Comparison of Methodology Proposed by the SFAR for the Detection by Videoconference of Obstructive Sleep Apnea.
The Aim of This Study is to Determine the Accuracy of the Self-reported Parameters (Compared to Measurement Performed by the Physician) and the Influence of OSA Screening Scores.
1 other identifier
observational
210
0 countries
N/A
Brief Summary
The SFAR (French society of anesthesiology and ICU) proposed a method to detect OSA (Obstructive Sleep Apnea) patients via videoconference. The aim of this study is to compare the result of this method with the results of polysomnography (PSG) which remains the gold standard in the detection of OSA patients.
Trial Health
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participants targeted
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Started Nov 2024
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Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 24, 2023
CompletedFirst Posted
Study publicly available on registry
February 3, 2023
CompletedStudy Start
First participant enrolled
November 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedApril 23, 2024
April 1, 2024
11 months
January 24, 2023
April 22, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
Validation of the method proposed by the SFAR by comparison with results of polysomnography.
Validation (or not) of the method proposed by the SFAR to detect OSA patient va videoconference. The SFAR proposed a method to detect OSA patients throughout a videoconference. This method consists in requesting the patient to go around his neck with his two hands. However, this method has not been validated. The outcome of the study is to validate or invalidate the method proposed by the SFAR in comparison with the results of polysomnography (which remains the gold standard for the diagnosis of OSA patients).
1 month
Study Arms (1)
All patients
Patients in this group will serve to validate the accuracy of the French method to detect OSA patients in comparison with PSG results.
Interventions
We will validate the accuracy of the method proposed by the SFAR to detect OSA patients via videoconference (in comparison with the results of the PSG).
Eligibility Criteria
Population to validate the method proposed by the SFAR to detect OSA patients via videoconference.
You may qualify if:
- All patients admitted in the Clinique Saint-Luc of Bouge for a polysomnography
You may not qualify if:
- Patient's refusal
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Asteslead
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Eric Deflandre, MD, PhD
Astes
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Head of Department
Study Record Dates
First Submitted
January 24, 2023
First Posted
February 3, 2023
Study Start
November 1, 2024
Primary Completion
September 30, 2025
Study Completion
December 31, 2025
Last Updated
April 23, 2024
Record last verified: 2024-04
Data Sharing
- IPD Sharing
- Will not share