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CompletedNCT02530333Updated Jan 8, 2016

Differential Biomechanical Effects of an ACL Injury Prevention Program in Women's Basketball and Soccer Players

An interventional study of Neuromuscular Prevention Program in Anterior Cruciate Ligament Injury, sponsored by High Point University. Completed at 1 site in United States. Open to female participants aged 12 Years to 19 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-01-08.

Sponsored by High Point University · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
99
Allocation
Randomized
Ages
12 Years to 19 Years
Sex
Female
01

Study summary

Anterior cruciate ligament injury programs are less successful in women's basketball than soccer players, yet the reason for this discrepancy is unknown. Thus, this study will recruit high school aged girl's basketball and soccer players, randomized teams into control and experimental groups, administer an ACL injury prevention program in the experimental group and compare the two groups on their lower extremity biomechanics before and after completion of the program. Biomechanical analyses will help determine the extent to which women's basketball and soccer players respond differently to a uniform injury prevention program, and whether this prevention program provides an adequate stimulus to improve lower extremity biomechanics during basketball-specific tasks.

Read the detailed description

Anterior cruciate ligament (ACL) injury prevention programs are considerably less successful in women's basketball than women's soccer. Women's basketball and soccer are each characterized by distinct sport-specific demands, where women's basketball players perform significantly more frequent jumping (2- and 1-legged landings) and frontal plane movements than women's soccer players. Despite varying sport-specific demands, ACL injury prevention programs have been uniformly administered in both sports, and emphasize improving high-risk biomechanics during 2-legged sagittal plane tasks. As such, they may not provide the appropriate stimulus to reduce ACL injury risk during the high-risk demands associated with women's basketball. To date, the differential biomechanical adaptations that result from ACL injury prevention programs in women's basketball and soccer have never been investigated.

This study will use a cluster randomized controlled trial using a repeated measures design. Participants will be randomized (by team) in to control and intervention groups. Participants in the control group will be asked to continue their normal daily and athletic activities (practices, games) without participating any distinct injury prevention training. Participants in the intervention group will complete at 6 week ACL injury prevention program previously described in the literature as being effective at reducing ACL injury risk. The prevention program lasts 20-25 minutes in duration and will take place as a warm-up prior to any practice. The frequency will depend solely on the number of practices each team holds throughout the given 6-week time period. A member of the research team plans to be at each intervention session. All participants will complete pre- and post-testing approximately 1 week before the onset and after the completion of the prevention program, respectively. As stated previously, all pre- and post-testing will be performed at the High Point University Human Biomechanics and Physiology Laboratory.

The following are Specific Aims and Hypotheses. Specific Aim 1. To determine the extent to which women's basketball and soccer players employ distinct lower extremity movement strategies during sagittal and frontal plane jump landing tasks.

Hypothesis 1. Prior to training, women's basketball athletes will exhibit no significant differences in high-risk hip and knee kinematics, but will generate higher hip and knee joint moments during jump landing activities than women's soccer players.

Specific Aim 2. To determine the response of women's basketball and soccer athletes to a 6-week ACL injury prevention program, as measured by changes in multi-planar hip and knee biomechanics of jump landings during sagittal and frontal plane jump landing tasks.

Hypothesis 1. After 6 weeks of training, high-risk biomechanics will improve to a larger extent during sagittal plane than frontal plane jump landing tasks.

Hypothesis 2. After 6 weeks of training, there will be no significant differences in biomechanical changes in women's basketball compared to women's soccer players.

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Conditions studied

  • Anterior Cruciate Ligament Injury
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In context

Wounds and Injuries

5,056 studies on the registry are indexed under Wounds and Injuries; 861 are open to participants now.

This study's enrollment of 99 is above the median of 52 across 3,239 interventional studies indexed under Wounds and Injuries.

Browse Wounds and Injuries studies →

Lead sponsor

High Point University is the lead sponsor of 12 studies on the registry; 1 is open to participants now.

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

04

Who can participate

Ages eligible
12 Years to 19 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • Participants will need to be participating in high school aged, competitive-level basketball and/or soccer and are medically cleared to participate in sports.

Exclusion criteria

Exclusion Criteria:

  • Participants will be excluded if they have a history of lower extremity surgery in the past 6 months, or have been diagnosed with a vestibular, balance, or cardiovascular disorders that may preclude safe participation during landing and jumping activities.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
99 participants (actual)

Study arms

  • No intervention
    Basketball Control

    Control group of basketball players

  • Experimental
    Basketball intervention

    Intervention group of basketball players

    Other: Neuromuscular Prevention Program

  • No intervention
    Soccer Control

    Control group of soccer players

  • Experimental
    Soccer Intervention

    intervention group of soccer players

    Other: Neuromuscular Prevention Program

Interventions

  • OtherNeuromuscular Prevention Program

    Participants in the intervention group will complete at 6 week ACL injury prevention program previously described in the literature as being effective at reducing ACL injury risk. The prevention program lasts 20-25 minutes in duration and will take place as a warm-up prior to any practice. The frequency will depend solely on the number of practices each team holds throughout the given 6-week time period.

06

What researchers measure

Primary outcomes

  1. Lower Extremity Angular Kinematics (hip flexion, hip adduction, hip internal rotation, knee flexion, abduction, knee internal rotation, knee external rotation)

    Time frame: 6-8 weeks

  2. Lower Extremity Kinetics (hip flexion, hip adduction, hip internal rotation, knee flexion, abduction, knee internal rotation, knee external rotation external moments)

    Time frame: 6-8 weeks

Secondary outcomes

  1. Triple Jump Distance

    Time frame: 6-8 weeks

  2. Maximal Vertical Jump Height

    Countermovement jump

    Time frame: 6-8 weeks

  3. Agility

    T-test

    Time frame: 6-8 weeks

07

Study locations

1 site
  • High Point University
    High Point, North Carolina 27268, United States
08

References and documents

Publications

  • Taylor JB, Nguyen AD, Shultz SJ, Ford KR. Hip biomechanics differ in responders and non-responders to an ACL injury prevention program. Knee Surg Sports Traumatol Arthrosc. 2020 Apr;28(4):1236-1245. doi: 10.1007/s00167-018-5158-1. Epub 2018 Sep 27. PubMed 30259145 ↗
  • Taylor JB, Ford KR, Schmitz RJ, Ross SE, Ackerman TA, Shultz SJ. Sport-specific biomechanical responses to an ACL injury prevention programme: A randomised controlled trial. J Sports Sci. 2018 Nov;36(21):2492-2501. doi: 10.1080/02640414.2018.1465723. Epub 2018 Apr 19. PubMed 29671383 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 8, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02530333
Lead sponsor
High Point University
Collaborators
University of North Carolina, Greensboro
Responsible party
Sponsor
First posted
Aug 21, 2015
Start date
May 2015
Primary completion
Nov 2015
Completion
Nov 2015
Last update
Jan 8, 2016

Study contacts

Jeffrey B Taylor, DPT
principal investigator · High Point University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2016. You cannot join it, but the record below documents what was studied.

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