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Clinical Trial Summary

The purpose of this study is to determine whether:

1. Progressive resistance training improves pain and disability

2. Progressive Resistance training improves muscular strength, ability to walk and quality of life


Clinical Trial Description

Patients in experimental group participated in a 12-week progressive resistance training using a repetition maximum (RM) exercise in which patients performed 1RM with the maximum bearable weight. Once the 1RM was determined, training was divided into the following regimen: 2 series of 8 repetitions, the first with 50% and the second with 70% of 1RM.

The exercises were knee extension and flexion and hip abduction and adduction, all performed in machines. The 1RM load was reevaluated every 2 weeks.

The control group remained on a three-month waiting list for physiotherapy. Patients were assessed for pain, function, quality of life, muscle strength and six-minute walk test. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01099371
Study type Interventional
Source Federal University of São Paulo
Contact
Status Active, not recruiting
Phase Phase 2/Phase 3
Start date February 2009
Completion date February 2011

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