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REX (Application of Rex Rehabilitation Robot in the Rehabilitation of Patients with Central Nervous System Injury)

REX (Application of Rex Rehabilitation Robot in the Rehabilitation of Patients with Central Nervous System Injury)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068398
Enrollment
Unknown
Registered
2023-02-17
Start date
2023-02-17
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

Stroke

Interventions

Experimental group:Routine rehabilitation + REX rehabilitation robot
Control group:Routine rehabilitation

Sponsors

Wuxi Mental Health Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Patients with hemiplegia after stroke are in line with the "Key Points for the Diagnosis of Various Cerebrovascular Diseases" revised by the National Conference on Cerebrovascular Disease of the Chinese Medical Association in 2019, and all have the imaging diagnosis basis of head CT or MRI; (2) Stroke patients with the first onset, the course of the disease is within 2 weeks to 3 months; (3) There is obvious lower limb motor dysfunction: patients with stage 3 BRUNSTROM grade = lower limb on hemiplegic side, Berg = 20 points; (4) The patient's vital signs are stable, and the neurological symptoms no longer progress; and can tolerate REX robotic therapy; Be between 40 and 75 years of age; (5) Lower limb muscle tone = grade 2; (6) Ability to understand and communicate simply (MMSE score= 21); (7) Patients signed informed consent for treatment.

Exclusion criteria

Exclusion criteria: (1) Severe arthritis or other serious musculoskeletal system diseases; (2) Those suffering from systemic immune diseases, blood system diseases and other diseases; (3) Patients with severe mental status abnormalities, unable to cooperate with the completion of treatment, or poor compliance; (4) Those with orthostatic hypotension, lower extremity deep vein thrombosis, unstable hypertension, severe heart or cardiopulmonary diseases who cannot participate in exercise; (5) Those with severe osteoporosis in bone density examination; (6) Patients who refuse to sign informed consent.

Design outcomes

Primary

MeasureTime frame
Berg balance scale;

Secondary

MeasureTime frame
Postural Assessment Scale for Stroke Patients;Modified Barthel Index;Surface electromyography;Tecnobody balancer;Fugl-Meyer Assessment Scale for Lower Extremity;

Countries

china

Contacts

Public ContactWenjuan Ding

Wuxi Mental Health Center

dingwenjuan921@163.com18921104665

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026