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Sport Cord Test Following ACL Reconstruction

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified May 2015 by The Hawkins Foundation.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT01937403
First Posted: September 9, 2013
Last Update Posted: May 5, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
The Hawkins Foundation
  Purpose

The primary purpose of this study is to determine the interrater reliability and validity of the Sportcord Test as a measure of physical performance following anterior cruciate ligament (ACL) reconstruction. A secondary purpose is to systematically track subjective and objective outcomes on patients following ACL reconstruction to help identify differences between those who have subsequent knee problems and those who do not. The study hypotheses are the following:

1) The Sportcord Test will provide a valid and reliable measure of functional performance following ACL reconstruction. 2) Patients who have subsequent knee problems in the 12 month study period will exhibit different scores on clinical special tests compared to those who do not.


Condition
Anterior Cruciate Ligament (ACL) Reconstruction

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: The Use of the Sport Cord Test as a Measure of Physical Performance Following Anterior Cruciate Ligament Reconstruction

Resource links provided by NLM:


Further study details as provided by The Hawkins Foundation:

Primary Outcome Measures:
  • Sportcord Test [ Time Frame: one year ]

    The Sportcord Test measures physical performance following an ACL reconstruction. The Sportcord test consists of the following:

    1. single-leg squats
    2. lateral (side-to-side) agility
    3. forward running
    4. backward running


Estimated Enrollment: 200
Study Start Date: October 2009
Estimated Study Completion Date: August 2016
Estimated Primary Completion Date: August 2015 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   10 Years to 50 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients receiving physical therapy/rehabilitation for an ACL surgery and are returning to participation in sports.
Criteria

Inclusion Criteria:

  • Undergoing surgical reconstruction for a torn ACL.
  • Returning to participation in a sport(s).
  • Will receive physical therapy/rehabilitation after surgical reconstruction for a torn ACL.
  • Between ages of 10 and 50.

Exclusion Criteria:

  • Non-weight bearing.
  • At least 12 weeks removed from surgery.
  • Unable to walk, squat, or jump/land without pain in the surgically repaired knee.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01937403


Contacts
Contact: Carlisle Shealy, BS 864-454-7458 carlisle.shealy@hawkinsfoundation.com

Locations
United States, South Carolina
Proaxis Therapy Recruiting
Greenville, South Carolina, United States, 29615
Contact: Carlisle Shealy, BS    864-454-7458    carlisle.shealy@hawkinsfoundation.com   
Principal Investigator: Ellen Shanley, PT, PhD, OCS         
Sub-Investigator: Chuck Thigpen, PT, PhD, ATC         
Sub-Investigator: Ryan Geary, DPT, CSCS         
Sub-Investigator: Melissa Stelmacki, DPT         
Sub-Investigator: Mike Osler, DPT, SCS         
Sub-Investigator: Lane Bailey, DPT         
Sub-Investigator: Harmony Noda, DPT         
Sponsors and Collaborators
The Hawkins Foundation
Investigators
Principal Investigator: Ellen Shanley, PT, PhD, OCS, CSCS Proaxis Therapy
  More Information

Responsible Party: The Hawkins Foundation
ClinicalTrials.gov Identifier: NCT01937403     History of Changes
Other Study ID Numbers: Pro00003653
First Submitted: September 4, 2013
First Posted: September 9, 2013
Last Update Posted: May 5, 2015
Last Verified: May 2015

Keywords provided by The Hawkins Foundation:
Physical Therapy
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