Launched in 2018 in response to the legalization of cannabis for non-medical use, the CIHR Integrated Cannabis Research Strategy (ICRS) supports research and knowledge mobilization to provide essential knowledge about the use of cannabis, both medical and non-medical, its health and safety effects, and the behavioural, social, cultural, ethical and economic implications of legalization both nationally and across jurisdictions. As part of a renewed ICRS, the current funding opportunity will create the Canadian Cannabis and Brain Health Consortium (CCBHC) to respond to several urgent priorities and knowledge gaps identified in the Legislative Review of the Cannabis Act Report tabled in Parliament in March 2024.
To better understand the impact of cannabis exposures and regular, heavy or high-potency cannabis use on population health, Canada requires a consortium of cannabis and brain health cohorts to measure cannabis use and the impact on brain health across the lifespan, and to provide the mechanism to facilitate data harmonization, data pooling, and data access across provinces and territories. The current funding opportunity brings about the opportunity to leverage existing research infrastructure and expertise in Canada to create an integrated data collection and clinical trials infrastructure that will be accessible to all Canadian researchers to investigate key questions about cannabis harms and benefits to the population across the lifespan.
Consortium Structure and Application Requirements
The Canadian Cannabis and Brain Health Consortium (CCBHC) will be created through a sequential three-step process:
Population-Based Cohort Studies (Current Funding Opportunity)
The current funding opportunity will support up to ten linked population-based cohort studies to address pressing issues on cannabis use and associated impacts on brain health from a lifespan perspective. Each funded team must contribute at least one additional cannabis-focused research study that capitalizes on the research infrastructure, assessment framework and/or database provided by the CCBHC. Research studies should address one of the priority areas: (a) interventions to reduce cannabis-related harms; (b) controlled trials of cannabis for medical purposes; (c) populations with rare, and/or clinically, complex contexts; (d) scaling of novel cannabis-related measurement methods; (e) parallel pre-clinical cannabis/cannabinoid studies; and (f) Indigenous Peoples' health and cannabis.
Please refer to the Health Canada webpage for information on the requirements of conducting research with cannabis, including clinical trials.
Applicants are required to ensure equitable access of diverse researchers, including First Nations, Inuit, and Métis peoples, and persons with lived or living experience (PWLLE) to opportunities available within the research team that will be established with program funding. This includes ensuring the research environment is supportive and any systemic barriers are addressed effectively and swiftly (see the Best Practices in Equity, Diversity and Inclusion in Research for guidance and examples of systemic barriers).
Applicants are expected to adopt data management best practices to enable reproducible science and to enable successful sharing across the Consortium (e.g., the FAIR principles – Findable, Accessible, Interoperable, Reusable). See Additional Information section for more details.
Research Areas
This funding opportunity will support harmonized projects that:
Population-based cohort study
Applications must include a population-based cohort study to address pressing issues on cannabis use and brain health from a lifespan perspective. Applicants must contribute to the Canadian Cannabis and Brain Health Consortium, an accelerated longitudinal study, by contributing data to a collaborative study whose goal is to pool data on over 3000 participants recruited from sites across Canada. Each application must significantly contribute to a brain health cohort in the following ways:
Cannabis Research Study
Applications must also propose at least one cannabis research study in one of the following priority areas (note that multisite designs are encouraged) particularly in relation to the health research gaps highlighted in Legislative Review of the Cannabis Act. As far as possible, cannabis and brain measures and design features must overlap significantly with those of the Canadian Cannabis and Brain Health Consortium cohort but can include other clinically relevant measures and design features.
Role and Contributions of Applicant Partners:
CIHR recognizes that a broad range of partners may be relevant to this opportunity and it is expected that applicant(s) describe the role of all applicant partners and how/if they will contribute to research and research related activities. Any consideration of risk and/or conflict of interest should also be explained, as appropriate.
Funds Available
CIHR and partner(s) financial contributions are subject to availability of funds. Should CIHR or partner(s) funding levels not be available or decrease due to unforeseen circumstances, CIHR and partner(s) reserve the right to reduce, defer or suspend financial contributions to grants received as a result of this funding opportunity.
CIHR reviewers heavily weight methodological rigor, including:
Strong theoretical framework
Clear hypotheses or research questions
Robust study design
Adequate controls, power calculations, and statistics
Reproducibility & transparency practices
Clear milestones and contingency plans
Predictor: Methodological strength is the #1 determinant across all CIHR committees.
CIHR prioritizes research that benefits:
The health of people living in Canada
Canadian healthcare systems and policies
Vulnerable or underserved populations
Chronic disease burdens in Canadian demographics
Predictor: Clear articulation of Canadian relevance dramatically improves scores.
Successful CIHR proposals:
Have 2–3 well-defined aims
Present realistic deliverables within the grant period
Include detailed methodologies for each aim
Avoid overambitious or unfocused scope
Demonstrate precise timeline and project management
Predictor: Feasibility + clarity of approach = high reviewer confidence.
Reviewers value:
Publications relevant to the field
Prior successful funding
Expertise aligned to each aim
Multi-disciplinary teams (clinicians, statisticians, biomedical scientists, policy experts)
For early-career investigators: mentorship, protected time, and institutional support
Predictor: A well-matched, credible team is essential.
Highly competitive CIHR proposals commonly include:
Pilot experiments or feasibility data
Retrospective analyses
Early mechanistic insights
Proof-of-concept findings
For high-risk or exploratory programs, strong rationale can substitute, but evidence is still preferred.
Predictor: Preliminary data significantly boosts chances.
CIHR explicitly evaluates EDI in:
Team composition
Training environment
Research design (sex, gender, intersectionality, inclusive sampling)
Barriers to participation or recruitment
Engagement with under-represented or Indigenous populations
Predictor: Meaningful EDI integration is essential; weak EDI sections lower scores.
CIHR places high value on:
How findings will reach clinicians, policymakers, communities, or the public
Realistic KT activities (briefs, publications, engagement, partnerships)
Integrated knowledge translation when applicable (co-design with stakeholders)
Predictor: Strong KT plan with defined stakeholders and products.
High success when aligned with:
Indigenous health
Digital health & AI
Aging and dementia
Chronic disease (cancer, cardiovascular, neurological)
Rare disease
Implementation science
Mental health, substance use
Health system strengthening
Predictor: Direct strategic alignment increases competitiveness.
CIHR reviewers look for feasibility evidence:
Confirmed clinical recruitment sites
Existing cohort or biobank access
Computational / lab infrastructure
Letters of support verifying data access
Agreements for collaboration or sharing
Predictor: Proven resource availability reduces perceived risk.
Successful budgets:
Are lean and proportional to aims
Avoid unnecessary equipment or inflated salaries
Align with Canadian Tri-Council rules
Include justification for trainees, supplies, analyses
Predictor: A clear, efficient budget strengthens feasibility.
| Pitfall | Why It Hurts |
|---|---|
| Vague or overly ambitious aims | Feasibility concerns |
| Weak or missing preliminary data | Too speculative |
| Poor methodology or unclear analytic plan | Low rigor |
| Minimal relevance to Canadian health | Weak significance |
| Poor EDI integration | Fails mandatory criteria |
| No KT or weak dissemination plan | Low potential impact |
| Unclear roles of team members | Execution risk |
| Overinflated budget | Reviewer concerns |
For an application to be eligible, all the requirements stated below must be met and clearly identified in the Participant Table (see How to Apply section):
The NPA must have successfully completed one of the sex- and gender-based analysis training modules available online through the CIHR Institute of Gender and Health and have submitted a Certificate of Completion (see How to Apply section): Select and complete the training module most applicable to your research project.
Note: A NPA can submit a maximum of 1 application under this funding opportunity. If the NPA submits more than 1 application, CIHR will automatically withdraw any subsequent application(s) based on time-stamp of submission. However, collaboration is encouraged and will be fostered in the Strengthening Workshop. As such, there is no limit of participation for other applicant roles.
Sponsor Institute/Organizations: Canadian Institutes of Health Research
Sponsor Type: Corporate/Non-Profit
Address: 234 Laurier Ave West, Ottawa, ON K1A 0K9
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Jan 22, 2026
Jan 22, 2026
$1,704,000
Affiliation: Canadian Institutes of Health Research
Address: 234 Laurier Ave West, Ottawa, ON K1A 0K9
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