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Operation of Locobot for Improvement of Postoperative Balance Function in Patients With Cervical Spondylotic Myelopathy

Operation of Locobot for Improvement of Postoperative Balance Function in Patients With Cervical Spondylotic Myelopathy - Operation of Locobot for Improvement of Postoperative Balance Function in Patients With Cervical Spondylotic Myelopathy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000055658
Enrollment
40
Registered
2024-09-28
Start date
2024-10-01
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

cervical spondylotic myelopathy

Interventions

weight-shifting-based robot control system (&quot
locobot&quot
) is used as balance training for postoperative patients with cervical spondylotic myelopathy. Conventional methods will be used as balance training for postoperative patients with cervical spondyloti

Sponsors

Rehabilitation Unit, University of Miyazaki Hospital, Miyazaki, Japan
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients who are 20 years of age or older at the time of consent; (2) Patients who underwent vertebroplasty during hospitalization; (3) Patients who were able to perform all endpoints before and after surgery; (4) Patients who have been fully informed about their participation in this study, and who have given their free, written consent based on their full understanding.

Exclusion criteria

Exclusion criteria: (1) Subjects with traumatic spinal cord injury, spinal cord infection, pathological musculoskeletal disease, or other neurological disease (2) Subjects with orthopedic problems that may affect the performance of the assessment items (3) Subjects with balance disorders not caused by CSM such as vestibular dysfunction (4) Subjects who cannot perform all assessment items during preoperative and postoperative assessments (5) Subjects with higher brain dysfunction or cognitive impairment (6) Subjects with other conditions that make them unsuitable as research subjects(5) Subjects with higher brain dysfunction or cognitive impairment (6) Other subjects deemed inappropriate as research subjects by the principal investigator

Design outcomes

Primary

MeasureTime frame
Movement of the center of gravity of the body in the open eye and close eye standing position Twice of preoperative and on day 11 or 12 postoperative

Countries

Japan

Contacts

Public Contacttsubasa kawaguchi

Rehabilitation Unit, University of Miyazaki Hospital, Miyazaki, Japan Rehabilitation Unit, University of Miyazaki Hospital, Miyazaki, Japan

tsubasa_kawaguchi@med.miyazaki-u.ac.jp0985-85-9849

Outcome results

None listed

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