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Clinical Trials/NCT01351311
NCT01351311
Completed
N/A

Assessment of Effectiveness of Resistance Training Exercise Using the Swiss Ball in Patients With Ankylosing Spondylitis

Federal University of São Paulo1 site in 1 country60 target enrollmentMarch 2011

Overview

Phase
N/A
Intervention
Not specified
Conditions
Ankylosing Spondylitis
Sponsor
Federal University of São Paulo
Enrollment
60
Locations
1
Primary Endpoint
Bath Ankylosing Spondylitis Functional Index (BASFI)
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

The aim of the present study is to assess the effectiveness of resistance training with swiss ball in the treatment of patients with ankylosing spondylitis.

Detailed Description

A randomized, controlled, single-blind, prospective trial being conducted involving 54 patients with ankylosing spondylitis, selected from outpatient clinics - UNIFESP. They will be randomized in intervention group (n = 27) conduct training for muscle strengthening with the aid of the Swiss ball and in the control group (n = 27) did not undergo any intervention. Eight exercises will be conducted with intent to engage all muscle groups.

Registry
clinicaltrials.gov
Start Date
March 2011
End Date
November 2012
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

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

Marcelo Cardoso de Souza

MsC

Federal University of São Paulo

Eligibility Criteria

Inclusion Criteria

  • Patients with established diagnosis of AS steinbrocker functional class I-II
  • Basic medication stable for at least three months
  • Agreed to participate and signed term of informed consent

Exclusion Criteria

  • Uncontrolled hypertension
  • Coronary artery disease
  • History of revascularization
  • History of syncope or arrhythmias induced by exercise
  • Decompensated diabetes mellitus
  • Severe psychiatric illness
  • Fibromyalgia
  • Another medical condition more disabling than AS
  • History of exercise regular (at least 30 minutes 2 times per week)

Outcomes

Primary Outcomes

Bath Ankylosing Spondylitis Functional Index (BASFI)

Time Frame: 16 weeks

Functional capacity assessed by BASFI

Secondary Outcomes

  • 6-MINUTE WALK TEST(16 weeks)
  • TIME UP AND GO TEST(16 weeks)
  • LIKERT SCALE(16 weeks)
  • 1 REPETITION MAXIMUM TEST(16 weeks)
  • Bath Ankylosing Spondylitis Disease Activity Index (BASDAI)(16 weeks)
  • Bath Ankylosing Spondylitis Metrology Index (BASMI)(16 weeks)
  • erythrocyte sedimentation rate (ESR)(16 weeks)
  • Short form-36 (SF-36)(16 weeks)
  • QUANTITY OF ANALGESICS AND ANTI-INFLAMATORY USED(16 weeks)
  • Health Assessment Questionnaire (HAQ) Health Assessment Questionnaire(16 weeks)

Study Sites (1)

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