Walking practice with a robotic support suit
This study compares supported walking practice using the HAL device with conventional training for parkinsonism.
Testing a treatment or activity · Study reference: JPRN-UMIN000046222
Plain-language introduction written with AI from the registry; not independently checked by a clinician. Read the original details below ↓
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Results reported
- Start (reported date)
- 2020-12-07
- Study finished (reported date)
- 2023-11-30
Planned dates can move. A study finishing does not tell us when a paper will be published.
Read the results reported in the registry
Changes we have recorded
- 2026-10-11 — recruiting
These are dates we observed a change, not necessarily the dates it happened.
Papers connected to this study
No connected paper has been found yet. The tracker checks the growing library for study identifiers and registry-linked publications.
Who can join?
Age 20years-old and over · Ask the team who can join
These are starting points, not the full rules. The research team can tell you whether the study is right for your situation.
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Sex eligibility reported by registry: male and female
Full study name & original research details
Official study title
Clinical effects of the robot suits Hybrid Assistive Limb assisted gait training in patients with Parkinsonism.: randomized controlled trial - Clinical effects of the robot suits Hybrid Assistive Limb assisted gait training in patients with Parkinsonism.
Short title used by the registry
Clinical effects of the robot suits HAL in Parkinsonism.
Original description
Conditions reported: Parkinson's disease Progressive supranuclear palsy Corticobasal degeneration Multiple system atrophy Vascular Parkinsonism
Registry records for this study
Records are joined using registration identifiers. Titles alone do not establish that two studies are the same.
- JPRN · JPRN-UMIN000046222 ↗ — Recruiting; WHO ICTRP processed 2026-06-29; checked 2026-10-11
- Study type
- Interventional
- Interventions
- Intervention will be provided daily during 4 weeks. Intervention will be provided 40 minutes including 20 minutes of gait training. Intervention group, they will be gait training with HAL for 5 days and conventional training other 2 days. Control group, they will be conventional training for 7 days. Control group will be provided 40 minutes of training including 20 minutes of gait training.
- Phases
- Not selected
- Sponsor
- Akita Prefectural Center for Rehabilitation and Psychiatric Medicine.
- Start date reported by registry
- 2020-12-07 (reported)
Registry updated: Not reported · Status last verified by the registry submitter: Not reported
Registry records retrieved 2026-10-11 (UTC). Individual records may have older updates. Recruitment and eligibility must be confirmed with the study team.
Contact the research team
Public study contacts supplied to the registry. Ask whether recruitment is still open and what participation involves.
Toru Takeda · 018-892-3751 · takeda-toru@akita-rehacen.jp
Study locations
Site status can differ from overall study status. “Status not reported” means local availability needs confirmation. Remote participation and travel arrangements must be checked with the team.
Facility not reported
Japan
Status not reportedThe original descriptions and participation rules come from the registry. Participation is voluntary and does not guarantee benefit.