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临床试验/NCT06867159
NCT06867159招募中不适用

Comparison of Effects of Autogenic Inhibition and Reciprocal Inhibition Muscle Energy Techniques on Iliotibial Band Syndrome

Foundation University Islamabad1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年7月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
40
试验地点
1
主要终点
Pain severity

研究概览

简要总结

Comparison of effects of autogenic inhibition and reciprocal inhibition muscle energy techniques on iliotibial band syndrome

详细描述

A single-blinded randomized control trial will be conducted over a period of one year in Foundation University Islamabad. Forty participants will be assigned to two groups: Group A (AI) and Group B (RI), with 20 participants each. The AI technique will involve a maximal isometric contraction of the target muscle followed by a stretch, while the RI technique will involve a maximal isometric contraction of the antagonist muscle followed by a similar stretching protocol. Both groups will perform the exercises 3 times per week for 2 weeks. Pain, Hip range of motion (ROM) and lower extremity function will be assessed using Numeric Pain Rating Scale (NPRS), goniometer and Lower Extremity Functional Scale (LEFS) respectively.

The outcomes will be measured in terms of improvements in pain score (NPRS), hip range of motion (ROM), and overall lower extremity function.

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 (Outcomes Assessor)

盲法说明

It will be a single blinded RCT in which assessor will be blinded to the group allocation of participants.

入排标准

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

入选标准

  • •Both male and female participants
  • •Age : 19-45years (8)
  • •Lateral knee pain (>3 months)
  • •Tenderness over lateral femoral condyle
  • •Positive Flexibility Tests
  • •Modified Ober's test (9)
  • •Length assessment of Tensor Fasciae Latae and Iliotibial Band (10)
  • •Positive Pain Provocation Tests
  • •Renne's test
  • •Noble's Compression test (11) *(individuals with 3 positive tests out of above mentioned 4 tests will be included)

排除标准

  • •Recent lower limb or pelvic girdle surgery within the past 3 months
  • •Lower limb fractures or trauma within the past year.
  • •Multiple lower limb surgeries (>2)
  • •Presence of any structural or postural disorders (kyphosis or severe scoliosis)
  • •Neurological disorders
  • •Hip and knee Osteoarthritis
  • •Rheumatoid Arthritis
  • •Pregnancy

研究组 & 干预措施

Autogenic Inhibition (AI) MET Group

Experimental

Autogenic Inhibition (AI) MET (Post Facilitation Stretch)

  1. The shortened muscle (Tensor Fascia Latae) is placed in a mid-range position about halfway between a fully stretched and a fully relaxed state.
  2. The patient contracts the muscle isometrically, using a maximum degree of effort for 5-10 seconds while the effort is resisted completely.
  3. On release of the effort, a rapid stretch is made to a new barrier, without any 'bounce', and this is held for at least 10 seconds.
  4. The patient relaxes for approximately 20 seconds and the procedure is repeated between three and five times more.

干预措施: Autogenic Inhibition (AI) MET (Post Facilitation Stretch) (Procedure)

Reciprocal Inhibition (RI) MET Group

Experimental

Reciprocal Inhibition (RI) MET

  1. The shortened muscle (Tensor Fascia Latae) is placed in a mid-range position about halfway between a fully stretched and a fully relaxed state.
  2. The patient contracts the antagonist muscles (hip adductors), using a maximum degree of effort for 5-10 seconds while the effort is resisted completely.
  3. On release of the effort, a rapid stretch to TFL is made to a new barrier, without any 'bounce', and this is held for at least 10 seconds.
  4. The patient relaxes for approximately 20 seconds and the procedure is repeated between three and five times more.

干预措施: Reciprocal Inhibition (RI) MET (Procedure)

结局指标

主要结局

Pain severity

时间窗: 2 weeks

Pain will be assessed using Numeric Pain Rating Scale (NPRS),

Range of motion

时间窗: 2 weeks

Hip range of motion (ROM) will be assessed using goniometer

Functional status of lower limb

时间窗: 2 weeks

Lower extremity function will be assessed using Lower Extremity Functional Scale (LEFS)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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