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Gait Analysis Using OneStep Smartphone Application

NCT05012891 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 12

Last updated 2022-04-08

No results posted yet for this study

Summary

OneStep technology is a smartphone application, utilizing smartphone sensors to provide ongoing gait diagnostics. In this longitudinal study, 50 consecutive patients with lower-extremity disability or chronic pain, will be using the One-Step App, downloaded to their personal smartphones, in parallel with the usual rehabilitation treatments, during a one-month period. Analyzed gait data from the App will be linked with clinical data collected by a team of experts, in order to evaluate the potential use of this App as an objective means to characterize and quantify patients' gait characteristics along the follow-up period, and to objectively assess the patients' adherence and compliance with the rehabilitation regime.

Conditions

  • Chronic Pain of Left Foot (Finding)
  • Chronic Pain of Right Foot (Finding)

Interventions

OTHER

OneStep Smartphone Application

OneStep technology is a smartphone application (app) utilizing smartphone sensors to provide ongoing gait diagnostics. The eligible study participants will be asked to download and install the app on their own smartphones and carry the smartphone in their front pants pocket at all times. The app will collect the required gait parameters but, will not present them (or any summary thereof) to the study participants or their physiotherapists, in order not to influence the rehabilitation plan.

Sponsors & Collaborators

  • Reuth Rehabilitation Hospital

    lead OTHER

Principal Investigators

  • Dana Gefen Doron, MD · Reuth Rehabilitation Hospital

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-07-01
Primary Completion
2022-03-01
Completion
2022-09-30

Countries

  • Israel

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05012891 on ClinicalTrials.gov