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临床试验/NCT05392283
NCT05392283已完成不适用

Vacuum Cupping for Chronic Neck and Back Pain - a Feasibility Study

Jena University Hospital2 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2022年5月2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
5
试验地点
2
主要终点
Pain intensity (Numeric rating scale (NRS))

研究概览

简要总结

Small clinical pilot studies have shown that vacuum massage-related techniques such as traditional dry cupping can reduce musculoskeletal pain such as back and neck pain. At the same time, little is yet known about the potential mechanisms of action of these therapies. A vacuum pump induces a massaging effect of the skin including the deeper tissue layers. The resulting massage technique corresponds to a kind of tissue manipulation similar to dry cupping. In this procedure, suction force and air flow can be individually adjusted. This is an advantage that can be used for patients with varying degrees of sensitivity or who are preloaded by patients with varying degrees of sensitivity or a history of pain. The aim of this study was to test the feasibility of the study design.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • chronic neck or back pain
  • mean pain intensity ≥ 40 mm VAS

排除标准

  • neurological symptoms or neuropathic pain
  • vertebral column surgery less than 12 months prior to the study
  • TENS, acupuncture, osteopathy, or a chiropractic maneuvre or infiltration at the area within 4 weeks prior to the inclusion in the study
  • congenital deformation of the spine

结局指标

主要结局

Pain intensity (Numeric rating scale (NRS))

时间窗: measured at baseline (week 1) and weekly during treatment (week 2 to 5) and 1 month after last treatment

NRS is a 11-point pain scale for self-reporting of pain ("0" meaning "no pain" and "10" meaning "worst pain")

次要结局

  • Quantitative sensory testing (QST)(measured at baseline (week 1) and weekly during treatment (week 2 to 5) and 1 month after last treatment)
  • Neck Disability Index (NDI)(measured at baseline (week 1), at the end of treatment (week 5) and after 1 month after last treatmentekly during treatment (week 2 to 5) and 1 month after last treatment)
  • Oswestry Disability Index (ODI)(measured at baseline (week 1), at the end of treatment (week 5) and after 1 month after last treatment)
  • Pain diary(filled in from baseline (week 1) until last treatment (week 5))

研究者

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

Winfried Meißner

Principal investigator

Jena University Hospital

研究点 (2)

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