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临床试验/NCT07661485
NCT07661485尚未招募不适用

Effect of Myofascial Release as Compared to Post Isometric Relaxation in Improving Pain and Lower Extremity Function in Piriformis Syndrome

University of Faisalabad1 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2026年6月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
26
试验地点
1
主要终点
Visual analogue scale

研究概览

简要总结

Piriformis Syndrome is a neuromuscular condition with symptoms of pain, numbness and tingling tracing the route of the sciatic nerve, due to the nerve impingement by the piriformis muscle. Two common manual therapy techniques used to treat musculoskeletal conditions are myofascial release and post-isometric relaxation. The intent of the research is to evaluate the effects of myofascial release (MFR) as compared to post-isometric relaxation (PIR) in improving pain and lower extremity function in piriformis syndrome (LEFS). The study population involved 32 individuals aged between 20 to 50 years who will be randomly assigned to two groups; a group that received MFR and a group that received PIR. Both groups received the baseline treatment for four weeks. The Visual Analog Scale (VAS) will be employed to gauge the amount of pain, while the LEFS was used to measure functional mobility

详细描述

This is Multiple-center, randomized controlled trail. Participants age 20-50 years with diagnosed piriformis syndrome will be referred from neuro physician and orthopedic department of Madina Teaching hospital (MTH) to Physiotherapy ward, Jafar Physiotherapy Clinic and Madina Specilaists Clinic. After informed consent Participants will be randomly assign to one of two parallel groups using a random number generator. Group A (Experimental): Receive MFR 3 sessions per week for total duration 4 weeks. Group B (Active Comparator) receive the PIR 3 sessions per week for total duration 4 weeks. Outcome measures (pain via VAS, functional status via LEFS) are taken at baseline and end of treatment. Data will be analyzed using Spss version 20.

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
20 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Positive Lasegue sign
  • Positive FAIR test
  • Grade 1-3 tenderness on palpation of piriformis between sacrum and greater trochanter of femur
  • 4 or more pain intensity on the VAS scale

排除标准

  • Lower extremity injuries including ligament, tendon injuries, muscle strains as well as nerve injuries
  • Systemic diseases including tuberculosis, multiple sclerosis, Parkinson's disease as well as chronic inflammatory conditions
  • Congenital deformities including hip dysplasia, limb length discrepancy, scoliosis and congenital pelvic asymmetry
  • Cognitive issues including dementia, severe depression and severe psychotic disorders
  • Lumbar Radiculopathy
  • SIJ Dysfunction
  • Lower Extremity Fractures
  • Pregnancy
  • Malignancy

研究组 & 干预措施

Myofascial release

Experimental

Myofascial release was then performed with the patient positioned in prone lying. The piriformis muscle was identified. Sustained pressure was applied directly to the trigger point/piriformis muscle for 10-100 seconds while the patient actively moved the affected limb repeatedly from internal to external rotation. Kneading strokes parallel to the muscle fibers were then performed for 5 minutes to promote elongation. This sequence was repeated three times.

干预措施: Myofascial Release (Other)

Post Isometric Relaxation

Experimental

The patient is in supine and the hip in neutral rotation. The affected hip was passively moved into horizontal adduction until a mild stretch was felt, while the lumbar spine was stabilized. The patient performed a gentle isometric contraction into hip abduction for 7-10 seconds, followed by 2-3 seconds of relaxation. The leg was then moved into further adduction to a new barrier.

This contraction-relaxation-stretch cycle was performed for 3 sets of 5 repetitions.

干预措施: Post Isometric Relaxation (Other)

结局指标

主要结局

Visual analogue scale

时间窗: Baseline and 4 week post intervention

Comparison on effect of pain. The Visual Analog Scale is a self-reported measure of pain intensity. Participants rate their pain on a 10-cm scale ranging from 0 to 10, where 0 indicates "no pain" and 10 indicates "worst imaginable pain."

次要结局

  • Lower Extremity Functional Scale(Baseline and 4 week of post intervention)

研究者

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

Muhammad Muneeb Jafar

Assistant Professor, Department of Rehabilitation Sciences

University of Faisalabad

研究点 (1)

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