Recruiting NCT06563258
Efficacy of Biodex Balance Training Versus Whole Body Vibration Training in Patients With Knee Osteoarthritis
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Biodex Balance Training, A vibration device, traditional exercises.
- Who it may be relevant to
- Registry conditions: Knee Osteoarthritis. Basic parameters: 40 years — 60 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Egypt
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
This study will be conducted to answer the research question: Are there differences between the effect of Biodex balance training and Whole-body vibration training on Knee osteoarthritis?
Detailed description
The purpose of this study is to compare the effects of biodex training balance versus whole body vibration training on Knee osteoarthritis on:
* Pain intensity * static balance * dynamic balance * Functional ability level
Interventions
- Device Biodex Balance Training
Sixty Subjects of both genders aged 40-60 years old with grade 2 knee osteoarthritis years will diagnosed by orthopedists they will assigned randomly into three groups: * Group A Will receive WBV Training with frequency of 35 Hz, peak-to-peak amplitude of 4- to 6-mm Vertical sinusoidal vibration, and the total exposure time of 30 minutes (vibration 60 seconds, interval rest 60 seconds) in addition to traditional exercises,3 sessions per week for four weeks. , A vibration device (My7™ model Pers - Device A vibration device
WBV Training with frequency of 35 Hz, peak-to-peak amplitude of 4- to 6-mm Vertical sinusoidal vibration, and the total exposure time of 30 minutes (vibration 60 seconds, interval rest 60 seconds) in addition to traditional exercises,3 sessions per week for four weeks. , A vibration device (My7™ model Personal Plate, Power Plate, Northbrook, IL, USA) will used in all WBVT sessions. - Other traditional exercises
1. Stretch exercises (flexibility exercise) Rectus femoris, Iliotibial band, Hamstring and self-stretch for calf muscle (3sets, each stretch 30 sec hold, between each set 5sec rests). 2. Strengthen exercises(resistance exercise) 1. Isometric Exercises for quadriceps (10 rep,3sets) 2. Hip abductors strengthening 45 degree (10 rep,3sets) 3. Hip extensor strengthening 15 degree (10 rep,3sets) 4. Straight leg raising 45-70 degree (10 rep,3sets) 5. Short arc knee extension (10 rep,3se
Primary outcome measures
- Pain intensity [Time frame: one month]
- static balance [Time frame: one month]
- Dynamic balance [Time frame: one month]
- .Functional abilities [Time frame: one month]
Eligibility criteria
Inclusion criteria
- Subjects age between (40-60) years old.
- Radiologic findings had to be compatible with knee OA grade 2 in a simple X ray.
- Tenderness on medial tibial plateau
- Intensity of pain: visual analogue scale equal to 5 or greater
- Failure of two or more types of previous conservative treatment (medication, anti-inflammatory drugs, physical therapy, stretching, acupuncture, orthotics and others) in the last three months
Exclusion criteria
- Neurological and vestibular system disorder, systematic inflammatory disease, steroid injections in the last six months
- Subjects with diabetes mellitus.
- acute symptomatic arthritis
- other conditions (such as osteomyelitis, tuberculosis, and tumor) that affect their walking function; had a contraindication to exercise; and exhibited cognitive impairment
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
Egypt · 1 center
- Mti University — Cairo
Identifiers
NCT: NCT06563258 · P.T.REC/012/005293