Skip to content

A randomized controlled clinical trial of exoskeleton robot assisted training in the treatment of functional impairment after spinal cord injury

A randomized controlled clinical trial of exoskeleton robot assisted training in the treatment of functional impairment after spinal cord injury

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039064
Enrollment
Unknown
Registered
2020-10-15
Start date
2020-11-01
Completion date
Unknown
Last updated
2021-01-18

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

Conditions

Spinal cord injury

Interventions

experimental group:Exoskeleton robot assistant training group, exoskeleton robot assistant training + routine training
Healthy adult group :No Intervention

Sponsors

The Third Affiliated Hospital of Sun Yat-Sen university
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients aged 18-65 years; 2. Patients with spinal cord injury caused by trauma; 3. Patients with a course of 2 months to 1 year were in stable condition; 4. Asia spinal cord injury grade a-c patients; 5. Patients with thoracolumbar spinal cord injury; 6. Patients without contraindications of MRI examination; 7. Right handed patients; 8. Patients with height between 150cm and 185cm; 9. Patients weighing less than 85kg; 10. Patients with informed consent voluntarily participated in the experiment.

Exclusion criteria

Exclusion criteria: 1. Patients with brain injury, ankylosing spondylitis, malignant tumor, neurodegenerative disease or neuropathy, mental disease, hemorrhagic disease or coagulation dysfunction, active or gradually aggravating infectious disease, 2. Patients with serious heart disease or wearing pacemaker; 3. Patients with severe spasm; 4. Patients with active pressure ulcer; 5. Patients with unstable fracture and nonunion of fracture; 6. Patients with hip subluxation; 7. Patients with acute deep venous thrombosis; 8. Patients with limited range of motion due to heterotopic ossification of lower limbs; 9. Patients with severe osteoporosis; 10. Patients with damaged skin in contact with the equipment; 11. Patients with cognitive impairment; 12. Objects of pregnancy or lactation; 13. Patients with poor compliance or incorrect understanding and cooperation that cannot complete the follow-up.

Design outcomes

Primary

MeasureTime frame
AISA score;

Secondary

MeasureTime frame
SCIM-III, Spinal Cord Independence Measure-III;IANR-SCIFRS score;ISAFSCI score;MAS;Penn score;Quality of life assessment;Low frequency oscillation amplitude ALFF analysis;Functional connectivity;VBM;Fractional Anisotropy;Mean Diffusivity;F wave detection;H reflex;The average time;Axial Diffusion;Radial Diffusivity;

Countries

China

Contacts

Public ContactRong Limin

The Third Affiliated Hospital of Sun Yat-Sen University

ronglimin@21cn.com+86 13609780973

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026