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临床试验/NCT03466008
NCT03466008已完成不适用

Whole-Body Cryotherapy (WBC) as an Adjunct Treatment on Pain in Fibromyalgia Persons: Short Time Effect.

Haute École Robert Schuman Libramont0 个研究点目标入组 24 人开始时间: 2017年1月1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
24
主要终点
pain status at 1 month from baseline

研究概览

简要总结

Our aim was to determine whether Whole Body Cryotherapy (WBC) can result in improved pain status, perceived health, and quality of life in patients with fibromyalgia. It is hypothesized that this positive effect can be achieved through increased functional mobility and decreased pain intensity resulting from cold-induced modulation of the inflammation-immune axis.

详细描述

24 patients with fibromyalgia were randomized into 2 groups (n=11 in the WBC group, n=13 in the control group). In the WBC group, 10 sessions of WBC were performed (in addition to usual care) in a standard cryotherapy room over a duration of 8 days. Patients in the control group did not change anything in their everyday activities. Several self-reported variables relating to perceived health were measured repeatedly (pain intensity, functional mobility, and quality of life).

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Fibromyalgia diagnosis

排除标准

  • cardiorespiratory disorder current pregnancy cold intolerance Embolic diseases

研究组 & 干预措施

Whole body cryotherapy arm

Experimental

intervention consisted of 10 sessions of WBC (three minutes for each session) which were performed in addition to usual care in a standard cryotherapy room over a duration of 8 days.

干预措施: Whole-Body Cryotherapy (Behavioral)

Usual treatment arm

No Intervention

usual care

结局指标

主要结局

pain status at 1 month from baseline

时间窗: change from baseline at one month follow-ups

pain score on a numerical scale (Subjective Numerical scale) likert rating 0 to 10 by the fibromyalgia patient 0 indicate no pain, 10 maximal pain value

次要结局

  • functional status : the Oswestry Disability Index (ODI)(change from baseline at one month follow-ups)
  • functional status : the Disability of the Arm, Shoulder and Hand (DASH) score(change from baseline at one month follow-ups)
  • functional status : Lower Extremity Functional Scale (LEFS)(change from baseline at one month follow-ups)
  • health related quality of life (HRQoL)(change from baseline to one month follow-ups)
  • pain status at 2 weeks from baseline(change from baseline at two weeks follow-ups)
  • functional status : the Oswestry Disability Index (ODI), subjective low back pain questionnaire(chnage from baseline at two weeks follow-ups)

研究者

发起方
Haute École Robert Schuman Libramont
申办方类型
Other
责任方
Principal Investigator
主要研究者

François Tubez

Physical Therapist, PT, PhD Student, Principal investigator

Haute École Robert Schuman Libramont

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