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Enrolling by invitation NCT07478861

Whole-body Vibration Training on the Elderly With Combined Bilateral Knee Osteoarthritis

No phase Interventional Knee OA Sarcopenic Obesity Whole Body Vibration

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: Whole-body vibration training.
Who it may be relevant to
Registry conditions: Knee OA, Sarcopenic Obesity, Whole Body Vibration. Basic parameters: 60 years — 75 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 →
Official title

Impact of Whole-body Vibration Training (WBVT) on the Elderly With Combined Bilateral Knee Osteoarthritis (KOA) and Sarcopenic Obesity

Overview

This study will aim to evaluate the effects of whole-body vibration training (WBVT) on body composition, muscle strength (hand grip strength), and physical performance \[gait speed (GS), 5-time chair stand test (5CST), and short physical performance battery (SPPB), pain intensity, triglycerides in older people with knee OA and sarcopenic obesity in a group of Men compared to group of females.

Detailed description

Both groups received the intervention 3 times a week for 12 weeks. WBVT group. Each intervention lasted 30 min, which included 5 min of warm-up, 20 min of vibration training, and 5 min of relaxation.

Interventions

  • Other Whole-body vibration training
    Whole-body vibration therapy stimulates muscle contraction. It can increase muscle function to a level like that of classical resistance training, but with the advantage of being more convenient and safer

Primary outcome measures

  • Physical performance [Time frame: 8 weeks]

Eligibility criteria

Inclusion criteria

  • Patients with KOA were graded based on the Kellgren-Lawrence grading criteria (K-L grading)
  • only grades 3 and 4 will be included in this study
  • Sarcopenia obesity based on with SMI with SMI < 7 kg/m2
  • PBF ≥ 30% into the SO group
  • BMI ≥ 28%, or waist circumference ≥ 85 cm in men and ≥ 80 cm in women
  • able to communicate

Exclusion criteria

  • Inability to walk
  • Knee joint underwent drug treatment or intra-articular injection
  • Uncontrollable angina pectoris induced by exercise
  • Uncontrolled hypertension, acute or chronic renal failure, or dyspnea in the resting state
  • Neurological or respiratory conditions or injuries (ie, dementia, Alzheimer's disease, multiple sclerosis, chronic obstructive pulmonary disease), rheumatoid arthritis and clinical depression.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Beni Suef University Hospital — Banī Suwayf

Identifiers

NCT: NCT07478861 · Faculty of Physical Therapy · Mariam Abdel Rahman

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗