HIIT Effects on Table Tennis Players (HIIT-TTP)

February 4, 2026 updated by: Alirıza Han Civan, Karabuk University

Comparative Effects of High-Intensity Interval Training Modalities on Physical Performance and Physiological Responses in Competitive Table Tennis Players

This study aims to investigate the effects of two different Tabata-based high-intensity interval training (HIIT) modalities on neuromuscular and physiological performance in competitive table tennis players. Participants will be randomly assigned to either a calisthenic/plyometric HIIT group or a kettlebell-based HIIT group. Both groups will perform their respective training protocols in addition to regular table tennis training for eight weeks. Physical performance and physiological variables will be assessed before and after the intervention.

Study Overview

Detailed Description

This study is designed as a randomized parallel-group interventional trial to examine the effects of two different Tabata-based high-intensity interval training (HIIT) modalities on neuromuscular and physiological parameters in competitive table tennis players.

Twenty-four male athletes aged between 18 and 24 years will be randomly assigned to one of two groups: a calisthenic/plyometric HIIT group or a kettlebell-based HIIT group. Both groups will continue their regular table tennis training and additionally perform their assigned HIIT protocol three times per week for a total duration of eight weeks.

The calisthenic/plyometric HIIT program consists of bodyweight and plyometric exercises performed in a Tabata format, while the kettlebell HIIT program consists of resistance-based exercises using kettlebells performed in the same interval structure. Each training session lasts approximately 20-30 minutes.

Outcome measures will be assessed before and after the intervention period and will include agility, flexibility, vertical jump performance, sprint performance, peak and average power output, and maximal oxygen uptake (VO₂max).

Study Type

Interventional

Enrollment (Actual)

24

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Male table tennis athletes aged 18-24 years.
  • Minimum of 2 years of regular competitive table tennis experience.
  • Currently performing structured training at least 3 days per week.
  • Medically cleared for high-intensity exercise.
  • Voluntary participation and signed informed consent.

Exclusion Criteria:

  • Any chronic illness or cardiovascular/metabolic disorders.
  • Musculoskeletal injury within the last 6 months that limits physical activity.
  • Participation in other high-intensity training programs outside the study protocol during the intervention.
  • Inability to complete at least 90% of the scheduled intervention sessions.
  • Signs of acute injury, excessive fatigue, or cardiovascular abnormalities during screening.

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

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Calisthenic/Plyometric HIIT Group
Participants in this group perform a Tabata-based high-intensity interval training program focused on calisthenic and plyometric exercises, in addition to their regular table tennis training. Sessions are conducted three times per week for eight weeks.
Participants perform a high-intensity Tabata protocol focusing on calisthenic and plyometric exercises designed to improve agility, flexibility, vertical jump performance, and neuromuscular function. Each session lasts 20-30 minutes, three times per week for eight weeks, in addition to regular table tennis training.
Other Names:
  • Tabata-style Calisthenic HIIT
Participants perform a high-intensity Tabata protocol focusing on kettlebell exercises designed to improve sprint performance, VO₂max, and overall physiological adaptations. Each session lasts 20-30 minutes, three times per week for eight weeks, in addition to regular table tennis training.
Other Names:
  • Tabata-style Kettlebell HIIT
Experimental: Kettlebell HIIT Group
Participants in this group perform a Tabata-based high-intensity interval training program focused on kettlebell exercises, in addition to their regular table tennis training. Sessions are conducted three times per week for eight weeks.
Participants perform a high-intensity Tabata protocol focusing on calisthenic and plyometric exercises designed to improve agility, flexibility, vertical jump performance, and neuromuscular function. Each session lasts 20-30 minutes, three times per week for eight weeks, in addition to regular table tennis training.
Other Names:
  • Tabata-style Calisthenic HIIT
Participants perform a high-intensity Tabata protocol focusing on kettlebell exercises designed to improve sprint performance, VO₂max, and overall physiological adaptations. Each session lasts 20-30 minutes, three times per week for eight weeks, in addition to regular table tennis training.
Other Names:
  • Tabata-style Kettlebell HIIT

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Agility Performance (seconds)
Time Frame: Pre-intervention and post-intervention (8 weeks)
Agility will be assessed using a standardized T-test protocol to measure change-of-direction speed.
Pre-intervention and post-intervention (8 weeks)
Flexibility (cm)
Time Frame: Pre-intervention and post-intervention (8 weeks)
A sitting and reaching test will be used to assess lower body flexibility.
Pre-intervention and post-intervention (8 weeks)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Vertical Jump Height (cm)
Time Frame: Pre-intervention and post-intervention (8 weeks)
Vertical jump performance will be measured using a countermovement jump test performed on a jump mat.
Pre-intervention and post-intervention (8 weeks)
Sprint Performance - 10 m (seconds)
Time Frame: Pre-intervention and post-intervention (8 weeks)
Sprint performance will be assessed over a distance of 10 meters using electronic timing gates.
Pre-intervention and post-intervention (8 weeks)
Peak Power Output (Watts)
Time Frame: Pre-intervention and post-intervention (8 weeks)
Peak power output will be measured using a standardized lower-body power assessment.
Pre-intervention and post-intervention (8 weeks)
Maximal Oxygen Uptake (VO₂max) (ml/kg/min)
Time Frame: Pre-intervention and post-intervention (8 weeks)
Maximal oxygen uptake (VO₂max) will be assessed using a graded exercise test performed on a treadmill or cycle ergometer.
Pre-intervention and post-intervention (8 weeks)

Collaborators and Investigators

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

Investigators

  • Study Director: 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

February 4, 2026

First Posted (Actual)

February 11, 2026

Study Record Updates

Last Update Posted (Actual)

February 11, 2026

Last Update Submitted That Met QC Criteria

February 4, 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

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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