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Feasibility of Wearable Sensors to Determine Gait Parameters

Sponsor
University of South Florida (Other)
Overall Status
Completed
CT.gov ID
NCT01620021
Collaborator
(none)
10
Enrollment
1
Location
38
Duration (Months)
0.3
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Hypotheses:

• A wearable sensor system can be used to accurately monitor three common gait parameters: gait speed, stride length, and torso motion.

Objectives:

This study will examine the feasibility of using wearable sensors to monitor common gait parameters: gait speed, stride length and torso motion. A wearable sensor system of 8 commercially available inertial measurement units (IMU) will be composed. These sensors will work in unison to monitor the gait parameters.

Technical Objectives

  • Gather information on commercially available IMUs

  • Use computer software to monitor and record data from IMUs

  • Develop an algorithm that can monitor volunteer gait speed, stride length and torso motion

  • Develop a graphical algorithm that compares healthy patient data to potential mild traumatic brain injury (mTBI ) candidates

  • Determine if there is a potential for mTBI determination using the wearable sensors

  • Accurately validate the wearable sensor system to the gait parameters measured using a Vicon motion analysis system

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This study will examine the feasibility of using wearable sensors to monitor common gait parameters. A sensor system consisting of 8 wearable inertial measurement units (IMU) that include accelerometers, gyroscopes and magnetometers will be examined. These sensors will be programmed to work in unison to monitor gait parameters. The wearable sensor suite will have the capability to collect and store gait parameter data. The size and weight of each sensor should be similar to a standard metal wrist watch. The sensor suite will monitor three gait parameters: gait speed, stride length, and torso motion. These gait parameters are important for monitoring and detection of mild traumatic brain injury and as well as other neurological and vestibular disorders.

    The wearable sensor suite will have the following design parameters:

    • Devices must be able to both stream data real-time and record data onboard for later transfer to a computer.

    • Data must be processed using a software analysis package such as MATLAB®

    • Device must be no heavier than the size of a metal wrist watch

    • Device must be easily put on and be easily operated by clinicians and users

    • Device must have a battery life of greater than 4 hours The wearable sensor suite will then be validated using an eight camera Vicon infrared optical capture motion analysis system for comparison. Ten healthy volunteers will be asked to complete four different types of gait trials 5 times for each trial type while being monitored by the Vicon motion analysis system and the wearable sensor system.

    The types of gait trials will be the following:

    • Walk down a 20 ft path at self-selected normal stride length and cadence

    • Walk down a 20 ft path with increased stride length while decreasing gait speed

    • Walk down a 20 ft path with increased stride length while increasing gait speed

    • Walk down a 20 ft path with decreased stride length while decreasing gait speed

    • Walk down a 20 ft path with decreased stride length while increasing gait speed

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    10 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Feasibility of Wearable Sensors to Determine Gait Parameters
    Study Start Date :
    Apr 1, 2011
    Actual Primary Completion Date :
    Jun 1, 2014
    Actual Study Completion Date :
    Jun 1, 2014

    Arms and Interventions

    Arm Intervention/Treatment
    Healthy

    Ten healthy volunteers with no history of gait and balance issues will be recruited to participate in the study.The participants must be between 18 and 65 years of age.

    Outcome Measures

    Primary Outcome Measures

    1. gait speed [60 seconds]

    2. stride length [60 seconds]

    3. Torso motion [60 seconds]

    4. Head motion [60 seconds]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:

    • no history of gait and balance issues

    • 18-65

    Exclusion Criteria:

    • younger than 18

    • older than 65

    • problems with gait and balance

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of South Florida Motion Analysis Laboratory Tampa Florida United States 33620

    Sponsors and Collaborators

    • University of South Florida

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Stephanie L. Carey, Assistant Research Professor, University of South Florida
    ClinicalTrials.gov Identifier:
    NCT01620021
    Other Study ID Numbers:
    • Pro00003205
    First Posted:
    Jun 15, 2012
    Last Update Posted:
    May 7, 2015
    Last Verified:
    May 1, 2015
    Keywords provided by Stephanie L. Carey, Assistant Research Professor, University of South Florida
    wearable sensors
    kinematics
    gait

    Study Results

    No Results Posted as of May 7, 2015