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An Observational Study of Electromyographic Biofeedback Combined with Rood Therapy for Central Facial Palsy Following Ischemic Stroke

An Observational Study of Electromyographic Biofeedback Combined with Rood Therapy for Central Facial Palsy Following Ischemic Stroke

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123082
Enrollment
Unknown
Registered
2026-04-21
Start date
2025-07-31
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

stroke

Interventions

experimental group:electromyographic biofeedback therapy and Rood stimulation Electromyographic biofeedback therapy and Rood stimulation
Control group A:Sham electromyographic biofeedback therapy and Rood stimulation
Control group B:Electromyographic biofeedback therapy and sham Rood stimulation

Sponsors

Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.  Meets all of the above diagnostic criteria. 2.  Age 18–70 years (inclusive), any sex. 3.  First occurrence of ischemic stroke. 4.  Stroke duration > 2 weeks. 5.  Development of central facial paralysis after ischemic stroke. 6.  No other facial paralysis–related rehabilitation treatments within the past month. 7.  Stable vital signs, clear consciousness, able to understand instructions, cooperate with treatment, and communicate clearly. 8.  Voluntarily agrees to participate in this study and to comply with the treatment protocol.

Exclusion criteria

Exclusion criteria: 1. Concurrent severe dysfunction of major organs such as the heart, liver, or kidneys. 2. History of traumatic brain injury, skull defects, or cranial surgery. 3. History of psychiatric illness, epilepsy, or dementia. 4. History of severe systemic disease with mental or cognitive impairment. 5. History of peripheral facial paralysis. 6. Presence of intracranial tumors, metallic foreign bodies, or implanted cardiac pacemakers.

Design outcomes

Primary

MeasureTime frame
Facial muscle electromyographic activity;Facial symmetry;House-Brackmann grading system;Facial disability index;

Countries

China

Contacts

Public ContactDan Yuzhuo

Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China

yuzhuodan1207@outlook.com+86 186 8308 3611

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026