Clinical study for the recovery of brain injury function by the end effect robot assisted gait training

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000028735

Enrollment

Unknown

Registered

2020-01-01

Start date

2020-02-01

Completion date

Unknown

Last updated

2020-01-06

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

Conditions

brain injury

Interventions

Control group:conventional rehabilitaiton

GEO group:conventional rehabilitaiton+robot training

Eligibility

Sex/Gender

All

Age

30 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. the first onset of the disease is in accordance with the diagnosis and classification criteria for stroke formulated by the Chinese Neuroscience Association and the Chinese society of Neurosurgery at the Sixth National Conference on cerebrovascular diseases in 2004; 2. the brain hemorrhage or cerebral infarction is confirmed by CT or MRI, and the focus is located in one side of the cerebral hemisphere (cortex, subcortical); 3. the vital signs are stable, the consciousness is clear, and there is no serious aphasia, and the treatment is coordinated; 4. included in this study is within 2 to 6 months after the onset of the disease; 5. Aged 30 and 70 years old; 6. the height is between 1.1 and 2 meters; 7. hemilateral limb motor dysfunction; 8. signed informed consent with the patient or family members before treatment.

Exclusion criteria

Exclusion criteria: (1) unstable condition, progressive or secondary brain injury; (2) unable to keep the upper body upright for 7 minutes; (3) unable to sit alone for 3 seconds without assistance; (4) unilateral neglect; (5) postural hypotension; (6) previous cerebrovascular disease, brain injury or peripheral neuropathy; (7) previous serious organ dysfunction such as heart and lung; (8) limb motor dysfunction due to other causes, including Including nerve, muscle and bone injury; (9) weight > 150kg; (10) severe osteoporosis.

Design outcomes

Primary

Measure	Time frame
functional ambulation category scale;FA;	—

Secondary

Measure	Time frame
Velocity;Barthel Index;Fugl Meyer lower extremity movement scale;MEP latentperiod;MEP Amplitude;central motor conduction time;	—

Countries

China

Contacts

Public ContactMou Xiang

Department of Rehabilitation medicine,Xijing Hospital,Fourth Military Medical University

pro.mu@fmmu.edu.cn+86 13991168060

Outcome results

None listed

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