Biomechanics/Motion Analysis Laboratory Data Bank

June 30, 2025 updated by: University of Florida

University of Florida Biomechanics/Motion Analysis Laboratory Data Bank

The purpose of the data bank is to collect data on joint motion.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

Biomechanical aspects, including ground reaction forces, range of motion of involved extremities, EMG data and videotape records of human motion will be collected and stored as part of the normal clinical care of patients seen in the UF Biomechanics/Motion Analysis Laboratory. All persons seen in motion analysis laboratory will be told of study and asked to participate. Those agreeing to participation will give informed consent.

Study Type

Observational

Enrollment (Estimated)

10000

Contacts and Locations

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

Study Contact

Study Locations

  • United States
    • Florida
      • Gainesville, Florida, United States, 32611
        • Recruiting
        • UF Orthopaedics and Sports Medicine Institute
        • Contact:
        • Principal Investigator:
          • Heather Vincent, Ph.D

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

2 years to 75 years (Child, Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Biomechanical/Motion Analysis Laboratory

Description

Inclusion Criteria:

  • Any person having joint analysis done for medical or personal need

Exclusion Criteria:

  • None, any person having joint analysis done for medical or personal need and interested in participation will be asked to sign informed consent.

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

  • Observational Models: Other
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Joint Motion Analysis
Joint motion will be recorded for analysis.
Behavioral: Joint Motion Analysis
Joint motion will be recorded for analysis.
Other Names:
  • No other names

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Range of Motion values
Time Frame: one day
Joint range of motion is measured in degrees for the hips, knees, ankles, shoulders and elbows
one day

Collaborators and Investigators

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

Sponsor

University of Florida

Investigators

  • Principal Investigator: MaryBeth Horodyski, Ed.D., University of Florida

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 (Actual)

January 1, 2005

Primary Completion (Estimated)

October 1, 2026

Study Completion (Estimated)

October 1, 2026

Study Registration Dates

First Submitted

September 8, 2005

First Submitted That Met QC Criteria

September 11, 2005

First Posted (Estimated)

September 12, 2005

Study Record Updates

Last Update Posted (Actual)

July 2, 2025

Last Update Submitted That Met QC Criteria

June 30, 2025

Last Verified

June 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • IRB201501196

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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