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临床试验/NCT07286669
NCT07286669尚未招募不适用

Positional Release Technique of Iliotibial Band and Pes Anserine Versus Proprioception Exercise on Patients With Knee Osteoarthritis

Cairo University0 个研究点目标入组 60 人开始时间: 2025年12月15日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
60
主要终点
knee disabiity

研究概览

简要总结

this studty was conducted to compare the effect of the positional release technique of the iliotibial band and Pes Anserine Versus Proprioception Exercise on Patients with knee osteoarthritis.

详细描述

Osteoarthritis (OA) is one of the most common chronic diseases in the world. It is frequently accompanied by high levels of persistent pain. Osteoarthritis is the most common degenerative disease, primarily affects the articular cartilage and the subchondral bone of a synovial joint, eventually resulting in joint failure. It is a disease involving multiple alterations on the joint tissues, including cartilage degradation, bone remodeling, and osteophyte formation; this leads to clinical manifestations, including pain, stiffness, swelling, and limitations in joint function. The positional release technique is a type of manual therapy that can be used effectively in treating pain and disability that is associated with musculoskeletal dysfunctional conditions and decrease tissue tenderness by altering nociceptor activity in the soft tissues. The positional release appears to affect inappropriate proprioceptive activity, thus helping to normalize tone and set the normal length-tension relationship in the muscle. Proprioceptive exercise is an effective way to strengthen knee joint muscle function and reduce pain in patients with knee osteoarthritis. The current study, it may be useful to compare the effect of the positional release technique, as it is a new modality and has proven its effectiveness in several studies on decreasing pain and dysfunction and increasing range of motion, versus the proprioception exercises which also have an improvement on pain, range, and function. The knee proprioception and pain pressure threshold will be also tested to compare these techniques on knee osteoarthritis patients

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
Double (Investigator, Outcomes Assessor)

盲法说明

opaque sealed envelope

入排标准

年龄范围
45 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Both genders with knee osteoarthritis will participate in this study according to the American College of Rheumatology criteria
  • An average pain intensity of ≥3 on a 10-cm visual analogue scale (VAS).
  • Patients with unilateral knee osteoarthritis, for those patients with bilateral knee -Patients with grade II &lll chronic knee osteoarthritis (clinical and imaging diagnosis X-ray.
  • Patients were referred by orthopedic physician.
  • Patients with body mass index <30Kg/cm2.

排除标准

  • Previous knee surgery
  • Serious valgus or varus deformity
  • Past or present vascular disorder.
  • Acute or chronic low back pain.
  • Upper motor neuron lesion and lower motor neuron lesion.
  • A history of rheumatoid arthritis.
  • Presence of malignancy.

结局指标

主要结局

knee disabiity

时间窗: up to 6 weeks

The Western Ontario and McMaster Universities Arthritis Index (WOMAC) was widely used in the evaluation of Hip and Knee Osteoarthritis. It is a self-administered questionnaire consisting of 24 items divided into 3 subscales;Pain (5 items),Stiffness (2 items), Physical Function (17 items): The test questions are scored on a scale of 0-4, which correspond to: None (0), Mild (1), Moderate (2), Severe (3), and Extreme (4). The scores for each subscale are summed up, with a possible score range of 0-20 for Pain, 0-8 for Stiffness, and 0-68 for Physical Function. Usually a sum of the scores for all three subscales gives a total WOMAC score, however there are other methods that have been used to combine scores. Higher scores on the WOMAC indicate worse pain, stiffness, and functional limitations

次要结局

  • knee joint position error(up to six weeks)
  • pain intensity(up to 6 weeks)
  • range of motion(up to six weeks)
  • pressure pain threshold(up to six weeks)

研究者

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

Nabil Mahmoud Ismail Abdel-Aal

principle investigator : nabil mahmoud ismail

Cairo University

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