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This study will be conducted to examine the superiority of effectiveness between muscle energy technique combined with physical therapy, strain counterstrain combined with physical therapy, and physical therapy alone in terms of pain intensity, pain pressure threshold, cervical lateral flexion and rotation range of motion, and neck function for patients with upper trapezius myofascial trigger points.
Myofascial pain syndrome represents a common, overlooked, and under-diagnosed disorder that have very critical negative effects on people's lives. In addition, it overloads the societies and causes several burdens on healthcare systems. However, this disorder is usually dismissed by many clinicians keeping the patients in pain for long periods. The central feature of myofascial pain syndrome is the myofascial trigger points that when managed properly, the painful symptoms disappear. Muscle energy technique and strain counterstrain immediate effects were compared in a recent comparative study for patients with upper trapezius myofascial trigger points in terms of pain intensity, pain pressure threshold, and neck mobility. The results showed that there were improvements of both techniques with no significant differences between them. Regarding the evidence of the two techniques; muscle energy technique and strain counterstrain in the management of patients with upper trapezius myofascial trigger points, there is lack of high-quality evidence investigating the effectiveness and safety of both techniques for this population and there is a need for well-developed randomized controlled trial to take a step in the pyramid of levels of evidence for the use and applicability of them. After reviewing the available literature, it was found that there is no study directly combined both techniques with physical therapy protocol in a randomized clinical trial for patients with upper trapezius myofascial trigger points; this will enable us to compare the effects of them in a controlled design to examine and find out the differences between the three treatment protocols.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Group A | Experimental | Experimental group 1. |
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| Group B | Experimental | Experimental group 2. |
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| Group C | Experimental | Experimental group 3. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Muscle energy technique combined with the physical therapy program. | Procedure | A manual therapy technique |
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| Measure | Description | Time Frame |
|---|---|---|
| Change in pain intensity. | Measurement of pain intensity using the visual analogue scale. | Change from Baseline pain intensity at one month. |
| Change in the right side pain pressure threshold. | Measurement of right side pain pressure threshold using the pressure algometer. | Change from Baseline right side pain pressure threshold at one month. |
| Change in the left side pain pressure threshold. | Measurement of left side pain pressure threshold using the pressure algometer. | Change from Baseline left side pain pressure threshold at one month. |
| Change in cervical flexion range of motion. | Measurement of cervical flexion range of motion using the cervical range of motion device. | Change from Baseline cervical flexion range of motion at one month. |
| Change in cervical extension range of motion. | Measurement of cervical extension range of motion using the cervical range of motion device. | Change from Baseline cervical extension range of motion at one month. |
| Change in cervical right lateral flexion range of motion. | Measurement of cervical right lateral flexion range of motion using the cervical range of motion device. | Change from Baseline cervical right lateral flexion range of motion at one month. |
| Change in cervical left lateral flexion range of motion. |
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Inclusion Criteria
Patients will be included in the study if they fulfil the following criteria:
Patients will be excluded from the study if they fulfil the following criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Haytham Morsi, M.Sc. | Contact | +201013657738 | 10722019485962@pg.cu.edu.eg |
| Name | Affiliation | Role |
|---|---|---|
| Bassem El Nahass, PhD | Professor of Orthopaedic Physical Therapy, Faculty of Physical Therapy, Cairo University | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The Outpatient Clinics, Faculty of Physical Therapy Kafrelsheikh University | Recruiting | Kafr ash Shaykh | Egypt |
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Randomized controlled trial
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Firstly, the research assistant, another qualified physical therapist, performing the assessment process, pre and post-treatment, will be blinded regarding the patients allocation into the three treatment groups. Secondly, the patients themselves will be blinded regarding which treatment group they will be allocated into. So the research assistant won't know the randomization results, and the main investigator won't know the assessment results which will make it a double-blinded study.
| Strain counterstrain technique combined with the physical therapy program | Procedure | A manual therapy technique |
|
| The physical therapy program | Procedure | Electrotherapy and exercise. |
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Measurement of cervical left lateral flexion range of motion using the cervical range of motion device. |
| Change from Baseline cervical left lateral flexion range of motion at one month. |
| Change in cervical right rotation range of motion. | Measurement of cervical right rotation range of motion using the cervical range of motion device. | Change from Baseline cervical right rotation range of motion at one month. |
| Change in cervical left rotation range of motion. | Measurement of cervical left rotation range of motion using the cervical range of motion device. | Change from Baseline cervical left rotation range of motion at one month. |
| Change in neck function. | Measurement of neck function using the neck disability index-Arabic version. | Change from Baseline neck function at one month. |