Exercise Program for Knee Recovery in Football Players with ACL Injuries

February 5, 2025 updated by: Norah A. Alshehri, King Saud University

Effect of an Exercise Program on Knee Joint Rehabilitation in Football Players with Anterior Cruciate Ligament Injuries: an Experimental Trial

This study aims to evaluate the effectiveness of a structured exercise program in improving knee function, muscle strength, and range of motion in football players recovering from anterior cruciate ligament (ACL) injuries. The study seeks to answer whether a rehabilitation program can restore the performance of the injured leg to levels comparable to the uninjured leg and significantly improve knee functionality over time.

Study Overview

Status

Completed

Conditions

Detailed Description

Anterior cruciate ligament (ACL) injuries are among the most common and challenging injuries faced by athletes, particularly football players. These injuries can significantly impact knee stability, muscle strength, and range of motion, making effective rehabilitation essential for a full recovery and return to sports.

This study investigates the impact of a structured exercise program on knee rehabilitation in male football players aged 18-22 years with ACL injuries. The goal is to understand whether this program can restore knee function and strength in the injured leg to levels comparable to the uninjured leg.

The rehabilitation program is designed to be implemented over 22 weeks, starting with five sessions per week and tapering to three sessions per week in the later stages. The program focuses on progressively strengthening the thigh and leg muscles, improving knee flexibility, and enhancing overall joint function.

The study uses a pre- and post-measurement experimental design with a single group of participants. The results will help determine whether structured exercise programs can effectively rehabilitate the knee after ACL injuries, enabling football players to regain performance and reduce the risk of future knee problems.

The findings will contribute valuable insights for sports medicine professionals, physiotherapists, and trainers in developing evidence-based rehabilitation protocols for athletes.

Study Type

Interventional

Enrollment (Actual)

9

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

      • Riyadh, Saudi Arabia, 11362
        • King Saud University

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
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Confirmed injury to the Anterior Cruciate Ligament (ACL).
  • Currently active in playing football.

Exclusion Criteria:

  • History of previous surgery to the knee.
  • Presence of other musculoskeletal injuries.
  • Diagnosis of chronic health 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: Supportive Care
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Rehabilitation Exercise Program for ACL Injury

This arm includes a structured rehabilitation exercise program designed to improve knee function, muscle strength, and range of motion in football players with anterior cruciate ligament (ACL) injuries.

The program is conducted over 22 weeks. Measurements of thigh and leg muscle strength, as well as knee range of motion, are taken at baseline, midway, and post-intervention to evaluate the program's effectiveness.

This arm aims to assess whether the exercise program restores knee function and supports a safe return to sports.

Rehabilitation Program Description:

The rehabilitation program was designed to restore knee function and strength progressively in football players recovering from anterior cruciate ligament (ACL) injuries. Key elements of the program are detailed below:

Program Components:

Session Structure:

Each session lasted 60 to 90 minutes. Sessions were performed multiple times weekly, progressively adjusted throughout the program.

Session Breakdown:

Warm-Up and Jump Exercises (Part 1):

Focused on preparing the body for physical activity and improving jump dynamics.

Dynamic Exercises (Part 2):

Included drop-jumps, side-hops, and crossover-hops for dynamic knee stabilization and balance.

Strength Exercises:

Targeted muscle groups included hamstrings, quadriceps, and calves. Exercises consisted of one-legged leg press, eccentric leg press, squats, one-legged squats on a balance mat, one-legged leg curls, Nordic hamstring, one-legged toe-raises, and lunge exercises.

Resistance training was i

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Outcome Measure: Muscle Strength of the Injured Leg
Time Frame: 22 weeks

Outcome Measure: Muscle Strength of the Injured Leg Description: Improvement in muscle strength of the injured leg, specifically targeting hamstrings and quadriceps.

Method of Measurement: Measured using an isokinetic dynamometer at 60°/second angular velocity.

Unit of Measure: Peak torque (Newton-meters, Nm).

22 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Comparison of Injured and Uninjured Leg Strength
Time Frame: 22 weeks

Outcome Measure: Comparison of Injured and Uninjured Leg Strength

  • Description: Change in the strength discrepancy between the injured and uninjured legs.
  • Method of Measurement: Measured via isokinetic testing.
  • Unit of Measure: Percentage difference in peak torque between the legs.
  • Time Frame: Baseline, mid-program (11 weeks), and post-program (22 weeks).
22 weeks

Collaborators and Investigators

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

January 24, 2024

Primary Completion (Actual)

July 28, 2024

Study Completion (Actual)

August 1, 2024

Study Registration Dates

First Submitted

January 21, 2025

First Submitted That Met QC Criteria

January 29, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 5, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

There is no plan to share individual participant data (IPD) collected in this study due to data privacy regulations, ethical considerations, and institutional policies.

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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