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临床试验/NCT06171022
NCT06171022已完成不适用

The Effect of Cherry Seed Pillow on Pain and Quality of Life in Patients With Fibromyalgia

Hasan Gerçek1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2023年12月6日最近更新:
适应症
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
72
试验地点
1
主要终点
Change from baseline in pain at 4 weeks

研究概览

简要总结

In this study, the effects of 4-week Cherry seed pillow application on pain and quality of life in individuals diagnosed with fibromyalgia will be examined.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Over 18 years of age
  • •Diagnosis of Fibromyalgia according to ACR classification criteria
  • •Neuromuscular system examination is normal
  • •Pain (vas-visual anologous scale) level of at least 5 points
  • •No communication problems
  • •Willingness to participate in the practice of using cherry seed cushion
  • •To be capable of answering the data collection tools to be used in the research
  • •Not having made hot, cold etc. applications at home

排除标准

  • •-No diagnosis of Fibromyalgia according to ACR classification criteria
  • •Normal examination of the neuromuscular system
  • •Pain (vas-visual anologous scale) level between 0-5
  • •Communication problems
  • •Failure to accept the practice of using cherry seed cushion and failure to finish the implementation process
  • •Having a musculoskeletal disorder other than fibromyalgia
  • •Pregnant or lactating
  • •To be capable of answering the data collection tools to be used in the research
  • •Having made hot, cold etc. applications at home

研究组 & 干预措施

Cherry seed pillow

Experimental

4 Weeks, 5 days a week, 20 minutes, in addition to the physiotherapy application of the routine, a heated cherry seed pillow will be applied.

干预措施: Cherry seed pillow (Other)

Control

Active Comparator

4 Weeks, 5 days a week, 20 minutes, in addition to the physiotherapy application of the routine, a hot-pack will be applied.

干预措施: Control (Other)

结局指标

主要结局

Change from baseline in pain at 4 weeks

时间窗: Baseline and 4 weeks

he rest, activity and night pains of the participants will be evaluated with a 10 cm Visual Analog Scale before the treatment and at the end of the 4-week application. "0" means no pain, "10" means excruciating pain. Results will be recorded in cm.

次要结局

  • Change from baseline in function at 4 weeks(Baseline and 4 weeks)

研究者

发起方
Hasan Gerçek
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Hasan Gerçek

Lecturer

KTO Karatay University

研究点 (1)

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