Education and Training

ICECAP

Education and Training

Welcome to the ICECAP Education and Training Page! This page provides essential training materials and certification requirements for ICECAP study team members. Here, you’ll find protocol training, regulatory guidance, data management instructions, Human Subjects Protection (HSP), and Good Clinical Practice (GCP) resources. Training is required for all study personnel, with re-training sessions available as needed. Follow the steps outlined in each section to complete your certifications and ensure compliance with study protocols.

Regulatory Parameters Document
This document shows the regulatory requirements (including training) for each role in the study. Use this to understand what training you need to complete.

The Protocol training consists of the following THREE requirements:

1. Review the Protocol.

2. Watch the Protocol Introduction and Rationale, Protocol Review AND ICECAP Game videos.

Protocol Introduction and Rationale – Will Meurer

Protocol Review – Robert Silbergleit and Will Meurer

ICECAP Game – ICECAP Leadership

3. Complete the Attestation.

NOTE: Upon completion of all three requirements save the attestation and send it to your Study Coordinator to upload to WebDCU. There is no expiration for this certification.

SIREN WebDCU User Manual

Data Training

NOTE: Click on the arrows for full screen mode.

Complete the Training Certificate after the video is viewed and upload it to WebDCU.

WebDCU Data Training Certificate

Regulatory Document Management Training

NOTE: Click on the arrows for full screen mode.

Complete the Training Certificate after the video is viewed and upload it to WebDCU.

WebDCU Regulatory Training Certificate

Optional Training:

WebDCU General Overview

DOA Log Training – How to Update Your Site’s DOA Log

Regulatory Document Module Training Video (specific to only the regulatory document module in WebDCU)

A free option for GCP training is available at the National Institute of Allergy and Infectious Diseases (NIAID). Click here to access the NIAID training.

NOTE: Effective January 1, 2017 – NIH expects all NIH-funded clinical investigators and clinical trial staff who are involved in the design, conduct, oversight, or management of clinical trials to be trained in Good Clinical Practice (GCP). Recipients of GCP training are expected to retain documentation of their training. GCP training should be refreshed at least every three years in order to stay up to date with regulations, standards, and guidelines.

https://grants.nih.gov/policy/clinical-trials/good-clinical-training.htm

Attention: You only need to complete the training module below if your institution does NOT provide HSP training.

Collaborative Institutional Training Initiative (CITI)

The University of Chicago Cardiac Arrest Service provides this free demonstration on how to place the esophageal temperature probe using the Seldinger technique.