ClinicalTrials.gg
CompletedNCT07270614Updated Aug 21, 2026

Eight-week Sports Injury Prevention Program

An interventional study of 8-Week Sports Injury Prevention Program in Health Adult Subjects, sponsored by Princess Nourah Bint Abdulrahman University. Completed at 1 site in Saudi Arabia. Open to female participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-21.

Sponsored by Princess Nourah Bint Abdulrahman University · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 9 months after the study started (first participant enrolled Feb 2025, registered Nov 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
37
Allocation
Not applicable
Ages
18 Years to 45 Years
Sex
Female
01

Study summary

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.

Read the 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.

02

Conditions studied

  • Health Adult Subjects

Keywords

  • Injury prevention program
03

In context

Lead sponsor

Princess Nourah Bint Abdulrahman University is the lead sponsor of 31 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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 and complete all study assessments

Exclusion criteria

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
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
37 participants (actual)

Study arms

  • 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.

    Behavioral: 8-Week Sports Injury Prevention Program

Interventions

  • Behavioral8-Week Sports Injury Prevention Program

    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.

06

What researchers measure

Primary outcomes

  1. Change in Lower-Extremity Functional Performance

    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.

    Time frame: From enrollment to the end of treatment at 8 weeks

  2. Change in Lower-Body Explosive Power

    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).

    Time frame: From enrollment to the end of treatment at 8 weeks

  3. Change in Dynamic Balance

    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.

    Time frame: From enrollment to the end of treatment at 8 weeks

07

Study locations

1 site
  • PNU- Students gym
    Riyadh, Riyadh Region 12341, Saudi Arabia
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 21, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07270614
Lead sponsor
Princess Nourah Bint Abdulrahman University
Responsible party
Monira Aldhahi (Principal Investigator, Princess Nourah Bint Abdulrahman University) — Principal investigator
First posted
Dec 8, 2025
Start date
Feb 16, 2025
Primary completion
Nov 30, 2025
Completion
Jan 30, 2026
Last update
Aug 21, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion