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Comparative Effects of Conventional Physical Therapy, Kinesio Taping and ESWT in Upper Trapezius MPS.

Not Applicable
Completed
Conditions
Trapezius Muscle Strain
Interventions
Device: Extracorporeal Shock Wave Therapy
Other: Kinesiotaping
Other: 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
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.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Extracorporeal Shock Wave TherapyExtracorporeal Shock Wave TherapyExtracorporeal shock wave therapy (ESWT) is a noninvasive treatment that involves delivery of shock waves to injured soft tissue to reduce pain and promote healing.
KinesiotapingKinesiotapingThe Kinesiotaping method is a therapeutic taping technique which alleviates pain.
Conventional Physical TherapyConventional Physical TherapyHotpack, therapeutic ultrasound and tens applications.
Primary Outcome Measures
NameTimeMethod
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
NameTimeMethod
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

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