Trapezius Muscle Strain Clinical Trial
Official title:
Comparative Effects of Conventional Physical Therapy, Kinesio Taping and Extracorporeal Shock Wave Therapies in Upper Trapezius Myofascial Pain Syndrome.
Verified date | May 2022 |
Source | Yuzuncu Yil University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
There is no study in the literature comparing both kinesiotaping and Extracorporeal Shock Wave Therapy (ESWT) with conventional physical therapy in upper trapezius myofascial pain syndrome. In this study, we aimed to make this comparison.
Status | Completed |
Enrollment | 99 |
Est. completion date | May 2, 2022 |
Est. primary completion date | April 18, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 16 Years and older |
Eligibility | Inclusion Criteria: - Presence of at least 1 active trigger point in the upper trapezius muscle, exacerbation of pain when this point(s) is pressed, painful limitation of cervical lateral flexion and extension. Exclusion Criteria: - Having a history of spine and upper extremity surgery, neuromuscular disease, active rheumatologic disease, active infection, malignancy, having previously applied ESWT or Kinesio Taping to the back and neck region. |
Country | Name | City | State |
---|---|---|---|
Turkey | Yuzuncu Yil University | Van |
Lead Sponsor | Collaborator |
---|---|
Yuzuncu Yil University |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Visual Analogue Scale (VAS) | patient's self-assessment of pain, in the range of 0 to 10, higher scores mean a worse outcome. | at baseline (before the treatment) | |
Primary | Visual Analogue Scale (VAS) | patient's self-assessment of pain, in the range of 0 to 10, higher scores mean a worse outcome | 2 weeks after baseline (at the end of treatment) | |
Primary | Visual Analogue Scale (VAS) | patient's self-assessment of pain, in the range of 0 to 10, higher scores mean a worse outcome | 6 weeks after baseline (one month after the end of treatment) | |
Primary | Neck Disability Index (NDI) | a self-report questionnaire used to determine how neck pain affects a patient's daily life and to assess the self-rated disability of patients with neck pain. The total score ranges from 0 (no disability) to 50 (total disability). | at baseline (before the treatment) | |
Primary | Neck Disability Index (NDI) | a self-report questionnaire used to determine how neck pain affects a patient's daily life and to assess the self-rated disability of patients with neck pain. The total score ranges from 0 (no disability) to 50 (total disability). | 2 weeks after baseline (at the end of treatment) | |
Primary | Neck Disability Index (NDI) | a self-report questionnaire used to determine how neck pain affects a patient's daily life and to assess the self-rated disability of patients with neck pain. The total score ranges from 0 (no disability) to 50 (total disability). | 6 weeks after baseline (one month after the end of treatment) | |
Secondary | Measurement of Cervical range of motion (Cervikal ROM) | Measuring cervical lateral flexion and cervical extension with a manual goniometer. | at baseline (before the treatment) | |
Secondary | Measurement of Cervical range of motion (Cervikal ROM) | Measuring cervical lateral flexion and cervical extension with a manual goniometer. | 2 weeks after baseline (at the end of treatment). | |
Secondary | Measurement of Cervical range of motion (Cervikal ROM) | Measuring cervical lateral flexion and cervical extension with a manual goniometer. | 6 weeks after baseline (one month after the end of treatment) |
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