Presentation of tools made available to CRIR researchers and students
REDCap (Research Electronic Data Capture) is a web-based software program created by Vanderbilt University and supported by the REDCap Consortium to facilitate research and data collection.
CRIR offers the use of the service and support to researchers and clinicians associated with the network. Using REDCap significantly improves data quality and security by enforcing an authorization matrix, that allows different members of the study team to have specified levels of access to the data.
For more details, we invite you to consult the latest presentation (in English) from Samir Sangani, Ph.D., our REDCap Project Manager.
Network of Networks (N2)
The Network of Networks (N2) is a not-for-profit incorporated organization and an alliance of Canadian research networks and organizations working to enhance national clinical research capability and capacity.
N2 membership offers networking opportunities with universities, academic organisations, pharmaceutical and biotech companies, charities, etc. N2 members are also offered training seminars, conferences, and tool kits.
Please contact CRIR administration for login information: [email protected]
ClinicalTrials.gov gov is a free resource provided by the U.S. National Library of Medicine. It is a web-based data entry system allowing the registration of clinical trials.
For researchers, it permits searching the database to stay up to date on developments in their field, to find collaborators, and identify unmet needs. Increasingly, scientific journals will only accept to publish clinical trials that have been registered before initiation of participant recruitment.
For patients and families, it provides current information about clinical research studies.
A single CRIR organization account exists for registering CRIR research with ClinicalTrials.gov.
To register your study with ClinicalTrials.gov you must be the principal researcher.For Login information, please contact Sabine Leunens: [email protected]
The following conditions apply:
- The principal researcher is responsible for the completeness and accuracy of the data submitted to ClinicalTrials.gov
- Only data for studies that are in conformance with applicable human subjects or ethics review regulations (or equivalent) and applicable regulations of the national (or regional) health authority (or equivalent) may be submitted
- Notice of changes in recruitment status must be provided as soon as possible, but no later than 30 days after such changes. All other submitted data must be reviewed, verified, and updated as necessary and no less than every 12 months
- Study data must be submitted in English
- Previous versions of study data will be available to the public, although the default view will be the most recent version
COVID-19 Communities of Practice in Rehabilitation – 1st Edition
As an extension to our Talking Research/Parlons recherche lunchtime seminars, the JRH Feil-Oberfeld Research Centre of the CISSS Laval is proud offer this bulletin as well as encouraging words.
“If we fight hard now, we will curb the deaths. We will relieve our healthcare system. We will prepare better. We will learn.
The world has never learned as fast about anything, ever. And we need it, because we know so little about this virus. All of this will achieve something critical: Buy Us Time. If we choose to fight hard, the fight will be sudden, then gradual.
We will be locked in for weeks, not months. Then, we will get more and more freedoms back… It might not be back to normal immediately. But it will be close, and eventually back to normal…’’
Practical guidelines adapted to COVID-19 ex. Telerehabilitation
COVID-19 Research project initiatives which are underway, etc.
Resources to support all during these challenging times