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Recruiting NCT05581680

NCT05581680 Multimodal Quantified Analysis of Facial Movements: Comparison Between Pathological and Control Subjects

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Clinical Trial Summary
NCT ID NCT05581680
Status Recruiting
Phase
Sponsor Centre Hospitalier Universitaire, Amiens
Condition Electromyography
Study Type INTERVENTIONAL
Enrollment 720 participants
Start Date 2022-10-12
Primary Completion 2027-10

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
dental impressionsSimultaneous MoCap and EMG acquisitionEye-tracking acquisition for pathological subjects

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 720 participants in total. It began in 2022-10-12 with a primary completion date of 2027-10.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The facial palsy is a frequent disease with a lot of etiologies. It has variable severities with sometimes heavy functional repercussions and different recovery potentials. The proposed treatments are based on surgery, physiotherapy and botulinum toxin injections. However, when recovery is incomplete, acceptance is more difficult, with an impacted quality of life. Thanks to Motion Capture and Electromyography, a quantification of the facial mimicry is now possible with a great precision. In addition with the quantification of the facial mimicry, eye-tracking, wich is widely used in the marketing field, but it also finds medical applications including head and neck lesions and facial palsy in particular, will be used to evaluate the visio of the patients on their pathology in function of the movement quantification measured with MoCap and Electromyography. The aim of this research is to measure in a combined way the action potentials by sEMG and the amplitudes of displacement of the markers in motion capture, for movements determined in a population of patients presenting a facial pathology, in order to compare them with reference values obtained in healthy subjects. In a second step, the aim will be to study if there is a link between the way the patient looks at his pathology and the results of his management (treatment, rehabilitation) which will be quantitatively evaluated thanks to MoCap and sEMG.

Eligibility Criteria

Inclusion Criteria: * Subjects with no known facial pathology (healthy volunteers) OR * Patients with peripheral facial palsy, irrespective of grade, whether or not previously treated * Subject with written informed consent * Subject over 18 years of age * Subject affiliated to a social security scheme Exclusion Criteria: * Subjects with severe skin disorders that do not allow the application of electrodes or photo reflective markers * Subjects with speech disorders making it impossible to pronounce the sounds \[o\] and \[pu\] * Subject unable to provide written informed consent * Subjects under guardianship, curators or safeguard of justice

Contact & Investigator

Central Contact

Stéphanie Dakpé, Pr

✉ dakpe.stephanie@chu-amiens.fr

📞 03 22 08 90 50

Frequently Asked Questions

Who can join the NCT05581680 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Electromyography. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05581680 currently recruiting?

Yes, NCT05581680 is actively recruiting participants. Contact the research team at dakpe.stephanie@chu-amiens.fr for enrollment information.

Where is the NCT05581680 trial being conducted?

This trial is being conducted at Amiens, France.

Who is sponsoring the NCT05581680 clinical trial?

NCT05581680 is sponsored by Centre Hospitalier Universitaire, Amiens. The trial plans to enroll 720 participants.

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