Applying Actigraphy to quantify delirium, withdrawal syndrome, and depth of sedation in childre

• Conditions: F13.4; F13.3

• Registration Number: DRKS00024532
• Lead Sponsor: Robert-Enke-Stiftung

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2022-06-17
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

Treatment in pediatric intensive care unit of Charité Universitaetsmedizin Berlin.

Exclusion Criteria

No limb available for Actigraphy.

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Primary aim of the study: identification of the most appropriate method for the analysis of raw actigraphic data

Secondary Outcome Measures

Name	Time	Method
Secondary aim of the study: Determination of the correlation of the quantity of patient movements (determined by different methods of raw actigraphic data analysis) with semiquantitative scores.