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Effect of gait assessment and training system based on visual feedback mode on walking function of stroke patients

Effect of gait assessment and training system based on visual feedback mode on walking function of stroke patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900024253
Enrollment
Unknown
Registered
2019-07-03
Start date
2019-08-01
Completion date
Unknown
Last updated
2019-07-15

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 + Walker View system training
control group:Routine rehabilitation

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) In line with the diagnostic criteria for "stroke" (the fourth diagnostic criteria for the study of the fourth cerebrovascular disease conference in 1995, all cases require clinical diagnosis and CT or MRI to confirm cerebral infarction or cerebral hemorrhage); 2) The vital signs are stable; 3) Aged 30 to 70 years; 4) The onset time is >= 1 month, there is walking dysfunction of lower limbs, the balance of standing position reaches Second level, and the knee strength of lower limbs reaches the third level; 5) Brunnstrom staged lower extremity II-III; 6) Those who are willing to sign "informed consent" by themselves or their immediate family members.

Exclusion criteria

Exclusion criteria: 1) There are more serious complications (including liver and kidney dysfunction, cardiac infarction, heart failure, malignant tumor, gastrointestinal bleeding, serious infection, mental disorder and dementia, epilepsy, osteoarthritis and pulmonary dysfunction, etc.); 2) There are more serious cognitive disorders (including severe aphasia, attention disorder, memory or communication problems, etc.). 3) Patients during pregnancy; 4) Those who participated in other clinical trials during the same period; 5) The patient has serious vision problems and cannot see the screen; 6) The condition is unstable, and there may be new bleeding or ischemic lesions; 7) Poor compliance and difficulty in following up.

Design outcomes

Primary

MeasureTime frame
FMA-LE;6 minute walk test;Berg Balance Scale;Evaluation of biomechanical parameters of lower limbs in patients with ipsilateral step, average knee flexion and extension angle, and average touchdown duration;Trunk average lateral angle assessment;

Countries

China

Contacts

Public ContactDongyan Xu

Huashan Hospital, Fudan University

xudy07@163.com+86 13585864623

Outcome results

None listed

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