Actively Recruiting
Multimodal Quantified Analysis of Facial Movements Comparing Patients with Facial Palsy and Healthy Volunteers
Led by Centre Hospitalier Universitaire, Amiens · Updated on 2025-05-28
720
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying facial palsy, a condition with various causes that can affect facial movement and quality of life. This trial aims to measure facial muscle activity and movement using surface electromyography (sEMG) and motion capture technology. Additionally, eye-tracking will be used to observe how patients view their facial condition and relate it to their treatment outcomes. The study compares these measurements between patients with facial palsy and healthy volunteers. Participants include healthy volunteers and patients with peripheral facial palsy, regardless of severity or prior treatment. The study involves several procedures like dental impressions, simultaneous motion capture and electromyography recordings, eye-tracking for patients, and follow-up visits. These methods will help quantify facial movement and eye gaze patterns over time. During the study, participants will undergo baseline measurements over one month for healthy volunteers and up to one year for patients. Researchers will track the maximum range of facial movement and eye-tracking data to analyze treatment effects and patient responses. Participants must provide informed consent and be monitored throughout to ensure accurate and safe data collection.
CONDITIONS
Brief Title
Multimodal Quantified Analysis of Facial Movements: Comparison Between Pathological and Control Subjects
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Subjects with no known facial pathology (healthy volunteers) OR patients with peripheral facial palsy, regardless of severity or prior treatment
- Subjects aged 18 years or older
- Subjects must provide written informed consent
- Subjects must be affiliated with a social security scheme
You will not qualify if you...
- Subjects with severe skin disorders preventing application of electrodes or reflective markers
- Subjects with speech disorders making it impossible to pronounce the sounds 'o' and 'pu'
- Subjects unable to provide written informed consent
- Subjects under guardianship, curatorship, or safeguard of justice
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 year
Participants undergo dental impressions and simultaneous motion capture (MoCap) and electromyography (EMG) acquisition. Pathological subjects also have eye-tracking acquisition.
1 baseline visit and 1 follow-up visit for pathological subjects
Trial Site Locations
Total: 1 location
1
CHU Amiens Picardie
Amiens, Picardie, France, 80054
Actively Recruiting
Research Team
S
Stéphanie Dakpé, Pr
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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