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N/A N=33 Randomized Double-blind Treatment

Kinesiotaping in Lateral Epicondylitis

Lateral Epicondylitis

Enrolled (actual)
33
Serious AEs
0.0%
Results posted
Oct 2019
Primary outcome: Primary: Patient Rated Tennis Elbow Evaluation (PRTEE) — 49; 53.75; 49.25; 26.5 units on a scale — p=0.643

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Kinesiotaping (Device); Sham taping (Other); Exercise (Other)
Age
Adult · 18+ yrs
Sex
All
Sponsor
Marmara University
Primary completion
Apr 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
Patient Rated Tennis Elbow Evaluation (PRTEE)
49; 53.75; 49.25; 26.5; 50.25; 46.25 0.643
SECONDARY
The Disabilities of the Arm, Shoulder and Hand Score (QuickDash)
50; 46.57; 46.59; 29.5; 47.72; 39.77 0.633
SECONDARY
Visual Analogue Scale (VAS) at Rest
1.5; 1.5; 3; 0; 1.5; NA 0.715
SECONDARY
Visual Analogue Scale (VAS) at Daily Activity
6.5; 7.5; 7; 5; 7; NA 0.103
SECONDARY
Visual Analogue Scale (VAS) at Night
2.5; 2.5; 3.5; 0; 2; 1 0.837
SECONDARY
Painless Grip Strength
14; 12; 13; 17; 13; NA 0.897
SECONDARY
Grip Strength
20; 19.5; 23.5; 22; 19.5; NA 0.958

Summary

The aim of this study is to compare the effects of kinesiology taping with exercise, sham taping with exercise and exercise alone for lateral epicondylitis.

Eligibility Criteria

Inclusion Criteria

  • Having had symptoms less than 12 weeks
  • Tenderness and pain over lateral epicondylitis
  • Provocation of the lateral elbow pain with at least one of the following tests - resisted middle finger extension (Maudley's test), resisted wrist extension or passive stretch of wrist extensors (Mill's test).

Exclusion Criteria

  • Cervical spondylosis or radiculopathy
  • Diabetes mellitus
  • Neuropathy
  • Arthritis in the upper extremities
  • History of injection and physical therapy for lateral epicondylitis within the last three months
  • Pregnancy
  • History of surgery or acute trauma in the elbow
  • Allergy to tape
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03074500). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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