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Research on the Evolution, Geometry, and Alterations of the Periorbital Region Based on Age and Deformations (REGARD)

C

Centre Hospitalier Universitaire, Amiens

Status

Not yet enrolling

Conditions

Aging
Periorbital Region
Facial Skin
Motion Capture
Vertical Jump
Skin Movement

Treatments

Other: MoCap

Study type

Interventional

Funder types

Other

Identifiers

NCT07080320
PI2025_843_0101

Details and patient eligibility

About

The periorbital region of the face is a critical area affected by aging. Motion Capture (MoCap) allows the precise measurement of the mechanical properties of skin in this region. This study will validate MoCap as a tool for quantifying these properties, comparing it to traditional reference tools, and exploring how these properties evolve with age and external treatments. It will also assess MoCap's ability to detect the effects of various treatments such as tightening products and massages. Ultimately, this research will provide a deeper understanding of skin dynamics in the periorbital region and offer insights into both medical and cosmetic applications.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Female participants
  • Caucasian, Fitzpatrick skin types I-III
  • BMI between 18.5 and 27, healthy participants
  • Aged 18 to 65 years (inclusive)
  • Not under guardianship or curatorship
  • Informed written consent
  • Social security affiliation
  • Non-smokers for at least 5 years
  • No excessive UV exposure (artificial or natural) in the last 3 weeks prior to the study or during the study

Exclusion criteria

  • Severe skin disorders preventing the application of electrodes or photo-reflective markers
  • Neurovascular history affecting the face
  • Ongoing treatments influencing facial tissues (e.g., corticosteroids)
  • Current sleep disorders
  • Psychiatric conditions or social interaction impairments
  • Inner ear or balance disorders
  • Osteoporosis, recent fractures, or fragile bone conditions
  • Pregnant or breastfeeding women
  • Under guardianship, curatorship, or legal protection

Trial design

Primary purpose

Other

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

subjects aged 18-33 years
Experimental group
Treatment:
Other: MoCap
subjects aged 50-65 years
Experimental group
Treatment:
Other: MoCap

Trial contacts and locations

1

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Central trial contact

Stéphanie Dakpé, Pr

Data sourced from clinicaltrials.gov

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