Trends in Low-Value Health Service Use and Spending in the US Medicare Fee-for-Service Program, 2014-2018.
John N Mafi, Rachel O Reid, Lesley H Baseman...
https://pubmed.ncbi.nlm.nih.gov/33591365/Actively Recruiting
Led by Karolinska Institutet · Updated on 2025-12-02
10000
Participants Needed
2
Research Sites
52 weeks
Total Duration
Researchers are evaluating the introduction of the Choosing Wisely campaign in intensive care units ICUs to determine if it can be used without harming critically ill patients. This campaign aims to reduce unnecessary diagnostic testing, which is common in ICUs and contributes to high healthcare costs. The study focuses on adult patients treated in Swedish ICUs and assesses whether this new care strategy affects 30-day mortality and other important clinical outcomes. The study compares two groups one following the Choosing Wisely protocol, which minimizes the number of arterial blood gases, venous tests, and chest x-rays, and the other receiving regular ICU care without this protocol. It is a registry-based cluster randomized controlled trial involving multiple Swedish ICUs. The study phases include a control period and an intervention period, with monitoring of diagnostic test use during both phases. Participants outcomes will be tracked using the Swedish Intensive Care Register, focusing on 30-day mortality as the primary outcome. Secondary outcomes include ICU length of stay, time on invasive and non-invasive mechanical ventilation, time on continuous renal replacement therapy, and unplanned ICU readmissions within 72 hours. Data collection for outcomes may extend up to one year after ICU admission, allowing comprehensive monitoring of patient safety and resource use.
CONDITIONS
Wise Choices in the Intensive Care Unit
M
Max B Bell, MD, PhD
E
Emma Larsson, MD, PhD
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here
Karolinska Institutet
Lead Sponsor
Uppsala-Örebro Regional Research Council
Collaborating Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Participants 18 years or older treated in Swedish ICUs are eligible.
Duration - Duration of ICU stay, up to one year after ICU admission
Participants receive either the Choosing Wisely protocol, which aims to minimize the number of arterial blood gases, venous tests, and chest x-rays, or regular critical care in the ICU.
Clinical monitoring during ICU stay and assessments at 6 and 12 months
Duration - Up to one year after ICU admission
Participants are monitored for outcomes including 30-day mortality, ICU length of stay, time on mechanical ventilation, continuous renal replacement therapy, and unplanned ICU readmissions within 72 hours of discharge.
Outcomes assessed using registry data; no additional visits required
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
SEQUENTIAL
Primary Purpose
TREATMENT
Number of Arms
2
Have more questions? Get in touch with our team for quick support
John N Mafi, Rachel O Reid, Lesley H Baseman...
https://pubmed.ncbi.nlm.nih.gov/33591365/Thomas Bodley, Olga Levi, Maverick Chan...
https://pubmed.ncbi.nlm.nih.gov/36657786/William H Shrank, Teresa L Rogstad, Natasha Parekh
https://pubmed.ncbi.nlm.nih.gov/31589283/Jerry J Zimmerman, Lori A Harmon, Pamela L Smithburger...
https://pubmed.ncbi.nlm.nih.gov/33555779/Scott D Halpern, Deborah Becker, J Randall Curtis...
https://pubmed.ncbi.nlm.nih.gov/25271745/Adam C Salisbury, Kimberly J Reid, Karen P Alexander...
https://pubmed.ncbi.nlm.nih.gov/21824940/Alicia Costante, Xi-Kuan Chen, Alexey Dudevich...
https://pubmed.ncbi.nlm.nih.gov/36826234/Karolinska Institutet
Lead Sponsor
Uppsala-Örebro Regional Research Council
Collaborating Sponsor