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Development and Clinical Evaluation of a Gluteus Medius Assistive Device for Abnormal Gait Correction

Development and Clinical Evaluation of a Gluteus Medius Assistive Device for Abnormal Gait Correction - Development and Clinical Evaluation of a Gluteus Medius Assistive Device for Abnormal Gait Correction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000059999
Enrollment
48
Registered
2025-12-05
Start date
2026-02-01
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

None listed

Interventions

Participants will walk for 10 minutes at a unified walking cadence of 100 bpm while wearing the device. The examiner will give the start and stop instructions, and lateral knee acceleration, pelvic fr

Sponsors

Waseda University
Lead Sponsor
Yokohama Seishinkai Hospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Individuals who request to participate in training using the motion-assist orthosis, have been diagnosed with an abnormal gait, require the use of a corrective orthosis, and are deemed eligible for participation by both the attending physician and the physical therapist. - Healthy older adults who request to participate in training using the motion-assist 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 infectious disease 7. Thrombophlebitis 8. Ventricular tachycardia or refractory ventricular arrhythmia 9. Severe left ventricular outflow tract obstruction 10. Uncontrolled arterial hypertension or pulmonary hypertension 11. Participation in another interventional study during the same period (to be verbally confirmed with the responsible physical therapist) * The exclusion criteria will be determined by the attending physician.

Design outcomes

Primary

MeasureTime frame
- Lateral knee acceleration - Gait data

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