ClinicalTrials.Veeva

Menu

The Anti-snoring Bed

F

Federal Institute of Technology (ETH) Zurich

Status

Completed

Conditions

Snoring

Treatments

Device: Anti-snoring bed

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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..

Enrollment

22 patients

Sex

All

Ages

18 to 100 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

22 participants in 2 patient groups

Baseline
No Intervention group
Description:
Participants slept in the anti-snoring bed in the laboratory, but the bed did not provide any intervention
Anti-snoring Intervention
Experimental group
Description:
Participants slept in the anti-snoring bed in the laboratory, and the bed moved the trunk of the participant
Treatment:
Device: Anti-snoring bed

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems