Frequently Asked Questions (FAQ)

A clinical trial is a research study that tests treatments. To compare treatments, clinical trials often assign patients or treatment centers to a specific treatment approach. Clinical trials may help doctors answer many questions about diseases and their treatments.

This trial is being done to see if two different strategies help ICU teams follow the ABCDEF bundle and improve patient outcomes. The two strategies are: 

• An ICU dashboard that reminds ICU teams when they need to do something for a patient.
• A nurse facilitator who helps the ICU team with tasks.

If you have any questions or concerns about this trial, please contact the Project Coordinator at this phone number: 402-559-4345

You are included in this trial because your ICU has agreed to participate. Like all other patients in this ICU who meet the following criteria, you will be part of this trial unless you choose not to participate. We will collect data on all patients in this unit who are:

1. Over 19 years old at the time of ICU admission.
2. Receiving invasive mechanical ventilation in the ICU.
3. Staying in the ICU for at least 24 hours.

All patients in this trial will keep getting the care ordered by their ICU providers. Depending on when you are admitted, your ICU will randomly receive either a dashboard or a nurse facilitator.

Your participation in this study will be for as long as you are in the hospital.

If you move to another ICU, they might not be part of the BEST ICU study. We will continue to include you in the study, but the new ICU may not have the dashboard or RN facilitator. If you do not want your information included in the study after you move, please call the number below.

There is a risk that your information could be seen by people other than the researchers. Keeping your data private is very important to us, and we will do everything we can to keep all information collected in this trial confidential.

There is no direct benefit from participating in this research. However, the findings from this trial could help patients in the future.

You are being included in this trial because your ICU has agreed to participate and you currently work in this ICU.

All patients in this trial will continue to receive care as ordered and delivered by their ICU providers. Depending on when you work, the ICU you practice in will randomly receive either a dashboard or a RN facilitator.

This clinical trial will last for 30 months.

There is a risk that your patients’ information could be seen by people other than the researchers. The confidentiality of your data is very important to us and we will make every effort to keep all information collected in this trial strictly confidential.

There is no direct benefit from participating in this research. It is possible that findings from this trial could help patients in the future.

Should you suspect your patient had an unfavorable outcome related to BEST ICU study participation please contact the site principle investigator at your institution or click the link on this website.