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Clinical Trials/NCT06267027
NCT06267027
Completed
Not Applicable

Comparison Of The Effects Of Kinesiotaping And High Intensity Laser Therapy In Patients With Lateral Epicondylitis: A Randomized Controlled Study

Bakirkoy Dr. Sadi Konuk Research and Training Hospital1 site in 1 country55 target enrollmentStarted: February 7, 2023Last updated:

Overview

Phase
Not Applicable
Status
Completed
Sponsor
Bakirkoy Dr. Sadi Konuk Research and Training Hospital
Enrollment
55
Locations
1
Primary Endpoint
Patient Rated Tennis Elbow Evaluation (PRTEE)

Overview

Brief Summary

Comparison of the effects of kinesiotaping and high intensity laser therapy in patients with lateral epicondylitis: a randomized controlled study

Detailed Description

In this study, it was aimed to compare the effects of exercise therapy, kinesiology taping and high-intensity laser therapy on pain, muscle strength and functional status in patients with LE. Patients who applied to the outpatient clinic of the Sadi Konuk Training and Research Hospital Physical Medicine and Rehabilitation clinic due to elbow pain and were diagnosed with unilateral LE will be included. The study was planned as randomized, prospective and controlled. Patients will be randomized using a random (randomized) numbers table and distributed equally to the groups. Only exercise will be applied to the first group, high-intensity laser therapy and exercise to the second group, and kinesiology taping and exercise treatments to the third group. Sixty people will be included in the study. Patients will be evaluated before treatment, immediately after treatment, and at 4 weeks post-treatment. In the evaluation of the patients, the severity of pain during rest and activity measured with the Visual Analogue Scale (VAS), Quick Disability of the Arm, Shoulder and Hand (QuickDASH), Patient Based Lateral Epicondylitis Evaluation Test - Patient Rated Tennis Elbow Evaluation (PRTEE), Jamar' Hand grip strength will be evaluated with the hand dynamometer.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Investigator)

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Volunteer patients diagnosed with unilateral lateral epicondylitis

Exclusion Criteria

  • Those who have previously received treatment for lateral epicondylitis
  • Current extremity fracture or surgical history
  • Presence of congenital deformity in the upper extremity
  • Cervical radiculopathy, myelopathy, plexopathy, entrapment neuropathies
  • Presence of neurological disease such as stroke, Parkinson's, multiple sclerosis, epilepsy and muscle disease
  • Presence of skin lesion, infection and open wound on the affected extremity
  • Presence of metal implant in the affected extremity
  • Rheumatological disease
  • Pregnancy
  • Pacemaker presence

Outcomes

Primary Outcomes

Patient Rated Tennis Elbow Evaluation (PRTEE)

Time Frame: Initial, Week 3, Week 7

It consists of pain and function subscales that assess the level of pain in the affected arm in the last 1 week and the degree of difficulty experienced during specific and daily activities. The pain assessment consists of 5 questions and the functional assessment consists of 10 questions, totaling 15 questions. The questions are evaluated with a 10-point Likert scale, as in the VAS, with numbers written side by side from 0 to 10. It is calculated by averaging the pain score and functional score. The total score ranges from 0-100, with a higher score indicating an increase in pain and functional loss. Validation of turkish version is available.

Secondary Outcomes

  • Jamar's handheld dynamometer(Initial, Week 3, Week 7)
  • Visual Analogue Scale (VAS)(Initial, Week 3, Week 7)
  • Quick Disabilities of the Arm, Shoulder and Hand (qDASH)(Initial, Week 3, Week 7)

Investigators

Sponsor
Bakirkoy Dr. Sadi Konuk Research and Training Hospital
Sponsor Class
Other Gov
Responsible Party
Principal Investigator
Principal Investigator

Sibel Caglar Okur

Principal Investigator

Bakirkoy Dr. Sadi Konuk Research and Training Hospital

Study Sites (1)

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