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Effects of Extracorporeal Shockwave Therapy Versus Dry Needling on Jumpers Knee

Effects of Extracorporeal Shockwave Therapy Versus Dry Needling on Jumpers Knee

Recruiting
18-35 years
All
Phase N/A

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Overview

The study is randomized and single-blinded. Ethical approval is taken from ethical committee of Riphah International University, Lahore. Participants who meet the inclusion criteria will be enrolled and allocated in group A \& B through sealed envelope method by Non-probability Convenient random sampling technique. Subjects in Group A will receive Shock wave therapy. Group B will receive Dry needing.

Description

Patellar tendinopathy (Jumper's knee) remains, nowadays, a therapeutic challenge because of the unclear mechanism that induces this condition and related symptoms. Overloading or incorrect training, hard playing surfaces, and inadequate equipment are implicated as extrinsic risk factors, while age, sex, biotype, internal load, lower limb length discrepancy or abnormality (alignment defects or lower limb rotational defect, foot abnormalities and constitutional laxity) have been considered predisposing factors. The aim of present study is to compare the effects of Extracorporeal Shockwave Therapy versus Dry needling for Pain Management, knee function and QOL in Jumpers Knee. The aim of the study is to compare the effects of Extracorporeal Shockwave Therapy versus Dry needling for Pain Management, knee function and QOL in Jumpers Knee.

This study will be randomized clinical trial in which 48 individuals will be randomized through non-probability convenient sampling by lottery method into 2 groups. Group A will undergo Extracorporeal Shockwave Therapy and group B will receive Dry needling. To evaluate the acute effects of the training protocols, assessments will be conducted pre- and post-intervention using the measures relevant to on Pain (NPRS), knee function (VISA-P score) and Quality of Life (KOS-ADL) are performed before and after the training sessions. The duration of training sessions will be 10 weeks with 2-3 treatment sessions per week.

Eligibility

Inclusion Criteria:

  • Participants of either gender between the age of 18-35 years with a confirmed diagnosis of jumper's knee for more than 1 month.
  • Confirmed diagnosis of jumper's knee for more than 1 month.
  • Pain NPRS (Numeric Pain Rating Scale) score greater than 4 at the first evaluation.

Exclusion Criteria:

  • Surgery around the knee joint within the last 6 months.
  • Chronic knee joint disease.
  • Knee pain management with corticosteroid injections in the last 3 months.
  • Trauma history
  • Systemic illness

Study details
    Pain
    Quality of Life
    Jumper's Knee

NCT07756918

Riphah International University

15 August 2026

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