Ways to Give

The Aging, Mobility, & Cognitive Health Laboratory is conducting a study to determine whether high-intensity interval training (HIIT), a popular form of exercise, will benefit cognitive function and brain health in those going through menopause transition.

The study is 12 weeks in duration and participants will receive free, supervised exercise sessions 3 times a week. HIIT training will be performed on the treadmill.

In order to be eligible for the study, you must:

• Be a biological female, as assigned at birth
• Be between 40 and 55 years of age
• Be perimenopausal
• Have an intact uterus
• Have completed high school education
• Read, write, and speak English
• Be able to walk independently

We are recruiting participants on an ongoing basis, and can schedule screening sessions with you Monday through Friday. If you are interested, would like to see if you may be eligible, or would like more information, please contact:

Sarah Heath, Recruitment Coordinator

Phone: 604-875-4111 ext. 69313

Email: cogmob.research@ubc.ca

Who: Healthy volunteers over 50, normal or corrected to normal vision

What: Simple computer gambling games and questionnaires

When: Two separate morning sessions; 3.5 hours total time

Where: Vancouver General Hospital campus

Compensation: Cash bonuses earned on the gambling games

Contact: eflynn02@mail.ubc.ca

A UBC research team supervised by Prof. Dongwook Yoon is looking for individuals who would be interested in participating in an interview about the importance of self in therapy and the potential of the different clinical intervention methods to be used in conjunction with AI self-clone chatbots.

You may be eligible to participate if:

• Are over 19 years of age (self-consent)
• Have a higher education degree in clinical psychology
• Have at least two years of experience as a mental health clinician and/or researcher in the related fields

What is involved: A one hour interview that would be audio/video recorded with permission. You would receive an honorarium of CA $100 per hour.

What is this study about? The goal is to identify promising intervention techniques that will be later used in the development of the AI chatbot for a thesis project.

To participate or inquire: Please contact mehrshi@cs.ubc.ca.

SOSTOS is a clinical research study that may find out if patients who have not had a relapse within the past 6 months might benefit from switching to ofatumumab (study drug) compared to continuing on their current MS treatment. The study will also look at neurofilament light (NfL) which is a biomarker that may indicate a neurological decline. The study will look to see if patients with an elevated NfL may have a greater benefit from switching to study drug compared to staying on current treatment.

You may be eligible to participate if:

• Have been diagnosed with RRMS
• Are 18-45 years of age
• Are on a current treatment for MS for at least 6 months
• Have not had a relapse within the last 6 months
• Agree to wear a study watch if selected
• Are willing to have 3 magnetic resonance imaging scans

What is involved: If you qualify and agree to join SOSTOS, you will be in the study for approximately 22 months and asked to come in for office visits about 12 times. You will be randomly selected to either continue on your current MS therapy or switch to ofatumumab treatment during that time. When you attend study visits, activities will include MRI scans, blood draws, physical and neurological exams, and other testing designed to measure your health and MS disease.

Location: This study takes place in the Djavad Mowafaghian Centre for Brain Health, 2215 Wesbrook Mall, Vancouver, BC V6T 1Z3.

To participate or inquire: please the MS Clinical Trials Group at MS.NMO_Research@ubc.ca or 604-822-1756.

Principal investigator: Dr. Alice Schabas, Department of Medicine

Study sponsor: Novartis Pharmaceuticals Canada Inc.

More information: https://clinicaltrials.gov/ct2/show/NCT05090371 

Do you binge drink and use cannabis? You may be eligible to participate in a cannabis research study!

The Behavioural Reward Affect + Impulsivity Neuroscience (B.R.A.I.N.) Lab at the University of British Columbia is conducting an exciting study investigating the short-term effects of cannabis consumption!

Study title: Cannabis and Polysubstance Use: Response Inhibition and Stress Exposure

Principal Investigator: Dr. Christian Schütz, MD, PhD

What is this study about? 

The goal of the study is to assess the effects of cannabis oil in individuals who use cannabis recreationally and binge drink.

Who can participate?

You may be able to participate if you:

• Have no major physical or mental health diagnoses
• Used cannabis at least once per week for the past month. Two of these times must be oral cannabis
• Binge drink at least once per month for the past year. Binge drinking is defined as 4 or more drinks (women) or 5 or more drinks (men)

Additional screening will be completed via phone interview.

What does my participation involve? 

The study involves taking cannabis oil during three sessions and completing MRI scans, computer tasks, questionnaires, and biological samples. If you participate, you will attend 5 in-person sessions and complete a daily survey at home for approximately 24 hours. You will receive a paid honorarium and an image of your brain for your participation.

How do I get involved? 

If you are interested, please contact the B.R.A.I.N. Lab at brainlab.cannabis@ubc.ca, reply to this posting through email, or phone us at 604-827-4287.

Researchers from the University of British Columbia are recruiting individuals who have been recently diagnosed with early stage Parkinson’s disease (less than 6 years duration), as well as healthy individuals to participate in a study at the Djavad Mowafaghian Centre for Brain Health.

What is involved:

PET/MRI imaging will be used to investigate changes in the brain in Parkinson’s disease, by comparing patterns of altered connections in people with Parkinson’s disease versus healthy controls.

If you choose to join, you will be asked to commit up to 14 hours; a single visit of two hours for screening and assessments and two visits of approximately 6 hours each to scan. These visits can be conducted on either consecutive or non-consecutive days.

Who can participate:

Parkinson’s disease participants:

• Recently diagnosed with early stage Parkinson’s Disease (less than 6 years duration)
• Between the ages of 50 to 85

Healthy Controls:

• Healthy male between the ages of 50 and 85
• Healthy female between the ages of 50 and 85

Exclusion Criteria:

1. No current or past major psychiatric disorders (e.g. depression, anxiety disorders) or major neurological disease secondary to Parkinson’s disease.
2. No current or past substance use problems.
3. No serious head injury with loss of consciousness for ≥ 5 minutes.
4. No MRI contra-indicators (e.g. claustrophobia, non-MRI safe metal implants and devices, injury to eye with metal object).
5. No history of exposure to high doses of radiation (e.g. radiation therapy for cancer)

For more information contact:

Nurse Coordinator: Jess McKenzie at 604-822-7764 or by email at jess.mckenzie@ubc.ca

The purpose of our study is to explore the use of two separate non-medication treatments, light therapy and ion therapy, as maintenance treatment in major depression. We are interested in exploring factors affecting the two treatments as maintenance treatments (to help prevent the return of symptoms) instead of medications in people with Major Depressive Disorders who wish to stop their antidepressant treatment.

Participation would include daily use of a bright light device or ion device provided by our clinic for 6 months, as well as regularly completing self-rated scales and meeting the study doctor for assessments. However, half of the treatment devices have been modified so that they are inactive (placebo). You have a 1 in 2 chance (like flipping a coin) of receiving an active or an inactive device.

You may be eligible for our study if you:

• are 19-65 years old
• meet criteria for major depressive disorder (not bipolar disorder) and have had two or more episodes of depression
• are currently taking an antidepressant for depression, and have taken it continuously for at least 3 months and no more than 12 months, with no dose change in the past month
• are interested in or are considering stopping your antidepressant
• are feeling well (no longer depressed) and in remission, according to a clinical interview
• do not have a seasonal pattern of depressive episodes (seasonal affective disorder)
• have no other major medical conditions or psychiatric conditions (except for major depressive disorder);
• do not have a problem with substance use currently or within the past 6 months.

For more information about this study and how to enroll, please contact: Lam.MDDResearch2@ubc.ca

Location: UBC Hospital

Compensation: an honorarium for each in-person visit

This study is being conducted by Dr. Raymond Lam at the Mood Disorders Centre, UBC Hospital.

This study is being conducted by Dr. Vesna Sossi and her team at UBC and is aimed at investigating brains of people with Parkinson’s at varying levels of exercise and comparing them against each other over a six-month period.

What is involved:

You will be asked to complete three baseline study visits and two follow up study visits after six months. Each set of visits includes a PET/MRI scan to learn more about brain behaviour and a VO2 max bike test of aerobic fitness. You will be reimbursed for travel or provided with transportation.

Who can participate:

• Have a diagnosis of Parkinson’s Disease
• Ages 40-80
• Currently participating in less than 120 minutes of high-intensity exercise per week.
• Able to maintain and report activity levels for 24 weeks
• Able to tolerate laying down on their back for about 90 minutes for PETMR scanning and not have claustrophobia or a fear of needles

Exclusion Criteria:

• Hypertension
• Diabetes
• Depression treated with antidepressants
• Serious head injury with loss of consciousness for ≥ 5 minutes

For more information contact:

Nurse Coordinator: Jess McKenzie at 604-822-7764 or by email at jess.mckenzie@ubc.ca

Are you interested in getting your brain scanned? We’re recruiting able bodied participants (ages 18 – 60) not diagnosed with chronic pain, spinal cord injury, or other major health conditions for an Magnetic resonance imaging (MRI)/Magnetic resonance spectroscopy (MRS) scan to investigate pain sensitivity. Participation will involve 2 hours of testing at the Blusson Spinal Cord Centre (recording electroencephalogram (EEG) activity with laser exposure) and 1.5 hours at DMCBH (for the MRI and MRS scan).

If you are interested in participating or have any questions, please contact Cassie Choles (ccholes@student.ubc.ca) for further details!

The Mood Disorders Centre at UBC is recruiting people who:

• Are between 19-65 years of age
• Have a diagnosis of Bipolar Disorder
• Are clinically stable on current medication
• Are not currently in a manic or depressed episode

Study visits will be at the UBC, Vancouver campus.

Contact us at bipolar.research@ubc.ca with Subject line “ ELICE-BD study”

This study is looking at changes in cognitive function in bipolar patients who are treated with 1.5mg/day of cariprazine vs Placebo add on therapy over a 6 week period.

Who can participate:

• Males and females between 19-65 years of age
• Have a diagnosis of Bipolar Disorder
• Are clinically stable on current medication
• Not currently in a manic or depressed episode
• No changes will be made to your current medications.

What is involved: 

The study involves 4 clinical visits and four telephone calls. Participants will complete neurocognitive (e.g. memory, reasoning and attention) testing and give blood samples. Participants with cognitive impairment will be randomly allocated, to either receive cariprazine or placebo added to their current medications for six weeks.

For more information contact:

Study Coordinator Email: bipolar.research@ubc.ca

This study is looking at changes in cognitive function in bipolar patients who are treated with 20 to 80mg/day of Lurasidone vs Placebo adjunctive therapy over a 6-week period.

Who can participate:

• Males and females between 19-65 years of age
• Have a diagnosis of Bipolar Disorder
• Are clinically stable on current medication
• Not currently in a manic or depressed episode
• No changes will be made to your current medications.

What is involved: 

The study involves 4 clinical visits and four telephone calls. Participants will complete neurocognitive (e.g. memory, reasoning and attention) testing and give blood samples. Only participants with cognitive impairment will be randomised into the study to receive either Lurasidone or placebo added to their current medications for six weeks.

For more information contact:

Study Coordinator Email: bipolar.research@ubc.ca

The purpose of this study is to determine if there are differences between individuals with bipolar disorder (BD) and healthy individuals in the position and density of nerve cells in the brain, and if they are related to inflammation. Magnetic resonance imaging (MRI) and Positron Emission Tomography (PET) will be used to obtain this information.

What’s Involved:

Participants, who are eligible after the screening visit, will be scheduled to come in for a second visit for a PET/MRI scan. In addition, there will be two blood tests (one at each visit) and a cognitive test.

Eligibility: 

Age: 19 Years – 50 Years Old

Patient participants must have had a diagnosis of Bipolar Disorder Type 1 for more than 5 years.

Control participants must have no history of any psychiatric diagnosis.

For more information contact:

Study Coordinator bipolar.research@ubc.ca

Do you use stimulants and cannabis? You may be eligible to participate in a cannabis research study!

The Behavioral Reward Affect + Impulsivity Neuroscience (B.R.A.I.N.) Lab at the University of British Columbia is conducting an exciting study investigating the short-term effects of cannabis consumption!

Study title: Cannabis and Polysubstance Use: Response Inhibition and Stress Exposure

Principal Investigator: Dr. Christian Schütz, MD, PhD

What is this study about? 

The goal of the study is to assess the effects of cannabis oil in individuals who use both stimulants and cannabis recreationally.

What does my participation involve? 

The study involves taking cannabis oil during three sessions and completing MRI scans, computer tasks, questionnaires, and biological samples. If you participate, you will attend 5 in-person sessions and complete a daily survey at home for approximately 24 hours. You will receive a paid honorarium and an image of your brain for your participation.

How do I get involved? 

If you are interested, please contact the B.R.A.I.N. Lab by email at brainlab.cannabis@ubc.ca, or phone us at 604-827-4287.

Call for research participants! Help shape the future of ethical social media use in dementia prevention research.

We are looking for participants who:

• Have a lived experience of dementia;
• Are a researcher or expert working in dementia research; or
• Are simply interested in dementia research and social media

We invite you to take part in a 30-45min virtual interview conducted by Dr. Julie Robillard and her research team at the University of British Columbia.

To participate or inquire, please email Viorica Hrincu at viorica.hrincu@ubc.ca

At this time, we do not accept whole-brain donations. Please contact the Biobank about other ways to get involved in research by donating samples.

The UBC Body Program does accept donations, with the majority used for teaching purposes although some are used specifically for medical and research training. The program can be reached at body.program@ubc.ca or (604) 822-2578.

No, we appreciate any and all donations. You can donate online by clicking here.
If you are looking to make a larger donation, please connect with Development or VGH + UBC Hospital Foundation. Their contact information can be found under the “Donate Funds” section of this page.

No, not always. Please reach out to the contact person for each study to receive specific information about what is required to participate.