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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03080402
Other study ID # R44HD068054
Secondary ID 5R44HD068054
Status Recruiting
Phase N/A
First received March 9, 2017
Last updated March 9, 2017
Start date February 20, 2017
Est. completion date December 31, 2017

Study information

Verified date March 2017
Source University of Delaware
Contact Martha Callahan
Phone (302) 831-6202
Email mcall@udel.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A prospective trial will be used to evaluate the efficacy of prophylactic mechanical perturbation training program. 24 female athletes who are regular participants in activities that involve cutting, pivoting, jumping, and lateral movements prior to injury who range in age from 15-30 year are eligible. Using a prospective risk stratification design, female athletes with knee abduction moment (KAM) > 25.25 Nm from drop jump motion analysis will be classified as high KAM and will receive 12 sessions of mechanically-driven perturbation training and female athletes with KAM < 25.25 Nm from drop jump motion analysis will be classified as normal KAM and only participate in baseline performance testing, followed 6 weeks later by another session of drop jump motion analysis and performance testing.


Description:

Anterior cruciate ligament (ACL) injuries are prevalent in sports with female athletes at particularly high risk. Female athletes have 2-4x higher risk of ACL injury compared to their male counterparts in the same high-risk sports. Modifiable and non-modifiable risk factors play a role in the high incidence of ACL injuries in female athletes. High knee abduction moment (KAM), is a known modifiable risk factor for ACL injury risk. Female athletes with a KAM greater than 25.25 Nm have been identified as at high risk for an ACL injury. The ability to classify female athletes who are at a high risk for an ACL injury, highlights the importance of identifying modifiable risk factors that can be readily addressed by physical therapists and developing targeted treatments to potentially reduce ACL injury risk while improving functional performance.

Neuromuscular training programs are treatments designed to help improve coordination, strength, and control. Such training programs have been designed to alter biomechanical and neuromuscular measures, in particular high KAM, in order to improve performance and function and thereby reduce the risk of ACL injury. Neuromuscular training programs involving plyometric exercises can reduce dynamic lower extremity valgus and limb-to-limb asymmetries in healthy female athletes. Despite the reductions in injury rates seen with performance of neuromuscular training programs, incidence of ACL injuries is remains higher than acceptable. Novel training methods are currently in development to optimize these current ACL injury prevention programs. As unanticipated perturbations may contribute to ACL injury risk, incorporating a mechanical platform device that provides unanticipated surface compliance changes (i.e. the floor lowering down below a subject's feet) into an ACL injury prevention program has the potential to optimize knee biomechanics and neuromuscular performance, including during unanticipated perturbations.

Mechanical perturbation has been advocated for as an effective training method to modify the sensorimotor system and restore normal neuromuscular coordination through exposing the subjects to controlled, progressive perturbations. Furthermore, mechanical perturbation has the potential to improve dynamic postural stability and control, and enhance muscle activation patterns. One advantage of mechanical perturbation devices is that they can be utilized while performing a variety of dynamic tasks such as hopping and jumping compared to static loading tasks such as standing and balancing activities. Dynamic tasks may place a greater demand on the knee joint, promoting joint stability as the subject overcomes the perturbation. Additionally, mechanical perturbation may allow physical therapists to administer random perturbations at different phases of the activities (i.e. as the subject is landing from a hop, or taking-off from a jump) that simulate real-life perturbations which occur during different functional or sporting activities.

The goal of this study is to assess the effectiveness of an intensive neuromuscular training program to reduce risk factors associated with ACL injury


Recruitment information / eligibility

Status Recruiting
Enrollment 24
Est. completion date December 31, 2017
Est. primary completion date December 31, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 15 Years to 30 Years
Eligibility Inclusion Criteria:

- Female athletes will be eligible if they are: 1) regular participants in Level 1 and 2 sports (cutting and pivoting type sports, and 2) ages 15-30 years

Exclusion Criteria:

- History of major injury or surgery to the legs.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Mechanical Perturbation Training
The training program will consist of three stages and subjects will progress through each neuromuscular training stage.The training will consist of double- to single-limb movements with progression of jumping, hopping, and pivoting maneuvers on the perturbation device with an emphasis on proper technique and landing. The initial four sessions will focus on primarily on jumping and hopping maneuvers on double- and single-limb in the sagittal plane. The intermediate four sessions will incorporate additional medial and lateral maneuvers with the plyometric tasks. The final four sessions will incorporate rotational and pivoting activities with the maneuvers. The resultant protocol has been derived and optimized from previous published research studies and prevention techniques.

Locations

Country Name City State
United States University of Delaware, Physical Therapy Department Newark Delaware

Sponsors (3)

Lead Sponsor Collaborator
University of Delaware Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Simbex, LLC

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Vertical Jump Vertical jump for height baseline and 6 weeks after baseline testing
Primary Peak knee abduction moment Peak knee abduction moment during a drop jump landing task as assessed via motion analysis baseline and 6 weeks after baseline testing
Secondary Peak Quadriceps torque 60 degrees/sec Peak Quadriceps torque 60 degrees/sec baseline and 6 weeks after baseline testing
Secondary Peak Quadriceps torque 240 degrees/sec Peak Quadriceps torque 240 degrees/sec baseline and 6 weeks after baseline testing
Secondary Peak Hamstrings torque 60 degrees/sec Peak Hamstrings torque 60 degrees/sec baseline and 6 weeks after baseline testing
Secondary Peak Hamstrings torque 240 degrees/sec Peak Hamstrings torque 240 degrees/sec baseline and 6 weeks after baseline testing
Secondary Single hop for distance LSI Single hop for distance limb symmetry index baseline and 6 weeks after baseline testing
Secondary Crossover hop for distance LSI Crossover hop for distance limb symmetry index baseline and 6 weeks after baseline testing
Secondary Triple hop for distance LSI Triple hop for distance limb symmetry index baseline and 6 weeks after baseline testing
Secondary 6m Timed Hop LSI 6 meter Timed Hop limb symmetry index baseline and 6 weeks after baseline testing
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