NCT07420764

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
150

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Apr 2022

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
1.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2023

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2024

Completed
1.7 years until next milestone

First Submitted

Initial submission to the registry

January 25, 2026

Completed
25 days until next milestone

First Posted

Study publicly available on registry

February 19, 2026

Completed
Last Updated

February 19, 2026

Status Verified

February 1, 2026

Enrollment Period

1.8 years

First QC Date

January 25, 2026

Last Update Submit

February 11, 2026

Conditions

Keywords

lateral epicondylitistennis elbowkinesiotapingwrist splintrehabilitation

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

OTHER

Participants received kinesiotaping treatment in addition to standard cold application and a home exercise program.

Other: KinesiotapingOther: Conservative treatment

Wrist-Hand Splint

OTHER

Participants used a static wrist-hand splint in addition to standard cold application and a home exercise program.

Device: Wrist-Hand SplintOther: Conservative treatment

Control Group

OTHER

Participants received conservative treatment consisting of cold application and a home exercise program.

Other: Conservative treatment

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.

Kinesiotaping

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.

Wrist-Hand Splint

Participants received standardized cold application and a home exercise program without kinesiotaping or splint use.

Control GroupKinesiotapingWrist-Hand Splint

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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)

Location

MeSH Terms

Conditions

Tennis Elbow

Interventions

Conservative Treatment

Condition Hierarchy (Ancestors)

Elbow TendinopathyTendinopathyMuscular DiseasesMusculoskeletal DiseasesElbow InjuriesArm InjuriesWounds and InjuriesTendon Injuries

Intervention Hierarchy (Ancestors)

Therapeutics

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
Model Details: Participants were randomized into three parallel groups receiving kinesiotaping, wrist splint, or control interventions.
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.

Locations