Speed, Agility, and Quickness Training (SAQ)

August 6, 2024 updated by: SUN MIN

Effects of Speed, Agility, and Quickness Training on Physical, Cognitive, and Skill Performance Among University Soccer Major Students in China

This study aims to evaluate the effects of Speed, Agility, and Quickness (SAQ) training on the physical, cognitive, and skill performance of university soccer major students in China. The hypothesis is that SAQ training will significantly improve students' physical fitness (e.g., speed, agility), cognitive functions (e.g., reaction time, decision-making), and soccer skills (e.g., ball control, passing). The study will recruit 52 university soccer major students, randomly assigned to an intervention group and a control group, with 26 students in each group. The study will last for 12 weeks, and tests will be conducted before, during, and after the intervention. The expected outcome is that the intervention group will show superior performance in various tests compared to the control group, thereby validating the effectiveness of SAQ training.

Study Overview

Detailed Description

This study adopts a cluster randomized controlled trial (CRCT) design to evaluate the impact of SAQ training on the physical, cognitive, and skill performance of university soccer major students. The study will recruit 52 eligible university soccer major students, randomly assigned to the intervention group and the control group, with 26 students in each group. The study will last for 12 weeks, with the intervention group undergoing SAQ training three times a week, while the control group continues their regular training.

The SAQ training program includes the following components:

Warm-up and Cool-down: Each training session begins and ends with a 10-minute warm-up and cool-down to ensure safety.

Training Content: The SAQ training includes speed runs, agility exercises, and quick reaction drills, each session lasting 60 minutes.

Assessment Metrics: The study will assess students' physical fitness (speed, agility), cognitive functions (reaction time, decision-making), and soccer skills (ball control, passing).

Testing Time Points:

Pre-test: Initial assessment of all participants before the intervention. Mid-test: Mid-term assessment after 6 weeks of intervention. Post-test: Final assessment after the completion of the intervention.

Data Collection and Analysis:

Data Collection: Standardized testing methods will be used to assess all participants before, during, and after the intervention.

Data Analysis: Data will be analyzed using SPSS software, employing independent sample t-tests and ANOVA to compare differences between the intervention and control groups across various metrics.

Quality Assurance and Data Validation:

Quality Assurance Plan: An independent quality control team will oversee data collection and entry to ensure accuracy and completeness.

Data Validation: Data will be validated by comparing it with external sources (e.g., medical records, paper reports) to ensure authenticity and representativeness.

Sample Size Estimation and Statistical Analysis Plan:

Sample Size Estimation: Based on preliminary studies, the required sample size is estimated to be 52 to ensure statistical significance of the results.

Statistical Analysis Plan: Multivariate regression analysis and other methods will be used to control for confounding variables and analyze the impact of SAQ training on various metrics in detail.

Study Type

Interventional

Enrollment (Estimated)

52

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 Contact

Study Contact Backup

Study Locations

    • Selangor
      • Kuala Lumpur, Selangor, Malaysia
        • Faculty of Educational Studies

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 major students (age ≥18 years old)
  • At least 3 years of professional soccer training
  • No recent history of surgery or injury
  • No participation in SAQ training programs within 8 weeks prior to the study
  • Able to provide written informed consent and willing to participate in the entire study and complete all assessments

Exclusion Criteria

  • Recent history of fractures or other injuries
  • Currently participating in an SAQ training program

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental Group: SAQ Training
Participants in the experimental group will undergo Speed, Agility, and Quickness (SAQ) training three times per week, with each session lasting 60 minutes, for a duration of 12 weeks. The training intensity will range from 70% to 100% of the participants' maximum effort. This program is designed to enhance physical fitness, cognitive abilities, and soccer-specific skills.
The SAQ training will include exercises designed to improve speed, agility, and quickness, such as ladder drills, cone drills, sprint drills, and reaction drills.
Active Comparator: Control Group: Regular Training
Participants in the control group will engage in their regular training routine, which does not include the specific SAQ training regimen. The training intensity for the control group will also range from 70% to 100% of the participants' maximum effort. This routine will last for 12 weeks, with training sessions occurring three times per week for 60 minutes each session.
Participants in the control group will follow a standard soccer training regimen, which includes general conditioning exercises, skill drills, and tactical training.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Flexibility
Time Frame: Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
Measured by the sit-and-reach test. Results are recorded in centimeters (cm), with higher scores indicating better flexibility.
Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
Agility
Time Frame: Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
Measured by the Arrowhead Agility Test. Results are recorded in seconds (s), with shorter times indicating better agility.
Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
Sprint
Time Frame: Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
Measured by sprints at 5m, 10m, 20m, and 30m. Results are recorded in seconds (s), with shorter times indicating better speed.
Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
Upper Body Strength
Time Frame: Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
Measured by pull-ups. Results are recorded as the number of completed pull-ups, with more pull-ups indicating greater upper body strength.
Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
Lower Limb Explosiveness
Time Frame: Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
Measured by vertical jump. Results are recorded in centimeters (cm), with higher jump heights indicating greater explosiveness.
Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
Aerobic Endurance
Time Frame: Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
Measured by the Yo-Yo Intermittent Recovery Test Level 2 (Yo-Yo2). Results are recorded as maximum distance covered(m), with higher distances indicating better aerobic endurance.
Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
Reaction Time
Time Frame: Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
Measured by a computerized reaction time test. Results are recorded in milliseconds (ms), with shorter reaction times indicating faster responses.
Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
Selective attention
Time Frame: Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
Through the computer flanker task, the results are recorded in milliseconds (ms), with higher accuracy and shorter reaction time indicating better decision-making ability.
Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
Dribbling Agility
Time Frame: Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
Measured by the 22-meter slalom dribble test. Results are recorded in seconds (s), with shorter times indicating better dribbling skills.
Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
Passing performance
Time Frame: Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
When measuring passing performance using the Loughborough Soccer Passing Test (LSPT), results are recorded as total time and passing accuracy. Total time is measured in seconds (s) and includes the time from the start of the test to the completion of the last pass, including all penalty time. Shorter total times indicate better performance. Passing accuracy is recorded by the number of successful passes into target areas, with more successful passes indicating better passing skills. Penalties are applied as follows: five seconds for completely missing the target area or passing to the wrong target, three seconds for missing the target area, three seconds for handling the ball, two seconds for passing from outside the designated area, and two seconds for the ball touching any cone.
Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Height
Time Frame: Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
The height of the participant is recorded, typically measured to two decimal places, in meters (m).
Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
Weight
Time Frame: Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12
The weight of the participant is recorded, measured to one decimal place, in kilograms (kg).
Pre-intervention: Week 0 Mid-intervention: Week 6 Post-intervention: Week 12

Collaborators and Investigators

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

Sponsor

Investigators

  • Principal Investigator: Min Sun, Faculty of Educational Studies

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 (Estimated)

September 1, 2024

Primary Completion (Estimated)

December 25, 2024

Study Completion (Estimated)

February 15, 2025

Study Registration Dates

First Submitted

July 30, 2024

First Submitted That Met QC Criteria

August 6, 2024

First Posted (Actual)

August 9, 2024

Study Record Updates

Last Update Posted (Actual)

August 9, 2024

Last Update Submitted That Met QC Criteria

August 6, 2024

Last Verified

August 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

individual participant data will not be shared. The data is intended solely for research purposes and will only be accessible to the research team. Data confidentiality will be maintained, and no individual data will be made available to external parties.

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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