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临床试验/NCT05577403
NCT05577403已完成不适用

Effect of Mulligan's Mobilization With Movement Added With Isometric Exercises on Muscle Strength Pain and Disability Associated With Knee Osteoarthritis: A Randomized Controlled Study

Majmaah University2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2022年11月5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
50
试验地点
2
主要终点
Range of Motion

研究概览

简要总结

To evaluate the effect of Mulligan's mobilization with movement in osteoarthritis of the knee.

详细描述

Patients with knee OA diagnosed at the orthopaedic clinic of Tumair general hospital and referred to the physiotherapy department who attended the rehabilitation centre of Majmaah university will be recruited.

Patients will be excluded if they have had a knee or hip injury, sensory deficits in the lower extremity, a history of lower-extremity surgery, a history of a quadriceps or hamstring muscle injury, low back-related leg pain, or any contraindication to manual therapy.

The protocol was submitted to and approved by the Rehabilitation Research Chair, King Saud University Research Ethics Committee (RRC-2021-17)

Participants will be requested to sign a written informed consent form approved by the institutional ethics committee. A total of 60 participants were randomly assigned to group A (experimental group): Mulligan's mobilization with movement MWM added isometric strength training, and group B (control group): Sham MWM added isometric strength training. Pre and post-test readings were taken at baseline, week 2, and week 4, respectively. The outcome measures for this study will be maximal voluntary isometric contraction of quadriceps strength (measured by ISOMOVE dynamometer), ROM, and Western Ontario and McMaster universities osteoarthritis (WOMAC) index.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
40 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient with knee OA with radiological evidence of grade 2 or 3 of the Kellgren and Lawrence scale.
  • Age between 40-65 years, unilateral or bilateral involvement (in the case of bilateral involvement, the more symptomatic knee was included), and pain in and around the knee.

排除标准

  • Patient will be excluded, if they had any deformity of the knee, hip, or back, had any central or peripheral nervous system involvement.
  • They had received steroids or intra-articular injection within the previous three months, uncooperative patients.

结局指标

主要结局

Range of Motion

时间窗: 6 weeks

Standard goniometer.

pain intensity

时间窗: 6 weeks

Visual Analogue scale on 0 to10 cm

Western Ontario and McMaster universities osteoarthritis (WOMAC) index

时间窗: 6 weeks

Western Ontario and McMaster universities osteoarthritis scale

次要结局

未报告次要终点

研究者

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

Shahnaz Hasan, PhD

Associate Professor

Majmaah University

研究点 (2)

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