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临床试验/NCT03588208
NCT03588208已完成不适用

Evaluation of the Effectiveness of a Progressive Resistance Training Program for Patients With Fibromyalgia: a Randomized Controlled Trial

Federal University of São Paulo0 个研究点目标入组 60 人开始时间: 2016年2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
60
主要终点
Change in pain

研究概览

简要总结

Patients in the experimental group underwent a progressive resistance training program, performed twice a week for 12 weeks. The charge intensity was progressively increased from 40% to 80% of 1 repetition maximum. The following muscle groups were worked: trunk flexors and extensors, elbow flexors and extensors, knee flexors and extensors, hip abductors and adductors and shoulder abductors. In addition to strength training, the experimental group also conducted a structured education program in one hour class once a week for five weeks. Patients in the control group performed the same education program.

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
Single (Outcomes Assessor)

入排标准

接受健康志愿者

入选标准

  • Diagnosis of fibromyalgia according to the criteria of the American College of Rheumatology;
  • Feminine gender;
  • Age between 18 and 65 years;
  • Pain between 3 and 8 cm in the Numerical Pain Scale (END);
  • Have not changed treatment for fibromyalgia in the past three months;
  • Agree to participate in the study and sign the informed consent form.

排除标准

  • Cognitive deficit that does not allow the understanding of the evaluation instruments;
  • Other diseases that make it impossible to perform the exercises;
  • Physical activity started or changed in the last three months;
  • Physical therapy in the last six months;
  • In litigation.

研究组 & 干预措施

Control Group

Active Comparator

干预措施: Educational Program (Other)

Intervention Group

Experimental

干预措施: Progressive resistance training program (Other)

Intervention Group

Experimental

干预措施: Educational Program (Other)

结局指标

主要结局

Change in pain

时间窗: Baseline and after 6 and 12 weeks

Measured by numerical pain scale

次要结局

  • Change in Functional capacity(Baseline and after 6 and 12 weeks)
  • Change in Health related quality of life(Baseline and after 6 and 12 weeks)
  • Change in strength(Baseline and after 6 and 12 weeks)
  • Change in Generic quality of life(Baseline and after 6 and 12 weeks)

研究者

发起方
Federal University of São Paulo
申办方类型
Other
责任方
Principal Investigator
主要研究者

Anamaria Jones

Professor

Federal University of São Paulo

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