Comparative Effects of Conventional Physical Therapy, Kinesio Taping and ESWT in Upper Trapezius MPS.
- Conditions
- Trapezius Muscle Strain
- Interventions
- Device: Extracorporeal Shock Wave TherapyOther: KinesiotapingOther: Conventional Physical Therapy
- Registration Number
- NCT05277259
- Lead Sponsor
- Yuzuncu Yıl University
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 99
- 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.
- 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.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Extracorporeal Shock Wave Therapy Extracorporeal Shock Wave Therapy Extracorporeal shock wave therapy (ESWT) is a noninvasive treatment that involves delivery of shock waves to injured soft tissue to reduce pain and promote healing. Kinesiotaping Kinesiotaping The Kinesiotaping method is a therapeutic taping technique which alleviates pain. Conventional Physical Therapy Conventional Physical Therapy Hotpack, therapeutic ultrasound and tens applications.
- Primary Outcome Measures
Name Time Method Neck Disability Index (NDI) 6 weeks after baseline (one month after the end of treatment) 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).
Visual Analogue Scale (VAS) 6 weeks after baseline (one month after the end of treatment) patient's self-assessment of pain, in the range of 0 to 10, higher scores mean a worse outcome
- Secondary Outcome Measures
Name Time Method Measurement of Cervical range of motion (Cervikal ROM) 6 weeks after baseline (one month after the end of treatment) Measuring cervical lateral flexion and cervical extension with a manual goniometer.
Trial Locations
- Locations (1)
Yuzuncu Yil University
🇹🇷Van, Turkey