NCT00327275
Completed
Not Applicable
The Strength Training and Remicade Study
ConditionsRheumatoid Arthritis
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.
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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