Actively Recruiting
Intensive Care Decision-making, Survival and Dying Well
Led by University of Manchester · Updated on 2025-01-16
50
Participants Needed
1
Research Sites
117 weeks
Total Duration
On this page
Sponsors
U
University of Manchester
Lead Sponsor
T
The Royal College of Anaesthetists
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this study is to investigate how the experiences of intensive care patients and their end-of-life wishes affect their willingness to accept intensive care treatment at different chances of survival. The main questions it aims to answer are: * What can ICU survivors' experiences of ICU treatment tell us about what it would be like to die whilst receiving ICU treatment? * How do ICU survivors' reflections about what it might be like to die on ICU relate to their own preferences for their end-of-life care? * What chance of survival would make ICU survivors willing to go through ICU treatment again, in light of the fact that the alternative chance is dying whilst experiencing ICU treatment? * How does the possibility of reduction in health-related quality of life and functional decline as a result of critical illness impact ICU survivors' willingness to accept ICU treatment again? Participating in this study will involve filling out a questionnaire and then taking part in an interview. Participants will be recruited through ICU review clinics and ICU steps groups. The study will last for two years and will be conducted at locations convenient to the participants or via zoom.
CONDITIONS
Official Title
Intensive Care Decision-making, Survival and Dying Well
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be 18 years or older
- Have previously been a patient on an intensive care or critical care unit
- Be willing to discuss experiences of intensive care treatment and end-of-life wishes
- Be willing to meet in person or have access to a device with video and stable internet for Zoom conversations
You will not qualify if you...
- Under 18 years of age
- Had a planned admission to an intensive care or critical care unit (e.g., after elective surgery)
- Unable to consent to participate in the research
- Have a significant language barrier without available translation support
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Manchester
Manchester, United Kingdom, M13 9PL
Actively Recruiting
Research Team
T
Thomas M Donaldson, MB/BChir
CONTACT
S
Soren Holm
CONTACT
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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