跳至主要内容
临床试验/NCT06769958
NCT06769958已完成不适用

The Effect of Reflexology on Pain, Comfort and Breastfeeding Self-Efficacy in Post-Cesarean Headache Due to Spinal Anesthesia

Yuzuncu Yıl University2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
60
试验地点
2
主要终点
Visual Analog Scale

研究概览

简要总结

This study was conducted to determine the effects of reflexology applied to mothers with headache due to spinal anesthesia after Cesarean delivery on pain, comfort and breastfeeding self-efficacy levels. The study, which was conducted with a single-blind, randomized controlled experimental design, was conducted between April 2024 and August 2024 at the Department of Obstetrics and Pediatrics, SBU Van Training and Research Hospital with mothers who had cesarean delivery under spinal anesthesia and had postpartum headache (Intervention group=30, Control group=30). Foot reflexology was applied to the mothers in the intervention group for a total of 30 minutes, 15 minutes on each foot. The control group was not subjected to any intervention other than routine nursing practices. Personal Information Form, Visual Analog Scale (VAS), Postpartum Comfort Scale (PPSC) and Breastfeeding Self-Efficacy Scale (BSSE) were used as data collection tools.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Health Services Research
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

  • 18 years and older,
  • performing SD under spinal anesthesia,
  • experiencing postpartum headaches,
  • Caesarean section performed at 37-42 weeks of gestation,
  • giving only one live birth,
  • open to written or oral communication,
  • at least a primary school graduate,
  • no complications during pregnancy,
  • mothers who agreed to participate in the study

排除标准

  • Performing a cesarean section at periods other than 37-42 weeks of gestation,
  • caesarean section under general anesthesia,
  • have health problems such as fractures, dislocations, phlebitis, arthritis, burns, wounds, eczema, fungus or inflammation in the foot tissue,
  • with disease of the cardiovascular system,
  • with chronic diseases such as hypertension or diabetes mellitus,
  • Postpartum controlled analgesia administered,
  • mothers with psychiatric diagnoses such as anxiety and depression

结局指标

主要结局

Visual Analog Scale

时间窗: pre-test post-test (approximately eight months), reduce pain

min-max (0-10), an increased score is a bad result

Postpartum Comfort Scale

时间窗: pre-test post-test (approximately eight months), Increasing Postpartum Comfort

min-max (34-170), increased score is a good result

Breastfeeding Self-Efficacy Scale

时间窗: pre-test post-test (approximately eight months), Increasing breastfeeding self-efficacy

min-max (14-70), increased score is a good result

次要结局

未报告次要终点

研究者

发起方
Yuzuncu Yıl University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Veysel Can

Asst. Prof.

Yuzuncu Yıl University

研究点 (2)

Loading locations...

相似试验