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Effects of Electromyography Bridge on Upper Limb Motor Function Rebuilding in Stroke Patients

Effects of Electromyography Bridge on Upper Limb Motor Function Rebuilding in Stroke Patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051957
Enrollment
Unknown
Registered
2021-10-10
Start date
2020-05-14
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

Stroke

Interventions

experimental group:Electromyography Bridge treatment
control group:neuromuscular electrical stimulation treatment

Sponsors

Second Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 73 Years

Inclusion criteria

Inclusion criteria: 1. Stroke diagnosis that was confirmed by evidence on computed tomography (CT) or magnetic resonance imaging (MRI) scans 3 days to 12 months prior to the study; 2. Patient aged between 18 and 75 years; 3. Poor upper limb function11, though the contralateral upper limb functioned well; 4. No progressive stroke and vital signs were stable; 5. AROM of carpal extension was 0 degree; 6. The ability to understand and agree to the trial procedures and to sign an informed consent form in accordance with national legislation.

Exclusion criteria

Exclusion criteria: 1. Severe cognitive disorders12 (Mini-Mental State Examination score = 24); 3. A modified Ashworth scale (MAS) score of two or more points for spasticity in extension carpal; 4. Carpal contracture; 5. New York Heart Association (NYHA) cardiac function was classified as Level 4; 6. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were twice higher than the upper limit of normal; 7. Severe heart, liver, kidney or lung diseases, or cancer; 8. Cardiac pacemakers and various implantable electronic devices; 9. Pregnant or lactating women; 10. Muscles do not respond to functional electrical stimulation (FES); 11. Concurrent participation in another similar clinical study during the 3 months before enrollment; 12. Other reasons deemed by the investigators to render the subject unsuitable for this trial.

Design outcomes

Primary

MeasureTime frame
active range of motion of wrist dorsal extension;

Secondary

MeasureTime frame
extensor carpi radialis muscle strength;extensor carpi ulnaris muscle strength;extensor digitorum communis muscle strength;Barthel index;Fugl-Meyer assessment for upper extremity;

Countries

China

Contacts

Public ContactTan Botao

Department of Rehabilitation Medicine, the Second Affiliated Hospital of Chongqing Medical University

300895@cqmu.edu.cn+86 13896179179

Outcome results

None listed

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