MedPath

The study of the whole body vibration therapy effects on the patients with knee osteoarthritis.

Phase 2
Conditions
Knee Osteoarthritis.
Other primary gonarthrosis
Registration Number
IRCT201601171637N5
Lead Sponsor
Vice chancellor for research-Tarbiat Modares University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
45
Inclusion Criteria

The inclusion criteria:
Knee OA with Kellgren–Lawrence grade II and III in simple X-ray;
between 55-75 years old;
no previous or concomitant injury on the knee and other lower extremity joints; no previous history of serious knee trauma, surgery and arthroplasty;
no history of knee intra-articular injection of hyaluronic acid or steroid in the last 6 months;
no history of surgery or traumatic injuries to the lower limbs;
no history of medical problems such as cardiopulmonary diseases, neurologic diseases, malignant diseases, chronic diseases such as diabetes;
no history of newly repaired fracture and bone implants;
no pacemaker and no history of WBVT contraindications for participants of the WBVT group;

The exclusion criteria:
Any systemic disorder in the body, according to the patient and physician;
taking any medication according to the patient;
incomplete treatment and assessment;
WBVT intolerance for the WBVT group;

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Pre and post intervention. Method of measurement: Visual Analogue Scale for pain( 100 mm Ruler).;Knee Range of Motion. Timepoint: Pre and post intervention. Method of measurement: Goniometery in degree.;Time up & Go test. Timepoint: Pre and post intervention. Method of measurement: Chronometer ( sec).;6 minute walk test. Timepoint: Pre and post intervention. Method of measurement: Meter.;Electromyographic (EMG) root mean square (RMS) response of some lower limb muscles during maximum voluntary isometric contraction. Timepoint: Pre and post intervention. Method of measurement: Electromygraphy.;Overall Sway Index. Timepoint: Pre and post intervention. Method of measurement: Biodex Balance System.;Antroposterior Sway Index. Timepoint: Pre and post intervention. Method of measurement: Biodex Balance System.;Medilateral Sway Index. Timepoint: Pre and post intervention. Method of measurement: Biodex Balance System.
Secondary Outcome Measures
NameTimeMethod
Anteroposterior Sway. Timepoint: pre andp post intervention. Method of measurement: Forceplate.;Sway Average Velocity. Timepoint: pre andp post intervention. Method of measurement: Forceplate.;Mediolateral Sway. Timepoint: pre andp post intervention. Method of measurement: Forceplate.
© Copyright 2025. All Rights Reserved by MedPath