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Influence of Using Physical Therapy Resources for Knee Osteoarthritis

Not Applicable
Completed
Conditions
Osteoarthritis
Physical Therapy Modalities
Interventions
Other: exercise
Device: Ultrasound therapy
Device: short-wave diathermy
Device: Low level laser therapy
Device: interferential current
Registration Number
NCT02636764
Lead Sponsor
University of Nove de Julho
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
100
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.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
exercise group + interferential currentexerciseBesides the intervention of the exercise group after the exercises will be applied to interferential current through the device. Will be positioned 4 electrodes (8x5 cm), two upper and two lower (forming a square) around the center of the knee.
exercise groupexerciseAn exercise protocol drawn up with the objective will be held to strengthen the musculature: flexor and extensor of the knee; extension, abduction, hip side rotator, using the weight and the elastic band.
exercise group + Ultrasound therapyUltrasound therapyApart from intervening in the exercise group, an ultrasound device is used .
exercise group + short-wave diathermyshort-wave diathermyBesides the intervention of the exercise group after the exercises will be applied diathermies short wave in continuous mode. For that will be used apparatus, 27.12 megahertz, by means of vulcanized rubber electrodes (12x17 cm) with gentle warming for 30 minutes.
exercise group + Low level laser therapyLow level laser therapyApart from intervening in the exercise group, will be applied to Low level laser therapy, through the laser unit, Class 3b, gallium-aluminum-arsenide, continuous mode, wavelength: 830 nanometer, power: 30 watts.
exercise group + Ultrasound therapyexerciseApart from intervening in the exercise group, an ultrasound device is used .
exercise group + interferential currentinterferential currentBesides the intervention of the exercise group after the exercises will be applied to interferential current through the device. Will be positioned 4 electrodes (8x5 cm), two upper and two lower (forming a square) around the center of the knee.
exercise group + Low level laser therapyexerciseApart from intervening in the exercise group, will be applied to Low level laser therapy, through the laser unit, Class 3b, gallium-aluminum-arsenide, continuous mode, wavelength: 830 nanometer, power: 30 watts.
exercise group + short-wave diathermyexerciseBesides the intervention of the exercise group after the exercises will be applied diathermies short wave in continuous mode. For that will be used apparatus, 27.12 megahertz, by means of vulcanized rubber electrodes (12x17 cm) with gentle warming for 30 minutes.
Primary Outcome Measures
NameTimeMethod
painChange from Baseline in The Western Ontario and McMaster Universities Arthritis Index at 8 weeks

The Western Ontario and McMaster Universities Arthritis Index (WOMAC) is widely used in the evaluation Knee Osteoarthritis.

stiffnessChange from Baseline in The Western Ontario and McMaster Universities Arthritis Index at 8 weeks

The Western Ontario and McMaster Universities Arthritis Index (WOMAC) is widely used in the evaluation Knee Osteoarthritis.

physical functionalChange from Baseline in The Western Ontario and McMaster Universities Arthritis Index at 8 weeks

The Western Ontario and McMaster Universities Arthritis Index (WOMAC) is widely used in the evaluation Knee Osteoarthritis.

Secondary Outcome Measures
NameTimeMethod
intensity of painChange from Baseline in The Numerical rating pain scale at 8 weeks

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'.

Self-perceived fatigueChange from Baseline in The question of F2.2 instrument for assessing quality of life World Health Organization (WHOQOL-100) at 8 weeks

The question of F2.2 instrument for assessing quality of life World Health Organization (WHOQOL-100).

Functional capacity for sitting and standingChange from Baseline in The Functional capacity for sitting and standing at 8 weeks

sitting-rising test

level of pressure painChange from Baseline in ThePressure Pain Threshold at 8 weeks

Pressure Pain Threshold in the knee with algometer dynamometer.

Trial Locations

Locations (1)

University of Nove de Julho

🇧🇷

São Paulo, São Paulo, São Paulo, Brazil

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