Comparison of Methodology Proposed by the SFAR for the Detection by Videoconference of Obstructive Sleep Apnea.

Obstructive Sleep Apnea Clinical Trial

Official title:

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.

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT05711329
• Other study ID #: Visio-PSG
• Status: Not yet recruiting
• Start date: November 1, 2024
• Est. completion date: December 31, 2025

Study information

• Verified date: April 2024
• Source: Astes
• Contact: Eric Deflandre, MD, PhD
• Phone: 003281209563
• Email: eric.deflandre[@]gmail.com
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

Description:

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.

Other methods, such as a predictive score, also exist. The accuracy of the French method compared to PSG and the predictive scores is to be determined.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 210
• Est. completion date: December 31, 2025
• Est. primary completion date: September 30, 2025
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• All patients admitted in the Clinique Saint-Luc of Bouge for a polysomnography

Exclusion Criteria:

• Patient's refusal

Related Conditions & MeSH terms

• Obstructive Sleep Apnea
• Sleep Apnea Syndromes
• Sleep Apnea, Obstructive

Intervention

Other:
• Accuracy
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).

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Astes

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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