The increasing reliance on the Internet for health information has raised concerns about patients using unreliable and potentially harmful content. This study aimed to establish quality criteria to assist patients, caregivers, and the public in evaluating the reliability of online health information. We conducted focus group workshops with 25 participants recruited across Canada, proficient in either English or French.
View Article and Find Full Text PDFArtificial Intelligence (AI) systems are gaining momentum in complementing and/or replacing performing tasks typically done with the aid of human ability. AI systems, inherently human creations, are, however, beset by, wittingly or unwittingly, so-called male chauvinism, despite all the advancements made in the progress of civilization to make inroads for women's equitable participation in the labor force, particularly in relation to the digital economy, and more importantly, AI. In regards to the Canadian context, this perspective has examined the evidence to find research highlighting gender representation in the Canadian AI ecosystem.
View Article and Find Full Text PDFThe current pandemic of COVID-19 has changed the way health information is distributed through online platforms. These platforms have played a significant role in informing patients and the public with knowledge that has changed the virtual world forever. Simultaneously, there are growing concerns that much of the information is not credible, impacting patient health outcomes, causing human lives, and tremendous resource waste.
View Article and Find Full Text PDFPurpose: In-the-field projects aiming to improve quality in cancer control provide a valuable complement to health services and knowledge translation (kt) research studies. The present paper describes the methods used to develop the Knowledge Translation for Cancer Control in Canada: A Casebook and its results.
Methods: Nominations for in-the-field projects were accepted from individuals and organizations across Canada.