Kristen Jacklin, Ph D.
Northern Ontario School of Medicine at Laurentian University
935 Ramsey Lake Road
Canada P3E 2C6
Associate Professor, Medical Anthropology, Northern Ontario School of Medicine
Faculty, School of Rural and Northern Health, Laurentian University
Faculty Investigator, Centre for Rural and Northern Health Research, Laurentian University
Education and Training
2007 - Ph.D. McMaster University (Hamilton, ON)
Medical Anthropology, Department of Anthropology
1998 - M.A. McMaster University (Hamilton, ON)
Medical Anthropology, Department of Anthropology
1996 - Hons. B.A. University of Waterloo (Waterloo, ON)
Anthropology and International Studies
Kristen Jacklin joined the Northern Ontario School of Medicine (NOSM) in 2005 as part of its founding faculty. She was trained as a medical anthropologist with a focus on Indigenous health at McMaster University. Dr. Jacklin brings a social science and health equity perspective to her
teaching and research. Her teaching portfolio includes significant contributions to the development and delivery of the socio-cultural and Aboriginal health content for undergraduate medical students. She has previously served as Chair of the Northern and Rural Health Course Curriculum
Committee at NOSM is currently a member of the committee. Dr. Jacklin has been involved in national initiatives to develop core competencies in the area of Aboriginal health in medical education. Dr. Jacklin is also affiliated with
Laurentian University and accepts graduate students through the School of Rural and Northern Health (
Ph.D and Masters) and the
Masters of Indigenous Relations programs.
Dr. Jacklin is committed to research that is participatory and action-oriented. She leads and collaborates on several research projects which aim to improve chronic disease care and outcomes for Indigenous peoples in Canada including investigations on
age-related dementias and national and community-based projects on culturally safe diabetes care. She is one of the principal investigators on the CIHR funded
Canadian Consortium on Neurodegeneration in Aging and co-leads the team concerned with Indigenous dementia care. Dr. Jacklin is also a Faculty Investigator with the
Centre for Rural and Northern Health research where she contributes to their MOHLTC funded work concerning the unique health care needs of communities in Northern Ontario.
Specific areas of expertise include:
Indigenous health research; age-related dementias and cognitive decline in Indigenous populations; healthy aging, rural and remote health care delivery; Indigenous health systems and policy research; community-based (participatory) research; qualitative methods; cultural and social constructions of health and illness;
cross-cultural medicine and Indigenous health medical education.
Selection of Current Research
- The Canadian Consortium on Neurodegeneration in Aging
(CCNA) (Principal Applicant, 2014-2019): The CCNA is
led by Dr. Howard Chertkow, McGill University in conjunction with 37 Principal
Applicants and +300 Collaborators. Dr. Jacklin is the Co-Lead of Team 20: Issues in Dementia Care for Rural
and Indigenous populations: Indigenous Projects along with Dr. Carrie Bourassa
(First Nations University) and Dr. Debra Morgan
(University of Saskatchewan). Team 20 investigators and leads have various
research programs addressing quality of life and dementia care needs in
Indigenous populations. CCNA Team 20
Program of Research Overview https://vimeo.com/139010506.
- Unlocking health information for older
First Nations populations (Principal
Investigator, 2015-2018): This project is led by CCNA and CRaNHR Investigator Dr.
Jennifer Walker and has been funded through the CIHR Transitional
Operating Grants. This project includes investigators from universities, the
Chiefs of Ontario and The Institute of Clinical and Evaluative Sciences (ICES).
This project will result in the first population-level profile of the wellbeing
of First Nations seniors in Ontario and their health care experiences. Our dual
aim is 1) to assess gaps and limitations of existing data sources as they apply
to older populations and 2) to enable First Nations people to describe their
experiences with aging using existing data sources. Specifically, our
objectives will assess and quantify the opportunities and limitations in the
use of existing data to understand the wellbeing of older First Nations
populations in Ontario; refine a First Nations approach to measuring “vitality”
or “thriving” for older First Nations people in Ontario; describe the patterns
and outcomes of vitality/thriving in the adult First Nations population in
Ontario by selected demographic and social characteristics, using the First
Nations Regional Health Survey (FNRHS) (on-reserve) and the administrative
health data available at ICES (on and off-reserve).
- Reducing the burden of diabetes on First
Nations people in Ontario: using population level data to inform policy and
practice. (Principal Investigator,
2015-2017): This project is led by Dr. Michael
Green, Queen’s University in partnership with the Chiefs of Ontario. We are funded
by the Ontario SPOR Support Unit (OSSU) IMPACT Awards. In close partnership
with the Chiefs of Ontario, this study is designed to examine the health care
experiences of First Nations people with diabetes in Ontario. We will describe
in detail changes in the rates of diabetes and its complications over the past
20 years, how access to healthcare for First Nations people compares to other
Ontarians, and how particular policies have impacted either health outcomes or
access to care for First Nations people with diabetes. By working closely with
patients and key stakeholders from federal, provincial and First Nations
organizations, we will identify and evaluate key policy changes that are
important and where data is needed to improve decision making.
- Rural/Remote Indigenous Technology Needs
Exploration (Principal Investigator, 2015-2018). This
project is lead by Dr. Megan O’Connell at the University of Saskatchewan and is
funded by AGE-WELL National Centre of Excellence.
Dr. Jacklin and Dr. Wayne Warry
lead the investigations in Ontario. The research in Ontario is comprised of two
phases. Phase 1 will look at technology use and needs of older Indigenous
adults. Phase 2 will explore how technologies may need to be adapted to improve
- Developing Educational Materials for
Community Based Dementia Care (Principal Investigator,
2014-2017). This project is funded by Health Canada to address the need for
culturally relevant health promotion materials and training concerning dementia
for First Nations (with Dr. Wayne Warry, CRaNHR).
Health Equity for Northern Ontarians: Applied Health Research with
Vulnerable Populations (co-investigator): Centre for Rural and Northern Health Research. (2013-2016) Dr. Jacklin
leads a program of research called The Best of Both Worlds. The Best of
Both Worlds is a three year, multiphase project that seeks to create a
culturally safe care model that will improve the quality of care for
Aboriginal patients with complex co-morbid chronic illness. Working in
partnership with The Wikwemikong
Health Centre, The Best of Both Worlds project will develop,
implement, and evaluate a cultural safety training module for all health
service workers who provide care to individuals from Wikwemikong. (NPI Dr.
Wayne Warry, CRaNHR)
Indigenous Dementia Research Network (IIDRN): In 2009, I founded and
continue to lead the International Indigenous Dementia
Research Network. This network connects academic researchers,
graduate students, new investigators, community members, and policy
workers interested in the study of dementia in Indigenous populations from
Canada, New Zealand, Australia and the United States. The network
facilitates research collaborations and sharing of knowledge between
researchers, policy makers and community-based workers. Most communication
among network members occurs on a secure web-based platform. Our website
for the network is currently in transition (to be completed in early
2016), individuals sharing this research interest may request to join the
network by contacting Dr. Kristen Jacklin.
- The Indigenous
Health Research Development Program (role Co-PI): One
of nine national Network Environment for Aboriginal Health Research
centres funded by CIHR until 2016. The IHRDP is committed to a
student-centered and community capacity building approach to
community-based Aboriginal health research. We assist with building a career
structure for students in Aboriginal health research and focus our
resources on community-driven research projects and knowledge translation
concerning health-related issues in First Nations communities.
- Educating for
Equity: Exploring how health professional education can reduce
disparities in chronic disease care and improve outcomes for Indigenous
populations (role co-PI): This is a multi-national initiative aimed at improving
health outcomes for Aboriginal peoples through improved approaches to
medical and health education. The Canadian team will seek to research,
design, deliver and evaluate a medical educational approach for practicing
physicians (CME) that seeks to enhance physician’s understandings of
cultural and structural issues affecting the provision of appropriate
diabetes care for Aboriginal peoples in Canada. (2010-2016)
Jacklin, K., Pace
J.E., & Warry, W (2015) Informal Dementia Caregiving among Indigenous
Communities in Ontario, Canada. Care Management Journals 16(2):106-120.
Strasser, R. and Peltier, I. (2014) From the Community to the Classroom: The
Undergraduate Aboriginal Health Curriculum at the Northern Ontario School of
Medicine. The Canadian Journal of Rural Medicine 19(4), 143-150.
Jacklin, K., J. Walker and M. Shawande. (2013)
The emergence of Alzheimer’s disease and dementia as a health concern among First Nations populations in Canada. The Canadian Journal of Public Health 104(1):e39-e44.
Jacklin K., and W. Warry (2012)
Forgetting and Forgotten: Dementia in Aboriginal Seniors. Anthropology and Aging Quarterly 33(1):13
Jacklin, Kristen and Wayne Warry (2011) Chapter 18:
Decolonizing First Nations Health. In Rural Health: A Canadian Perspective. Judith C. Kulig & Allison Williams Editors. University of British Columbia Press.
Jacklin, Kristen (2009) Diversity Within: Deconstructing Aboriginal Health. Social Science and Medicine Volume 68, Issue 5, Pages 980-989
Minore, Bruce; Jacklin, Kristen; Boone, Margaret; Cromarty, Helen. (2009) Realistic expectations; The changing role of paraprofessional health workers in First Nation communities in Canada'. Education for Health. 22(2):1-9.
Jacklin, Kristen and Phyllis Kinoshameg (2008). Developing a Participatory Aboriginal Health Research Project: “Only if it’s going to mean something.” Journal of Empirical Research of Human Research Ethics 3(2):53-68.
Lightfoot, N., Strasser, R., Maar, M. and Jacklin, K. (2008). Challenges and rewards of conducting research with northern, rural, and remote communities. Annals of Epidemiology 18: 507-514.
Farmer, T and Jacklin, K (2007).
Matching Research With Evidence: Reorienting Aboriginal Tuberculosis Research in Canada. In Multiplying and Dividing: Tuberculosis in Canada and Aotearoa New Zealand. RAL-e (Research in Anthropology and Linguistics), University of Auckland, Department of Anthropology’s, refereed monograph series. Chapter 6 page 38, June 2008.
Jacklin, K. (2007) Medical Anthropology.
The Canadian Encyclopedia. Historica Foundation of Canada, (Invited Submission).
Jacklin, Kristen and Wayne Warry (2004).The Indian Health Transfer Policy: Toward Cost Containment or Self-Determination? In Unhealthy Health Policy: A Critical Anthropological Examination, edited by Merrill Singer and Arachu Castro. Walnut Creek, CA: Altamira Press.
Selected Technical Reports and Community Publications
Jacklin, K. and Warry W. (2015) Developing First Nations Dementia Factsheet Material: Methodology Report. For Health Canada, First Nations and Inuit Health, Home and Community Care Program, Health Funding Contribution Agreement HQ150013.
Kristen Jacklin, W. Warry and Melissa Blind (February 2014) Perceptions of Alzheimer’s Disease and Related Dementias in Aboriginal Peoples in Ontario: Sudbury Community Report (64 pages). Submitted to: Sudbury-Manitoulin Alzheimer’s Society; N’Swakamok Indian Friendship Centre.
Kristen Jacklin, W. Warry and Melissa Blind (January 2014) Perceptions of Alzheimer’s Disease and Related Dementias in Aboriginal Peoples in Ontario: Six Nations Community Report (57 pages). Submitted to: Six Nations Health Services.
Kristen Jacklin, W. Warry and Melissa Blind (November 2013) Perceptions of Alzheimer’s Disease and Related Dementias in Aboriginal Peoples in Ontario: Moose Cree First Nation Community Report (58 pages). Submitted to: Moose Cree First Nations Health Services
Kristen Jacklin, W. Warry and Devin Dietrich (October 2013) Perceptions of Alzheimer’s Disease and Related Dementias in Aboriginal Peoples in Ontario: Thunder Bay Community Report (51 pages). Submitted to: Thunder Bay Indian Friendship Centre and Anishinaabe Mushkiki Health Centre.
Kristen Jacklin and Jennifer Walker. (2012) Trends in Alzheimer’s Disease and related dementias among First Nations and Inuit. Prepared for Health Canada, First Nations and Inuit Health, Home and Community Care Program (70 pages).
Kristen Jacklin (2012)
International Indigenous Dementia Research Network Meeting Report. Ancillary Meeting of the Alzheimer’s Association International Conference July 16, 2012.
Warry, W. and K. Jacklin 2005. Aboriginal Relationship Development and Training Manual for the Aboriginal Unit, Cancer Care Ontario.
Selected Media Coverage
- The Scope (Inaugural Edition) (November 2014). “
NOSM Researcher Participating in 55.5M National Dementia Initiative.”
- CBC Radio “Up North” Interview (October 16th, 2014) “
NOSM researcher gets funding for dementia project.”
- Q92/ 105.3 KISS FM Sudbury News (September 17th, 2014). “
NOSM Professor Part of National Dementia Research Studies.”
- Alzheimer’s Society Ontario Media Relations Interview (June 20, 2014) “
Learning how Aboriginal culture affects dementia care.”
- Press Interview (2011). "
Need for ‘Culturally Competent’ Dementia Assessment and Care ."
(Print versions November 30, 2011)
Alzheimer’s Society Canada Communications Interview. March 31, 2011.
- Press Interview. Giving Alzheimer’s patients a voice at
the table. The Star. Judy Gerstel Published on Friday, March 25, 2011.