Trapezius Muscle Strain Clinical Trial
Official title:
Comparison Of Bowen's Technique And Myofascial Release Technique On Pain And Disability In Patients With Trapezitis
Verified date | April 2022 |
Source | Riphah International University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The aim of this research is to compare the effects of Bowen's technique and Myofascial Release technique on pain and disability in patients with trapezitis.Randomized controlled trials done at Islamabad Physiotherapy and Rehabilitation Centre(IPRC) and Benazir Bhutto Hospital. The sample size was 66. The subjects were divided in two groups, 33 subjects in Bowen's Technique group and 33 subjects in Myofascial Release Technique group. Study duration was of 6 months. Sampling technique applied was non probability purposive sampling technique. The patients aged 20-40 years and clinicaly diagnosed with Trapezitis(spasm,trigger points,tenderness,stiffness) were included in the study. Tools used in the study are Cervical ROMs, NPRS, NDI, Isometric Scapular Pinch Test and Lateral Scapular Slide Test.
Status | Completed |
Enrollment | 66 |
Est. completion date | February 1, 2022 |
Est. primary completion date | January 1, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years to 40 Years |
Eligibility | Inclusion Criteria: - Both male and female. - Age 20-40 years. - Clinically diagnosed with Trapezitis.(Spasm,stiffness,Tenderness,Trigger Points,Taut band) - Cummulative trauma disorder - Occupational overuse syndrome Exclusion Criteria: - Any medical conditions or diseases that could interfere with intervention performance. - Any traumatic neck injury - Cervical vertebral fracture - Cervical spinal cord compromise/ cervical myelopathy - Cervical radiculopathy - Cervical Spondylolisthesis - Any tumour - Any degenerative diseases |
Country | Name | City | State |
---|---|---|---|
Pakistan | Benazir Bhutto Hospital | Rawalpindi | Punjab |
Lead Sponsor | Collaborator |
---|---|
Riphah International University |
Pakistan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Neck Disability Index | It is a 10-item questionnaire each them of having 6 possible answers. The score of each item lies between 0 to 5, where 0 means no pain/ limitation in activities) and 5 means 'as much pain as possible or maximal limitation in activities'.[19] Thus the Total scores range between 0 - 50 points. | 3rd day | |
Primary | Isometric Scapular Pinch Test | In ISPT the patient actively performs maximal scapular retraction and holds it for 2 seconds. If the pain is present after 15-20 seconds or patient fails to hold it then the test is positive. | 3rd day | |
Secondary | Lateral Scapular Slide Test | LSST is a test that assesses the excessive scapular movement with respect to thoracic spine. A total of three measurements are taken in three positions:
From scapular spine to T2/T3 level From Inferior scapular angle to T7/T9 level From superior scapular angle to T2 level. Measurments are taken 3 times in 3 positions |
3rd day | |
Secondary | NPRS | pain is measured with the help of numeric pain rating scale that is 11 point scale from 0-10 with 0 referring no pain and 10 represent max pain. | 3rd day | |
Secondary | Cervical flexion range of motion | The range of motion will be measure by goniometer at baseline, after first day treatment and after 3rd day. | 3rd day | |
Secondary | Cervical extension range of motion | The range of motion will be measure by goniometer at baseline, after first day treatment and after 3rd day. | 3rd day | |
Secondary | Cervical Rt side flexion range of motion | The range of motion will be measure by goniometer at baseline, after first day treatment and after 3rd day. | 3rd day | |
Secondary | Cervical Lt side flexion range of motion | The range of motion will be measure by goniometer at baseline, after first day treatment and after 3rd day. | 3rd day | |
Secondary | Cervical Rt side Rotation range of motion | The range of motion will be measure by goniometer at baseline, after first day treatment and after 3rd day. | 3rd day | |
Secondary | Cervical Lt side Rotation range of motion | The range of motion will be measure by goniometer at baseline, after first day treatment and after 3rd day. | 3rd day |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
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