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Taking people in CanadaNo phase

Comprehensive Assessment of Neurodegeneration and Dementia

Key facts

Where
Calgary, Edmonton, Halifax, Hamilton, London, Montreal, Ottawa, Peterborough, Québec, Sherbrooke, Toronto, Vancouver, Victoria, and Waterloo, CanadaSee the 19 sites

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 50 and 90 years old?

Where in Canada

  • University Of CalgaryCalgary, CanadaTaking people
  • University of Alberta HospitalEdmonton, CanadaTaking people
  • Veteran's Memorial BuildingHalifax, CanadaTaking people
  • Hamilton General HospitalHamilton, CanadaTaking people
  • Gait and Brain LabLondon, CanadaTaking people
  • St. Joseph's Health Care LondonLondon, CanadaTaking people
  • Clinique de cognition Institut universitaire de gériatrie de MontréalMontreal, CanadaTaking people
  • Jewish General Hospital/McGill Memory ClinicMontreal, CanadaTaking people
  • Research Institute of the McGill University Health CentreMontreal, CanadaNo longer taking part
  • Bruyère Research InstituteOttawa, CanadaNo longer taking part
  • Kawartha CentrePeterborough, CanadaNo longer taking part
  • Hôpital Enfant-JésusQuébec, CanadaTaking people
  • Centre de recherche sur le vieillissement CIUSSS de l'Estrie-CHUSSherbrooke, CanadaNo longer taking part
  • Baycrest Clinical UnitToronto, CanadaTaking people
  • Sunnybrook Health Sciences CentreToronto, CanadaNo longer taking part
  • University Health Network Memory ClinicToronto, CanadaNo longer taking part
  • Djavad Mowafaghian Centre for Brain HealthVancouver, CanadaTaking people
  • Island HealthVictoria, CanadaNot yet recruiting
  • University of WaterlooWaterloo, CanadaNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
McGill University
Trial code
NCT03402919
Record updated
20 January 2026
Original description
This is a longitudinal observational study recruiting individuals between the ages of 50 and 90 with different types of dementia as well as a comparison group without cognitive deficits. Participants are/will be recruited at sites across Canada and will undergo assessments, neuroimaging, and biological sample collection.Read full original descriptionShow less

The Comprehensive Assessment of Neurodegeneration and Dementia Study

This is a longitudinal observational study recruiting individuals between the ages of 50 and 90 with different types of dementia as well as a comparison group without cognitive deficits. Participants are/will be recruited at sites across Canada and will undergo assessments, neuroimaging, and biological sample collection.

Inclusion: Has subjective or objective cognitive impairment; Written informed consent must be obtained and documented (from the patient or, where jurisdictions allow it, from a caregiver/family member); Sufficient proficiency in English or French to undertake self report and neuropsychological testing; Geographic accessibility to the study site; Must have a study partner who can participate as required in the protocol (provide corroborative information); Up to 12 years of education; Fits into one of the following groups: Cognitively Unimpaired, Subjective Cognitive Impairment, Mild Cognitive Impairment, Vascular Mild Cognitive Impairment, Parkinson's Disease, Parkinson's Disease with Mild Cognitive Impairment.

Exclusion: The presence of other significant known chronic brain disease such as: moderate to severe chronic static leukoencephalopathy (including previous traumatic injury), multiple sclerosis, a serious developmental handicap, malignant tumors, Parkinson's disease (other than for the Parkinson's cohort), and other rarer brain illnesses; Ongoing alcohol or drug abuse which in the opinion of the investigator may interfere with the subject's ability to comply with the study procedures; Symptomatic stroke within the previous year; Unable to undergo MRI scan due to medical contraindications or inability to tolerate the procedure.

ClinicalTrials.gov NCT03402919