CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 56 enrolled
Drug / intervention
Cutaneous stimulationdevice
Likely dose
Not stated in record
Key inclusion· 3
  • BMI less than 35 kg/m²
  • Full weight-bearing status
  • For knee pathology subjects: diagnosis of knee osteoarthritis, ACL injury, or similar knee pathology and/or knee pain
Key exclusion· 5
  • Non-ambulatory
  • Use of walking aid
  • For healthy volunteers: history of surgical intervention at any joint of the lower extremity
  • For healthy subjects: any diagnosis of knee osteoarthritis or knee pain

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02884414
NCT02884414N/ACompleted

Analysis of Joint Mechanics in Response to Gait Modifications and Cutaneous Stimulation

Stanford University·interventional·Posted Aug 31, 2016·Updated Jan 8, 2021

In Brief

A clinical study evaluating Cutaneous stimulation for Osteoarthritis, Knee. Completed, enrolled 56 participants across 1 site.

Detailed Summary

The purpose of this study is to quantify differences in joint mechanics between different types of walking in healthy individuals and individuals with knee pathology. The investigators will determine how modifying gait through feedback and/or cutaneous stimulation changes joint loading.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedAug 31, 2016
Enrollment StartAug 1, 2016
Primary CompletionFeb 1, 2019
TodayJul 2, 2026
Enrollment to primary: 2.5 yearsPosted 9.8 years ago

Interventions

Cutaneous stimulationdevice

A non-invasive external device that will be placed on the leg of the subject. The device consists of a sensing module to determine specific points in the gait cycle, a processor to analyze signal from the sensor, and a stimulus module to provide feedback to the subject.