Actively Recruiting

Age: 18Years +
All Genders
ID06756542

Utilizing Large Language Models to Augment Family Conversations in the Intensive Care Unit

Led by Davy van de Sande · Updated on 2025-02-25

40

Participants Needed

2

Research Sites

17 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating how artificial intelligence (AI), specifically large language models like GPT-4, can help doctors in intensive care units (ICUs) save time and improve communication with families of adult patients. This observational study aims to see if AI-generated summaries of family conversations can reduce the time doctors spend documenting notes while making the information clearer and easier for families to understand. The study involves ICU doctors and adult family members of patients, all providing informed consent, and focuses on improving interactions in the ICU setting. During the study, family conversations occurring in Dutch will be observed and analyzed. Both the ICU healthcare professionals and participating family members must provide consent. The study does not involve experimental treatments but observes the use of AI technology in documenting these conversations. There are no specified intervention groups or treatments being administered. Participants will be involved in family conversations documented by ICU staff, with researchers assessing the quality of documentation within 30 days after each conversation. They will also measure the time ICU clinicians spend on documentation within one day following the conversation and evaluate family satisfaction within 30 days. The study focuses on adult patients admitted to the ICU and their families, with data collection centered on communication and documentation practices rather than clinical treatment.

CONDITIONS

Brief Title

Evaluating the Use of Artificial Intelligence to Improve Family Conversations for Intensive Care Patients and Their Families

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Informed consent is signed by all participating family members during the conversation
  • Informed consent is signed by the ICU healthcare professionals
  • The patient of the family must be admitted to the adult ICU
  • All participating family members must be 18 years or older
  • The family conversation must be in Dutch
Not Eligible

You will not qualify if you...

  • Trained to interpret medical jargon and/or intensive care terminology specifically
  • Difficulty reading and/or writing in the Dutch language

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Monitoring

Duration - Up to 30 days after the family conversation

Participants who undergo routine care are observed during family conversations in the intensive care unit.

1 family conversation observation and follow-up within 30 days

Trial Site Locations

Total: 2 locations

1

Erasmus University Medical Center

Rotterdam, South Holland, Netherlands, 3015GD

Not Yet Recruiting

2

Erasmus University Medical Center

Rotterdam, Netherlands, 3015GD

Actively Recruiting

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Research Team

D

Davy van de Sande, PhD

M

Michel E. van Genderen, MD PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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