Predictability of OSA With a Subjective Screening Scale (OSASSS1)

Center for Sleep Medicine - Clinique André Renard

Status: Completed

Conditions: OSA; Obstructive Sleep Apnea

Treatments: Diagnostic Test: neuro-sensorial subjective evaluation of the airways collapsibility

Study type: Observational

Funder types: Other

Identifiers

NCT06092710

OSASSS1

Details and patient eligibility

About

the study aims to evaluate the accuracy correlation between subjective perception of the air flow through airways from patients and survey and/or polysomnography they spent, using a brief clinical protocol they answered with a manual therapist

Full description

The subjects in the study are 18 to 77 years old and present the following conditions:

• polysomnography and sleep survey realized at the Center for Sleep Medicine André RENARD, without any informations of the results for the experience group
• sleep survey with no sleep trouble found for the control group

Enrollment: 112 patients

Sex: All

Ages: 18 to 77 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Female or male subjects aged 18 to 77 years old
• subjects who have performed a PSG at the sleep medicine center André Renard for the study group
• subjects with no sleep disorder on sleep survey for the control group
• Subjects who agree to comply with the requirements of the study.
• Subjects who are of age (and know how to read and write) who have given their informed, explicit consent in advance to any procedure related to the trial, the study or the investigation conducted on human beings, with the objective of developing knowledge specific to the exercise of health care professions, as set out in Royal Decree No. 78 of 10 November 1967 on the practice of the health care professions (Act of 27 December 2005)

Exclusion criteria

• subjects with acute infections
• subjects with trauma within the last 72 hours
• subjects who already benefit from OSA treatment
• subjects with known perceptual disorders, for example post-stroke
• subjects with current or recent chemotherapy and radiotherapy treatment
• Pregnant women
• Criteria related to prior or concurrent treatments:

Treatment with antipsychotics, anxiolytics, soporifics or muscle relaxants started within the two months preceding the study.

Treatment with intraoral implants during the study or in the two months preceding the study

Trial design

112 participants in 2 patient groups

study group with PSG and sleep survey

Description:

the study group will be recruited after their polysomnography but before its results, so patients and investigators will not have any data about Apnea Hypopnea Index (AHI) and sleep survey. they will experiment their subjective perception of air flow through their airways with the guidance of a manual therapist during a 15 minutes protocol

Treatment:

Diagnostic Test: neuro-sensorial subjective evaluation of the airways collapsibility

control group with sleep survey

Description:

the control group will be recruited after a sleep survey with no sleep disorder. they will experiment their subjective perception of air flow through their airways with the guidance of a manual therapist during a 15 minutes protocol

Treatment:

Diagnostic Test: neuro-sensorial subjective evaluation of the airways collapsibility