INMOTION study on contactless monitoring of vital signs in a sleep laboratory

INMOTION study on contactless monitoring of vital signs in a sleep laboratory - INMOTION

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00040061

Enrollment

500

Registered

2026-04-22

Start date

2026-01-19

Completion date

Unknown

Last updated

2026-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

G47

Interventions

Group 1: Prospective, interventional study. In addition to the routine measurement for therapeutic purposes (PSG), a second, non-invasive measurement is carried out for scientific purposes. The clini

Eligibility

Sex/Gender

All

Age

6 Months to 18 Years

Inclusion criteria

Inclusion criteria: Included are patients for whom a polygraph test or polysomnography has been ordered.

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

Measure	Time frame
The primary aim of the study is the AI-assisted analysis of measurement data for the contactless recording of vital signs. As part of an exploratory pilot study, AI models will be trained in order to conduct a preliminary assessment of the feasibility and methodology in children.	—

Countries

Germany

Contacts

Public ContactMatthias Jahn

Hochschule für angewandte Wissenschaften Landshut

matthias.jahn@haw-landshut.de+49 (0)871 - 506847

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 29, 2026