Opti Gait Wearable Gait Tracker
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Gait Tracker.
- Who it may be relevant to
- Registry conditions: Seniors. Basic parameters: from 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Opti Gait Wearable Gait Tracker: Pilot Trial l With Healthy Older Adults
Overview
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.
Detailed 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.
Interventions
- Device Gait Tracker
Opti Gait is a wearable gait tracker
Primary outcome measures
- Change in walking speed [Time frame: 3 hours]
- Change in natural gait [Time frame: 3 hours]
- Gait height [Time frame: 3 hours]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Case-only
Study locations
United States · 1 center
- University of Wisconsin - Madison — Madison
Identifiers
NCT: NCT07158580 · 2025-1220 · R33AG061699-06 · ENGR/ELECTRICAL & COMPUTER ENG · AS · Protocol Version 8/13/2025