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临床试验/NCT07756918
NCT07756918招募中不适用

Effects of Extracorporeal Shockwave Therapy Versus Dry Needling on Pain, Knee Function and Quality of Life in Jumpers Knee

Riphah International University1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2025年10月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
48
试验地点
1
主要终点
numeric pain rating scale

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •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.

排除标准

  • •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

研究组 & 干预措施

Extracorporeal Shockwave therapy

Experimental

Extracorporeal Shockwave therapy

干预措施: Extracorporeal Shockwave therapy (Other)

Dry needling

Experimental

Dry needling

干预措施: Dry Needling (Other)

结局指标

主要结局

numeric pain rating scale

时间窗: Pre and 6 week post interventional

pain will be evaluated through numeric pain rating scale, The Numeric Pain Rating Scale (NPRS) is an 11-point scale from 0 to 10. Patients select a whole number matching their pain intensity, where 0 means no pain and 10 means the worst pain imaginable. Scores are grouped into mild (1-3), moderate (4-6), and severe (7-10) pain levels

Victorian Institute of Sport Assessment - Patella

时间窗: Pre and 6 week post interventional

Knee Function measured through the VISA-P (Victorian Institute of Sport Assessment - Patella) score has a maximum value of 100 points for a healthy, pain-free individual, with a theoretical minimum of 0. It consists of eight questions assessing pain, functional severity, and sports capacity. You can calculate your score interactively using online tools like the VISA-P Questionnaire.

Quality Of life measure through KOS-ADLS

时间窗: Pre and 6 week post interventional

The Knee Outcome Survey Activities of Daily Living Scale (KOS-ADLS): The KOS-ADLS is a 14-item self-reported questionnaire designed to evaluate symptoms and limitation during activities of daily living among patients with various knee disorders

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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