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临床试验/NCT07403045
NCT07403045已完成不适用

Effects of McGill Strengthening Exercises Program With and Without Integrated Neuromuscular Inhibition Technique on Pain, Range of Motion and Function in Patients With Piriformis Syndrome

Riphah International University1 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2025年5月26日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
56
试验地点
1
主要终点
Numeric Pain Rating Scale

研究概览

简要总结

The study was conducted to determine the effects of McGill strengthening exercises program with and without integrated neuromuscular inhibition technique on pain, range of motion and function in patients with piriformis syndrome.

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 (Participant, Outcomes Assessor)

入排标准

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

入选标准

  • Both genders with age ranged from 25 and 45 years
  • Sedentary
  • Non-traumatic
  • Idiopathic
  • External tenderness near the greater sciatic notch
  • Pain for more than 1 month's duration
  • NPRS ranging from >3 to ≤ 6
  • Positive results on three of the following five tests:

排除标准

  • Acute low back pain and/or acute lumbar radiculopathy
  • History of Stroke or any other neurological disorders
  • Recent buttock trauma
  • Inflammatory, infectious or tumor diseases
  • Severe vascular disease
  • Osteoporosis
  • Pregnancy

研究组 & 干预措施

McGill strengthening exercises program with integrated neuromuscular inhibition technique

Experimental

干预措施: McGill strengthening exercises program (Other)

McGill strengthening exercises program with integrated neuromuscular inhibition technique

Experimental

干预措施: Integrated neuromuscular inhibition technique (Other)

McGill strengthening exercises program with integrated neuromuscular inhibition technique

Experimental

干预措施: Standardized physiotherapy treatment (Other)

McGill strengthening exercises program

Active Comparator

干预措施: McGill strengthening exercises program (Other)

McGill strengthening exercises program

Active Comparator

干预措施: Standardized physiotherapy treatment (Other)

结局指标

主要结局

Numeric Pain Rating Scale

时间窗: From enrollment to 6 weeks of intervention with follow-up at 14 weeks.

Numeric Pain Rating Scale (NPRS) was used to assess the patient's pain intensity. This scale ranges from 0 to 10, where 0 indicates "no pain" and 10 indicates "worst pain.

次要结局

  • Range of Motion (Hip Abduction)(From enrollment to 6 weeks of intervention with follow-up at 14 weeks.)
  • Range of Motion (Hip Internal Rotation)(From enrollment to 6 weeks of intervention with follow-up at 14 weeks.)
  • Lower Extremity Functional Scale(From enrollment to 6 weeks of intervention with follow-up at 14 weeks.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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