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.

Status

Not yet recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT05711329

Enrollment

210

Registered

2023-02-03

Start date

2024-11-01

Completion date

2025-12-31

Last updated

2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obstructive Sleep Apnea

Brief summary

Detailed 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.

Interventions

OTHERAccuracy

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).

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

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

Exclusion criteria

* Patient's refusal

Design outcomes

Primary

Measure	Time frame	Description
Validation of the method proposed by the SFAR by comparison with results of polysomnography.	1 month	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).

Contacts

Primary ContactEric Deflandre, MD, PhD

eric.deflandre@gmail.com003281209563

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026