跳至主要内容
临床试验/NCT04667091
NCT04667091已完成不适用

Comparing the Effects of Positional Release Technique Versus Myofascial Release Technique of Gluteus Medius in the Management of Patellofemoral Pain Syndrome - A Randomized Control Trial

Dow University of Health Sciences2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2020年12月7日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
2
主要终点
Visual Analog Scale

研究概览

简要总结

Patellofemoral pain syndrome is a condition of misleading diagnosis. It mostly affects individuals with ages between 18-40 years. It is believed that much work has been done on the joint itself in treating the Quadriceps muscles and triggers related to it but now literature is focusing on the segmental involvement, where weakness of the hip abductors and lateral rotators play a major role. Therefore, interventions used for treating this syndrome should include on focusing the hip muscles for trigger point therapy as well as strengthening them in increasing the stability of the hip and pelvis to reduce excessive valgus forces on the knee.

详细描述

Literature regarding Gluteus Medius trigger point is quite scarce especially in alleviating the pain related to Patellofemoral Pain Syndrome. The management of Patellofemoral Pain Syndrome includes a segmental treatment, giving special focus to the lateral rotators and abductors of the hip especially Gluteus Medius muscle, rather than treating the Patellofemoral Joint itself. It will help in improving the pain of the subjects suffering from this syndrome effectively, and within a shorter duration of time. It will also provide the practicing physiotherapist with an insight for treating such patients with better outcomes. Myofascial Trigger Points of the Gluteus Medius are important contributing factors in the management of Patellofemoral Pain Syndrome which is identified in a single study as per author's knowledge. But the treatment used to release the trigger point of Gluteus Medius in managing this syndrome has not yet been explored. So, this study will compare two well-known treatments in comprehending which one of the two techniques have better effects on the population to be studied. Written consent will be taken from all the study participants. Simple randomization technique will be used through "Randomization Main" software and randomization sheet will be generated. 60 participants with patellofemoral pain syndrome having Gluteus Medius trigger point will be randomly allocated in two equal group.

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 (Participant)

盲法说明

Single blinding will be used in which only the researcher doing the study knows which treatment or intervention the participant is receiving until the trial is over.

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Anterior knee pain >1month and <3 month
  • Pain in activities like ascending & descending stairs, running or sports activity & prolonged sitting
  • Presence of Gluteus Medius trigger point in the affected limb
  • Age group 18-40 years
  • Both genders

排除标准

  • Dislocation of Patella
  • Damaged cartilage and ligament of Knee Joint
  • Soft tissue injury related to Knee
  • Any knee or hip surgery
  • Lumbar spine dysfunction
  • Sacroiliac joint dysfunction
  • Pelvic malalignment
  • Flat foot
  • Chondromalacia patellae
  • Young onset Osteoarthritis

结局指标

主要结局

Visual Analog Scale

时间窗: Baseline and end of intervention (6th week)

A subjective psychometric response scale used to measure discrete behavioral or physiological phenomena based on linear numerical gradient in measuring the intensity of pain.

Pain Pressure Threshold

时间窗: Baseline and end of intervention (6th week)

It is the amount of direct pressure required in eliciting a response in pain on a selected area obtained by an Algometer in kilograms (kg.)

Anterior Knee pain Scale

时间窗: Baseline and end of intervention (6th week)

It is 13-item questionnaire with different categories relating various levels of individual's current knee function. Score ranges from 1 representing severe disability to 100 representing no disability.

次要结局

  • Muscle strength(Baseline and end of intervention (6th week))
  • World Health Organization Quality of Life Questionnaire- Brief(Baseline and end of intervention (6th week))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Priyanka Ratan Kumar

Dr. Priyanka Ratan Kumar (PT)

Dow University of Health Sciences

研究点 (2)

Loading locations...

相似试验