Thesis (Ph.D.)--McMaster University, 2003. / Includes bibliographical references (leaves 226-244). Also available via World Wide Web.

Many Inuit feel they are not benefitting from research activities that come from colonial research licensing practices and laws enabling state control over research. In Nunavut, research licensing also helped to increase community engagement in research. The Nunavut Research Institute (NRI), based in Iqaluit, Nunavut manages research and issues physical/natural, health, and social science research licenses in the Territory. In partnership with the NRI, we examined social science and Inuit knowledge research licensed between 2004-2019, to understand the scope of research trends in Nunavut. Using the 568 project summaries from social science research licenses, thematic content analysis was conducted to: i) identify research topics in social science and Inuit knowledge projects; ii) determine frequency and diversity of topics according to leadership, location, and timeframe; iii) develop new metrics to improve tracking of research topics; and, iv) contribute to the development of a Nunavut research portal making NRI research applications/reports public. Through this analysis we learned that social science research in Nunavut increased over time. Research projects are predominantly led by Canadian academics, with the highest concentration of research being in Iqaluit. Social science research is mainly focused on cultural topics, conducted using interviews, and shared in peer-reviewed journal articles. Community engagement has also increased over time in Nunavut, and research intensity appears to be connected to the availability of research-related capacity and infrastructure in a community. This research is an important starting point in making research trends more accessible to Nunavummiut (people of Nunavut), and more useable by decision-makers regarding research intensity and potential fatigue in some Nunavut communities. Long term, improving tracking of metrics such as funding sources and reporting mechanisms can contribute to policy reform and to advancing the NRI licensing database. This is an initial step contributing to Nunavut-specific approaches to Inuit self-determination in research. / Thesis / Master of Arts (MA) / Many Inuit feel they are not involved in the research process or seeing benefits from research outcomes. For my MA research, I am working with the Nunavut Research Institute (NRI) licensing database analyzing summaries of social science research applications from 2004-2019. The objectives are to: 1) Identify research topics addressed in social science projects; 2) Determine the variation of research topics across Nunavut over the past 16 years; 3) Develop new metrics to improve tracking of research topics; 4) Contribute to the development of a Nunavut research database making NRI research applications publicly accessible Through this analysis we learned that social science research in Nunavut has increased over time. Research projects are mainly led by Canadian academics, focused on cultural topics, and concentrated in Iqaluit. Community engagement has also increased over time in Nunavut and appears to be linked with the availability of research-related capacity and infrastructure in a community. This research is an important starting point in making research trends more accessible to Nunavummiut (people of Nunavut). This work is also an initial step contributing to Nunavut-specific approaches to Inuit self-determination in research.

This paper describes Inuit cultural considerations when defining and communicating electronic health concepts and personal health information services to urban Inuit audiences. Applying a two-eyed seeing model to build on and describe contextual meanings for Western and Inuit versions of health information and information communication technologies is critical to sustained relevance of electronic health information. Overarching concerns include reclaiming Inuit ownership and vision; sustainability; and; authority and capacity. It is within an electronic health space that Inuit can attain self-determination for the management of their own personal health data and develop a set of culturally safe and empowering practices for communicating ownership and cultural relevancy of health and health information in an evolving health care system.