Participants who take part will be provided with a stool sample collection kit at their in-home interview. They will bring the samples with them when they visit the Data Collection for physical assessments. At the Data Collection Site, they will complete some additional memory tests, which take about 20 minutes.

Following the Data Collection Site visit, a one-hour MRI appointment will be scheduled at an MRI facility located near the Data Collection Site.

The brain MRI, additional memory tests and stool samples are being collected with funding for a sub-study called the Healthy Brains Healthy Aging Initiative. The Healthy Brains, Healthy Aging Initiative is supported through a $12-million grant from the Weston Family Foundation. It will include 6,000 CLSA participants who will be asked to undergo brain imaging, additional memory tests and stool sample analysis. The initiative aims to collect data that, when added to the other data the CLSA is collecting, will shed light on how lifestyle factors – such as sleep, physical activity and diet – influence healthy cognitive aging.

You should not have an MRI if you have any of the following items implanted in your body:

  • Cardiac pacemaker, wires, or a defibrillator
  • Metal fragment in the eye or orbit
  • Brain aneurysm clip
  • Stainless steel Intrauterine Device (IUD)
  • Artificial heart valve
  • Eye or ear implant
  • Implanted drug infusion pump
  • Shunt
  • Electrical stimulator for nerves or bones
  • Coil, catheter or filter in any blood vessel
  • Orthopedic hardware (artificial joint, plate, screws, rods)
  • Other metallic prosthesis
  • Shrapnel, bullets, or other metallic fragments
  • Stent
  • Participants who have any of the implants listed above cannot participate in the study.
  • You should also not have an MRI if you are pregnant or suffer from claustrophobia.

If you are having issues with the web survey, please try the following:

  • Make sure you are not using Internet Explorer as certain parts of our questionnaires may not display correctly.
  • For questions requesting a numeric value, please do not write the value, instead use the keyboard numbers. For example, do not write two, use 2 instead.
  • If your tablet or smartphone is more than five years old, you may not be able to complete the survey using that device.
  • If the questionnaire does not move forward, make sure you have answered all the questions on the page.
  • You can select “Prefer not to answer” if you are not comfortable providing a response.
  • If there is an error or the questionnaire does not load, refresh the page.
  • If your web browser is not compatible with this application, please try using a different device, computer, or browser. If you cannot use a different device, computer, or web browser please contact the CLSA by email at info@clsa-elcv.ca or telephone at 1-866-999-8303. One of our team members will be able to place you on our calling lists for this questionnaire.

The purpose of this research study is to determine whether information that is collected through CLSA interviews can be used to correctly identify individuals who have memory problems and individuals without memory problems.

No, participants in the study will not receive a medical diagnosis. If the study clinician identifies a potential concern about your memory, you will be given a letter about the study and some of your individual results that you can share with your family doctor.

If you do not have a family doctor, the study clinician will provide you with some suggested resources regarding the potential concern about your memory.

There are no direct medical risks associated with participation in this study.

Some participants may feel tired or frustrated during the medical assessment with the study clinician. If you need a break during the medical assessment, please ask the study clinician.

Some participants may feel worried about if the study clinician will identify a potential concern about their memory. Participants identified as having a potential concern about their memory will have an opportunity to speak with the study clinician to discuss their concerns.