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Clinical Trials/NCT03588208
NCT03588208
Completed
Not Applicable

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

Federal University of São Paulo0 sites60 target enrollmentFebruary 1, 2016
ConditionsFibromyalgia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Fibromyalgia
Sponsor
Federal University of São Paulo
Enrollment
60
Primary Endpoint
Change in pain
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
February 1, 2016
End Date
March 25, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel

Investigators

Sponsor
Federal University of São Paulo
Responsible Party
Principal Investigator
Principal Investigator

Anamaria Jones

Professor

Federal University of São Paulo

Eligibility Criteria

Inclusion Criteria

  • 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.

Exclusion Criteria

  • 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.

Outcomes

Primary Outcomes

Change in pain

Time Frame: Baseline and after 6 and 12 weeks

Measured by numerical pain scale

Secondary Outcomes

  • 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)

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