Laser Shoes for Freezing in People With Parkinson's Disease

Sponsor
Northern Arizona University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05131906
Collaborator
FY2020 Research Bridge (Other), Arizona State University (Other)
15
1
1
19
0.8

Study Details

Study Description

Brief Summary

The purpose of this study is to assess the effectiveness of the visual cues of a wearable device in preventing freezing of gait (FOG) in those with PD.The aim is to investigate the impact of laser shoe attachments on gait in single and dual-tasking scenarios, as well as "real-world" mobility scenarios, in people with PD who freeze. For this study, participants will wear sensors on their feet, hips, chest, and head to show stride length, foot angle, and foot height, and head position during different gait assessments. The patients will do the gait assessments without the laser shoes and with the laser shoes to determine how the laser shoes affect freezing of gait. The gait assessments include having the patient complete a two minute walk, two minute walk with another task (reciting every other letter of the alphabet), obstacle course, obstacle course with another task (reciting every other letter of the alphabet), and quickly turning in place. The assessments are activities that are performed in everyday activities so there are no risks associated with these requested tasks. These activities will be done in a lab at the Phoenix Biomedical Campus. Safety for the participants will be monitored by placing a belt around the waist of the participant with a member of the research personnel close by in case the participant demonstrated a shift in their balance. The research member can use the belt to provide stability and secure the participant, preventing them from further loss of balance. Moreover, three different activities of daily living (ADL's) will be assessed with and without the laser shoes in a simulated apartment environment located at the Phoenix Biomedical campus. The ADL's include walking from the bed to the kitchen, walking from the living room to the kitchen and making tea in the microwave, and answering the door. The activities to be done in the apartment setting will be video-recorded and analyzed. Some participants will be given the laser shoes to take home and use for one week. The same protocol explained above will be used to assess freezing of gait after this one week in those selected participants. To assess retention of improvements, the participants who took the laser shoes home will also be given the same protocol two days later (after not having used the laser shoes during that time). Participants will also complete surveys for quality of life, freezing and gait and cognitive function. A standard test for balance will also be conducted.

Condition or Disease Intervention/Treatment Phase
  • Device: gait task and activity of daily living task
N/A

Detailed Description

15 individuals with Parkinson's Disease will complete two tasks: a gait task and an activity of daily living (ADL) task both with and without the use of laser shoe attachment. The gait task involves 5 separate scenarios: 2 min walk with a single and dual-task trial, obstacle course with a single and dual-task trial, and a quick turn-in-place. For the dual-task trials, participants will complete the 2 min walk and obstacle course scenarios in addition to a cognitive task (e.g. reciting the alphabet every other letter). During the single-task trials for the 2 min walk and obstacle course, participants will complete these activities without a cognitive task. Participants will also be required to fill out surveys for quality of life, balance and freezing of gait. A standard test for balance will be conducted (MiniBEST). Participants will be assessed using the UPDRS in order to categorize the level of Parkinson's Disease. Permission and training for use of the UPDRS will be obtained prior to testing participants.

The ADL task involves three "real-world" mobility scenarios, in which participants will be asked to: walk from the bedroom to the bathroom and also the kitchen, make tea in the kitchen, and move from the couch to answer the front door.

For both tasks, gait will be characterized during each scenario using inertial sensors (OPALs). Outcomes will include step length, foot angle and foot height (clearance from floor) and head movement. To characterize functional movements we will video movements during all scenarios for both tasks. Outcomes will be the number and temporal length of each freezing event, to be determined by a movement disorders neurologist.

A subset of participants (n=3) will use the sensors at home for 1 week, and return to the lab for gait and functional task assessment. They will return after a 2-day washout (no sensors) to assess retention of improvements from the 1-week exposure.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
15 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Assessing the Use of Lasers on Shoes for Freezing of Gait in People With Parkinson's Disease: A Pilot Study
Actual Study Start Date :
Dec 12, 2020
Anticipated Primary Completion Date :
Jul 14, 2022
Anticipated Study Completion Date :
Jul 14, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: People with Parkinson's disease on medication who freeze

We will be testing each of the 15 participants both with and without the removeable lasers on their shoes.

Device: gait task and activity of daily living task
use of lasers on shoes to potentially minimize freezing of gait
Other Names:
  • A gait task and activity of daily living task without laser shoe attachment
  • Outcome Measures

    Primary Outcome Measures

    1. Freezing Severity [4 hours]

      The severity of freezing during a gait task, as quantified by review of a video of the movement, assessed by a trained reviewer

    Secondary Outcome Measures

    1. Freezing of Gait Ratio [This outcome will be assessed during in-place turning with and without laser shoes (both collected within the same data collection). The time frame will be 2 hours with or without the lasers followed by 2 hours without or with the lasers.]

      Freezing of gait (FoG) ratio is calculated from acceleration of the shins (measured via inertial sensors, Opals by APDM) in-place turning. First, power spectral density from antero-posterior acceleration signals are calculated. Then, a FoG ratio is calculated as the ratio of total power in the "freezing band" (3-8 Hz) and the "locomotion band" (0.5-3 Hz). Higher freezing ratios indicate higher severity of FoG. (Tang et al., 2019).

    Other Outcome Measures

    1. Step length during gait [4 hours]

      The step length during gait as quantified by gait map recording.

    2. Foot angle during gait [4 hours]

      The foot angle during gait as quantified by gait map recording.

    3. Foot height during gait [4 hours]

      The foot height during gait as quantified by gait map recording.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • People with PD who exhibit freezing, on medications
    Exclusion Criteria:
    • People who are non-ambulatory

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Phoenix Biomedical Campus Phoenix Arizona United States 85004

    Sponsors and Collaborators

    • Northern Arizona University
    • FY2020 Research Bridge
    • Arizona State University

    Investigators

    • Principal Investigator: Cindy C Ivy, OTD, Northern Arizona University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Northern Arizona University
    ClinicalTrials.gov Identifier:
    NCT05131906
    Other Study ID Numbers:
    • 1550436-1
    First Posted:
    Nov 23, 2021
    Last Update Posted:
    Nov 23, 2021
    Last Verified:
    Nov 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Northern Arizona University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 23, 2021