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Clinical Evaluation of Gait Improvement Through Multisensory Plantar Pressure Feedback

Clinical Evaluation of Gait Improvement Through Multisensory Plantar Pressure Feedback - Clinical Evaluation of Gait Improvement Through Multisensory Plantar Pressure Feedback

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000058339
Enrollment
80
Registered
2025-07-03
Start date
2025-08-01
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

Stroke patients Elderly patients Post-orthopedic surgery patients

Interventions

Wearing a perception support device equipped with functions for measuring the center of foot pressure and load and for real-time FB of the values, the subject walks while perceiving his/her own center

Sponsors

Waseda University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who have been diagnosed with knee osteoarthritis and who wish to participate in training using sensory-assistive orthoses. Hemiplegic patients who request to participate in training with sensory supportive orthosis and meet the following criteria: 1. Patients with lower limb Brunnstrom stage III to VI 2. Patients with no higher brain dysfunction 3. Patients whose attending physicians and physical therapists can judge that there is no problem in performing the examination. Able-bodied elderly patients who have requested to participate in training using sensory supportive orthosis.

Exclusion criteria

Exclusion criteria: 1. uncontrolled heart failure 2. acute myocardial infarction 3. active myocarditis or pericarditis 4. unstable angina 5. acute systemic embolism or pulmonary embolism 6. acute infection 7. thrombophlebitis 8. ventricular tachycardia or refractory ventricular arrhythmia 9. severe ventricular outflow tract obstruction 10. uncontrolled arterial or pulmonary hypertension 10. Uncontrolled arterial or pulmonary hypertension 11. Contemporaneous inclusion in another interventional study (verbally check with your physiotherapist)

Design outcomes

Primary

MeasureTime frame
Lower extremity coordinates, force, gait data, blood pressure and heart rate, surface myoelectricity, acceleration, myoelectric potentials, ankle plane angle, video recording during test, vibration sensation Evaluation period: Before, during and after the 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