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临床试验/NCT05893355
NCT05893355已完成不适用

The Effect of Acupressure Applied in the Late Postpartum Period After Cesarean Section on Back Pain

Kocaeli University2 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2023年6月5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
70
试验地点
2
主要终点
Visual analog scale for assessing back pain

研究概览

简要总结

The study will be carried out in a randomized controlled manner in order to examine the effectiveness of acupressure applied in the late postpartum period in postpartum women who have had back pain and have had a cesarean delivery. The sample of the study will consist of 70 participants who applied to the family health center between 05.06.2023 and 05.12.2024, who had cesarean birth registered in the central family health center in Kocaeli province Kandıra district, who met the research criteria and agreed to participate in the research. Data in the research; It will be collected using the 'Participant Information Form', 'VAS (Visual Analog Scale for Evaluating Back Pain)', 'McGill Pain Questionnaire (Short Form)'. Participants in the acupressure group will be given 2 times acupressure application in the 1st week and 4th week postpartum. No application will be made to the participants in the control group. The research is planned to be carried out after obtaining the necessary institutional and ethical committee permissions.

详细描述

Aim: The study was planned to examine the effect of acupressure on back pain in the late postpartum period after cesarean section.

Hypothesis(s):

H0: Acupressure application applied to puerperant women who had a cesarean delivery in the late postpartum period has no effect on reducing the level of back pain.

H1: Acupressure application applied to puerperant women who had cesarean delivery in the late postpartum period reduces the level of back pain.

Type of Research: This study was designed as a randomized controlled experimental study.

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 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • 18-49 years old,
  • Able to read and write Turkish
  • Postpartum 1st week and within 4th week
  • Primiparous and multiparous
  • Those who had a registered cesarean section in the family health center where the study was conducted,
  • Able to speak and understand Turkish,
  • Back pain score above 4 according to VAS (Visual analog scale),
  • Participants who voluntarily agree to participate in the study will be included in the study.

排除标准

  • Congenital anomaly in the baby who gave a stillbirth, whose baby is hospitalized in the neonatal intensive care unit,
  • Use of cigarettes or alcohol
  • History of past or present mental illness,
  • Using antidepressants or anxiolytic drugs,
  • With rheumatoid arthritis, ankylosing spondylitis, Scheuermann's disease, Ehlers-Danlos syndrome, spinal surgeries, nerve root compression, spondylolisthesis comorbid disease,
  • Perineal edema, hematoma, wound dehiscence, bladder catheterization and serious postpartum complications (internal bleeding, femoral artery embolism, pelvic fracture),
  • With impaired tissue integrity in the area to be applied,
  • Vaginal delivery,
  • Taking painkillers in the last 6 hours,
  • In addition, those who want to leave the research at any stage of the research will be excluded from the research.

结局指标

主要结局

Visual analog scale for assessing back pain

时间窗: This scale will be filled in by the participants after the application is made at the end of the first week after birth.

The application will be made at the end of the first week after birth. The participant marks his or her own pain on a 10 cm ruler, which says no pain on one end and the most severe pain on the other end. The participant is told that there are two endpoints and to mark anywhere between these points that matches the severity of the pain. The distance between the onset of no pain and this point marked by the patient is measured and recorded in centimeters. It is stated that VAS is more sensitive and reliable than other unidimensional scales in pain severity measurement. The VAS is more sensitive than the simple descriptive scale.

次要结局

  • Visual analog scale for assessing back pain(This scale will be filled in by the participants after the application at the end of the first mounth after birth.)

研究者

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

sena dilek

Principal Investigator

Kocaeli University

研究点 (2)

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