跳至主要内容
临床试验/NCT07004881
NCT07004881招募中不适用

Comparison Between the Effects of Mulligan and Maitland Mobilization on Patellofemoral Pain Syndrome

Foundation University Islamabad1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年7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
40
试验地点
1
主要终点
Range of Motion

研究概览

简要总结

This study is a randomised control trial and the purpose of this study is to investigate and compare the "Effects of Maitland mobilizations and Mulligan Mobilization With Movement (MWM) in patients with Patellofemoral Pain Syndrome

详细描述

This study is a randomised control trial just used to investigate and compare the effects of maitland mobilizations and Mulligan's Mobilization With Movement ; with respect to:

  1. Pain
  2. Range of motion and
  3. Function in patients with Patellofemoral pain syndrome All males and females with ages of 18 to 40 years having the Patellofemoral pain syndrome can be included in this study.

A total number of 40 participants are equally and randomly divided into two groups i.e. group A and group B. Group A recieves the Mulligan Mobilization With Movement (MWM) and group B receives the Maitland's Patellar mobilizations.

Outcomes are recorded at 0 weeks and at end of 2 weeks. Outcome measure used for pain is Numeric Pain Rating Scale (NPRS), for knee ROM is goniometery and for knee function is Lower Extremity Function Scale (LEFS).

Pre and post intervention reading of all 3 measures will then be compared and data will be analysed

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)

盲法说明

It is a single blinded Randomized Controlled Trial, in which the data assessor will be blinded.

入排标准

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

入选标准

  • •Referred patients from rehabilitation, orthopedic and rheumatology department
  • •Both males and females of age 18-40 years
  • •Having pain from at least 2 months.
  • •Pain score ≥ 3 on NPRS.
  • •Pain on palpation of medial or lateral Patellar facet. (12, 13)
  • •Retro patellar pain in at least two of the following activities:
  • •Ascending , descending stairs
  • •Hopping / jumping
  • •prolonged sitting with flexed knees
  • •kneeling and squatting
  • •Patellar tilt test
  • •EXCLUSION CRIETERIA:
  • •Positive tests/findings on physical examination for knee menisci, ligaments and bursa.
  • •Chondromalacia patellae
  • •Individuals with Instability of tibiofemoral joint
  • •lower extremity surgery
  • •Rheumatoid arthritis, other connective tissue disorders and congenital deformities.

排除标准

  • 未提供

研究组 & 干预措施

Mulligan Mobilization with Movement

Active Comparator

Mulligan Mobilization with Movement This group will receive two techniques of mulligan i.e. Medial Patellar Glide relative to femoral trochlea and other is tibial internal rotation relative to femoral condyles.

Both the techniques are repeated 10 times with total 3 sets. 3 sessions are performed in a week on alternate days. Total duration of interventions is 2 weeks.

After mobilization, following exercises are to be performed all in 3 sets of 7 repetitions:

  1. Side-lying hip abduction
  2. Clamshell exercises
  3. Quadriceps setting exercise
  4. Vastus Medialis Oblique strengthening
  5. Mini squats
  6. Hamstring stretch
  7. Iliotibial band stretch

干预措施: Group A (Active Comparator) Mulligan's Mobilization With Movement (MWM) (Procedure)

Maitland Mobilization

Experimental

Maitland Mobilization This group recieves 4 patellar mobilization tehniques given by Maitland. For all the mobilizations the patient is positioned either in supine or sitting with 30-0 degree knee flexion or full knee extension.

The therapist holds patella between his/her thumb and index finger and glides it cranially (Superior Patellar glide), caudally (Inferior Patellar Glide) and medially (Medial Patellar Glide).

The fourth one i.e. Patellofemoral Distraction is given by grasping the patella between two fingers and lifting it above/away from underlying femoral trochlea. All 4 of these techniques are repeated 10 times with total 3 sets. 3 sessions are performed in a week on alternate days.

Total duration of interventions is 2 weeks.

After mobilization; 3 sets of 7 repetitions:

  1. Side-lying hip abduction
  2. Clamshell exercises
  3. Quadriceps setting exercise
  4. Vastus Medialis Oblique strengthening
  5. Mini squats
  6. Hamstring stretch
  7. Iliotibial band stretch

干预措施: Group B(Experimental) Maitland's Patellar Mobilizations (Procedure)

结局指标

主要结局

Range of Motion

时间窗: Variable will be assessed at before and after treatment for the total interval of 2 weeks.

Universal goniometer is used to measure knee flexion and extension ranges. Patient is positioned in supine with the knee straight and foot flat on the table. Therapist stabilizes the femur with one hand. Axis of goniometer is aligned with the lateral epicondyle of the femur, stationary arm is kept parallel to the femur and moving arm is aligned with long axis of tibia. The patient is then asked to flex and extend the knee to maximum range without pain, subsequently aligning moving arm of goniometer with new position of tibia. Angle of flexion/extension are then recorded from the goniometer and documented.

Patellofemoral Pain

时间窗: 2 weeks

It will be measured using numeric pain rating scale (NPRS). Subjects select a number ranging from 0-10 according to their intensity of pain where '0' indicates no pain while '10' indicates worst pain experienced.

Lower Extremity Function

时间窗: Variable will be assessed at before and after treatment for the total interval of 2 weeks.

It is measured using Lower Extremity Function Scale (LEFS). The LEFS is a questionnaire used to assess an individual's ability to perform daily activities and functional tasks related to the lower extremities (hips, knees, ankles, and feet). It comprises of total 20 questions and patients rate their ability to perform each activity on a scale from 0 (unable to perform) to 4 (able to perform without difficulty). The total score ranges from 0 to 80, with higher scores indicating better functional ability. The total sore before and after interventions of both groups is calculated and compared.

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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