Digital Smart Hub for Advanced Connected Care - DISTANCE

• Conditions: T88.8; T80.8; T88.5; Other specified complications of surgical and medical care, not elsewhere classified; Other complications following infusion, transfusion and therapeutic injection; Other complications of anaesthesia

• Registration Number: DRKS00030055
• Lead Sponsor: niversitätsklinikum der RWTH Aachen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-04-25
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 1000

Inclusion Criteria

All surviving patients who required an ICU stay > 72 hours or being mechanically ventilated for >24 hours.

Exclusion Criteria

Age below 18 years, patient that cannot give informed consent; Pregnancy

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Availability of complete, analyzable post ICU data from more than 25% of all discharged ICU patients over 12 weeks.

Secondary Outcome Measures

Name	Time	Method
It is expected to have a clearly reduced frequency of re-visits to the GP.<br>Compared to baseline assessment at ICU discharge, reduction of cognitive, emotional and physical<br>symptoms will be expected to be 20%.