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Real-time Optimized Biofeedback Utilizing Sport Techniques (ROBUST)

H

High Point University

Status and phase

Completed
Phase 2

Conditions

Knee Injuries

Treatments

Other: Hip Focused ROBUST Training
Other: Knee Focused ROBUST Training
Other: Neuromuscular Training

Study type

Interventional

Funder types

Other

Identifiers

NCT02754700
R21AR069873

Details and patient eligibility

About

This study will identify the most optimal, focused approach for biofeedback in adolescent females at high risk for anterior cruciate ligament (ACL) injury. A six-week randomized, pre/post-testing design will be used to identify biofeedback training effects. The investigators will also determine the effects of hip strategy on retention of decreased knee abduction load with focused biofeedback. A six-month follow-up design will be used to test retention of real-time biofeedback intervention.

Full description

Real-time Optimized Biofeedback Utilizing Sport Techniques (ROBUST) represents an innovative new approach to reduce traumatic anterior cruciate ligament (ACL) injuries. Over the last four decades, these debilitating injuries have occurred at a 2 to 10-fold greater rate in female compared to male athletes with the highest prevalence occurring between the ages of 16-18 years. As a consequence, there is a large population of females that endure significant pain, functional limitations and knee osteoarthritis (OA) as early as 5 years after the initial unintentional injury. To reduce the burden of OA, The National Public Health Agenda for Osteoarthritis recommends both expanding and refining evidence-based prevention of ACL injury. There currently is a gap in knowledge regarding how to maximize the effectiveness of injury prevention training in young female athletes. The long-term goal is to reduce ACL injuries in young female athletes. The objective of this application is to increase the efficacy of biofeedback training to reduce the risk of ACL injury. This proposal tests the central hypothesis that biofeedback methodology is needed to maximize the effectiveness of neuromuscular prophylactic interventions. The rationale supporting this proposal is that once the proposed research is completed, health professionals will be more successful at preventing devastating ACL injuries through properly optimized and targeted biofeedback training for young at-risk females. This research is innovative because it represents a new and substantive departure from the status quo by recognizing the need to optimize the application of biofeedback training. The work will contribute clinically relevant data in support of a future more robust clinical trial. The proposed research will be significant because it will lead to reduced rates of ACL injury in young females. Reduction of female injury rates to equal that of males would allow females annually to continue the health benefits of sports participation and avoid the long-term complications of osteoarthritis, which occurs with a 10 to 100-fold greater incidence in ACL-injured than in uninjured athletes.

Enrollment

150 patients

Sex

Female

Ages

9 to 19 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Currently participating on club or school sponsored soccer team

Exclusion criteria

  • Current injury that limits participating in sport
  • Male
  • Cannot participate in a 6-week intervention due to time or other constraints

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

150 participants in 3 patient groups

Biofeedback Hip
Experimental group
Description:
Hip focused biofeedback with neuromuscular training
Treatment:
Other: Hip Focused ROBUST Training
Biofeedback Knee
Experimental group
Description:
Knee focused biofeedback with neuromuscular training
Treatment:
Other: Knee Focused ROBUST Training
Neuromuscular Training
Active Comparator group
Description:
Neuromuscular Training component
Treatment:
Other: Neuromuscular Training

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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