The scale's Cronbach's alpha coefficient is .89 (Yalnız et al., 2016).

次要结局

未报告次要终点

研究者

发起方
NURTEN ÖZÇALKAP
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

NURTEN ÖZÇALKAP

Asistant Professor

Agri Ibrahim Cecen University

研究点 (1)

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