Sleep Quality Evolution: Dreem Under CPAP
Study Details
Study Description
Brief Summary
Continuous positive airway pressure (CPAP) has a caricatural effect in reducing nocturnal respiratory abnormalities and improving the micro-and macrostructure of sleep. Studies characterizing the improvement of acute sleep parameters after the initiation of CPAP are limited to one or two nights of polysomnographic recording. This is related to the cost of performing these studies with repeated recordings in the laboratory and to the acceptability by patients to perform multiple nights of recordings.
Investigators currently have powerful and reliable methods allowing us to carry out nights at home in the patient's ecosystem, in real-life conditions. The characterization of sleep parameters by these methods is equivalent to a polysomnographic recording.
These technological innovations will allow us to characterize sleep before the initiation of CPAP treatment during several nights performed at home. Investigators will then be able to characterize the kinetics and stability of the improvement of sleep parameters in patients with obstructive sleep apnea syndrome in whom continuous positive airway pressure is initiated.
These data will be original and will serve as exploratory data to judge whether the objective improvement of sleep parameters in the first weeks of treatment is associated with improvement in sleepiness, quality of life, and compliance with treatment.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
This study aims to evaluate the quality of sleep, principally the deep slow-wave sleep (sleep stage N3) before and after the initiation of continuous positive airway pressure (CPAP) treatment.
70 newly diagnosed patients with OSA requiring CPAP treatment, will be included.
For the study, they will wear the Dreem 3 headband and pulse oximeter at home before initiation of CPAP (for 7 nights) and during the first month of CPAP (for a minimum of 9 nights). They will be also equipped with a glucose sensor and a pedometer during the entire study period before and after CPAP treatment.
Patients will also complete questionnaires about their health status before CPAP treatment (at inclusion) and after one month of treatment
These devices will allow the measurements of different parameters: sleep stages, total sleep time, sleep measures derived from sleep stages, snoring, breathing rate, heart rate head movements, arterial hemoglobin oxygen saturation, pulse rate, continuous subcutaneous glucose level, and physical activity data (average daily steps, average distance walked per day).
This will generate interesting data on the sleep parameters and their evolution during the initiation of the CPAP treatment.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Technological innovations and CPAP Patients will be equipped with 4 devices: a Dreem 3 Headband, a pulse oximeter, a continuous glucose sensor, and a pedometer. In parallel they will be equipped by the CPAP at home by Icadom. |
Device: Deem 3 Headband
The patient will wear the Dreem 3 headband and pulse oximeter at home before initiation of CPAP (for 7 nights) and during a month of treatment (for a minimum of 9 nights), after the initiation of CPAP. He will also wear a glucose sensor and a pedometer during the entire study period before and after CPAP treatment.
|
Outcome Measures
Primary Outcome Measures
- Duration of deep slow-wave sleep (sleep stage N3) before and after initiation of continuous positive airway pressure (CPAP) treatment. [7 nights before CPAP initiation and for a month (minimum 9 nights) after CPAP initiation]
Time spent on the deep slow-wave sleep stage (stage N3 sleep), recorded by the Dreem 3 headband, from 7 nights before and 9 nights after initiation of CPAP treatment
Secondary Outcome Measures
- Duration of the other sleep stages (W, N1, N2 and REM) [7 nights before CPAP initiation and for a month (minimum 9 nights) after CPAP initiation]
Sleep stages (W, N1, N2 and REM) and total sleep time spent in each sleep stage, recorded by the Dreem 3. All the data units are in minutes
- Duration of different sleep times [7 nights before CPAP initiation and for a month (minimum 9 nights) after CPAP initiation]
Sleep parameters recorded by Dreem 3 headband: sleep times (bedtime, total sleep time (TST), sleep onset delay (SOD),time in bed (TIB), time awake after falling asleep (WASO), final wakefulness time)
- The percentage of time while sleeping [7 nights before CPAP initiation and for a month (minimum 9 nights) after CPAP initiation]
Sleep parameter recorded by Dreem 3 headband: sleep efficiency ((TST/TIB) x100)
- The frequences of sleep waves during the NREM sleep stage recorded by Dreem 3 headband [7 nights before CPAP initiation and for a month (minimum 9 nights) after CPAP initiation]
sleep spindle density expressed in Hertz recorded by the EEG sensors
- The frequence of snoring while sleeping recorded by Dreem 3 headband [7 nights before CPAP initiation and for a month (minimum 9 nights) after CPAP initiation]
snoring is expressed in decibel minute recorded by a microphone integrated in the Dreem3
- Respiratory rate measurment recorded by Dreem 3 headband [7 nights before CPAP initiation and for a month (minimum 9 nights) after CPAP initiation]
It is expressed in breathe per minute recorded accelerometer sensor
- Heart rate measurement while sleepingrecorded by Dreem 3 headband [7 nights before CPAP initiation and for a month (minimum 9 nights) after CPAP initiation]
Expressed in beats per minute recorded by accelerometer sensor
- The position of the head changes while sleeping recorded by Dreem 3 headband [7 nights before CPAP initiation and for a month (minimum 9 nights) after CPAP initiation]
Head movements are recorded by an accelerometer sensor in the Dreem 3 Headband
- Evolution of the nocturnal oximetry [7 nights before CPAP initiation and for a month (minimum 9 nights) after CPAP initiation]
Nocturnal oxygen saturation measured by a pulse oximeter
- Evolution of the subcutaneous glucose level [7 nights before CPAP initiation and for a month after CPAP initiation]
Continuous subcutaneous glucose level (measured by FreeStyle Libre 2 continuous glucose sensor)
- Evolution of glycemia [At inclusion and a month after CPAP initiation]
Blood glucose level by blood sampling
- Average daily number of steps [7 nights before CPAP initiation and for a month after CPAP initiation]
It will be measured by a Garmin Vivofit 3 pedometer expressed in steps/day
- Average distance walked per day [7 nights before CPAP initiation and for a month after CPAP initiation]
It will be measured by a Garmin Vivofit 3 pedometer expressed in Kilometer
- Sleep quality assessed by Pittsburg questionnaire [At inclusion and a month after CPAP initiation]
The PSQI includes a scoring key for calculating a patient's seven subscores, each of which can range from 0 to 3. The subscores are tallied, yielding a "global" score that can range from 0 to 21. A global score of 5 or more indicates poor sleep quality; the higher the score, the worse the quality.
- Severity of insomnia measured by the index sverety of insomnia questionnaire [At inclusion and a month after CPAP initiation]
The general ISI score varies between 0 and 28: -7 = No insomnia 8-14 = Sub-clinical insomnia (mild) 15-21 = Clinical insomnia (moderate) 22-28 = Clinical insomnia (severe)
- Evolution of the somnolence [At inclusion and a month after CPAP initiation]
Epworth Sleepiness Score (ESS): 0 = no chance of dozing or falling asleep = low chance of falling asleep = medium chance of falling asleep = high chance of falling asleep
- Evolution of the quality of life by the Short Form 36 health survey questionnaire [At inclusion and a month after CPAP initiation]
A score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability.
- Evolution of the compliance of CPAP treatment [For a month during CPAP treatment]
Collection of average CPAP treatment use (in hours/day) provided by telemonitoring
- Evolution of the effectiveness of CPAP treatment [For a month during CPAP treatment]
Collection of residual AHI provided by telemonitoring
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Patients newly diagnosed with OSA requiring CPAP treatment
-
Patients able to use a mobile application on a smartphone or tablet
-
Patients with access to a wi-fi internet connection at home
-
Patients agreeing to remote monitoring of CPAP compliance data by the home care provider
-
Patients who have signed consent to participate in the study
-
Subjects affiliated to a social security
Exclusion Criteria:
-
Patients already treated for OSA
-
Patients treated with a sleep aid (sleeping medications)
-
Patients with severe chronic obstructive or restrictive lung disease with or without oxygen
-
Patients with unstable cardiovascular disease or severe heart failure requiring hospitalization within the last three months or meeting New York Heart Association criteria, Class III or IV disease
-
Subjects listed in articles L1121-5 to L1121-8: pregnant women, feeding and parturients, subjects deprived of liberty by judicial or administrative decision, persons under legal protection
-
Persons in a period of exclusion from another study or ongoing participation in a drug study
-
Subjects likely, at the investigator's discretion, to be uncooperative or noncompliant with the obligations inherent to participation in the study
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Grenoble Alpes University Hospital | Grenoble | France |
Sponsors and Collaborators
- University Hospital, Grenoble
- Dreem
- AGIR à Dom
Investigators
- Principal Investigator: Jean Louis Pépin, MD, PhD, Grenoble Alpes University Hospital (CHUGA)
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 38RC21.0346