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临床试验/NCT06138288
NCT06138288已完成不适用

The Effect of Acupressure Applied After Cesarean Section on Postpartum Pain and Postpartum Comfort: A Randomized Controlled Study

Eastern Mediterranean University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年11月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
1
主要终点
visual analog scale

研究概览

简要总结

Pressure applied according to the principles of acupressure limits the pain limit, reduces the secretion of endorphins, which is a neurochemical, reduces the tension in the muscles, reduces the amount of oxygen in the blood flow, and finally provides duration and relaxation. Acupressure application is becoming more and more common nowadays because it is a noninvasive, safe, easy-to-apply and effective method without side effects. It seems that there is a limit to the study in which group acupressure applications in the literature are examined together on pain and comfort after cesarean section. In these basic points, the expectations of achieving postpartum pain and postpartum comfort of acupressure applied after cesarean delivery in this study. The circle of the research; There will be women who will have repeated cesarean section in a private Obstetrics Clinic in Famagusta. Women will be separated from two groups, one group will continue acupressure and the other group will do routine care. Visual analog scale and end-of-birth comfort procedure will be applied to women before and after the application.

详细描述

Pressure applied according to the principles of acupressure limits the pain limit, reduces the secretion of endorphins, which is a neurochemical, reduces the tension in the muscles, reduces the amount of oxygen in the blood flow, and finally provides duration and relaxation. Acupressure application is becoming more and more common nowadays because it is a noninvasive, safe, easy-to-apply and effective method without side effects. It seems that there is a limit to the study in which group acupressure applications in the literature are examined together on pain and comfort after cesarean section. In these basic points, the expectations of achieving postpartum pain and postpartum comfort of acupressure applied after cesarean delivery in this study. The circle of the research; There will be women who will have repeated cesarean section in a private Obstetrics Clinic in Famagusta. Women will be separated from two groups, one group will continue acupressure and the other group will do routine care. Visual analog scale and end-of-birth comfort procedure will be applied to women before and after the application.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Other

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

  • agreeing to participate in the research,
  • be between the ages of 18-49,
  • To give birth by cesarean section between 37-40 weeks,
  • Having a healthy and live birth at the end of a single pregnancy,
  • Receiving spinal anesthesia
  • Being able to read and write Turkish and be open to communication.

排除标准

  • Absence of pain in the 2nd hour postpartum
  • Having a cesarean delivery after a risky pregnancy,
  • Having a chronic illness
  • Having severe systemic disease
  • Not receiving spinal anesthesia
  • Having a body mass index over 25,
  • Have previous acupressure experience.

结局指标

主要结局

visual analog scale

时间窗: 5 minutes

VAS has been developed to convert some values that cannot be measured numerically into numeric values. The VAS, which is a generally accepted, safe and easily applicable measurement tool in the world literature, consists of a 10 cm long line and there are subjective descriptive statements at both ends of the scale (0 cm = no pain and 10 cm = unbearable pain). The individual marks the appropriate place for his/her pain on this 10 cm line on the scale. The distance from the beginning of the scale to the point where the individual marks is measured with a ruler, and the pain intensity of the individual is determined numerically in cm. A low score obtained from the VAS indicates that the individual's pain intensity is low/low, and a high score indicates high/severe. The VAS is sensitive to pharmacological and non-pharmacological modalities that alter the pain experience.

次要结局

  • postpartum comfort scale(15 minutes)

研究者

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

Hilal Begüm Çayır

Nurse

Eastern Mediterranean University

研究点 (1)

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