Skip to content

The effect of the Mirror Effect Plus protocol in acute Bell's palsy

Efficacy of the Mirror Effect rehabilitation in acute Bell’s Palsy: a pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN93896690
Enrollment
40
Registered
2020-11-25
Start date
2017-02-27
Completion date
Unknown
Last updated
2022-08-05

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

Conditions

Acute Bell's palsy Nervous System Diseases Bell palsy

Interventions

In the present study, the researchers are recruiting a small number of patients to be able to obtain an estimate of the effectiveness of the new therapy called “Mirror Effect”. The Mirror Effect thera

Sponsors

Centres Intégré Universitaires de Santé et de Services Sociaux
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 18 years and older 2. First episode of Bell's Palsy 3. Having persistent severe Bell's palsy 10 days post-onset 4. Received the recommended drug regimen for severe and total BP (1000 mg valacyclovir three times daily for 7 days and 50 mg prednisone once daily for 10 days) began within 72 hours of onset 5. Normal cognitive status based on the Montreal Cognitive Assessment

Exclusion criteria

Exclusion criteria: 1. History of trauma to the 7th cranial nerve 2. Having suffered from Bell's palsy previously or any other facial palsy of another origin (e.g. secondary to surgery or a syndrome 3. History of neurological disorders (e.g. stroke, neurodegenerative diseases) 4. Psychiatric illness on active treatment (e.g. schizophrenia, severe depression) 5. History of neoplastic diseases

Design outcomes

Primary

MeasureTime frame
Severity of facial palsy assessed using the Facial Nerve Grading System 2.0 (FNGS 2.0; also known as the House-Brackmann 2.0 score and the Sunnybrook Facial Grading System at the initial assessment (10 to 14 days after onset) as well as 1, 2, 3, 4, 5, 6 and 12 months after onset

Secondary

MeasureTime frame
Speech intelligibility measured using a visual analog scale at the initial assessment (10 to 14 days after onset) as well as 1, 2, 3, 4, 5, 6 and 12 months after onset

Countries

Canada

Contacts

Public ContactSarah Martineau
sarah.martineau.2@umontreal.ca+1 (0)514 338 2222 extension 7710

Outcome results

None listed

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