Clinical Validation of the Safety and Efficacy of a Sensory-motor Training System for Stroke Patients

Research and Development of Dynamic Quantitative Assessment and Intelligent Rehabilitation Training System for Limb Movement Dysfunction

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2200065040

Enrollment

Unknown

Registered

2022-10-26

Start date

2022-10-28

Completion date

Unknown

Last updated

2023-05-15

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

Conditions

Stroke

Interventions

Physical rehabilitation group:Sensory-motor training system

Control group:None

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Inclusion criteria are confirmed first stroke by CT or MRI;onset between two weeks and six months;the presence of mild to moderate motor dysfunction;the patient has no significant cognitive or speech dysfunction.

Exclusion criteria

Exclusion criteria: Exclusion criteria are history of previous stroke or traumatic brain injury or brain tumor;concurrent severe cardiac,pulmonary,hepatic or renal dysfunction or other serious physical disease;previous epilepsy and family history of epilepsy;metal implanted in the body such as pacemakers,metal in the skull,etc;the presence of new infarct foci or secondary hemorrhage with worsening of the condition;those with severe cervical spine pathology including severe cervical conus stenosis and cervical instability.

Design outcomes

Primary

Measure	Time frame
Measurement Scale;	—

Countries

China

Contacts

Public ContactYang Lv

The First Affiliated Hospital of Chongqing Medical Universitying 400016, China

yanglyu@hospital.cqmu.edu.cn13618236535

Outcome results

None listed

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