Toolbox
Recruitment Materials
POST-ICECAP Study Flyer (Please use your site-specific version with IRB stamp)
Contact
For immediate emergency assistance during enrollment, please use the 24/7 ICECAP Principal Investigator Hotline at 1-833-4-ICECAP (1-833-442-3227).
Getting Started
Education and Training
POST-ICECAP
FAQs
Q: Who is eligible for POST-ICECAP?
A:
- Age ≥ 18 years
- Coma after resuscitation from OHCA
- Patients who were either screened or enrolled in the ICECAP trial
- Received targeted temperature management
- Patient survived to 1 month
- Signed ICF by a patient or an authorized representative
Q: What is the definition of “Received targeted temperature management” in the inclusion criteria?
POST-ICECAP
Patterns Of
AutoBOOST
AutoBOOST is a BOOST-3 ancillary study under a separate grant. The study looks at machine learning analytics of heart rate variability on the Moberg collected waveforms as predictors of other parameters thought to be related to cerebrovascular reactivity and outcome.
Please note:
- There are additional analyses of existing data collected for BOOST-3.
- There are no additional contracts.
- There are no site payments.
- There are no consent forms.
Intensivists Working Group
The mission of the Intensivist Investigator Working Group is to provide a forum for SIREN investigators and trainees who practice intensive care to: 1) provide feedback on SIREN trial proposals and ideas in the pipeline, 2) discuss and develop new ideas for SIREN trials and ancillary studies, and 3) promote academic collaboration for publication and dissemination.
Trauma Working Group
The mission of the Trauma Working Group is to support multidisciplinary, multi-center trauma care research to promote excellence in trauma care. We provide expertise to develop and fund pragmatic trauma care research proposals.
E-mail the group
Human Subjects Protection Working Group
The mission of the Human Subjects Protection Working Group (HSP) is to help advance research efforts in the SIREN Network while keeping the human research participants’ interests, rights, justice, and wellbeing at the forefront. The group advocates for human research participant welfare, and to maintain ethical standards in clinical trials. HSP also has an interest in fostering opportunities to better participants’ experience in research; as well as LARs, families, and clinical treating teams.