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A randomized controlled trial for Effects and Mechanism of Intelligent Functional Electrical Stimulation on Ambulation of Stroke Patients

A randomized controlled trial for Effects and Mechanism of Intelligent Functional Electrical Stimulation on Ambulation of Stroke Patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17013339
Enrollment
Unknown
Registered
2017-11-10
Start date
2017-11-01
Completion date
Unknown
Last updated
2017-11-13

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

Conditions

Stroke

Interventions

1-hour intelligent group:1-hour intelligent multi-channel FES
30-minute multi-channel group:30-minute intelligent multi-channel FES
single channel group :30-minute single channel FES

Sponsors

Sun Yat-sen Memorial Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. First stroke with stable vital signs and symptoms of neurological system have stopped progressing; 2. Aged 40 to 80 years old; 3. Hemiplegic but with the ability of standing and walking; 4. No sensory disorder and severe cognition dysfunction (AMT=7 scores); 5. No contraindications for electrical stimulation; 6. No severe diseases of heart, lung or kidney; 7. Agree to sign the informed consent form.

Exclusion criteria

Exclusion criteria: Progressing stroke; subarachnoid hemorrhage (SAH); recurrent stroke; dysfunction of bilateral limbs; sensory disorder; severe cognition dysfunction (AMT?7 scores); with other musculo-orthopeadic disorders affecting ambulation (e.g. fractures, OA) or neurological diseases(e.g. tremor, involuntary movement, PD); With contradiction of electrical stimulation (e.g. cardiac pacemaker, local metal internal fixation); severe diseases of heart, lung and kidney; cranio-cerebral injuries or tumors; with a history of epilepsy or already diagnosed with epilepsy; refuse to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
Walking velocity;step length;

Secondary

MeasureTime frame
Somatosensory evoked potential;Motor evoked potential;cocontracion index of paretic antagonisitic muscle;

Countries

China

Contacts

Public ContactJingjing Xue

Sun Yat-sen Memorial Hospital of Sun Yat-sen University

xuejing0384@163.com+86 13570501891

Outcome results

None listed

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