- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07403461
HIIT Effects on Table Tennis Players (HIIT-TTP)
Comparative Effects of High-Intensity Interval Training Modalities on Physical Performance and Physiological Responses in Competitive Table Tennis Players
Study Overview
Status
Intervention / Treatment
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Merkez
-
Karabük, Merkez, Turkey (Türkiye), 78000
- Karabuk University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
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
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:
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:
|
|
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:
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:
|
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
Sponsor
Investigators
- Study Director: Alirıza Han Civan, Dr, Karabük Üniversitesi Hasan Doğan Spor Bilimleri Fakültesi Spor Yöneticiliği Bölümü
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- / E-77192459-050.99-376986
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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