- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03035994
Effect of Altered Mechanical Loading in ACLR
April 17, 2017 updated by: University of North Carolina, Chapel Hill
Effect of Altered Mechanical Loading on Lower Extremity Biomechanics and Biochemical Markers in Individuals With an Anterior Cruciate Ligament Reconstruction
Altered loading is a causative factor for the development of knee osteoarthritis following anterior cruciate ligament reconstruction (ACLR), and real-time biofeedback may be an effective intervention to manipulate altered mechanical loading about the knee.
The purpose of this study is to 1) determine if ACLR participants are able to acquire and retain various loading patterns using real-time biofeedback, 2) determine the effect of altered loading on lower extremity biomechanics during walking gait, and 3) determine the effect of altered loading on biochemical markers of collagen turnover and inflammation during walking gait.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Participants will attend 4 testing sessions.
Lower extremity biomechanical outcomes and blood samples will be taken before and following the participant walking at a self-selected speed for 20 minutes.
During the 20 minutes of treadmill walking real-time biofeedback will be displayed in an attempt to alter mechanical loading.
Participants will complete a control, overloading, under-loading, average loading testing session.
Order of loading condition will be randomized.
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
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
18 years to 35 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Have a history of a primary, unilateral ACLR using either a hamstring or patellar tendon autograft, cleared by a physical for full return to physical activity with no limitations, and participate in at least 30 minutes of physical activity 3 times per week
Exclusion Criteria:
- History of injury to either leg, other than ACLR (e.g. ankle sprain, muscle strain), within 6 months prior to participation in the study, history of lower extremity surgery other than ACLR, history of osteoarthritis or current symptoms related to knee osteoarthritis (e.g. pain, swelling, stiffness), currently pregnant, or planning to become pregnant while enrolled in the study, cardiovascular restrictions that limit the participant's ability to participate in physical activity.
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: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Overloading
Participants will walk on a force-instrumented treadmill for 20 minutes and will be provided visual biofeedback consisting of bilateral vertical ground reaction force.
A target will be placed at 10% greater than the participant's baseline vertical ground reaction force.
Participants will be asked to alter their walking gait in an attempt to reach the target line with each step.
|
A custom written MatLab script will sample bilateral peak vertical ground reaction forces and display the magnitude in real time on a screen placed in front of the participant.
A target line will be placed in the middle of the screen which corresponds to one of the three loading conditions.
Participants will be instructed to alter their movement in an attempt to match each limb's vertical ground reaction force to the target line.
|
|
Experimental: Underloading
Participants will walk on a force-instrumented treadmill for 20 minutes and will be provided visual biofeedback consisting of bilateral vertical ground reaction force.
A target will be placed at 10% lower than the participant's baseline vertical ground reaction force.
Participants will be asked to alter their walking gait in an attempt to reach the target line with each step.
|
A custom written MatLab script will sample bilateral peak vertical ground reaction forces and display the magnitude in real time on a screen placed in front of the participant.
A target line will be placed in the middle of the screen which corresponds to one of the three loading conditions.
Participants will be instructed to alter their movement in an attempt to match each limb's vertical ground reaction force to the target line.
|
|
Experimental: Average
Participants will walk on a force-instrumented treadmill for 20 minutes and will be provided visual biofeedback consisting of bilateral vertical ground reaction force.
A target will be placed at the average of each participant's baseline vertical ground reaction force between limbs.
Participants will be asked to alter their walking gait in an attempt to reach the target line with each step.
|
A custom written MatLab script will sample bilateral peak vertical ground reaction forces and display the magnitude in real time on a screen placed in front of the participant.
A target line will be placed in the middle of the screen which corresponds to one of the three loading conditions.
Participants will be instructed to alter their movement in an attempt to match each limb's vertical ground reaction force to the target line.
|
|
No Intervention: Control
Participants will walk for 20 minutes on a force-instrumented treadmill and will not be provided biofeedback.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Difference in acquisition as measured in root mean square error (RMSE) between loading conditions
Time Frame: Change in acquisition over 20 minute intervention
|
Change in acquisition over 20 minute intervention
|
|
Difference in joint loading as measured in peak vertical ground reaction force normalized to body weight (xBW) between loading conditions
Time Frame: Change in joint loading over 20 minute intervention
|
Change in joint loading over 20 minute intervention
|
|
Difference in cartilage turnover as measured in serum concentration of cartilage oligomeric matrix protein (pg/mL) between loading conditions
Time Frame: Chance in cartilage turnover over 20 minute intervention
|
Chance in cartilage turnover over 20 minute intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Brian Pietrosimone, PhD, University of North Carolina, Chapel Hill
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.
General Publications
- Luc-Harkey BA, Franz J, Hackney AC, Blackburn JT, Padua DA, Schwartz T, Davis-Wilson H, Spang J, Pietrosimone B. Immediate Biochemical Changes After Gait Biofeedback in Individuals With Anterior Cruciate Ligament Reconstruction. J Athl Train. 2020 Oct 1;55(10):1106-1115. doi: 10.4085/1062-6050-0372.19.
- Luc-Harkey BA, Franz JR, Blackburn JT, Padua DA, Hackney AC, Pietrosimone B. Real-time biofeedback can increase and decrease vertical ground reaction force, knee flexion excursion, and knee extension moment during walking in individuals with anterior cruciate ligament reconstruction. J Biomech. 2018 Jul 25;76:94-102. doi: 10.1016/j.jbiomech.2018.05.043. Epub 2018 Jun 15.
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
July 1, 2016
Primary Completion (Actual)
February 1, 2017
Study Completion (Actual)
April 1, 2017
Study Registration Dates
First Submitted
January 22, 2017
First Submitted That Met QC Criteria
January 26, 2017
First Posted (Estimate)
January 30, 2017
Study Record Updates
Last Update Posted (Actual)
April 19, 2017
Last Update Submitted That Met QC Criteria
April 17, 2017
Last Verified
April 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- 16-0409
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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