Digitalized Clinical Decision Support for the Prevention of Postoperative Delirium (POD)

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The project aims to improve patient safety, reduce barriers to the implementation of current guideline recommendations, reduce workload in clinics, increase efficiency in work processes and close gaps in care. Subprojects regarding delirium are implementes as well.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 70
Healthy Volunteers: f
View:

• Age ≥ 70 years

• Male and female patients

• Patients who are insured through statutory health insurance

• Patients capable of giving consent for inclusion: by the patient, preoperatively

• Patients under guardianship for inclusion: written declaration of consent by guardian

• Operation (elective)

• Age ≥ 18 years

• Male and female relatives

• Relatives capable of giving consent for inclusion

• All inpatients ≥ 18 years of age who have undergone delirium screening with a validated delirium screening instrument

Locations
Other Locations
Germany
Institut für Anästhesiologie und Schmerztherapie-Herz- und Diabeteszentrum NRW- Universitätsklinik der Ruhr-Universität Bochum
RECRUITING
Bad Oeynhausen
CARITAS Klinik Maria Heimsuchung
RECRUITING
Berlin
Department of Anaesthesiolgy and Intensive Care Medicine CCM/CVK, Charite- University Berlin
RECRUITING
Berlin
Klinikum im Friedrichshain - Vivantes - Netzwerk für Gesundheit GmbH
RECRUITING
Berlin
Contact Information
Primary
Claudia Spies, MD, Prof.
claudia.spies@charite.de
+49 30 450 55 11 02
Time Frame
Start Date: 2024-06-03
Estimated Completion Date: 2026-07-30
Participants
Target number of participants: 800
Treatments
No_intervention: Control phase
Control phase: in this phase, all study patients receive the standard therapy of the respective study center.
Experimental: Intervention phase
In this phase, the intervention with Digi-POD is made available as Clinical Decision Support System. The intervention consists of providing patients, relatives and caregivers with Digi-POD decision support for the prevention of delirium and treatment decisions for delirium in accordance with the recommendations from the guidelines in addition to the standard therapy of the respective study center.
Related Therapeutic Areas
Sponsors
Collaborators: Freie Universität Berlin, Universitätsklinik der Ruhr-Universität Bochum, BARMER, Technische Universität Berlin
Leads: Charite University, Berlin, Germany

This content was sourced from clinicaltrials.gov