contactless breathing motion
Conditions
Interventions
Group 1: The main purpose of this prospective data collection study is to collect data (RGB and depth images) from healthy volunteers obtained via a 3D camera integrated into a commercially released X
CE marked device, FDA cleared device) and, as a reference, from a commercially released breathing belt (Philips Respironics Alice NightOne
CE marked and FDA cleared device). Volunteers will stand in several positions in front of a wallstand detector and are asked to do free breathing and breathhold maneuvres. This will be done in several
Sponsors
Philips Medical Systems DMC GmbH
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: • Apparently healthy volunteers • Age between 18 and 70 years • BMI between 16 and 40 kg/m² • Subject is able to read, write, and follow instructions in simple German language • Subject provides informed consent for the study
Exclusion criteria
Exclusion criteria: • Vulnerable populations (e.g., age 70 years, not able to consent by themselves, immunocompromised, or pregnant women) • Inability/Refusal to stand for at least 10 mins to 15 mins • Inability/Refusal to wear a breathing sensor belt during the study • Inability/ Refusal to follow simple instructions with respect to controlling ones breathing pattern • Inability/Refusal to maintain a certain posture or pose during the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective of this study is to collect data with the intent to later3 evaluate the agreement of the contactless measurement of the breathing motion using the 3D-camera-based Breathing Monitor, with the existing breathing belt device as reference. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary objectives of this study are to: • collect data to test the technical limitations of the Breathing Monitor approach, e.g. long hair, clothing, positioning technique (hands on handles or on hips), patient motion, • collect data for future development of user assistance functions for stitching exams and ankle and knee radiography exams on the table • collect data for general R&D purposes by DXR BU, related to workflow improvements in Philips’ X-ray systems. | — |
Countries
Germany
Contacts
Public ContactNataly Wieberneit
Philips Medical Systems DMC GmbH
Outcome results
None listed