Motion Capture and Analysis of NYIT Athletes

October 10, 2017 updated by: New York Institute of Technology

The purpose of this research is to:

  1. determine the normal or existing dynamic biomechanics of college athletes and
  2. test the effectiveness of osteopathic manipulative medicine in the treatment of athletic injuries.

Motion capture using Vicon systems allows researchers to quantify characteristics of a body such as the range of motion of the hip or shoulder during an athletic technique such as kicking or shooting a basketball into the basket. The quantified information has been used before to better understand human mobility and performance. Osteopathic manipulative medicine (OMM) is manual medicine applied to joints, muscles, and connective tissue with a goal of improved body functions. Research demonstrating effectiveness of OMM on the musculoskeletal and associated connective tissue systems health includes, among others, prospective clinical trials of OMM for treatment of neck pain, low back pain, and acute first- and second-degree ankle sprains.

Study Overview

Status

Withdrawn

Conditions

Detailed Description

Volunteers for the study will be recruited through their Athletic director, coach, or physician by an announcement made verbally or via email. The motion capture will be performed under Matthew Cornelius, MS using the Vicon Bonita Motion Capture system in the Fine Arts Department of NYIT. Following the motion capture, body biomechanics will be analyzed to determine the range of motion of each joint in sagittal, frontal, and horizontal planes as well as the timing and sequence of the movements. The motion analysis will be compared to the Sports Physical exam, including the general, structural/neuromusculoskeletal, and central neurological (ImPACT) exams. The comparison will add validity to the physical exam. In addition, determining if the quantitative, 3-dimensional motion analysis can be correlated with information from the physical exam with regards to restrictions to motion may be useful for athletes to optimize their abilities in the future. If during the course of the athlete's training and competition season s/he sustains an injury, s/he will be evaluated by the NYIT athletics physician, who will randomly assign the injured athletes to either the 'standard of care without OMM' or 'standard of care with OMM' cohorts when medically appropriate. OMM will be performed by an NYITCOM physician specializing in family medicine and OMT or neuromusculoskeletal systems and OMM. "Return to play' time and post-intervention/post-control quantitative motion analysis of biomechanics during the athletes demonstration of the same athletic maneuvers as before the injury.

Study Type

Interventional

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

    • New York
      • Old Westbury, New York, United States, 11568
        • New York Institute of Technology
      • Old Westbury, New York, United States, 11568
        • New York Institute of Technology College of Osteopathic Medicine Academic Health Care Center

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 30 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • athlete at new York Institute of Technology
  • approval by NYIT Athletics Physical for participation in sports
  • no current injury

Exclusion Criteria:

  • illness preventing participation in sports
  • any current injury
  • younger than 18 years of age
  • pregnancy
  • allergy to spandex, nylon, or polyester

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: Non-Randomized
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: injured athlete for OMM
Participating athletes who sustain an injury will receive standard of care with the Intervention osteopathic manipulative medicine (OMM)
Osteopathic manipulative medicine includes all types of manual therapies to gently restore and/or optimize one's natural joint, muscle, and other soft tissue balance.
Other Names:
  • osteopathic manual therapy
No Intervention: injured athlete no OMM
Participating athletes who sustain an injury will receive standard of care withOUT osteopathic manipulative medicine (OMM)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
change in joint angles (degrees)
Time Frame: 1 year
quantitative biomechanical testing will be performed before and after OMM or control
1 year

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Jayme D Mancini, DO PhD, New York Institute of Technology

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

February 1, 2015

Primary Completion (Actual)

October 1, 2017

Study Completion (Actual)

October 1, 2017

Study Registration Dates

First Submitted

February 12, 2015

First Submitted That Met QC Criteria

April 1, 2016

First Posted (Estimate)

April 4, 2016

Study Record Updates

Last Update Posted (Actual)

October 12, 2017

Last Update Submitted That Met QC Criteria

October 10, 2017

Last Verified

October 1, 2017

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • BHS1064

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

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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