Skip to content

Randomized controlled study of the efficacy of lower limb rehabilitation robot on the improvement of lower limb walking function in patients with incomplete spinal cord injury

Randomized controlled study of the efficacy of lower limb rehabilitation robot on the improvement of lower limb walking function in patients with incomplete spinal cord injury

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070068
Enrollment
Unknown
Registered
2023-03-31
Start date
2020-11-12
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Incomplete spinal cord injury

Interventions

Experimental group:Lower limb rehabilitation robot-assisted walking training group

Sponsors

Zhejiang Rehabilitation Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 56 Years

Inclusion criteria

Inclusion criteria: (1) according to the American Spinal Injury Association (Asia) International Standard for neurological classification of Spinal cord Injury, there are definite clinical manifestations of Spinal cord Injury and Spinal cord lesions diagnosed by CT or MRI; (3) Asia was classified as C/D grade, (4) the injured segment was T10-L2, (5) the muscle tone of each muscle group of both lower limbs was =2 grade, (6) there was no cognitive, visual and auditory dysfunction, able to communicate with the therapist and follow the therapist's advice on rehabilitation exercise, (7) patients can walk with the help of walking or walking independently.

Exclusion criteria

Exclusion criteria: (1) patients with complete spinal cord injury, (2) patients with fracture, contracture or deformity of lower limbs, (3) patients with other basic diseases of multiple organs and systems injury, (4) patients with other medical diseases affecting walking function training, and (4) patients with other medical diseases; (5) communication barriers and non-compliance with medical advice, patients (6) half-way withdrawal.

Design outcomes

Primary

MeasureTime frame
Surface electromyography;

Secondary

MeasureTime frame
10m walking time;Holden walking function;Asia assessment scale;Berg balance function score;

Countries

China

Contacts

Public Contactlining

Zhejiang Rehabilitation Medical Center

310649500@qq.com18868913541

Outcome results

None listed

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