Alzheimer's Disease Trial, By Invitation NCT06843109 Sponsor: London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's Condition: Alzheimer's Disease
Back to Alzheimers Disease

Alzheimer's Disease Trial, By Invitation

NCT06843109
By Invitation Not Applicable

voxsanity.com.au · Eligibility summary from public government registries · 18 August 2026 · not medical advice

Who may and may not be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who may be able to join

  • People who have been diagnosed with Mild Cognitive Impairment (MCI), or who have not yet been diagnosed but are showing memory changes as measured by a test called the MoCA.
  • People whose MoCA test score falls between 18 and 28 (inclusive).
  • People aged between 55 and 80 years (inclusive).
  • People who have a "study partner" (such as a family member or friend) who is willing to take part by providing information about the person, and who has roughly weekly contact with them — whether in person, by phone, or electronically — with enough contact that the trial investigator feels the study partner can speak meaningfully about how the person manages day-to-day.
  • Group A: People who have a clinical memory assessment appointment already scheduled at Parkwood Institute within 18 months of the study start date.
  • Group B: People who have already had a clinical memory assessment appointment at Parkwood Institute within 18 months of the study start date.

Who may not be able to join

Each point below is a reason the trial team may not be able to accept someone. It is not a list of requirements to meet.

  • People whose memory or thinking difficulties are thought to be caused by a condition other than Alzheimer's disease — for example, conditions such as frontotemporal dementia, Lewy body disease, Parkinson's disease, stroke-related changes, normal pressure hydrocephalus, head injury, or drug or alcohol use.
  • People who have a neurological, psychiatric, or medical condition that is associated with a long-term risk of significant cognitive decline or dementia, including (but not limited to) pre-symptomatic Huntington's disease, multiple sclerosis, Parkinson's disease, Down syndrome, active drug or alcohol misuse, schizophrenia, schizoaffective disorder, bipolar disorder, or a current episode of major depression.
  • People who currently have, or have had within the past 2 years, a psychiatric diagnosis or symptoms — such as hallucinations, major depression, or delusions — that in the investigator's opinion could interfere with study procedures.
  • People who have had epilepsy, seizures, or unexplained blackouts (other than a simple faint) within the 10 years before the screening visit.
  • People who have had a malignant cancer within the past 3 years (skin cancers such as basal cell or squamous cell carcinoma in situ are excepted).
  • Women who are able to become pregnant, or who are currently breastfeeding.
  • People who would need sedation in order to complete a PET scan.
  • People who are unable to complete the study assessments in the English language.
  • People who are unable to provide their own consent to participate.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 10 August 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
By Invitation
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
11 June 2024
Est. completion
1 September 2025

This date has passed while the registry still lists the trial as open to participants. Sponsors often update a trial's status without revising its projected end date, so it may well still be recruiting — but the record is out of date in at least one respect. Check with the study contact before relying on either.

Where this trial is recruiting

🇨🇦 Canada

Primary endpoints

Determine the feasibility of integrating a CSF biomarker into diagnostic decision making for AD.

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 10 August 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov