Skip to content

HAL-SJ Pilot study

HAL-SJ for acute stroke patients with upper extremity motor deficits - HAL-SJ

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs052180010
Enrollment
20
Registered
2018-11-28
Start date
2019-01-08
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

Acute stroke with upper extremity motor deficit Stroke, Upper extremity motor deficit

Interventions

Motor training of affected upper extremity using Hal-SJ for 20 minutes + conventional motor training for 20 minutes Conventional motor training of affected upper extremity for 40 minutes Each group

Sponsors

Miyamoto Susumu
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: -Acute stroke patients (except for subarachnoid hemmorrhage and transient ischemic attack) with unilateral upper extremity motor deficits -Brunnstrom stage of upper extremity of deficit side between II and V -Patients who can start intervention between 10 and 16 days after stroke onset, and who can be followed-up throughout study period

Exclusion criteria

Exclusion criteria: -Any upper extremity paresis caused by previous stroke -Diagnosed as stroke due to cerebral arteriovenous malformation, dural arteriovenous fistula, moyamoya disease, sinus thrombosis or cavernous malformation -Severe contracture of affected upper extremity

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer Assessment score of upper extremity

Secondary

MeasureTime frame
Efficacy measurements; (1)FMA proximal UE (total score of shoulder, elbow, forearm and wrist) (2)Brunnstrom stage, upper extremity and finger (3)Modified Ashworth Scale, elbow flexion and extension, forearm pronation and supination, wrist flexion and extension (4)Action Research Arm Test (5)Functional Independent Measure (6)Motor activity Log Safety measurements; (1)Occurrence rate of any adverse event or failure during three weeks after starting intervention

Contacts

Public ContactTakayuki Kikuchi

Kyoto University Hospital

tkik@kuhp.kyoto-u.ac.jp+81-75-751-3459

Outcome results

None listed

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