Optimizing Plyometric Training for Functional Recovery Post-ACL Reconstruction

April 24, 2019 updated by: Ryan Mizner, University of Montana

While surgical anterior cruciate ligament reconstruction (ACLR) of the knee restores passive stability, studies are showing consistently poor long-term outcomes. Unusually high risks of early-onset osteoarthritis and re-injury, and low rate of return to sport following ACLR all seem to be related to a chronic tendency to land stiff-legged from a jump or hop, which itself may be due to fear of re-injury. Decreased knee bending for force absorption simultaneously decreases performance level and increases risk for injury and arthritic changes.

The purpose of the proposed study is to compare a current best-practice plyometric training program to one utilizing body weight support to increase repetition and improve performance in the initial phases. The investigators hypothesize that we will see larger improvements in absorptive capacity of the knee and better confidence in activity immediately following body weight support training, as well as improved retention of training effects after a two-month period.

Study Overview

Study Type

Interventional

Enrollment (Actual)

47

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Montana
      • Missoula, Montana, United States, 59812
        • University of Montana, Movement Science Laboratory

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

12 years to 35 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • speak and understand English
  • age between 12-35 years
  • unilateral anterior cruciate ligament reconstruction between 6-48 months prior
  • activity level greater than or equal to level 5 on the Tegner Activity Scale

Exclusion Criteria:

  • Weight in excess of 300 pounds (136 kg)
  • contralateral/bilateral ACL reconstruction or an unreconstructed ACL injury
  • history of a posterior cruciate ligament injury
  • lower extremity of back injury or other condition (e.g. cerebral palsy) that has limited their normal activities of daily living within the last 6 months

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Standard Plyometric Training
Participants will undergo treatment 2 times a week for 8 weeks with plyometric exercises deemed to be consistent with best practice delivered at a standard dosage of sets and repetitions.
Participants will undergo individualized practice exercises of jumping, hopping, and cutting tasks consistent with standard published exercises.
Experimental: Plyometric Training with BWS
Participants will undergo treatment 2 times a week for 8 weeks with plyometric exercises deemed to be consistent with best practice with a treatment volume of sets and repetitions that exceeds standard practice. Higher number of practice trials will be completed with body weight support (BWS) to reduce load. Participants will start at 30 percent of body weight and will be slowly weaned away over time.
Participants will undergo individualized practice exercises of jumping, hopping, and cutting tasks consistent with standard published exercises while their body weight is supported via adjustable harness.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Change in sagittal plane knee kinetics and kinematics
Time Frame: Baseline and after 8 weeks of training
Baseline and after 8 weeks of training
Change in psychological readiness for sports activities via survey scores
Time Frame: baseline and after 8 weeks of training
baseline and after 8 weeks of training
Change in motor patterning via electromyography of quadriceps and hamstring muscles
Time Frame: Baseline and after 8 weeks of training
Baseline and after 8 weeks of training

Secondary Outcome Measures

Outcome Measure
Time Frame
Retention of Biomechanical Adaptions in Knee kinetics and kinematics
Time Frame: Change from end of 8 weeks of training to 2 month follow-up
Change from end of 8 weeks of training to 2 month follow-up
Retention of adaptations in Psychological Readiness for Sport via survey
Time Frame: Change from end of 8 weeks of training to 2 month follow-up
Change from end of 8 weeks of training to 2 month follow-up
Retention of adaptations in motor patterning via electromyography
Time Frame: Change from end of 8 weeks of training to 2 month follow-up
Change from end of 8 weeks of training to 2 month follow-up

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ryan L Mizner, PT, PhD, University of Montana

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2014

Primary Completion (Actual)

December 1, 2018

Study Completion (Actual)

December 1, 2018

Study Registration Dates

First Submitted

May 22, 2014

First Submitted That Met QC Criteria

May 27, 2014

First Posted (Estimate)

May 28, 2014

Study Record Updates

Last Update Posted (Actual)

April 25, 2019

Last Update Submitted That Met QC Criteria

April 24, 2019

Last Verified

April 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • UM IRB 282-13

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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