Comparative Effects of Tabata Training and Periodized Resistance Training in Sprinters

December 29, 2025 updated by: Riphah International University

Comparative Effects of Tabata Training and Periodized Resistance Training on Power, Speed and Agility in Sprinters.

This was a parallel group randomized control trail that utilized purposive sampling to recruit 32 participants. The 32 students are divided into 2 groups, namely the group of Tabata Training and Periodized Resistance Training. Periodized resistance training exercises will be performed three days a week during the eight-week period in group A. The periodized resistance training program started with warm up and continued by some exercises such as smith press, seated press, squat, lying dumbbell leg cruel, leg press, lying burble extension, sit up and finally the subjects cooled down. At the beginning of the study, the exercises will be conducted 60% intensity while eight maximum repetition and 10% intensity will be added after every week. The cycle will be repeated 1 times each exercise for a total of 8 repetitions. Each exercise will performed individually by each participant in a group activity. Tabata training will be performed in group B that included their Exercise sessions started with a general warm-up, and then stretching session followed by a specific warmup. The general warm-up consisted of 5 minutes of marching in place at 60% of the estimated maximal heart rate (HR max= 220 - age) measured with a heart rate monitor. The stretching session included major muscle groups and joints including triceps, deltoid, trapezius, neck extensors, pectoralis, biceps, latissimus dorsi, hamstrings, quadriceps, and gastrocnemius. Each stretch will maintained for 15 to 20 seconds. Then, a specific warm-up session followed that included 2 thruster repetitions of 30 seconds each, followed by 30 seconds of rest. Thrusters are a combination of 2 strength-training exercises: squat and overhead press. After the specific warm-up will be completed, the Tabata protocol began with participants performing thrusters as fast as possible for 20 seconds, followed by 10 seconds of resting. During the active part, participants will encouraged to reach near 100% of their HR max. Intensity will evaluated with heart rate monitors and also with the Borg rating of perceived exertion. The cycle will be repeated 7 times for a total of 8 repetitions in 4 minutes. After completing the protocol, a 5-minute cool-down period (slow walking and stretching exercises) was completed. Total duration of the Tab protocol will be approximately 19 to 20 minutes and will be completed 3 times per week for 8 consecutive weeks

Study Overview

Detailed Description

It will be a randomized clinical trial study. The sample size of study will be 38 participants (19 in each group) through non-probability purposive sampling technique. Data will be collected from Pakistan sports board coaching center, model town club Lahore, Sport complex phase 5 sector G DHA Lahore. Data will be collected within 10 months after approval of synopsis.

Inclusion Criteria:

Age group between 18 to 35year. Both male and female of sprinter athletes. Athletes currently performing Regular Training. 100m Sprinters. (should be registered Last 12 months.) [11] Shoe wear (heel drop minimum 1 inch and weight about 150g). [12]

Exclusion Criteria:

Athletes currently perform high resistance training. Injury report half a year ago. Non-sprinting populations. [13] Cardiac and metabolic disorder. Any diagnosed psychological condition that could affect participation. [14] The participants having any supplements or anabolic steroids that could effect performance.

Study Type

Interventional

Enrollment (Actual)

38

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

    • Punjab Province
      • Lahore, Punjab Province, Pakistan
        • Pakistan Sports Board

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:

  • Age group between 18 to 35year.
  • Both male and female of sprinter athletes.
  • Athletes currently performing Regular Training.
  • 100m Sprinters. (should be registered Last 12 months.) [11]
  • Shoe wear (heel drop minimum 1 inch and weight about 150g).

Exclusion Criteria:

  • Athletes currently perform high resistance training.
  • Injury report half a year ago.
  • Non-sprinting populations. [13]
  • Cardiac and metabolic disorder.
  • Any diagnosed psychological condition that could affect participation. [14]
  • The participants having any supplements or anabolic steroids that could effect performance.

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: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Group A
Group A were receiving periodized resistance training program started with warm up and continued by some exercises such as smith press, seated press, squat, lying dumbbell leg cruel, leg press, lying burble extension, sit up and finally the subjects cooled down.
Group A were receiving periodized resistance training program started with warm up and continued by some exercises such as smith press, seated press, squat, lying dumbbell leg cruel, leg press, lying burble extension, sit up and finally the subjects cooled down. At the beginning of the study, the exercises was conducted, 60% intensity while eight maximum repetition and 10% intensity were be added after every two weeks.
Other: Group B
Group B were receiving Tabata protocol began with participants performing thrusters as fast as possible for 20 seconds, followed by 10 seconds of resting. The cycle was repeated 7 times for a total of 8 repetitions in 4 minutes.
Group B were receiving Tabata training.the Tabata protocol began with participants performing thrusters as fast as possible for 20 seconds, followed by 10 seconds of resting. During the active part, participants will be encouraged to reach near 100% of their HR max. The cycle was repeated 7 times for a total of 8 repetitions in 4 minutes. After completing the protocol, a 5-minute cool-down period (slow walking and stretching exercises) was completed

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
30m sprint test
Time Frame: 8 weeks
The 30m sprint test is used to measure an athlete's acceleration, maximum speed, and speed endurance, assessing their overall sprint power and effectiveness for sports.
8 weeks
Agility T test
Time Frame: 8 weeks
The Agility T-test is commonly used to assess the ability of team sport athletes to change direction, including acceleration, deceleration, and lateral movement during preseason testing protocols
8 weeks
Vertical Jump Test
Time Frame: 8 weeks
A vertical jump test measures lower body explosive power by calculating the difference between your standing reach and the highest point you can touch in a jump, often using a wall with chalk or specialized equipment to assess athletic ability for sports
8 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Amina Amjad, DPT, Riphah International University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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 21, 2024

Primary Completion (Actual)

October 5, 2025

Study Completion (Actual)

November 5, 2025

Study Registration Dates

First Submitted

December 29, 2025

First Submitted That Met QC Criteria

December 29, 2025

First Posted (Actual)

January 9, 2026

Study Record Updates

Last Update Posted (Actual)

January 9, 2026

Last Update Submitted That Met QC Criteria

December 29, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • REC/RCR&AHS/24/0474

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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