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The development of intelligent hip-ankle linkage powered exoskeleton and its application for rehabilitation in hemiplegic patients with acquired brain injury

The development of intelligent hip-ankle linkage powered exoskeleton and its application for rehabilitation in hemiplegic patients with acquired brain injury

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084418
Enrollment
Unknown
Registered
2024-05-16
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-05-21

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

Conditions

Stroke or traumatic brain injury

Interventions

Observation group 1:conventional rehabilitation therapy+ intelligent ankle-assistance powered exoskeleton training
Observation group 2:conventional rehabilitation therapy+ intelligent hip-ankle linkage powered exoskeleton training

Sponsors

Beijing Bo'ai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: ?The patients met the diagnostic criteria for ischemic or hemorrhagic stroke in "Diagnostic Points of Various Major Cerebrovascular Diseases in China 2019" or patients with a definite history of traumatic brain injury who were confirmed by head CT or MRI. ? The course of stroke was =1 month, the age was 18-70 years old, ? Brunnstrom stage for the lower extremity was =III, and the modified Ashworth scale was =II. Patients can walk 10 meters independently, no ataxia and other extrapyramidal symptoms. ?No obvious cognitive function and speech impairment, MMSE score =22 points. ? Sign informed consent.

Exclusion criteria

Exclusion criteria: ?Patients with previous history of stroke or traumatic brain injury, past or current mental disorders and cognitive impairment. ?Patients with malignant tumors, severe infections, serious cardiopulmonary diseases, etc. ?Patients with fractures, serious deformity of limbs or joint contracture. ?There are metal foreign bodies or other devices implanted in the body, which makes the patient unable to undergo magnetic resonance examination. ?Those who are unwilling to cooperate and unable to test and evaluate.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer Assessment Lower Extremity;6-minute walking test;

Secondary

MeasureTime frame
Fugl-Meyer Assessment-Balance ;modified Ashworth Scale;Gait analysis;10-meter walking test;modified Barthel index;Satisfaction Questionnaire;functional magnetic resonance imaging;

Countries

China

Contacts

Public ContactLixu Liu

Beijing Bo'ai Hospital

liulixu2004@163.com+86 136 7126 2202

Outcome results

None listed

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