Facial Paralysis Clinical Trials

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Evaluation of the Effectiveness of Virtual Reality Self-rehabilitation in the Treatment of Facial Paralysis and Synkinesis

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Peripheral facial palsy affects 15 to 40 people per 100,000 inhabitants and induces important functional and social repercussions. Synkinesis is a frequent after-effect of facial palsy recovery, consisting of involuntary facial spasms that disturb the gestural harmony and can go as far as a painful hypertonic spasm. More than 55% of patients recovering from facial palsy will develop transient or permanent synkinesis. These facial hypertonias have two main causes: imperfect axonal regeneration, which is all the more important as the damage is proximal, and hyperexcitability of the facial nerve nucleus due to a lack of central control. Management is therefore essential for the functional restoration of the face, especially since synkinesis do not evolve spontaneously. The main treatments are currently botulinum toxin injection, acting on the motor plate, and functional rehabilitation, consisting on local muscle relaxation and central motor control work. In recent years, therapies based on biofeedback and acting on central motor control have shown interesting results, and technological advances in virtual reality have made it possible to deepen this treatment in patients suffering from stroke, limb trauma or Parkinson's disease. In this project, the investigators evaluate the contribution of virtual reality to the management of facial palsy, and hypothesize that self-rehabilitation using this technology will improve motor control of the skin muscles and reduce complications related to their hypertonia such as synkinesis.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
France
CHU Amiens Picardie
RECRUITING
Amiens
Contact Information
Primary
François-Régis SARHAN
sarhan.francois-regis@chu-amiens.fr
03 22 45 59 93
Time Frame
Start Date: 2022-08-02
Estimated Completion Date: 2029-08
Participants
Target number of participants: 100
Treatments
Experimental: Experimental arm
patients benefiting from rehabilitation associated with virtual reality
Active_comparator: Control arm
patients benefiting from rehabilitation without virtual reality
Sponsors
Collaborators: University Hospital, Rouen
Leads: Centre Hospitalier Universitaire, Amiens

This content was sourced from clinicaltrials.gov