Comparative Affects of Circuit Training and Complex Training on Agility, Power and Core Strength.

February 23, 2026 updated by: Riphah International University

Comparative Affects of Circuit Training and Complex Training on Agility, Power and Core Strength in Football Players.

Comparative Affects of Circuit Training and Complex Training on Agility, Power and Core Strength.

Study Overview

Detailed Description

Comparative Affects of Circuit Training and Complex Training on Agility, Power and Core Strength in Football Players.

Study Type

Interventional

Enrollment (Actual)

36

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

      • Lahore, Pakistan, 54782
        • Model Town Sports 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:

  • Age group between 18 to 26 years.
  • Both males and females.
  • At least 2 years of experience in competitive football
  • Regular participation in football training, at least 2 days per week.
  • Should be free from significant injuries in the last 6 months

Exclusion Criteria:

  • Chronic conditions (e.g., joint issues, cardiovascular diseases, history of severe neurological deficit)
  • Any recent core or back injuries (low back pain) within the past 6 months.
  • History of any fracture or trauma
  • Having any neurological disease
  • Any chronic musculoskeletal disorder
  • Any systemic illnesses

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: Experimental: Group A
Group A was administered Moderate-intensity Circuit Training protocol along with the baseline warm-up regime
Group A will engage in a circuit training protocol designed to enhance agility, power, and core strength over six weeks. Each session will commence with a 5-minute general warm-up to increase heart rate, followed by a static stretching routine targeting major muscle groups such as the hamstrings, quadriceps, and calves, with each stretch held for 15 to 20 seconds to improve flexibility and reduce the risk of injury.
Experimental: Experimental: Group B
Group B was administered Moderate-intensity complex training protocol along with the baseline warm-up regime.
Group B will undergo complex training protocol aimed at enhancing agility, power, and core strength for six weeks. Each session starts with a 5-minute general warm-up, followed by a static stretching protocol to enhance muscle flexibility, covering key muscle groups like the quadriceps, hamstrings, glutes, and calves, with each stretch held for 15-20 seconds.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
5-JUMP-TEST (FOR AGILITY):
Time Frame: 6 weeks
The 5-jump test is a simple physical assessment used to evaluate an individual's explosive power and agility, particularly in terms of lower body strength. It involves performing five consecutive horizontal jumps in a row, with
6 weeks
T TEST AGILITY (FOR AGILITY)
Time Frame: 6 weeks
The T-test for agility is a reliable and valid measure to assess an individual's quickness and directional change ability. To ensure reliability, the test should be administered multiple times (test-retest reliability) and checked for consistent scoring between trials, ideally resulting in an Intraclass Correlation Coefficient (ICC) above 0.75, which indicates good reliability. Additionally, inter-rater and intra-rater reliability should be examined if multiple evaluators are involved
6 weeks
1 Repetition Maximum (1RM) Test (Planks)
Time Frame: 6 weeks

The 1 Repetition Maximum (1RM) Test is commonly used to assess the maximum amount of weight an individual can lift for one complete repetition of an exercise.

However, when referring to planks, it typically isn't a traditional 1RM test since planks are a isometric exercise (where the body remains static rather than lifting weight). In the context of planks, the "1RM" concept could be adapted to measure how long a person can hold a plank position with correct form

6 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Ammar Hameed, MS SPT, Riphah International University
  • Principal Investigator: Maira Shaukat, 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)

October 4, 2025

Primary Completion (Actual)

November 21, 2025

Study Completion (Actual)

December 25, 2025

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

Other Study ID Numbers

  • REC/RCR & AHS/24/0478

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

product manufactured in and exported from the U.S.

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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