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临床试验/NCT07322185
NCT07322185Enrolling By Invitation不适用

COMPARATIVE EFFECTS OF STECCO-FASCIAL MANIPULATION AND ROLFING STRUCTURAL INTEGRATION IN PATIENTS WITH PIRIFORMIS SYNDROME; A RANDOMIZED CLINICAL TRIAL

Danyal Ahmad3 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2025年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
入组人数
42
试验地点
3
主要终点
Change From Baseline in Pain Intensity as Measured by the Numerical Pain Rating Rating Scale (NPRS)

研究概览

简要总结

This study aims to compare the effectiveness of Stecco Fascial Manipulation and Rolfing Structural Integration in treating Piriformis syndrome, focusing on special outcomes like pain severity and functional outcomes.

comparison will be done to check the effectiveness of Stecco-fascial Manipulation and Rolfing Structural Integration on patients of both groups.

participants will:

  1. get the treatment according to their respective groups
  2. Both groups were given 4 sessions for 4 weeks.

详细描述

This study will be a randomized clinical trial with a sample size of 42 participants as calculated with g power tool with 5% of attrition added. Subjects will be obtained by non- probability convenient sampling based on the inclusion and exclusion criteria. Participants will be randomly assigned into two groups, 21 subjects in each group. The group A will receive the stecco fascial manipulation along with the conventional therapy while group B will receive the rolfing structural integration along with conventional therapy. The conventional physiotherapy protocol will include TENS applied with a Hot- pack for 10 minutes that will be followed by piriformis stretch.The data analysis will be done by IBM SPSS 26.0 version. To check the normality Shaprio- Wilk test will be used.

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 (Participant)

入排标准

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

入选标准

  • •25 to 45 age group.
  • •For at least four weeks, there has been unilateral buttock discomfort, either with or without posterior thigh pain included buttock pain, pain that worsened when sitting.
  • •Positive slump test and fair test decrease ranges of hip NPRS greater than

排除标准

  • •Previous pelvic, ipsilateral hip, lumbar, or sacroiliac surgery that would have confused pain source.
  • •Evidence of lumbar radiculopathy or another spinal condition that could be the origin of the symptoms (matching MRI/CT revealing nerve root compression or disc herniation). progressive neurologic disease or neuromuscular disease (e.g., peripheral neuropathy, myopathy, neuromuscular junction diseases)
  • •During the research period, pregnancy or the planning of pregnancy (if interventions are employed) active pelvic or hip infection, malignancy, fracture, or systemic inflammation.

研究组 & 干预措施

GROUP A ( Stecco fascial Manipulation)

Experimental

GROUP A ( Stecco fascial Manipulation) containing 21 participants who will be given Stecco fascial Manipulation for 30 minutes along with the conventional physiotherapy.

干预措施: Experimental: GROUP A ( Stecco fascial Manipulation) (Other)

GROUP B (Rolfing Structural Integration)

Experimental

GROUP B (Rolfing Structural Integration) containing 21 participants who were given Rolfing Structural Integration for 30 minutes along with the conventional physiotherapy.

干预措施: Experimental: GROUP B (Rolfing Structural Integration) (Other)

结局指标

主要结局

Change From Baseline in Pain Intensity as Measured by the Numerical Pain Rating Rating Scale (NPRS)

时间窗: 4 Weeks

The Numerical Pain Rating Scale (NPRS) is a self-intensity on an 11-point scale, ranging from 0 (no pain) to 10 (worst possible pain). It is widely used in both clinical and research demonstrated strong reliability and validity in measuring Scale (NPRS) is a self-reported tool used to assess pain point scale, ranging from 0 (no pain) to 10 (worst possible pain). It is research settings for musculoskeletal conditions, strong reliability and validity in measuring both acute and chronic pain reported tool used to assess pain point scale, ranging from 0 (no pain) to 10 (worst possible pain). It is conditions, and it has both acute and chronic pain

Universal Goniometer

时间窗: 4 Weeks

A goniometer is an instrument used objective and reliable values that help evaluate mobility limitations i disorders such as piriformis syndrome used to measure joint range of motion (ROM). It provides objective and reliable values that help evaluate mobility limitations in musculoskeletal disorders such as piriformis syndrome.

次要结局

  • FAIR Test(4 Weeks)
  • Slump Test(4 Weeks)

研究者

发起方
Danyal Ahmad
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Danyal Ahmad

Head Of Department (HOD)

University of Management and Technology Sialkot Pakistan

研究点 (3)

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