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Pilot study of gait training with robot in acute hemiplegic patients

Feasibility of gait training with a robot in acute hemiplegic patients - Pilot study - GAR-P

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs052180129
Enrollment
40
Registered
2019-03-18
Start date
2019-07-16
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

Interventions

Participants are divided into two groups at an acute hospital
group A performing gait training with orthosis or group B performing gait training with robot. Participants perform gait training with orthosis or robot, 40 minutes a day, 5 days a week, in addition t

Sponsors

Mikami Yasuo
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Supratentorial intracerebral hemorrhage or cerebral infarction 2. Within 14 days after onset 3. SIAS lower extremity total score =6 before onset 5. FIM-walk =2 7. FIM-social interaction >=2 8. FIM-memory >=2 9. Patient whose weight is >=40 kg and =140 cm and <190 cm

Exclusion criteria

Exclusion criteria: 1.History of neuromuscular disease 2.Contracture of lower extremity disturbing walking 3.Participating other studies about function of lower extremity/trunk or walking 4.History of epileptic seizure within 2 years 5.History of myocardial infarction or existence of symptomatic angina, or existence of symptomatic arrhythmia 6.Using pacemaker 7. Uncontrollable hypertension; systemic blood pressure at rest >=180mmHg or diastolic blood pressure at rest =120bpm 9.Symptomatic pulmonary disease 10.Bone fragility of lower extremities or spine 11.Ectopic ossification of lower extremities causing limitation of range of motion of joints 12.Pregnancy or possibility of pregnancy 13.Patient who required isolation due to infectious diseases 14.Patient who cannot don WW-1000 due to oversize, deformity and swelling of lower extremity 15.When the number of intervention patients exceed the upper limit of each hospital 16.Patient judged unsuitable by the principal investigator or subinvestigator.

Design outcomes

Primary

MeasureTime frame
Improvement efficiency for gait independece

Secondary

MeasureTime frame
1.Functional Independence Measure (FIM) 2.Stroke Impairment Assessment Set (SIAS) 3.Walking performance 4.Dose of gait exercise 5.Length of stay 6.Time after onset at the discharge

Countries

Japan, None.

Contacts

Public ContactSuzuyo Ohashi

University Hospital, Kyoto Prefectural University of Medicine

reha@koto.kpu-m.ac.jp+81-75-251-5552

Outcome results

None listed

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