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Shock Wave Versus Traditional Physical Therapy for Adult Chronic Knee Osteoarthritis

Shock Wave Versus Traditional Physical Therapy for Adult Chronic Knee Osteoarthritis: A Prospective Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07468734
Enrollment
40
Registered
2026-03-13
Start date
2026-03-18
Completion date
2026-11-30
Last updated
2026-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Knee Osteoarthritis, Shock Wave, Traditional Physical Therapy

Brief summary

This study aims to compare the effectiveness of extracorporeal shock wave therapy (ESWT) versus structured therapeutic exercise in patients with chronic knee osteoarthritis (KOA), with respect to pain reduction and improvement of knee function.

Detailed description

Knee osteoarthritis (KOA) is a highly prevalent chronic degenerative joint disease characterized by progressive cartilage loss, chronic pain, stiffness, functional disability, and reduced quality of life in adults, particularly the elderly. Extracorporeal shock wave therapy (ESWT) has emerged as a non-invasive physical modality that delivers acoustic pressure waves to musculoskeletal tissues, stimulating biological responses such as enhanced microcirculation, anti-inflammatory cytokine modulation, neovascularization, cartilage and bone repair processes, and decreased pain transmission.

Interventions

OTHERExtracorporeal shock wave therapy

Patients will receive extracorporeal shock wave therapy.

Patients will undergo a structured exercise therapy program.

Sponsors

German International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults ≥ 40 years with clinical and radiographic diagnosis of chronic knee osteoarthritis (KOA) (Kellgren-Lawrence grade II-III). * Both sexes. * Persistent knee pain ≥ 3 months. * Ability to provide consent and participate in interventions.

Exclusion criteria

* Prior knee surgery within last 6 months. * Intra-articular injections in the last 3 months. * Systemic inflammatory arthritis or other neurological conditions affecting gait.

Design outcomes

Primary

MeasureTime frameDescription
Change in pain intensity5-week after interventionChange in pain intensity will be assessed using the Visual Analogue Scale (VAS) which is a 10-cm horizontal line used to measure pain intensity, ranging from (0) "no pain" to (10) "worst imaginable pain".

Secondary

MeasureTime frameDescription
Stiffness assessment5-week after interventionStiffness will be assessed using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). WOMAC will be recorded at baseline, at the end of the intervention period, and during follow-up. Higher scores indicate greater symptom severity.
Assessment of physical function5-week after interventionPhysical function will be assessed using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). WOMAC will be recorded at baseline, at the end of the intervention period, and during follow-up. Higher scores indicate greater symptom severity.
Knee range of motion5-week after interventionKnee range of motion (ROM) will be assessed.
Incidence of adverse events5-week after interventionIncidence of adverse events will be recorded.

Countries

Egypt

Contacts

CONTACTMagdy M Shabana, MD
magdy.shabana@giu-uni.de00201006053332

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 20, 2026