Healthy subjects Rehabilitation subjects
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Healthy subjects People who have no history of brain disease, neurological or muscular disease, and who have given informed consent for this study. 2)Rehabilitation subjects Patients who are currently in hospital or attending outpatient rehabilitation and who have given informed consent for this study.
Exclusion criteria
Exclusion criteria: 1)Healthy subjects People with a history of brain disease or neurological/muscular disease. People with orthopedic disorders that currently interfere with exercise. 2)Rehabilitation subjects Patients whose general condition is unstable and who may experience sudden changes. Patients who have difficulty following instructions when performing tasks due to impaired consciousness or cognitive function. Patients who currently have orthopedic conditions that interfere with movement.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Kinematic parameters (distance, speed, range of movement, etc.) of the COP. Questionnaire-based subjective assessment based on the Quebec User Evaluation of Satisfaction with assistive Technology (QUEST) and other methods. | — |
Secondary
| Measure | Time frame |
|---|---|
| Trunk Impairment Scale (TIS), Function In Sitting Test (FIST), Brunel Balance Assessment (BBA), Functional reach test in sitting position, etc. Kinematic indicators (posture and hand position) of the upper extremities and trunk during various movements in a sitting position. Subjective assessments of entertainment value and potential for continued use using the Numerical Rating Scale (NRS). Age, gender, body mass index. Basic information obtained during normal medical treatment and rehabilitation for rehabilitation subjects. | — |
Countries
Japan
Contacts
Fujita Health University Faculty of Rehabilitation, School of Health Sciences