THE EFFECTS OF CORRECTIVE EXERCISE AND KT APPLICATIONS IN YOUNG BASKETBALL PLAYERS (KT:KINESIOTAPE)

March 11, 2026 updated by: Vedat Göken

THE EFFECTS OF CORRECTIVE EXERCISE AND KİNESİOTAPE APPLICATIONS ON PERFORMANCE AND FUNCTIONAL MOBILITY IN YOUNG BASKETBALL PLAYERS

The main objective of this research is to comparatively examine the effects of corrective exercise programs and kinesio taping (KT) applications on performance parameters and functional mobility in adolescent male basketball players. Kinesio taping is used with the aims of regulating muscle tone, increasing proprioception, improving circulation, and supporting pain management. In this context, corrective exercises are applied to correct movement disorders, eliminate musculoskeletal imbalances, and improve the functional movement quality in athletes. Although the effects of both methods on the performance parameters and functional mobility of athletes have been examined separately in the literature, a direct comparative study in adolescent basketball players is noticeable.

Study Overview

Status

Recruiting

Detailed Description

Basketball is characterized by dynamic movement patterns involving high intensity, multi-plane, and sudden changes in direction. These characteristics require athletes to have highly developed physical parameters such as balance, strength, flexibility, and coordination. At the same time, the application of supportive methods to minimize the risk of injury without experiencing performance loss is of great importance in terms of training science and athlete health.

This research aims to achieve the following objectives:

Comparison of the effects of corrective exercise and chemotherapy on functional mobility in young basketball players, Analysis of the effects of both methods on fundamental performance parameters such as vertical jump, balance, acceleration, and change of direction, Measurement of pre- and post-application improvement levels through functional movement screening tests (e.g., Y-balance test, single-leg squat test, overhead squat, etc.), Evaluation of the effect of chemotherapy when combined with a corrective exercise program compared to applications performed alone, Providing concrete suggestions that can be used in planning preventive and performance-enhancing approaches for young basketball players. This research contains measurable objectives based on scientific data and is applicable in a short time, and aims to obtain important findings that will contribute to the performance development of young athletes in the field of sports science.

The study will include a total of 45 basketball players from Avrupa Karşıyaka Sports Club. The players will be divided into three groups using a simple lottery method: a kinesio taping group, a corrective exercise group, and a control group. Study timeline: The project will be completed within 12 months after obtaining ethical approval from the İstinye University Human Research Ethics Committee.

Sample and research group: Basketball players from Avrupa Karşıyaka Sports Club will be included in the study. 45 volunteer players meeting the inclusion criteria will be included. The sample size was calculated using *Power Version 3.1 software. For our study, with 80% power and a type 1 error of 0.05, and a moderate effect size (effect size = 0.54), it was found that a total of 45 people should be included in the study, with 15 people in each of the three different groups, to compare the effects.

Study Type

Interventional

Enrollment (Estimated)

45

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Istanbul, Turkey (Türkiye), 34800
        • Not yet recruiting
        • Istinye University
        • Contact:
    • Istanbul
      • Istanbul, Istanbul, Turkey (Türkiye), 34800
        • Recruiting
        • Istinye University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • The male athlete's sport must be basketball.
  • The male athlete must be between 9 and 16 years old.

Exclusion Criteria:

  • Having undergone any surgical operation within the last 6 months.
  • Having suffered a lower/upper extremity injury within the last 3 months.
  • The volunteer does not wish to continue the study.
  • Athletes for whom the necessary assessments or procedures could not be performed were excluded.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Corrective Exercise Group
Based on the athlete's initial assessment, in addition to routine training, a personalized exercise program will be designed for the athlete using artificial intelligence via a functional movement scanning system; this will be performed twice a week for 6 weeks.
These exercises are given to correct disrupted movement patterns and improve posture.
Active Comparator: Kinesiotape Group
Based on the athlete's initial assessment, in addition to routine training, kinesio taping was applied to the deltoid muscle and quadriceps femoris muscle twice a week for 6 weeks.
This is a drug-free elastic band application applied to the muscle to reduce pain, increase circulation, provide muscle support, and improve joint stability.
No Intervention: Control Group
After the initial assessment, the athletes continued their routine training for 6 weeks.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Y Balance Test
Time Frame: From enrollment to the end of treatment at 3 weeks and 6 weeks

The Y Balance Test is a widely used test in clinics and sports performance centers to assess dynamic balance in athletes. The test consists of a support platform with three PVC tubes attached in anterior, posteromedial, and posterolateral directions. The rear tubes are positioned at a 135-degree angle to the front tube, with a 45-degree angle between them. Each tube is marked at 5-millimeter intervals for measurement purposes.

During the test, the support foot is held in the center of the measurement mechanism, while the other foot pushes against targets in the anterior, posteromedial, and posterolateral reach directions of the system using the toes, without losing balance or stepping on the targets. The aim is to measure the longest distance the target can reach.

From enrollment to the end of treatment at 3 weeks and 6 weeks
Functional Movement System(FMS)
Time Frame: From enrollment to the end of treatment at 3 weeks and 6 weeks
Used in athletes to identify movement patterns, mobility and stability deficiencies, and to predict injury risk. FMA is a test battery that evaluates individuals in terms of dynamic and functional capacity, essentially aiming to assess basic movement performance. The exercises in the Functional Movement Assessment allow for the identification of asymmetries, limitations, and compensations not only at the joint level but also throughout the movement pattern, thus enabling the early prediction and prevention of injury risk during physical activity. The test consists of seven movements: deep squat, high step, cross step, shoulder mobility, active straight leg raise, trunk stability, and rotational stability. Separate scoring is provided for each side in some movements, and athletes can receive a score between 0 and 21 on this test. If the test score is below 14, it suggests a potential risk of injury and a decrease in functional mobility capacity. Each movement should be repeated at leas
From enrollment to the end of treatment at 3 weeks and 6 weeks
Agility T test
Time Frame: From enrollment to the end of treatment at 3 weeks and 6 weeks
This is a test that evaluates an athlete's agility, speed, sudden changes of direction, balance, and coordination. Agility is defined as the ability to move the body between two points and change direction as easily, quickly, fluidly, and controllably as possible, along with balance, speed, strength, and neuromuscular coordination. Agility is considered a significant determining factor affecting performance, especially in team sports such as basketball. Previous studies have indicated that when developing agility skills, it is more accurate to evaluate it as a kinetic chain function involving the active participation of the entire body, rather than focusing solely on the muscles of the lower extremities.
From enrollment to the end of treatment at 3 weeks and 6 weeks
My Jump 2
Time Frame: From enrollment to the end of treatment at 3 weeks and 6 weeks
This test, performed using a mobile application, assesses lower extremity strength and performance by calculating the athlete's jump height and flight time. In recent years, with advancements in technology, mobile applications aimed at improving, measuring, and analyzing athletic performance have continued to develop. One such application, My Jump 2, allows for a practical and rapid assessment of jump performance. The application aims to provide accurate calculations by considering flight time based on takeoff and landing frames. Since its introduction to the literature, the test has been used in numerous scientific studies.
From enrollment to the end of treatment at 3 weeks and 6 weeks
Seated Medicine Ball Throw Test
Time Frame: From enrollment to the end of treatment at 3 weeks and 6 weeks
This is a test used to measure an athlete's upper extremity strength. It is frequently used because it is easy to administer and inexpensive. Also known as the Medicine Ball Throw Test, it is a field test applied to evaluate upper extremity strength before and after training. There are various methods for evaluating upper extremity muscle strength. Compared to other tests, the Seated Medicine Ball Throw Test is frequently preferred due to its ease of application, cost, physical requirements, and practicality. In the SMBT test, the individual throws a shuttle ball as far as possible from a fixed seated position, and the test administrator measures the distance from the starting point of the throw to the point where the ball first touches the ground.
From enrollment to the end of treatment at 3 weeks and 6 weeks
The Closed Kinetic Chain Lower Extremity Stability Test
Time Frame: From enrollment to the end of treatment at 3 weeks and 6 weeks
It is a test designed to assess balance and endurance, evaluating an athlete's stability in a closed kinetic chain position. It provides performance-based, quantitative data aimed at assessing lower extremity stability within a closed kinetic chain context.
From enrollment to the end of treatment at 3 weeks and 6 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Principal Investigator: Vedat Göken, Vedat Goken/ Istinye University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 15, 2026

Primary Completion (Estimated)

May 7, 2026

Study Completion (Estimated)

July 16, 2026

Study Registration Dates

First Submitted

January 14, 2026

First Submitted That Met QC Criteria

January 14, 2026

First Posted (Actual)

January 22, 2026

Study Record Updates

Last Update Posted (Actual)

March 13, 2026

Last Update Submitted That Met QC Criteria

March 11, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

I haven't decided yet.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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