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Clinical Trials/NCT02401958
NCT02401958
Completed
Phase 4

Acute Effect of Resistance Training in Inflammatory Markers in Women With Rheumatoid Arthritis

Federal University of São Paulo1 site in 1 country34 target enrollmentMarch 2014

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Rheumatoid Arthritis
Sponsor
Federal University of São Paulo
Enrollment
34
Locations
1
Primary Endpoint
Change in one (or more) of the inflammatory markers
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

ABSTRACT Introduction: Rheumatoid arthritis (RA) is a systemic inflammatory, chronic and progressive disease that can lead to joint destruction and important functional disability. Chronic inflammation, with a substantial increase in the amount of pro-inflammatory cytokines in synovial joint, is one of the biggest challenges in controlling RA. Resistance exercise has been recognized for positively modulate inflammation in healthy subjects. Objective: To evaluate the effect of an acute bout of resistance exercise on serum concentrations of tumor necrosis factor alpha (TNF-α), interleukin 1 receptor antagonist(IL-1ra), interleukin 1 beta (IL-1β), C reactive protein (CRP), interleukin 6 (IL-6), interleukin 10 (IL-10), and cartilage oligomeric matrix protein (COMP) in postmenopausal women with RA and women without the disease. Methods: 17 volunteers with RA and 17 without the disease, with a mean age of 54.7 + 6.63 underwent a resistance exercise session with a set of 12 repetitions at 50% of one repetition maximum (1RM ) and a set of 8 repetitions at 75% of 1RM. The exercises performed were: knee extension, knee flexion, hip abduction and hip adduction. Blood samples were obtained 30 minutes before, 5 minutes before, immediately after, 1 hour, 2 hours and 24 hours after the exercise session. Serum glucose concentrations prior to exercise were also measured. The investigators used the Student's't test, the model of analysis of variance with repeated measures and Bonferroni method of multiple comparisons to analyze the data, being considered statistically significant levels of p <0.05.

Registry
clinicaltrials.gov
Start Date
March 2014
End Date
August 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

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

Ana Carolina Pereira Nunes Pinto

Physiotherapist

Federal University of São Paulo

Eligibility Criteria

Inclusion Criteria

  • Women classified acording to the American College of Rheumatology's criteria to rheumatoid arthritis
  • Post menopausal women
  • Stable medication three months before study

Exclusion Criteria

  • Women with rheumatoid arthritis with functional class IV, acording to ACR criteria
  • Women engaged in some type of regular exercise program;
  • Failure: heart, coronary, respiratory, renal and / or hepatic (uncompensated);
  • Uncompensated systemic hypertension;
  • Volunteers with other associated inflammatory diseases;
  • Unable to perform the exercises.
  • Control group We included in the control group of this study postmenopausal volunteers, without Rheumatoid Arthritis. Exclusion criteria were the same as those adopted for the participants of the Rheumatoid Arthritis Group

Outcomes

Primary Outcomes

Change in one (or more) of the inflammatory markers

Time Frame: 30 minutes before training; 5 minutes before training; 5 minutes after training; 1 hour after training; 2 hours after training; 24 hours after training

TNF-alfa, IL1-beta, IL1-ra, PCR, IL10, IL6

Secondary Outcomes

  • No change in inflammatory markers(30 minutes before training; 5 minutes before training; 5 minutes after training; 1 hour after training; 2 hours after training; 24 hours after training)

Study Sites (1)

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