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Clinical Trials/NCT00327275
NCT00327275
Completed
Not Applicable

The Strength Training and Remicade Study

University of Arizona1 site in 1 country35 target enrollmentMarch 2004

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Rheumatoid Arthritis
Sponsor
University of Arizona
Enrollment
35
Locations
1
Primary Endpoint
Strength
Status
Completed
Last Updated
19 years ago

Overview

Brief Summary

To assess the effects of a 16-week individualized, intensive strength training program in patients with rheumatoid arthritis. Primary and secondary outcomes include: strength and body composition, function, disease activity, pain, quality of life.

We hypothesized that improvements would be seen in all of the above outcomes.

Registry
clinicaltrials.gov
Start Date
March 2004
End Date
January 2005
Last Updated
19 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Males and females with RA
  • Over 18 years of age
  • ACR Functional Class I and II
  • Taking Remicade \>4 months

Exclusion Criteria

  • Presence of comorbid conditions contraindicated to exercise, including, but not limited to:
  • heart disease
  • severe osteoporosis: (if \>50 years): T score \< -3.0 for hip or spine excluded; T score \<-2.5 for hip or spine w/o current treatment)
  • (all potential subjects) previous non-traumatic fractures
  • uncontrolled BP
  • Regular use of assistive walking device which would interfere with ability to lift weights
  • Currently or within the last 3 months participating in aerobic exercise \> 150 minutes a week
  • Currently or within the last 3 months participating in any regular strength training activities
  • Presence of neurological impairment that directly limits ability to perform exercise
  • Participation in concurrent exercise study

Outcomes

Primary Outcomes

Strength

Body Composition

Function

Pain

Secondary Outcomes

  • Disease Activity
  • Fatigue
  • Quality of Life

Study Sites (1)

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