The Anti-snoring Bed

NCT ID: NCT04053738

Last Updated: 2019-08-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

22 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-01-01

Study Completion Date

2018-07-01

Brief Summary

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Habitual snoring is a widespread complication. Most snorers snore predominately when sleeping in supine position. Therefore, therapeutic interventions force snorers to avoid supine position. Devices that restrict the sleeping position or raise alarms when the user obtains the supine position cause discomfort or disrupt sleep resulting in low compliance. Therefore, anti-snoring mechanisms, which lift the trunk of the user without disturbing sleep, have been proposed.

We set out to investigate whether individual interventions provided by beds with lifting mechanisms are able to stop snoring within three minutes (success rate) and whether the bed reduces the snoring index (number of total snores divided by total time in bed). In addition, we investigat whether the trunk elevation provided by the bed is interfering with the subjective sleep quality assessed using the Groningen Sleep Quality Score.

Subjects are observed for four nights (adaptation, baseline, and two intervention nights). During intervention nights, the bed lifts the trunk of the user in closed-loop manner. Subjects are divided in three groups (non-snorers, snorer group one, and snorer group two). Non-snorers are lifted by the bed at random time points during the night. In snorer group one, a stepwise increase of the bed inclination is compared with going directly to a randomly selected angle. In snorer group two, the influence of a small inclination angle (10°) and a big inclination angle (20°) is compared..

Detailed Description

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Conditions

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Snoring

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants
Participants were not informed prior to going to bed whether the night would be an intervention night or not

Study Groups

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Baseline

Participants slept in the anti-snoring bed in the laboratory, but the bed did not provide any intervention

Group Type NO_INTERVENTION

No interventions assigned to this group

Anti-snoring Intervention

Participants slept in the anti-snoring bed in the laboratory, and the bed moved the trunk of the participant

Group Type EXPERIMENTAL

Anti-snoring bed

Intervention Type DEVICE

The mattress shape is adjusted using a custom made intelligent anti-snoring bed, which is able to detect snoring sound and change the position of the user whenever snoring occurs.

Interventions

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Anti-snoring bed

The mattress shape is adjusted using a custom made intelligent anti-snoring bed, which is able to detect snoring sound and change the position of the user whenever snoring occurs.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* none

Exclusion Criteria

* Pregnancy
* Previously diagnosed sleep-related breathing disorders
* Chronic lower back pain
* Heart insufficiency that might impede sleeping in supine position
* Inability to follow the procedures of the study, e.g. due to language problems
Minimum Eligible Age

18 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Zurich

OTHER

Sponsor Role collaborator

Swiss Federal Institute of Technology

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Robert Riener, Prof. Dr. Dr.-Ing.

Role: PRINCIPAL_INVESTIGATOR

University of Zurich

Locations

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Sensory-Motor Systems Lab, ETH Zurich

Zurich, , Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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ASB

Identifier Type: -

Identifier Source: org_study_id

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