Eval EarlySense Bet Lowenstein Sleeplab

EarlySense

Status: Withdrawn

Conditions: Sleep Disorders; Obese; Sleep Apnea, Obstructive; Central Apnea; Poor Quality Sleep

Study type: Observational

Funder types: Industry

Identifiers

NCT01978340

ES-CLC-2013_Prot_1

Details and patient eligibility

About

The study objective is to collect heart rate, respiration rate and motion data of patients admitted to sleep lab and to determine the accuracy level of the EarlySense system vs. the monitors used in sleep lab (e.g., Polysomnography, respiratory belts, ECG, etc..) . Data regarding sleep condition, scoring and quality of sleep and in and out of bed status, patient turns will also be collected and compared to data collected by EarlySense contactless monitor. Different patient population will be monitored including obese, morbidly obese, patients with or without obstructive/central apnea, patients with or without arrhythmia as well as healthy population who arrive to sleep lab for general evaluation will be monitored

Full description

EarlySense sensors will be placed under the mattress of subjects who have been included in the study. The sensors will not be in any contact with the patient. Two sensors will be utilized and placed under the subject's chest and pelvis area. Accuracy of the sensors will be compared to each other and to the reference device.

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Age 18 years or above
2. Is willing to sign the consent form

Exclusion criteria

1. Age < 18 years
2. Is not willing to sign the consent form

Trial design

0 participants in 1 patient group

sleeplab

Description:

Sleep Lab examined, usualy with some obesity or sleeping disorders.