Osteoarthritis Clinical Trial
— osteoarthritisOfficial title:
Influence of Using Physical Therapy Resources for Knee Osteoarthritis
Verified date | February 2018 |
Source | University of Nove de Julho |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Osteoarthritis is a chronic, multifactorial characterization, which changes in bone alignment, cartilage and structures that provide joint stability appear to be strongly correlated with the origin of this disease.This project will aim to verify the effectiveness of interferential current, short wave and low level laser therapy on an exercise program for mobility and pain in knee osteoarthritis. Blind randomized, placebo controlled. Five groups: exercise group, exercise group + Ultrasound therapy, exercise group + interferential current, exercise group + short-wave diathermy, exercise group + Low level laser therapy. Before and after the trial protocol by the following instruments: Western Ontario and McMaster Universities osteoarthritis index (WOMAC), numerical scale of pain assessment (END), Visual Analogue Scale Fatigue (VAS-F), issue F2.2 Instrument assessment of quality of life of the World Health Organization (WHOQOL-100) test sitting and standing + numerical rating pain scale, algometry. This project hypothesizes that the inclusion of photothermal and electrical agents in an exercise program will provide an improvement in pain, mobility and knee function in individuals diagnosed with knee osteoarthritis.
Status | Completed |
Enrollment | 100 |
Est. completion date | February 2018 |
Est. primary completion date | September 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 40 Years to 80 Years |
Eligibility |
Inclusion Criteria: - knee pain to at least six months and minimum of 4 points in pain scale - Diagnosed with osteoarthritis in unilateral knee according to the criteria established by the American College of Rheumatology and confirmed by radiographic examination for identification Kellgren-Lawrence grade 2 or 3 (Kellgren & Lawrence, 1957). Exclusion Criteria: - Any type of physical therapy - therapy with intra-articular corticosteroids or therapeutic chondroprotective drugs last year, before the start of the study. - history of trauma on his knees, cognitive disorder or psychological disorder, - neurological (sensory or motor) - cancer - diabetes, - or any state of adverse acute health osteoarthritis signs of hip - cardiopulmonary disease that prevents the conducting exercises - require auxiliary device for performing gait. - Yet who undertake physical activity in the last two months. Physical activity is defined as strength training and / or more than 20 minutes of aerobic activity twice a week. |
Country | Name | City | State |
---|---|---|---|
Brazil | University of Nove de Julho | São Paulo | São Paulo, São Paulo |
Lead Sponsor | Collaborator |
---|---|
University of Nove de Julho |
Brazil,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | pain | The Western Ontario and McMaster Universities Arthritis Index (WOMAC) is widely used in the evaluation Knee Osteoarthritis. | Change from Baseline in The Western Ontario and McMaster Universities Arthritis Index at 8 weeks | |
Primary | stiffness | The Western Ontario and McMaster Universities Arthritis Index (WOMAC) is widely used in the evaluation Knee Osteoarthritis. | Change from Baseline in The Western Ontario and McMaster Universities Arthritis Index at 8 weeks | |
Primary | physical functional | The Western Ontario and McMaster Universities Arthritis Index (WOMAC) is widely used in the evaluation Knee Osteoarthritis. | Change from Baseline in The Western Ontario and McMaster Universities Arthritis Index at 8 weeks | |
Secondary | intensity of pain | The Numerical rating pain scale, a simple, easily administered scale evaluates the perceived intensity of pain, using an 11-point scale from 0, representing 'no pain', to 10, which is the 'worst possible pain'. | Change from Baseline in The Numerical rating pain scale at 8 weeks | |
Secondary | Self-perceived fatigue | a visual analog scale (VAS-F). | Change from Baseline in the self-perceived fatigue at 8 weeks | |
Secondary | Functional capacity for sitting and standing | sitting-rising test | Change from Baseline in The Functional capacity for sitting and standing at 8 weeks | |
Secondary | level of pressure pain | Pressure Pain Threshold in the knee with algometer dynamometer. | Change from Baseline in ThePressure Pain Threshold at 8 weeks | |
Secondary | Self-perceived fatigue | The question of F2.2 instrument for assessing quality of life World Health Organization (WHOQOL-100). | Change from Baseline in The question of F2.2 instrument for assessing quality of life World Health Organization (WHOQOL-100) at 8 weeks |
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