Application of Transcranial Magnetic Stimulator, Upper Limb Robot and Lower Limb Robot for Patients with Spinal Cord Injury

The Effect of Combined Treatment of Upper and Lower Limb Rehabilitation Robot and Transcranial Stimulator for Spinal Cord Injury Patients

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0004443

Enrollment

Registered

2019-11-15

Start date

2019-05-10

Completion date

Unknown

Last updated

2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device, Others : ? This study is a randomized control trial (RCT) study divided into four groups. Group A: rTMS treatment + Armeo power + Erigo Pro Group B: Sham-rTMS Treatment + Armeo

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: -Adults over 19 -Cervical levels within 24 months of onset - Tetraplegia patients -American spinal injury association impairment scale (AIS) B-D patients -Patients with cognitive function enough to understand the research and follow the researcher's instructions -Patients who have decided to participate directly with their or their guardian's consent

Exclusion criteria

Exclusion criteria: -Patients with obvious diseases that may cause muscle weakness beyond the central nervous system other than spinal cord injury (Eg neuromuscular disease) -Patients with severe upper extremity stiffness of at least 3 points -Patients who are restricted from sitting in wheelchairs or chairs for more than 30 minutes -Patients with severe shoulder pain -Patients with a limit of 50% or more of upper limb ROM movement -Patients who have implanted electrical devices -Pregnant patients -Patients with neurological problems, including epilepsy -Osteoporosis patients -Patients with bedsores -Patients with serious limitations in ROM -Patients with Talipes equinus -Patients with acute periarticular ossification -Fracture patients

Design outcomes

Primary

Measure	Time frame
The Graded Redefined Assessment of Strength, Sensation and Prehension (GRASSP);lower extremity motor score(LEMS)	—

Secondary

Measure	Time frame
bone density test;DXA muscle mass;Modified ashworth scale;Korean version of spinal cord independence measure-3;Berg Balance scale(BBS);Trunk Impairment Scale (TIS);Functional Ambulation Categories(FAC);Number of occurrences of autonomic dysreflexia;Number of occurrences of Orthostatic hypotension;Visual analoge scale;Beck Depression Inventory (BDI-II);Pittsburgh sleep quality index	—

Countries

Korea, Republic of

Contacts

Public ContactJung-Eun Lim

National Rehabilitation Center

lje276020@korea.kr+82-2-901-1345

Outcome results