The First Nations Regional Health Survey (FNRHS, or RHS for short) is the only First Nations -governed, national health survey in Canada. It collects information about on reserve and northern First Nations communities based on both Western and traditional understandings of health and well-being.
1997: pilot survey (on-reserve First Nations and Inuit
2002/03: Phase 1 (238 First Nations communities [on-reserve]; no Inuit)2008/10: Phase 2
2014/16: Phase 3
includes Q's re: residential school attendance (under Health category, not Education), consumption of traditional foods, and community wellness, among many others.
The RHS National Team is located at the First Nations Information Governance Centre in Ottawa and coordinates the RHS on a national level. Our activities include preparing reports, serving as the data steward, and engaging in partnerships.
In addition, ten independent, RHS Regional Partners coordinate the RHS in their respective regions. The National Team and Regional Partners collaborate on collective issues as well as share ideas and knowledge.
The RHS National Team is mandated and authorized to report on national level statistics; we cannot provide or report on regional level statistics. Each Region is completely independent and is responsible for its own respective databases and reporting
‘Housing conditions and respiratory hospitalizations among First Nations people in Canada’. released April 19, 2017 by Statistics Canada. This Health Reports article examines whether First Nations Aboriginal identity is associated with a greater likelihood of hospitalization for selected respiratory conditions when adjusting not only for housing, but also for location (on or off reserves, urban or rural) and household income. The analyses are based on information from the 2006 Census linked to hospital discharge data from the Discharge Abstract Database.
Smoking prevalence among Inuit in Canada, 1991 to 2012’. was released on February 15, 2017. Using data from the 1991, 2001 and 2012 Aboriginal Peoples Survey, this study examines the prevalence of smoking among Inuit aged 15 or older, by location of residence, sex and age group.
Smoking correlates among Inuit men and women in Inuit Nunangat
On March 21, 2018, Statistics Canada released ‘Smoking correlates among Inuit men and women in Inuit Nunangat.’ Using data from the 2012 Aboriginal Peoples Survey, an Inuit-specific social determinants of health framework, and a gender-based analysis, this Health Reports article examines correlates of smoking among Inuit men and women aged 18 or older living in the four regions collectively known as Inuit Nunangat (Nunavik in Northern Quebec, Nunatsiavut in Northern Labrador, Nunavut, and the Inuvialuit region of the Northwest Territories).
The Daily: http://www.statcan.gc.ca/daily-quotidien/180321/dq180321e-eng.htm
“Social determinants of health for the off-reserve First Nations population, 15 years of age and older, 2012”, which explores the relationship between various social determinants of health and selected health outcomes for First Nations people aged 15 and older living off reserve. Specifically, the following social determinants are explored: health behaviours (smoking, alcohol consumption, obesity), physical environments (housing, mobility, employment, education, income, food security), access to health resources, cultural continuity (participation in traditional activities, Aboriginal language, social support), and residential school attendance. An integrated life course and social determinants model of Aboriginal health framework is used to guide the analysis. Released by Statistics Canada on April 12, 2016.
‘Acute care hospitalization by Aboriginal identity, Canada, 2006 through 2008’ was released on August 17, 2016. National data about acute care hospitalization of Aboriginal people are scarce. This Health Reports study addresses that information gap by describing patterns of hospitalization by Aboriginal identity for leading diagnoses for all provinces and territories except Quebec. The 2006 Census was linked to the 2006/2007- to 2008/2009 Discharge Abstract Database, which contains hospital records from all acute care facilities in Canada (excluding Quebec). With these linked data, hospital records could be examined by Aboriginal identity, as reported to the census.
Acute care hospitalizations for mental and behavioural disorders among First Nations people
On June 20, 2018, Statistics Canada released the article ‘Acute care hospitalizations for mental and behavioural disorders among First Nations people’ in Health Reports. This study describes acute care hospitalizations for mental/behavioural disorders among First Nations people living on and off reserve. The 2006 Census was linked to the Discharge Abstract Database from 2006/2007 through 2008/2009 for all provinces (except Ontario and Quebec) and the three territories. Hospitalizations for seven types of disorders were identified.
‘The influence of community well-being on mortality among Registered First Nations people’ was released July 20,2016. This Health Reports article examines associations between community socioeconomic characteristics and mortality among the First Nations population. The 1991-to-2006 Census Mortality and Cancer Cohort follow-up, which tracked a 15% sample of Canadians aged 25 or older, included 57,300 respondents who self-identified as Registered First Nations people or Indian band members. The Community Well-Being Index (CWB), a measure of the social and economic well-being of communities, consists of income, education, labour force participation, and housing components. This study uses the 1991-to-2006 Census Mortality and Cancer Cohort to assess the influence of community factors as measured by the CWB and individual characteristics on the mortality of individuals who identified as Registered First Nations people or Indian band members.
Assessing the social determinants of self-reported Inuit health in Inuit Nunangat.” was released on February 22, 2016. The study used data from the 2012 Aboriginal Peoples Survey to assess the relationship between various social, economic and cultural factors and excellent or very good self-reported health. The analysis was conducted for two age groups: those aged 15 to 24 years and those aged 25 to 54 years.
Among the findings:
‘Lifetime suicidal thoughts among First Nations living off reserve, Métis and Inuit aged 26 to 59: Prevalence and associated characteristics’. was released on January 19, 2016. Based on data from the 2012 Aboriginal Peoples Survey, this article presents prevalence estimates of suicidal thoughts among First Nations living off reserve, Métis and Inuit aged 26 to 59. It examines associations between suicidal thoughts and mental health, socio-demographic and other characteristics, many of which have been shown to be related to suicidal thoughts in other populations.
‘Past-year suicidal thoughts among off-reserve First Nations, Métis and Inuit adults aged 18 to 25: Prevalence and associated characteristics’. was released October 13, 2016. For decades, researchers have reported high suicide rates among Aboriginal youth, which are several times higher than rates among non-Aboriginal youth. Based on the 2012 Aboriginal Peoples Survey, this article presents estimates of prevalence of suicidal thoughts among off-reserve First Nations, Métis and Inuit adults aged 18 to 25. It examines associations between past-year suicidal thoughts and mental disorders and personality factors; childhood experiences and family characteristics; and socio-demographic characteristics, many of which have been shown to be related to suicidal thoughts in other populations.
'Reports Suicide among First nations people, Métis and Inuit (2011 – 2016): Findings from the 2011 Canadian Census Health and Environment Cohort (CanCHEC)' was released on June 28, 2019. It presents suicide rates for the 2011 to 2016 time period among selfidentifying First Nations, Métis, Inuit, and non-Indigenous people in private dwellings in Canada. It also explores the influence of socioeconomic factors in the disparity in risk of suicide between First Nations people, Métis, Inuit and non-Indigenous people in Canada
‘The 2006 Canadian Birth-Census Cohort’ was released on January 20, 2016. The purpose of the 2006 Canadian Birth-Census Cohort Database is to provide information on the nature and extent of variations in perinatal health across socioeconomic and ethnocultural groups.
Among the findings:
Tables 4 and 5 and Figure 2 contain data on the Aboriginal identity population.
‘Validation of the 10-item Kessler Psychological Distress Scale (K10) in the 2012 Aboriginal Peoples Survey’ was released on January 20, 2016. The 10-item Kessler Psychological Distress Scale (K10) is a short measure of non-specific psychological distress, which has been shown to be a sensitive screen for the Diagnostic and Statistical Manual of Mental Disorders criteria for anxiety and mood disorders. The scale has yet to be validated as a measure of psychological distress for Aboriginal peoples in Canada. Using the 2012 Aboriginal Peoples Survey, this study examined the psychometric properties of the K10 for First Nations people living off reserve, Métis, and Inuit aged 15 or older.
Health Research Working Paper Series
Government of Canada Publications