500 Participants Needed

Biomarker Modeling for Dementia

(CRND TorCA Trial)

Recruiting at 3 trial locations
CC
Overseen ByClaudia Clementi, HBSc
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: University Health Network, Toronto
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to create a model to predict the progression of neurodegenerative diseases that cause dementia. It focuses on conditions such as Mild Cognitive Impairment (MCI) and dementia due to Alzheimer's, Lewy Body Disease, Vascular Disease, and Frontotemporal degeneration. Candidates include those diagnosed with MCI or early dementia who have someone seeing them weekly. The goal is to enhance understanding of these diseases and assist doctors in making more informed patient care decisions. As an unphased study, this trial allows patients to contribute to groundbreaking research that could improve future care strategies.

Why are researchers excited about this trial?

Researchers are excited about this trial because it aims to improve the way we predict the progression of neurodegenerative diseases causing dementia, like Alzheimer's and Parkinson's. Unlike current methods that rely heavily on brain imaging and cognitive tests, this trial explores the use of peripheral biomarkers—substances that can be measured in blood or other body fluids—to provide insights. By integrating these biomarkers with advanced modeling techniques, the goal is to offer a more accurate and non-invasive way to track disease progression. This could lead to earlier and more personalized treatment plans, potentially improving patient outcomes significantly.

Who Is on the Research Team?

MC

Maria C Tartaglia, M.D.

Principal Investigator

Toronto Western Hospital, UHN; Tanz CRND

Are You a Good Fit for This Trial?

Inclusion Criteria

I have been diagnosed with mild cognitive impairment or early dementia.
I am between 40 and 95 years old.
I have someone who sees me weekly and can provide information about my health.
See 1 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Baseline Assessment

Participants undergo baseline assessments including brain imaging, body fluid samples, skin biopsy, cognitive ability, and behavioral questionnaires

4 weeks
1 visit (in-person)

Follow-up

Participants are monitored for changes in neurodegenerative protein levels, structural and functional brain differences, and cognitive phenotype

1 year
2 visits (6-month and 1-year follow-up)

What Are the Treatments Tested in This Trial?

Find a Clinic Near You

Who Is Running the Clinical Trial?

University Health Network, Toronto

Lead Sponsor

Trials
1,555
Recruited
526,000+

Baycrest

Collaborator

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46
Recruited
6,900+

Sunnybrook Health Sciences Centre

Collaborator

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693
Recruited
1,569,000+

Centre for Addiction and Mental Health

Collaborator

Trials
388
Recruited
84,200+

University of Toronto

Collaborator

Trials
739
Recruited
1,125,000+

Toronto Dementia Research Alliance (TDRA)

Collaborator

Trials
1
Recruited
500+
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