Comparison of Accentuated Eccentric and Concentric Resistance Training in Athletes.

December 29, 2025 updated by: Riphah International University

Comparison of Accentuated Eccentric and Concentric Resistance Training on Aerobic Capacity and Strength in Athletes.

This study will be randomized clinical trial and will recruit male soccer players aged 18-30yrs.Participants will be randomly divided into two groups with each group performing their program 3 times per week for 8 weeks.Group A will engage in Accentuated Eccentric resistance training ,using resistance bands and Group B will participate in Concentric Reistance training ,with similar resistance bands.

Study Overview

Detailed Description

Study Design: Randomized Clinical Trials Sample size: 78(39 for each group) Sampling technique: Non-probability, Purposive sampling technique

Study Setting:

  • Pakistan Football Federation, Lahore
  • Model town soccer club, Lahore

Inclusion criteria:

  • Male soccer players
  • Age 18 to 30 years.
  • A minimum of two years of experience in Regular training
  • Athletes with BMI 18.5kg/m2 -24.9kg/m2

Exclusion criteria:

  • History of lower extremity surgeries (e.g., ACL reconstruction or any major surgery) in the past year
  • Athletes having consumption of Drugs which may influence Athlete performance.
  • Any systemic illness
  • Any musculoskeletal disorder
  • Pre-existing Cardiovascular and respiratory (exercise-induced asthma) conditions

Tools:

  • Aerobic capacity:20-meter shuttle run test (ICC =0.96)
  • Muscle strength :1RM Back squat test (ICC=0.91-0.99)

Study Type

Interventional

Enrollment (Actual)

79

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, 54000
        • Model Town Football Club

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 soccer players

    • Age 18 to 30 years.
    • A minimum of two years of experience in Regular training
    • Athletes with BMI 18.5kg/m2 -24.9kg/m2

Exclusion Criteria:

  • • History of lower extremity surgeries (e.g., ACL reconstruction or any major surgery) in the past year

    • Athletes having consumption of Drugs which may influence Athlete performance.
    • Any systemic illness
    • Any musculoskeletal disorder
    • Pre-existing Cardiovascular and respiratory (exercise-induced asthma) conditions

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: Group A
The AERT group performed eccentric resistance training by Elastic Resistance bands for 3 sessions per week for 8 weeks. Each session included 3 sets of 10 repetitions with 2-3 mints of rest interval between each set. Participants in this group start with Yellow band (light resistance) and progressing through to purple band (high resistance). The level of exercise progressively increased throughout the 8-week program, by increasing the resistance of resistance bands. In group A, participants executed the Eccentric Phase for 2-4 seconds and Concentric phase for 1-2 seconds.
The AERT group performed eccentric resistance training by Elastic Resistance bands for 3 sessions per week for 8 weeks. Each session included 3 sets of 10 repetitions with 2-3 mints of rest interval between each set. Participants in this group start with Yellow band (light resistance) and progressing through to purple band (heavy resistance). The level of exercise progressively increased throughout the 8-week program, by increasing the strength of resistance bands. In group A, participants executed the Eccentric Phase for 2-4 seconds and Concentric phase for 1-2 seconds. 12 Comparison of accentuated eccentric and concentric resistance training in athletes
Experimental: Group B
The CRT group performed concentric resistance training by Elastic Resistance bands for 3 sessions per week for 8 weeks. Each session included 3 sets of 10 repetitions with 2-3 mints of rest interval between each set. Participants in this group start with Yellow band (light resistance) and progressing through to purple band (high resistance). The level of exercise progressively increased throughout the 8-week program, by increasing the resistance of resistance bands. In group B, participants executed the Concentric Phase for 2-4 seconds and Eccentric phase for 1-2 seconds.
The CRT group performed concentric resistance training by Elastic Resistance bands for 3 sessions per week for 8 weeks. Each session included 3 sets of 10 repetitions with 2-3 mints of rest interval between each set. Participants in this group start with Yellow band (light resistance) and progressing through to purple band (heavy resistance). The level of exercise progressively increased throughout the 8-week program, by increasing the strength of resistance bands. In group B, participants executed the Concentric Phase for 2 4 seconds and Eccentric phase for 1-2 seconds.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
1-RM Back Squat test
Time Frame: 8 weeks

a warm up of 10 repetitions using an empty barbell in back squat position. After rest of 2 mints, Participants will perform same protocol with addition of (35 pounds) weight and goal is to perform maximum repetitions. At final phase, weight (35 pounds) and the maximum repetitions performed are counted. This count is then used in Epley formula to calculate the individual 1RM (32).

Epley's Formula:

1RM = weight x (1 + (reps / 30))

8 weeks
20-MTR Shuttle Run test
Time Frame: 8 weeks
The 20-meter shuttle run test, often called the "beep" or "bleep" test, requires participants to run back and forth continuously between two lines 20 meters apart, with a rhythm imposed by audio(beep). Starting at a slow pace, they must turn when signaled by the beeps. After about a minute, the pace increased, with the beeps occurring more quickly, requiring the runners to speed up. The speed increases each minute(level), with beeps becoming closer together. If a participant reaches the line before the beep, they must wait; if not, they receive a warning and have two more chances to catch up to the pace. A second warning results in elimination from the test. Calculation: VO2max = 18.043461 + (0.3689295 x TS) + (- 0.000349 x TS x TS)
8 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: ayesha aslam, DPT, Riphah International University
  • Principal Investigator: Muhammad faheem Afzal, 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)

March 21, 2025

Primary Completion (Actual)

October 2, 2025

Study Completion (Actual)

November 2, 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/24/0481

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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