Functional Training in Adolescent Table Tennis (FT in Adolesce)

January 26, 2026 updated by: Alirıza Han Civan

The Effect of Functional Training on Speed, Balance, and Functional Capacity in Adolescent Table Tennis Players: A Randomized Controlled Trial

This randomized controlled trial aims to investigate the effects of an eight-week functional training program on physical performance parameters in adolescent table tennis players. Functional training involves multi-joint and multi-plane exercises designed to improve movement quality, strength, balance, and coordination.

Thirty adolescent table tennis players will be randomly assigned to one of three groups: Functional Training, Conventional Training, or Control (routine training). The Functional Training group will perform a structured functional exercise program in addition to regular table tennis training, while the Conventional Training group will continue standard training routines. The Control group will maintain regular practice only.

Physical performance variables including flexibility, agility, speed, vertical jump performance, functional movement patterns, and balance will be assessed before, during, and after the intervention period.

Study Overview

Detailed Description

This study is designed as a randomized controlled trial to examine the effects of an eight-week functional training program on physical performance in adolescent table tennis players. Functional training focuses on multi-joint, multi-planar exercises aimed at improving movement efficiency, balance, strength, and neuromuscular coordination.

Thirty adolescent table tennis players aged 12-16 years with at least three years of training experience will be recruited and randomly allocated to one of three groups: Functional Training, Conventional Training, or Control. The Functional Training group will perform a structured exercise program consisting of dynamic, whole-body movements designed to enhance agility, balance, speed, and movement quality. Training sessions will be conducted three times per week for eight weeks in addition to regular table tennis practice.

The Conventional Training group will continue standard technical and tactical training without additional functional exercises. The Control group will maintain routine training only.

Outcome measures will be collected at baseline, mid-intervention, and post-intervention. Assessments will include flexibility, agility, sprint speed, vertical jump performance, Functional Movement Screen scores, and static and dynamic balance measures. Outcome measures will be collected at baseline, mid-intervention, and post-intervention.

Study Type

Interventional

Enrollment (Actual)

30

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 Locations

    • Merkez
      • Karabük, Merkez, Turkey (Türkiye), 78000
        • Karabuk 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
  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Male and female adolescent table tennis players aged 12-18 years.
  • Actively training and competing in table tennis for at least 2 years.
  • Participating in at least 3 training sessions per week.
  • Free from injury or medical conditions affecting physical performance.
  • Voluntarily consent to participate in the study (parental consent required for minors).

Exclusion Criteria:

  • Any musculoskeletal injury, neurological disorder, or medical condition affecting training or performance.
  • Participation in another structured training program during the study period.
  • Non-compliance with study protocol or inability to attend scheduled sessions.

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Functional Training Group
Eight-week functional training program focusing on flexibility, agility, speed, balance, and movement quality. Training is performed three times per week alongside regular table tennis practice.
Eight-week functional training program focusing on flexibility, agility, speed, balance, and movement quality. Training is performed three times per week alongside regular table tennis practice.
Active Comparator: Conventional Training Group
Participants perform conventional table tennis training for eight weeks following standard club routines.
Standard table tennis training performed three times per week for eight weeks without additional functional exercises.
No Intervention: Control Group
Participants continue their usual routine table tennis training without any additional intervention.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Overall Physical Performance Score
Time Frame: Baseline (pre-test), mid-intervention (week 4), and post-intervention (week 8)

Overall physical performance will be assessed using a battery of standardized physical performance tests including flexibility, agility, speed, vertical jump height, balance, and Functional Movement Screen (FMS).

Flexibility: Sit-and-Reach Test (cm; higher values indicate better flexibility) Agility: T-test (seconds; lower values indicate better performance) Speed: 10-meter sprint test (seconds; lower values indicate better performance) Vertical Jump: Countermovement jump height (cm; higher values indicate better performance) Balance: Static and dynamic balance tests (test-specific scoring; higher scores indicate better balance) Functional Movement Screen (FMS): Composite score ranging from 0 to 21, with higher scores indicating better movement quality

Baseline (pre-test), mid-intervention (week 4), and post-intervention (week 8)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Flexibility (Sit-and-Reach Test)
Time Frame: Baseline (pre-test), mid-intervention (week 4), and post-intervention (week 8)

Flexibility will be assessed using a sit-and-reach test that measures the flexibility of the hamstring and lower back muscles.

Measurement: Sit-and-reach Test Unit: centimeters (cm) Range: Typically 0-50 cm Direction: Higher scores indicate better flexibility

Baseline (pre-test), mid-intervention (week 4), and post-intervention (week 8)

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Alirıza Han Civan, Dr, Karabük Üniversitesi Hasan Doğan Spor Bilimleri Fakültesi Spor Yöneticiliği Bölümü

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)

November 15, 2025

Primary Completion (Actual)

December 31, 2025

Study Completion (Actual)

January 3, 2026

Study Registration Dates

First Submitted

January 16, 2026

First Submitted That Met QC Criteria

January 26, 2026

First Posted (Actual)

February 3, 2026

Study Record Updates

Last Update Posted (Actual)

February 3, 2026

Last Update Submitted That Met QC Criteria

January 26, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Individual patient data will not be shared in this study. Study data were analyzed solely by the research team and will not be shared with third parties to protect participant confidentiality.

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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