Tabata vs Burn 2 Learn Program on Body Weight, Physical Performance and Mental Well Being in School Athletes. (TABATA)

February 23, 2026 updated by: Riphah International University

Effect of Tabata vs Burn 2 Learn Program on Body Weight, Physical Performance and Mental Well Being in School Athletes.

Physical activity is crucial for school-aged children. The comparison between Tabata training and the Burn 2 Learn (B2L) program on body weight, physical performance, and mental well-being in school athletes is an interesting research area. Both exercise protocols aim to improve physical fitness, but they differ in structure and focus, which could lead to varied impacts on school athletes.

The study design will be randomized clinical trial. This study will be conducted in divisional public schools. Tabata training and Burn 2 Learn program would be administered to school going to school athletes. Subjects meeting the predetermined inclusion criteria will be divided into two groups using lottery method. Sample size was 50 calculated by using Epitool which will be divided into 2 groups 25 in group A will be treated with Burn 2 Learn (B2L) program for 6 weeks, and 25 in group B will be treated with Tabata training for 3 times per week for 6 weeks. Assessment will be done using Digital Scale for body weight, waist to hip ratio, BMI,Beep Test, Standing Long Jump Test and 90-Degree Push-Up Test for Physical performance, Warwick-Edinburgh Mental Well-Being Scale (WEMWBS) for mental well-being at baseline after 6 weeks post treatment. Recorded values will be analyzed for any change using SPSS version 25

Study Overview

Study Type

Interventional

Enrollment (Actual)

50

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, 54790
        • Divisional public school

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

Yes

Description

Inclusion Criteria:

  • Age: 17-19 years
  • Participating in school sports teams
  • Athletes with body weight 70 and more will be selected

Exclusion Criteria:

  • Previous experience with Tabata or Burn 2 Learn programs
  • Current or recent (past 6 months) injury or illness affecting physical performance
  • Participation in other structured exercise programs
  • Failure to obtain parental/guardian consent

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
Experimental: Tabata
This group will receive Effect of Tabata on body weight, physical performance and mental well being
Body Mass Index (BMI) is a widely used metric to assess whether an individual has a healthy body weight in relation to their height. It's calculated by dividing a person's weight in kilograms by the square of their height in meters. BMI is commonly used to categorize individuals into different weight status groups (e.g., underweight, normal weight, overweight, and obesity). BMI provides a quick, simple screening method to identify potential weight-related health risks. Reliability coefficients or Intraclass Correlation Coefficient (ICC) range between 0.83 and validity or Correlation Coefficients r=0.79 showing high positive correlation.
Experimental: Burn 2 Learn program
This group will receive Effect of Burn 2 Learn program on body weight, physical performance and mental well being
A digital scale is a simple and widely used tool for measuring body weight, providing quick and precise readings suitable for most age groups. When placed on a flat surface and used barefoot at a consistent time of day, it offers reliable and valid measurements. High-quality digital scales show good reliability (0.78) and validity (0.67) when properly maintained.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Digital Scale for body weight:
Time Frame: 8 weeks
A digital scale is a standard and easy-to-use tool for measuring body weight. It provides precise, quick readings and is suitable for most age groups. Digital scales are widely available, user-friendly, and can accurately measure small weight changes. Place the scale on a flat, hard surface. Students should step on with bare feet, standing still until the measurement is complete. Ensure measurements are taken at the same time of day to maintain consistency. Digital scales can offer highly reliable and valid weight measurements when maintained and used properly. High-quality digital scales, especially those designed for medical or clinical use, tend to offer strong reliability and validity. Reliability coefficients range between 0.78 and validity of 0.67
8 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Muhammad Mudasir Mudasir, MS-SPT, Riphah International University
  • Principal Investigator: Dr. Eisha Mubarak, MS-SPT, 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 23, 2023

Primary Completion (Actual)

April 30, 2024

Study Completion (Actual)

May 30, 2024

Study Registration Dates

First Submitted

February 23, 2026

First Submitted That Met QC Criteria

February 23, 2026

First Posted (Actual)

February 27, 2026

Study Record Updates

Last Update Posted (Actual)

February 27, 2026

Last Update Submitted That Met QC Criteria

February 23, 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)?

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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