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Opti Gait Wearable Gait Tracker

University of Wisconsin (UW) logo

University of Wisconsin (UW)

Status

Not yet enrolling

Conditions

Seniors

Treatments

Device: Gait Tracker

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT07158580
R33AG061699-06 (U.S. NIH Grant/Contract)
Protocol Version 8/13/2025 (Other Identifier)
ENGR/ELECTRICAL & COMPUTER ENG (Other Identifier)
AS (Other Identifier)
2025-1220

Details and patient eligibility

About

The purpose of this observational study is to test a shoe mounted gait monitoring device that was refined with the input of older adults and assess the efficacy of the refinements through a series of tests that involve walking with and without the device.

Full description

In this testing, researchers seek to validate the precision, accuracy and robustness of the community-corefined device with healthy older adults, aged 65 years and above, by conducting walking tests on a state of the art GaitRite gaitmat to assess various gait metrics and on a flight of stairs to assess gait height. Following this, researchers will conduct a semi structured interview that will comprise a series of yes/no questions and open ended questions to understand the efficacy of the refinements and further refinement directions.

Enrollment

20 estimated patients

Sex

All

Ages

65+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Aged 65 years and older
  • Able to speak and understand English,
  • Able to provide consent

Exclusion criteria

  • Current or recent (< 1 year) major psychiatric condition
  • Significant medical condition such that usability evaluation could pose substantial health or safety risk
  • Individuals with an activated power of attorney will be excluded from the study

Trial design

20 participants in 1 patient group

No gait or mobility issues
Description:
Participants aged 65 or older who are able to walk for at least 10 minutes and can walk up and down a flight of stairs
Treatment:
Device: Gait Tracker

Trial contacts and locations

1

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Central trial contact

Kristen Pickett, PhD; Jayer Fernandes, PhD

Data sourced from clinicaltrials.gov

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