Comparison Of The Effectiveness Of Wrist Splint And Kinesiotaping Treatments In Patients With Lateral Epicondylitis
1 other identifier
interventional
150
1 country
1
Brief Summary
Lateral epicondylitis, also known as tennis elbow, is a common condition that causes pain in the elbow and forearm, especially in people who perform repetitive wrist movements. In most patients, symptoms improve over time, but in some cases, pain may persist for longer periods.Exercise programs are commonly used in treatment to reduce pain and improve arm function. Kinesiology taping is another method that may help reduce pain by improving blood circulation and supporting muscle movement. Wrist-hand splints are also used to allow the affected muscles to rest by keeping the wrist in a supported position, which may help reduce pain and improve daily activities.The aim of this study is to compare the effectiveness of kinesiology taping and wrist splint use in the treatment of patients with lateral epicondylitis.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Apr 2022
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2024
CompletedFirst Submitted
Initial submission to the registry
January 25, 2026
CompletedFirst Posted
Study publicly available on registry
February 19, 2026
CompletedFebruary 19, 2026
February 1, 2026
1.8 years
January 25, 2026
February 11, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pain intensity
Pain intensity was assessed using a 10-cm Visual Analog Scale (VAS), ranging from 0 (no pain) to 10 (worst imaginable pain).
All assessments were conducted by the same evaluator at baseline, at the end of the 3-week treatment period, and 4 weeks following treatment completion.
Secondary Outcomes (5)
Grip strength
All assessments were conducted by the same evaluator at baseline, at the end of the 3-week treatment period, and 4 weeks following treatment completion.
Upper extremity function
All assessments were conducted by the same evaluator at baseline, at the end of the 3-week treatment period, and 4 weeks following treatment completion.
Health-related quality of life
All assessments were conducted by the same evaluator at baseline, at the end of the 3-week treatment period, and 4 weeks following treatment completion.
Treatment satisfaction
All assessments were conducted by the same evaluator at the end of the 3-week treatment period, and 4 weeks following treatment completion.
Patient-Rated Forearm Evaluation Questionnaire) (PRFEQ)
All assessments were conducted by the same evaluator at baseline, at the end of the 3-week treatment period, and 4 weeks following treatment completion.
Study Arms (3)
Kinesiotaping
OTHERParticipants received kinesiotaping treatment in addition to standard cold application and a home exercise program.
Wrist-Hand Splint
OTHERParticipants used a static wrist-hand splint in addition to standard cold application and a home exercise program.
Control Group
OTHERParticipants received conservative treatment consisting of cold application and a home exercise program.
Interventions
Kinesiotaping was applied twice a week for a total of six sessions using muscle inhibition and epidermis-dermis-fascia (EDF) techniques. In addition, participants received standardized cold application and a home exercise program.
Participants were instructed to use a static wrist-hand splint for three weeks to maintain the wrist in a slightly extended position. Standardized cold application and a home exercise program were also provided.
Participants received standardized cold application and a home exercise program without kinesiotaping or splint use.
Eligibility Criteria
You may qualify if:
- Age 18-65 years
- Clinically diagnosed lateral epicondylitis
- Elbow pain for at least 3 months
- Ability to understand and comply with study procedures
- Written informed consent provided
You may not qualify if:
- Previous surgery to the affected elbow
- Corticosteroid injection to the affected elbow within the last 6 months
- Neurological disorders affecting the upper extremity
- Inflammatory rheumatic diseases and fibromyalgia
- Fracture or trauma of the upper extremity within the last 6 months
- Pregnancy
- Participation in another clinical study during the study period
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Konya Beyhekim Training and Research Hospital
Konya, Konya, 42200, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Masking Details
- Due to the nature of the interventions, including kinesiotaping and wrist splint use, masking of participants and investigators was not feasible. Therefore, the study was conducted as an open-label trial.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER GOV
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal İnvestigator/ Medical Doctor
Study Record Dates
First Submitted
January 25, 2026
First Posted
February 19, 2026
Study Start
April 1, 2022
Primary Completion
December 31, 2023
Study Completion
June 1, 2024
Last Updated
February 19, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared to protect patient confidentiality and in accordance with ethical regulations. The data were used solely for statistical analysis within the scope of the study.