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Assessing Dementia Risk in the Community: The Dementia Population Risk Tool (DemPoRT)

O

Ottawa Hospital Research Institute

Status

Completed

Conditions

Dementia

Study type

Observational

Funder types

Other

Identifiers

NCT03155815
CIHR FRN 142237

Details and patient eligibility

About

The purpose of this study is to develop and validate the Dementia Population Risk Tool (DemPoRT) algorithm to predict dementia incidence in the population setting.

Full description

The burden of disease from dementia is a growing global concern as incidence increases exponentially with age and average life expectancy has been increasing around the world. Planning for an aging population requires reliable projections of future dementia prevalence and resource requirements, however, existing population projections are simple and have poor predictive accuracy. The Dementia Population Risk Tool (DemPoRT) will predict incidence of dementia in the population setting using multivariable modeling techniques.

The derivation cohort will consist of elderly Ontario respondents of Canadian Community Health Survey (CCHS) (2001, 2003, 2005, 2007; approximately 19 000 males and 25 000 females). Pre-specified predictors include sociodemographic, general health, behavioral, functional and health condition variables. Incident dementia will be identified through individual linkage of survey respondents to population-level administrative health care databases. Using time of first dementia capture as the primary outcome and death as a competing risk, sex-specific proportional hazards regression models will be estimated. The 2008/2009 CCHS survey be used for validation (approximately 4 600 males and 6 300 females). Overall calibration and discrimination will be assessed as well as calibration within predefined subgroups of importance to clinicians and policy makers.

Enrollment

75,460 patients

Sex

All

Ages

55+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Respondents to the Canadian Community Health Surveys

Exclusion criteria

  • Less than 55 years of age at survey administration
  • Prior history of dementia
  • Not eligible for Ontario's universal health insurance program

Trial design

75,460 participants in 2 patient groups

Derivation Cohort
Description:
Eligible respondents to the combined 2001, 2003, 2005 and 2007 Canadian Community Health Surveys, conducted by Statistics Canada.
Validation Cohort
Description:
Eligible respondents to the 2008/2009 Canadian Community Health Survey.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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