Using virtual reality for self-rehabilitation of facial paralysis

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the effectiveness of virtual reality as a self-rehabilitation tool for patients suffering from peripheral facial palsy and associated synkinesis. It aims to improve functional recovery through interventions that include massages, motor stimulation, stretching, and virtual reality exercises. The study targets patients who have experienced recent onset facial palsy and assesses their progress over time. By utilizing innovative technology, the study seeks to enhance traditional rehabilitation methods and provide a more engaging recovery experience.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patient with recent onset peripheral facial palsy (≤ 12 months).
* Patient with peripheral facial palsy of grade ≥ III on the House \& Brackmann score
* Patient of legal age (≥ 18 years)
* Patient with appropriate information and informed consent

Exclusion Criteria:

* Patient with central facial palsy
* Patient with peripheral facial palsy of \> 12 months onset
* Patient with peripheral facial palsy of grade \< III House \& Brackmann score
* Patient who has previously undergone palliative surgery
* Patient undergoing a botulinum toxin injection protocol
* Patients benefiting from enhanced protection, i.e. minors, persons deprived of their liberty by a judicial or administrative decision, persons staying in a health or social institution, adults under legal protection, pregnant or breast-feeding women and patients in emergency situations
* Patients who have not provided informed consent
* Patients with cognitive disorders that do not allow them to follow the proposed self-education protocol
* Blind or visually impaired patients (visual acuity of the better eye after correction ≤ 4/10)

Where it's running

• CHU Amiens Picardie
  Amiens, Picardie, France Recruiting

Study contacts

• Study coordinator: François-Régis SARHAN
• Email: sarhan.francois-regis@chu-amiens.fr
• Phone: 03 22 45 59 93

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.