Core Stability vs Scapular Stabilization on Hand Grip Strength in Chronic Myofascial Neck Pain
Core Stability Exercises Versus Scapular Stabilization Exercises on Hand Grip Strength in Patients With Chronic Myofascial Neck Pain
研究概览
地位
条件
详细说明
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Adnan AA Gharib, PHD
- 电话号码:+201065798861
- 邮箱:dradnanpts@gmail.com
研究联系人备份
- 姓名:Magda Ramadan Zahran, Assistant Professor
- 电话号码:01065798861
- 邮箱:dradnanpts@gmail.com
学习地点
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Giza Governorate
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Giza、Giza Governorate、埃及、11432
- 招聘中
- Cairo University
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接触:
- Magda Ramadan Zahran, Assistant Professor
- 电话号码:01065798861
- 邮箱:dradnanpts@gmail.com
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接触:
- Adnan AA Gharib, PHD
- 电话号码:01065798861
- 邮箱:dradnanpts@gmail.com
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首席研究员:
- Adnan AA Gharib, PHD
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参与标准
资格标准
适合学习的年龄
- 成人
接受健康志愿者
描述
Inclusion Criteria:
- Patients diagnosed with chronic myofascial neck pain depending on referral, and physical examination.
- Sixty patients diagnosed with chronic myofascial neck pain for more than six months.
- Patients age range will 25-45 years
- Patients body mass index (BMI) will be 18.5-24.9 kg/m2
- Each patient suffering from all active MTrPs in the upper trapezius muscle with painful/ tender nodule.
- Patients have a constant neck pain with positive jump sign when palpating the upper trapezius muscle.
- Patients have referred pain, and symptoms of ipsilateral hand muscle weakness.
- No history of undergoing physiotherapy modalities or corticosteroid injection therapies in the past six months before the study
Exclusion Criteria:
- Presence of signs of severe pathology such as malignancies, mainly of the cervical region.
- Fracture of the cervical spine.
- Cervical radiculopathy or myelopathy.
- Diabetes mellitus.
- Trauma, cognitive anomalies, and surgery around neck, shoulders, or hand.
- Fibromyalgia or vascular syndromes such as vertebral basilar insufficiency.
- Pregnancy.
- Having undergone physical therapy within the past three months before the study.
- Having corticosteroid injection therapies in the past 3 months before the study.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:四人间
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Experimental Group A (Core Stability)
consists of 20 participants who receive core stability exercises, plus the traditional physical therapy program in the form of ischemic compression of upper trapezius muscle, strain-counter strain of upper trapezius muscle, and muscle energy technique of upper trapezius muscle, three sessions per week for 6 weeks.
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The core stability exercise protocol will be conducted to experimental group (A), only. The core stability exercise protocol will be conducted for 40-45 minutes (10 minutes worm-up 'stretch exercises', 25 minutes core stabilization exercises, and 5-10 minutes cool down exercises 'stretch exercises') 3 sections/ week for six weeks 1. Diaphragm Core '';360 degree expansion breathing, weighted breathing 2. Transverse abdominis 'Abdominal drawing in maneuver, supine vacuum, pelvic tilt'; 3. Multifidus 'quadruped altered leg/arm, bridge with leg extension'; 4. Pelvic Floor muscles/Kegel, bridging, and bridging dog, and squat Core stability exercise.
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实验性的:Experimental Group B (Scapular Stabilization)
consists of 20 participants who receive scapular stabilization exercise, plus the traditional physical therapy program, three sessions per week for 6 weeks.
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The scapular stabilization exercise protocol will be conducted to experimental group (B), only. The core scapular stabilization exercise protocol will be conducted for 40-45 minutes (10 minutes worm-up 'stretch exercises', 25 minutes scapular stabilization exercises, and 5-10 minutes cool down exercises 'stretch exercises') 3 sections/ week for six weeks a. Open chain stabilization exercises 'scapular elevation/depression, upward/downward rotation', b. Static closed chain stabilization exercises 'Protected weight bearing through both hands leaning against wall', c. Dynamic closed chain stabilization exercises 'scapular retraction' |
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有源比较器:Control Group C (Traditional Physical Therapy Program)
consists of 20 participants who receive the traditional physical therapy program, three sessions per week for 6 weeks, only
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Hand Grip Strength
大体时间:1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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Hand-held Dynamometer (SAMMONS PRESTON, INC.
Bolingbrook, IL604404989) will be used to measure it.
The patient will sit on a standard height chair with no armrest with his/ her forearm in a neutral position, and shoulder in adducted and neutral rotation, with elbow flexed 90 degrees (°).
The patient will be requested to squeeze the ipsilateral hand on the hand grip dynamometer handle accordingly to the ordered verbs 'i.e., one, two, three, squeeze…harder, harder'.
Three measures will be conducted with one minute a break in between, then the average will be recorded in value score.
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1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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Pinch Grip Strength
大体时间:1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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The pinch gauge (FEI, White plains, NY 10602, USA) will be used to measure the pinch grip strength, it is a valid and reliable tool.
The patient will sit on a standard height chair with no armrest with his/ her shoulder, elbow, forearm, and wrist in a neutral position.
The patient will be requested to squeeze the thumb pad as firm as possible against the lateral aspect of index fingers' middle phalanx, while the examiner will hold the distal end of the pinch gauge.
Three measures will be conducted with one minute a break in between, then the average will be recorded in a score value.
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1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Chronic Myofascial Neck Pain Intensity assessment using Numerical Pain Rating Scale:
大体时间:1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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Numerical Pain Rating Scale will be used to assess chronic myofascial neck pain intensity, The patient will be in a relaxed position then will be given the appendix which contains numerical pain rating scale.
It involves a 0-10 scale, where 0 represents "no pain" and 10 represents "the worst pain imaginable" The patient will be instructed to place a vertical mark on the line to indicate his/her pain.
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1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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Pressure Pain Threshold using electronic pressure algometer
大体时间:1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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The electronic pressure algometer 'force one gauge model FDI' (Wagner instruments, Greenwash, CT, USA) will be used to measure it, it is a valid and reliable tool.
Over trigger point recognized via jump sign clinically, a dial-style pressure algometry will be installed while a steady vertical pressure will be applied.
When the patient reported only mild pain, the patient will be asked to raise hand to indicate it.
Three measures will be conducted with one minute a break in between, then average will be recorded in value.
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1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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Whole Upper Extremity Functional Level using Arabic-Q-DASH scale
大体时间:1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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The whole upper extremity functional level will be evaluated using Arabic-Q-DASH it is a valid and reliable tool.
The Arabic-Q-DASH is like the original questionnaire.
Items have a rating scale ranged from 1 to 5. The patient will be instructed to place a score that the examiner will transform it into a value between 0 and 100.
The high score indicates better hand function outcomes with exception of pain, where high value indicates more intense pain score.
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1. At Baseline (Pre-procedure), 2. Post-treatment (Post 6 weeks of treatment program).
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合作者和调查者
调查人员
- 研究主任:Sohair Shehata Rezkallah, Professor、Cairo University; Faculty of Physical Therapy
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
关键字
其他研究编号
- P.T.REC/012/006550
计划个人参与者数据 (IPD)
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