ClinicalTrials.gg
Not yet recruitingNCT04095260Updated Feb 10, 2026

Identification of Neuromusculoskeletal Variables Associated With Injury Risk and Performance in High School Athletes.

An observational study in Athletic Injuries, sponsored by The University of Texas Medical Branch, Galveston. Not yet recruiting at 1 site in United States. Open to participants aged 14 Years to 18 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-10.

Sponsored by The University of Texas Medical Branch, Galveston · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
250
Ages
14 Years to 18 Years
Sex
All
01

Study summary

The purpose of this study is to complete a neuromuscular performance assessment of high school athletes who are participating in school based pre-season strength and performance training program. The performance assessment will screen for existing muscle imbalances and strength deficits known to increase risk for sports injury, and provide a baseline performance measurement. Athletes will be measured before the start of the program and then again at the end of the pre-season training period to measure changes in motor coordination, muscle strength, and performance and injury risk category. Internal and external training load will be measured weekly during the training program to track intensity of the training program. In addition to the pre and post measurements, sports injury occurrence and time away from sports participation will be tracked throughout the sport season/school year to evaluate training program outcomes and accuracy of risk assessment.

Read the detailed description

This study involves a test - re-test design. Subjects will be tested in their physical performance. These measures include a general assessment of joint mobility, muscle strength, motor coordination, and performance assessment utilizing functional movement screens. The physical examination is similar to a physical examination performed clinically in sports performance testing and also in the practice of Physical Therapy. The initial baseline measure will provide objective scores that can be utilized to assess for change over time. Additional information to be gathered includes demographic information on the subject including age, previous injury history, and level of exposure to physical performance training. These variables are associated with injury risk and also impact the potential for change with physical performance training. In addition, information on mental factors including stress, fear of failure, and burnout will be collected. It is hypothesized that these variables also factor into athletic performance. It is not known how these variables impact injury risk. Information on training load will be gathered weekly during the training period. Training load has a direct impact on muscle performance, and is hypothesized to impact injury risk. The subjects will be re-tested at the end of the training period to measure changes in physical performance and injury risk.

Project Procedures

Study population: High school athletes, ages 14 to 18, who are participating in an organized sports training program. The target subject enrollment is 250 high school athletes.

Inclusion criteria will be athletes who have completed a pre-participation sports physical, are enrolled in a sports elective or a member of a sports team, and have volunteered to participate in the study providing both verbal and written consent.

Exclusion criteria for participation include athletes who have not submitted a pre-participation sports physical to the high school training staff, student athletes who are currently suffering from an acute neuromusculoskeletal injury with restrictions on athletic participation, an athlete who has undergone surgery within a 3 month period of the program start date, an athlete who presents with a cardiovascular condition that would exclude exercise participation (systolic BP > 180, diastolic BP > 100), or athletes who are currently pregnant.

Study Methodology

Participants will complete a self-report questionnaire collecting demographic data including age, gender, primary and secondary sport activity, and previous injury history. Participants will also complete the Perceived Stress Scale to measure self-appraised stress, the Sports Mental Training Questionnaire to measure mental preparation skills, and the Athlete Burnout Questionnaire to assess emotional/physical exhaustion at the beginning and end of the 8 week program to assess psychological stressors associated with sport participation that may impact motivation to participate and perceived internal training load.

The structured physical performance assessment will include functional movement testing, motor coordination testing, joint mobility screen, muscle strength testing, and agility performance testing. Video analysis will be included with the functional movement testing utilizing software to assess reliability of the neuromuscular impairment screen.

Research project specific measures:

Functional movement testing includes:

  1. Forward flexion/hinge
  2. Standing trunk rotation
  3. Bilateral squat
  4. Forward lunge
  5. Lateral lunge
  6. Lower extremity functional reach test
  7. Upper extremity movement pattern (shoulder mobility test)
  8. Quadruped trunk rotary stability test

Mobility testing includes:

  1. Ankle mobility testing (DF, PF, IV, EV, first ray extension)
  2. Hip mobility testing (flexion, extension, abduction, IR, ER)
  3. Cervical mobility testing (flexion, extension, side bending, rotation, flexion rotation
  4. Thoracic mobility testing (seated trunk rotation)
  5. Shoulder mobility testing (flexion with scapular mobility assessment, abduction with scapular mobility assessment, IR, ER)
  6. Elbow mobility testing (flexion, extension, supination, pronation)
  7. Wrist mobility (flexion, extension)

Muscle strength testing:

  1. Hip strength (flexion, extension, abduction, ER, IR)
  2. Knee strength (flexion, extension)
  3. Ankle strength (PF, IV, EV)
  4. Shoulder strength (IR, ER, AB)
  5. Scapular strength (middle trap, lower trap)
  6. Elbow strength (flexion, extension)

Performance testing:

  1. Jump testing (bilateral long jump, unilateral jump, drop box jump)
  2. Upper extremity closed chain reach testing
  3. Shuttle run

Intrinsic and Extrinsic training load will be recorded weekly for subjects participating in the research study. Data will be utilized to calculate the training load associated with the school based strength and conditioning training program.

02

Conditions studied

  • Athletic Injuries

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03

In context

Athletic Injuries

258 studies on the registry are indexed under Athletic Injuries; 45 are open to participants now.

This study's planned enrollment of 250 is above the median of 100 across 91 observational studies indexed under Athletic Injuries.

Browse Athletic Injuries studies →

Lead sponsor

The University of Texas Medical Branch, Galveston is the lead sponsor of 257 studies on the registry; 38 are open to participants now.

Of its 32 completed or terminated interventional studies of FDA-regulated products, 26 (81%) have results posted.

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

04

Who can participate

Ages eligible
14 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

High school athletes, ages 14 to 18, who are participating in an organized sports training program. The target subject enrollment is 250 high school athletes.

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

  • athletes who have completed a pre-participation sports physical
  • are enrolled in a sports elective or a member of a sports team
  • have volunteered to participate in the study providing both verbal and written consent.

Exclusion criteria

Exclusion Criteria:

  • athletes who have not submitted a pre-participation sports physical to the high school training staff
  • student athletes who are currently suffering from an acute neuromusculoskeletal injury with restrictions on athletic participation
  • an athlete who has undergone surgery within a 3 month period of the program start date
  • an athlete who presents with a cardiovascular condition that would exclude exercise participation (systolic BP > 180, diastolic BP > 100)
  • an athletes who are currently pregnant.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
250 participants (estimated)
Patient registry
No

Groups and cohorts

  • high school athletes

    High school athletes, ages 14 to 18, who are participating in an organized sports training program.

    Other: Pre-season strength and conditioning program

Interventions

  • OtherPre-season strength and conditioning program

    The structured physical performance assessment will include functional movement testing, motor coordination testing, joint mobility screen, muscle strength testing, and agility performance testing. These measures will assess the effectiveness of pre-season strength and conditioning program to reduce musculoskeletal impairments and increase resistance to injury.

    Also known as: pre and post physical performance testing following a high school based strength and conditioning training program

06

What researchers measure

Primary outcomes

  1. Change in baseline movement quality as measured by the Selective Functional Movement Assessment (SFMA).

    The Selective Functional Movement Assessment is an assessment to score movement quality on 7 functional movements. The movement is categorically scored as: Functional and not painful (FN); Functional and painful (FP); Dysfunctional and not painful (DN); Dysfunctional and painful (DP)

    Time frame: Pre (initial baseline), and after week 8 of preseason strength and condition training program

  2. Change in muscle strength testing as measured by hand held dynamometer.

    Hand held dynamometer measures isometric force production in kilograms or pounds.

    Time frame: Pre (initial baseline) and after week 8 of preseason strength and condition training program

  3. Change in baseline movement quality as measured by the Anterior reach of the Y Balance Test.

    The Anterior reach of the Y Balance Test measures distance of limb reach in centimeters. Distance is compared from one side to the other to assess for symmetry. A difference of \> 4cm is a positive risk factor for lower extremity injury.

    Time frame: Pre (initial baseline) and after week 8 of preseason strength and condition training program

  4. Change in baseline in motor performance as measured by the Single Leg Hop jump distance.

    Single leg hop test measures hop distance in centimeters. Distance hopped is compared between limbs, comparing strength and power symmetry between the two limbs.

    Time frame: Pre (initial baseline) and after week 8 of preseason strength and condition training program

  5. Change in baseline in motor performance as measured by the Modified T-Test drill completion time (seconds).

    The Modified T-Test is an agility test that incorporates quick direction changes in a defined pattern. The test is measured in seconds. A reduction in the time to complete the drill represents improved motor performance and power.

    Time frame: Pre (initial baseline) and after week 8 of preseason strength and condition training program

Secondary outcomes

  1. Number of participants who experience a musculoskeletal sports related injury.

    Measuring occurrence of musculoskeletal injury that is reported by the athlete and/or impacts participation practice or playing time during the training and competition season. Number of missed days of practice and or sports competition will be recorded.

    Time frame: End of study (1 year)

  2. Intrinsic training load as measured by perceived effort of the training session (Rate of Perceived Exertion Scale)

    Rate of Perceived Exertion Scale is a 0 to 10 scale that measures the perceived difficulty of a training sessions.

    Time frame: Weekly, for 8 weeks during the strength and conditioning training program

07

Study locations

1 site
  • Clear Falls High School
    League City, Texas 77573, United States
    • Janna M McGaugh, ScD · Contact
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Aug 2028; primary completion for Aug 2029, 12 months later.

Of 35 non-industry observational studies under Athletic Injuries, half reached primary completion within 10 months of starting (the median), counting those still running; a quarter within 3 and three quarters within 12. This study's planned 12 months is above that.

Counting every sponsor, half of 35 studies reached it within 10 months; a quarter within 3 and three quarters within 12.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 16, 2019
First posted
Sep 19, 2019
StartEst.
Aug 1, 2028
Primary completionEst.
Aug 30, 2029
CompletionEst.
Sep 30, 2029
Last update
Feb 10, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04095260
Responsible party
Sponsor
First posted
Sep 19, 2019
Start date
Aug 1, 2028 (estimated)
Primary completion
Aug 30, 2029 (estimated)
Completion
Sep 30, 2029 (estimated)
Last update
Feb 10, 2026

Study contacts

Janna M McGaugh, ScD
Contact
jamcgaug@utmb.edu
409-772-3068
Janna M McGaugh, ScD
principal investigator · UTMB

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

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