Locomotive syndrome
Conditions
Interventions
HAL lumbar type or HAL mono-articular
Sponsors
ImPACT project by Cabinet Office, Goverment of Japan
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Patients who agree to participate in the current trial and from whom informed consent was obtained orally and in writing. 2. Patients who is possible to install HAL lumbar type and/or HAL mono-articular type 3. Patient who correspond to locomotive syndrome (with the criterion for locomotive syndrome made by Japanese Orthopedic Association)
Exclusion criteria
Exclusion criteria: 1. Patient who cannot install HAL because of skin disease 2. Patient who is not applicable to locomotor training due to severe comorbidity 3. Patient who cannot agree to participate in the current study due to consciousness disorder
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Adverse events related to locomotor training using HAL for locomotive syndrome | — |
Secondary
| Measure | Time frame |
|---|---|
| Alteration of vital signs pre- and post-locomotor training with HAL (vital signs will be measured using Vital sensor) | — |
Countries
Japan
Contacts
Public ContactMasao Koda
University of Tsukuba Department of Orthopedic Surgery
Outcome results
None listed