Knee Osteoarthritis Join Diseases
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The study will include individuals who have had osteoarthritis for at least 6 months; who experience movement-related join pain; morning stiffness lasting less than 30 minutes; the presence of crepitus or limited range of motion
Exclusion criteria
Exclusion criteria: Participants will be excluded if they have injuries to the upper or lower limbs that would prevent them from completing the proposed training; a history of orthopedic surgery within the past 12 months; patients with lower limb arthroplasty; pregnancy; inability to follow instructions or complete the questionnaire; individuals in the active phase of sistemic complications relates to other rheumatic diseases; severe cardiovascular disease; uncontrolled hypertension; cancer that limits participation in the protocol; participants who regularly engage in physical exercise at other locations or those already undergoing non-pharmacological treatment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected that patients will report a reduction in knee pain, as measured by the Numerical Pain Rating Scale (NRS) | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected that an improvement in quality of life will be observed using the Knee Injury and Osteoarthritis Outcome Store;It is expected that improvements will be observed in measures of functional ability, as assessed by the 30 second Chair Stand Test (30CST), Timed Up and Go (TUG), and 10 Meter Walk Test (10MWT);Assess medication use using a medication diary compiled by the study author;Assess maximum isometric strength using a handheld dynamometer | — |
Countries
BR
Contacts
Universidade Federal de Santa Catarina