Pilot study on contactless sleep monitoring of patients with different sleep disorders based on three-dimensional video signal and audio signal analysis (Kinect)

Not Applicable

• Conditions: G47.31; G25.81

• Registration Number: DRKS00009347
• Lead Sponsor: Charité-Universitätsmedizin Berlin, Interdisziplinäres Schlafmedizinisches Zentrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2015-11-27
• Study Completion: 2016-11-20
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

sex: male and female
- minimum age: 18 years
- maximum age: 70 years
- healthy sleep (control group) or
presence of one of the following diagnoses:
orestless legs syndrome
oobstructive sleep apnea
- comprehension of the study protocol
- written consent

Exclusion Criteria

- severe heart failure
- severe respiratory failure
- home ventilation (BiLevel or higher)
- acute psychiatric disorder like severe depression, - mania or psychosis
- body mass index > 40
- pregnancy
s- leep disorders (only relevant to control group)

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Comparison of the data on night time movements that are collected with Video-KinectTM with the parameters of polysomnography regarding to depth of sleep, quality of sleep and sleep disturbance.

Secondary Outcome Measures

Name	Time	Method
Compilation of a sleep profile (awake/sleep) based on the data of Kinect and comparison of these profile with the sleep profile that is calculated with polysomnography or actigraphy.