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Clinical evaluation of stimulus discrimination and gait improvement of perceptual co-sensory wear that shares foot pressure at the hip and back

An Assist Method for After-Surgery Orthopedic Patients using Perception Support to Prevent New Deformity on Knee Joint - An Assist Method for After-Surgery Orthopedic Patients using Perception Support to Prevent New Deformity on Knee Joint

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000051062
Enrollment
20
Registered
2023-05-15
Start date
2023-06-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee asteoarthrithrtis

Interventions

Gait rehabilitation while wearing the vibrating device Objective: To train the subject to become accustomed to the position of his/her foot by telling him which part of the foot he/she should put pre

Sponsors

Waseda University
Lead Sponsor
Saiwai Tsurumi Hospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who have requested to participate in training with a sensory-assistive orthosis and meet the following criteria 1. Lower limb Brunnstrom stage III to VI 2. Patients with no higher brain dysfunction 3. Patients whom the attending physician and physical therapist can judge that there is no problem in conducting the examination. Able-bodied older adults who have requested to participate in training using a sensory assistive device.

Exclusion criteria

Exclusion criteria: 1. uncontrolled heart failure 2. acute myocardial infarction 3. Active myocarditis or pericarditis 4. unstable angina pectoris 5. acute systemic embolism or pulmonary embolism 6. Acute infectious disease Thrombophlebitis Ventricular tachycardia or refractory ventricular arrhythmia 9. Severe ventricular outflow tract obstruction Uncontrolled arterial or pulmonary hypertension 11. being a participant in another interventional study at the same time (to be confirmed verbally with the physiotherapist in charge). Exclusion criteria are at the discretion of the physician in charge.

Design outcomes

Primary

MeasureTime frame
Plantar pressure (Pre-intervention, Post-intervention)

Countries

Japan

Contacts

Public ContactHiroyasu Iwata

Waseda University Faculty science and engineering

jubi@waseda.jp03-3203-4427

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026