Actively Recruiting
Strengthening Hope After ICU Discharge
Led by Oslo University Hospital · Updated on 2024-09-19
75
Participants Needed
3
Research Sites
311 weeks
Total Duration
On this page
Sponsors
O
Oslo University Hospital
Lead Sponsor
V
Vestre Viken Hospital Trust
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to evaluate an interventional program that aims to strengthen hope in intensive care unit (ICU) patients in the rehabilitation phase. The main questions it aims to answer are: To develop and implement a follow-up service to strengthen hope in ICU patients, and to evaluate the effect on hope in a stepped wedge randomized trial. To identify possible predictive factors (facilitators and barriers) associated with hope. Participants will be asked to take part in an ICU follow-up service, a "Hope Intervention" consisting of digital individual- and group conversations. The program will address topics that are important for hope, such as active involvement, social relationships, believes and thoughts of the future. We will compare the level of hope between participants who have completed the "Hope Intervention" to those that have not yet completed the program.
CONDITIONS
Official Title
Strengthening Hope After ICU Discharge
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18 years or older
- ICU stay longer than 48 hours
- Able to communicate verbally just after ICU stay
- Able to handle digital meetings
You will not qualify if you...
- Severe cognitive impairment
- Do not understand or speak Norwegian
- Major psychiatric challenges or suicidal attempts as reason for ICU stay
- Age over 85 years
AI-Screening
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Trial Site Locations
Total: 3 locations
1
Vestre Viken HF, Bærum Hospital
Drammen, Akershus, Norway
Not Yet Recruiting
2
Diakonhjemmet Hospital
Oslo, Norway
Not Yet Recruiting
3
Oslo University Hospital
Oslo, Norway
Actively Recruiting
Research Team
K
Kristin W Sunde, Msc
CONTACT
H
Hanne Birgit Alfheim, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
5
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