N/A N=56 Treatment

Gait Modifications and Cutaneous Stimulation

Osteoarthritis, Knee

Bottom Line

View on ClinicalTrials.gov: NCT02884414 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Jan 2021

Primary outcome: Primary: Change in Peak Knee Flexion Moment (%Bw*Ht) — 2.72 %Bw*Ht — p=0.44

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: Cutaneous stimulation (Device)
Age: Adult, Older Adult · 18+ yrs
Sex: All
Sponsor: Stanford University
Primary completion: Feb 2019

Outcome Measures

Outcome	Result	p-value
PRIMARY Change in Peak Knee Flexion Moment (%Bw*Ht)	2.72	0.44

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.

Eligibility Criteria

Inclusion Criteria

BMI < 35 kg/m^2
For knee pathology subjects: Diagnosis of knee pathology (e.g. knee osteoarthritis, ACL injury, etc) and/or knee pain
Full weight-bearing status

Exclusion Criteria

Non-ambulatory
Use of walking aid
For healthy volunteers - history of surgical intervention at any joint of the lower extremity
Inability to cooperate with study protocol due to medical or psychiatric reasons
Inability to provide informed consent
For healthy subjects: Any diagnosis of knee osteoarthritis or knee pain

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02884414). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.