Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID05581680

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

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Data Collection

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

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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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