Evaluation of Chest Wall Motion Symmetry During Ventilation in Healthy Subjects by Optoelectronic Plethysmography
NCT ID: NCT06774118
Last Updated: 2025-01-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
100 participants
OBSERVATIONAL
2025-02-01
2025-12-31
Brief Summary
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Conventional spirometry, the gold-standard reference method in ventilatory analysis, allows to measure the quantities of air mobilized at inspiration and expiration. This quantitative method does not provide information on the kinematics of the different areas of the thorax and abdomen involved during breathing.
Optoelectronic plethysmography (OEP) is a non-invasive technique for the analysis of the 3D motion of passive markers placed on the surface of the subject's chest, abdomen and back. This technique, validated as a reliable alternative to conventional spirometry, allows the combination of quantitative measurements of respiratory volumes with qualitative measurements of thoraco-abdominal kinematics. The OEP has the specificity of allowing to choose a segmentation of the trunk to analyze the kinematics of the different identified zones. The most commonly used method in research is segmentation into three compartments (pulmonary thoracic, abdominal and abdominal thoracic).
The OEP studies also suggested the use of segmentation in relation to the median plane of the body to compare the symmetry of the three compartments described above. This 6-compartment segmentation was rarely used in respiratory analysis to assess interventions such as surgery of pulmonary rehabilitation protocols. To our knowledge, there is no study in healthy subjects to assess the level of symmetry of pulmonary ventilation. This type of study is a fundamental preliminary step to be able to subsequently study the symmetry of the ventilatory kinematics in the case of pathologies giving deformities of the thorax, spine and abdomen (scoliosis for example).
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
CROSS_SECTIONAL
Study Groups
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healthy subjects
Consenting healthy subjects with no previous major surgical, traumatic or medical cardiopulmonary history.
Data collection
Data collection
Interventions
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Data collection
Data collection
Eligibility Criteria
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Inclusion Criteria
* with no prior major cardiopulmonary surgical, traumatic or medical history
* agreeing to participate in the study
Exclusion Criteria
* A major medical cardiopulmonary history included any pathology requiring hospital treatment or allopathic therapy lasting more than 3 months.
* Active smoker
* Protected by law (guardianship, curatorship, safeguard of justice)
* Refusing to take part in the study
10 Years
70 Years
ALL
No
Sponsors
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Université de Reims Champagne-Ardenne
OTHER
Responsible Party
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Central Contacts
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Other Identifiers
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2024_RIPH_21_EVAST
Identifier Type: -
Identifier Source: org_study_id
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