- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07270614
Eight-week Sports Injury Prevention Program
Effects of an 8-Week Injury Prevention Program on Lower Limb Performance in Female Athletes: Quasi-Experimental Evidence
This study aims to find out whether an 8-week sports injury prevention program can improve lower-body performance-such as power, agility, and balance-among female college athletes in Saudi Arabia.
Sports participation has increased among women in Saudi Arabia, but many injury-prevention programs were originally designed for male athletes and may not meet the specific needs of females. This study will help determine whether a tailored program can reduce injury risks and improve athletic performance.
Female athletes aged 18-35 years who have been training and competing for at least one year can participate. Athletes with recent injuries, pregnancy, or chronic medical conditions that could affect performance will not be included.
Participants will complete tests before and after the program, including jumping, balance, and agility assessments. The prevention program includes warm-up exercises, stretching, strengthening, jumping drills, balance work, and agility training.
By comparing results before and after the program, the study will show whether this type of training can help female athletes stay safer and perform better.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study will evaluate whether an 8-week sports injury prevention program can improve injury-related knowledge and lower-body performance in female college athletes. Sports participation among women in Saudi Arabia has increased in recent years, but female athletes often use injury-prevention programs originally designed for men. Because women have different physical and biomechanical characteristics, they may face a higher risk of sports injuries. This study aims to address this gap by testing a program tailored to their needs.
Participants will attend supervised injury-prevention sessions for eight weeks. Each session includes:
Warm-up drills (jogging, shuttle runs, backward running)
Stretching for major lower-body muscles
Strength training such as lunges and hamstring exercises
Plyometric drills (jumping and bounding)
Balance exercises on one leg
Agility drills such as directional running
Cool-down stretching and core exercises
This type of program is commonly used to reduce lower-limb injuries by improving strength, stability, coordination, and movement control.
How participation will be assessed
Before starting the program and again after the eight weeks, participants will complete several tests that measure:
Jumping power
Agility during multi-directional movement
Balance while reaching in different directions
These tests are widely used in sports medicine and have high reliability. They help identify injury risk and measure improvements in physical performance.
Why this study is important
The results will show whether a structured injury-prevention program can help female athletes:
Improve movement quality
Enhance lower-body strength, balance, and agility
Increase awareness of sports-injury risks
Potentially reduce the likelihood of future injuries
This research may support the development of safer and more effective training strategies for female athletes in Saudi Arabia as sports opportunities continue to expand.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Monira Aldhahi, Phd
- Phone Number: +966506215406
- Email: mialdhahi@pnu.edu.sa
Study Locations
-
-
Riyadh Region
-
Riyadh, Riyadh Region, Saudi Arabia, 12341
- Recruiting
- PNU- Students gym
-
Contact:
- Monira Aldhahi
- Phone Number: 0506215406
- Email: mialdhahi@pnu.edu.sa
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Female athletes aged 18-35 years
- Actively participating in organized sports in Saudi Arabia
- Minimum of one year of continuous experience in their sport
- Currently engaged in regular training and/or competition
- Able to perform physical activity safely as confirmed by self-report
- Willing to provide informed consent and complete all study assessments
Exclusion Criteria:
- Any recent injury within the past six months that limits performance
- Pregnancy at the time of enrollment
- Diagnosis of a chronic medical condition that may affect performance (e.g., uncontrolled diabetes, uncontrolled hypertension)
- Any condition that could interfere with safe participation in physical testing or training
- Refusal or inability to provide informed consent
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Exercise group
Participants will attend supervised injury-prevention sessions for eight weeks. Each session includes: Warm-up drills (jogging, shuttle runs, backward running) Stretching for major lower-body muscles Strength training such as lunges and hamstring exercises Plyometric drills (jumping and bounding) Balance exercises on one leg Agility drills such as directional running Cool-down stretching and core exercises This type of program is commonly used to reduce lower-limb injuries by improving strength, stability, coordination, and movement control. |
A structured 8-week injury prevention exercise program designed to improve lower-extremity strength, balance, agility, and movement control in female college athletes. Each supervised session includes: Warm-up: jogging, shuttle runs, backward running Stretching: calf, quadriceps, and hamstring stretches Strengthening: walking lunges, Russian hamstring exercise, single-leg toe raises Plyometrics: lateral, forward, and backward jumps; zigzag shuffle; bounding drills Balance training: single-leg stance with chest pass, forward bend, and figure-of-eight reach Agility drills: multidirectional shuttle runs, diagonal runs, bounding runs Cool-down: bridging, abdominal crunches, knee-to-chest stretches, and seated butterfly stretch Sessions follow a standardized protocol with prescribed repetitions, sets, or time durations for each component. The goal of the intervention is to enhance athletic performance and reduce the risk of lower-extremity sports injuries. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Lower-Extremity Functional Performance
Time Frame: From enrollment to the end of treatment at 8 weeks
|
Description: Assessed using the Lower Extremity Functional Test (LEFT), which evaluates multidirectional agility through eight standardized tasks (forward run, backward run, side shuffle, carioca, figure-8 run, 45° cuts, 90° cuts, and countermovement jump). Time Frame: Baseline and 8 weeks (post-intervention). Outcome Metric: Total completion time (seconds). Lower times indicate better performance. |
From enrollment to the end of treatment at 8 weeks
|
|
Change in Lower-Body Explosive Power
Time Frame: From enrollment to the end of treatment at 8 weeks
|
Description: Measured using the Countermovement Jump (CMJ) and Standing Long Jump (SLJ) tests, both widely validated for assessing lower-limb power. Time Frame: Baseline and 8 weeks. Outcome Metric: CMJ height (cm) and SLJ distance (cm). |
From enrollment to the end of treatment at 8 weeks
|
|
Change in Dynamic Balance
Time Frame: From enrollment to the end of treatment at 8 weeks
|
Description: Evaluated using the Star Excursion Balance Test (SEBT) in the anterior, posteromedial, and posterolateral directions. Outcome Metric: Max reach distance (cm), normalized to leg length. |
From enrollment to the end of treatment at 8 weeks
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- PNU-7
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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