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临床试验/NCT06277375
NCT06277375已完成不适用

Fibromiyalji Tanılı Kadınlarda Uygulanan Yavaş Vurumlu Sırt Masajının Ağrı ve Yorgunluk Üzerine Etkisi: Randomize Kontrolü Çalışma

TC Erciyes University1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2023年2月14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
48
试验地点
1
主要终点
Fatigue

研究概览

简要总结

Fibromyalgia syndrome (FM) is defined as a non-inflammatory chronic pain syndrome with widespread pain in the musculoskeletal system, tender points (PINs) on physical examination and no specific laboratory findings. T Sampling was calculated using Power power (G Power 3.1.9.4) analysis. The effect size of the study was calculated based on the mean pain scores and standard deviations of the control and experimental groups taken from the study conducted by Field, et al. (2002). Accordingly, when 25 patients were included in each group, it was determined that the power was 85% at 5% Type I error level. The application to the experimental group will be done 3 days a week for 10 minutes for a total of 30 minutes. data will be collected with patient information form, fatigue severity scale and vas.

详细描述

he research will be conducted experimentally with the aim of evaluating the effects of slow-stroke back massage in patients followed up in the physical therapy and rehabilitation unit with the diagnosis of fibromyalgia.

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
Single (Outcomes Assessor)

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

  • Able to communicate verbally,
  • Over 18 years of age,
  • no vision and hearing loss
  • who have received medical treatment,
  • who have never received a slow-stroke back massage before

排除标准

  • Initially volunteered to participate in the study, but did not like the application of slow-stroke back massage
  • who wants to leave the study for another reason

结局指标

主要结局

Fatigue

时间窗: The scale was filled in the baseline

It is a tenitem, self-administered questionnaire. Because each item has a maximum possible score of 10, the maximum possible total score is 100.

VAS

时间窗: The scale was filled in the baseline

VAS consisting of a 10-centimeter horizontal line, anchored evenly by numbers from 0 to 10, was used to assess the patient's pain and willingness to repeat the procedure. The number 0 was identical to having no pain while the number 10 corresponded to maximal pain that can be experienced by the patient.

次要结局

未报告次要终点

研究者

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

Dilek Efe Arslan

ErciyesU

TC Erciyes University

研究点 (1)

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