Actively Recruiting

Age: 18Years - 100Years
All Genders
Healthy Volunteers
ID05765162

Safe Brain Initiative - Advancing Anaesthesia and Perioperative Personalized Care Through Continuous Quality Improvement

Led by University of Southern Denmark · Updated on 2024-06-07

15000

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

U

University of Southern Denmark

Lead Sponsor

N

Nykøbing Falster County Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to improve the care of patients undergoing surgery and anesthesia by monitoring and reducing side effects such as nausea, severe pain, anxiety, stress, postoperative delirium (POD), and neurocognitive dysfunctions. These issues can lead to long-term cognitive problems, lower quality of life, and higher mortality. The Safe Brain Initiative (SBI) collects high-quality routine data to help healthcare providers understand and reduce these adverse effects, supporting patient-centered and precision care. The SBI platform includes 18 core, non-invasive recommendations designed to detect and prevent adverse outcomes during perioperative care. SBI-Muda focuses on improving operating room efficiency, reducing delirium, and enhancing patient-reported outcomes by providing detailed feedback on hospital metrics like surgery timing and recovery durations. SBI-Us collects anonymous feedback from healthcare staff and patients to benchmark and improve the quality of care from both perspectives. Participants aged 18 and older will be involved in this observational study, during which data on patient well-being, side effects, and postoperative delirium will be collected. Healthcare professionals will receive systematic feedback to guide care improvements. The study measures include postoperative delirium and patient-reported outcomes throughout the perioperative period. Participation may last through the surgical and immediate recovery phases, with continuous quality improvement efforts ongoing.

CONDITIONS

Brief Title

Safe Brain Initiative, Operationalizing Precision Anaesthesia

Who Can Participate

Age: 18Years - 100Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • All patients aged 18 years and older
Not Eligible

You will not qualify if you...

  • Patients younger than 18 years

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Perioperative period

Participants who undergo routine perioperative care are observed with continuous quality improvement measures to detect and prevent adverse outcomes related to surgery and anaesthesia.

Visits occur as part of routine care during the perioperative period

Trial Site Locations

Total: 1 location

1

Nykøbing Falster Hospital

Nykøbing Falster, Denmark, 4800

Actively Recruiting

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Research Team

F

Finn M. Radtke, Professor

K

Karina Jakobsen, MCN

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Published Research Related To This Trial

A first assessment of the safe brain initiative care bundle for addressing postoperative delirium in the postanesthesia care unit.

Basak Ceyda Meco, Karina Jakobsen, Edoardo De Robertis...

https://pubmed.ncbi.nlm.nih.gov/38972091