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Team Grant : Pan-Canadian Network : Emerging LHS in Perinatal Mental Health

Team Grant : Pan-Canadian Network : Emerging LHS in Perinatal Mental Health

Researchnet RecherchenetNew Zealand
8 hours ago
Job description

Team Grant : Pan-Canadian Network : Emerging LHS in Perinatal Mental Health

(Pan-Canadian Network : Emerging Learning Health System in Perinatal Mental Health)

Sponsor(s)

The Institute of Neurosciences, Mental Health and Addiction

The content of this funding opportunity has been updated

Date updated :

Section(s) updated : Important Dates

Tri-Agency CV

This funding opportunity uses the tri‑agency CV . This narrative‑style CV is more flexible and allows applicants to best highlight their wide range of outputs and expertise. The tri‑agency CV allows applicants to capture relevant information, describe their career trajectories in more detail, provide indicators of quality and impact, and provide context to their contributions in a narrative format to help peer reviewers assess their track record. More information on the new CV is available on the tri‑agency CV – frequently asked questions page.

As we gradually transition to the tri‑agency CV, the system may continue to display references to the CCV. Please note that all participants must follow the tri‑agency CV instructions as specified in the Funding Opportunity and complete and attach the tri‑agency CV. (Updated : )

For details on using the tri‑agency CV on this funding opportunity, see the How to Apply section.

This funding opportunity will support the development of a learning health system (LHS) network in perinatal mental health. The LHS approach integrates research, data, and knowledge for continuous improvement in care to help ensure that the most effective treatments are consistently updated and implemented equitably across Canada. This approach would also enable the rapid translation of research findings into clinical and care practice, providing a mechanism for evaluating program impacts and improving equitable service delivery. Furthermore, this approach would ensure continuous improvement in efficiency and effectiveness of the processes of the LHS. The network is expected to develop an LHS by : (i) collecting and synthesizing data from real‑world practice ('practice to data'), (ii) using that data to answer questions and generate new and useful knowledge ('data to knowledge'), and (iii) applying that knowledge to improve care to equitably meet the needs of people with lived / living experience (PWLLE), caregivers / families and communities served ('knowledge to practice'), which includes knowledge mobilization and implementation science; see Additional Information.

Excellent research and LHSs should incorporate open science practices that enable timely access and sharing of research findings, data, and other outputs, see Additional Information.

Perinatal mental health (PMH) is an area that has seen significant research and service delivery investment / advancement in recent years at the local and regional levels. Perinatal mental illness occurs during prenatal and postpartum periods and includes conditions such as depression, anxiety, and post‑traumatic stress disorder (PTSD). If untreated, these conditions can have long‑lasting effects, increasing the risk of chronic mental health issues for the parent and developmental challenges for the child. Despite the availability of evidence‑based treatments, barriers such as stigma, lack of knowledge, and limited access to care—especially in rural areas—create a gap in treating individuals to full remission. Additionally, First Nations, Inuit, and Métis Peoples, racialised people, persons with disability, and those that identify as 2SLGBTQI+ face higher rates of perinatal mental illness, with even less access to appropriate care.

Across Canada, there are several specialised PMH programmes located in academic centres that provide gold‑standard care, including psychological and pharmacological treatment, but they are often burdened with long waitlists. Referrals depend on geographic location and primary care provider knowledge, creating an inequitable system. Timely intervention can prevent long‑term negative outcomes and improve quality of life for both parent and child. Specialised programmes are already collaborating on clinical guidelines and quality indicators for care, as well as engaging Indigenous experts for culturally safe care. However, despite these efforts, there remains a lack of an integrated, equitable system for timely access to perinatal mental health services. The ability to link programmes and local networks to develop an LHS in PMH would improve health outcomes, health equity, service delivery, and cost. Additionally, an LHS would ensure proper integration of PWLLE and caregiver / family insights, which are key in PMH patient care.

Applicants are expected to ensure equitable access of diverse researchers, including First Nations, Inuit and Métis peoples, 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 network (e.g., the FAIR principles – Findable, Accessible, Interoperable, Reusable). Final data policies and procedures, for example data access procedures, are expected to be publicly available. See Additional Information for more details.

Research Areas

This funding opportunity will support a project relevant to the development of a pan‑Canadian learning health system network in perinatal mental health (PMH).

Role and Contributions of Applicant Partners : CIHR recognises 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 for this initiative are subject to availability of funds. Should CIHR or partner(s) funding levels not be available or are decreased 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.

  • The total amount available for this funding opportunity is $6,000,000, enough to fund one grant for up to five (5) years.

For more information on the appropriate use of funds, refer to Allowable Costs.

The specific objectives of this funding opportunity are to :

  • Develop a pan‑Canadian LHS network for PMH that integrates research, practice, and care to strengthen the implementation of evidence‑based practices.
  • Enhance equitable and timely access to specialised mental health services for PMH to improve the quality of life for affected individuals and to better reach underserved populations.
  • Facilitate multi‑site, multidisciplinary research and knowledge mobilization collaborations to generate and disseminate evidence for new treatment options and early intervention / prevention strategies, while also refining and improving existing treatments and models of care for PMH.
  • Develop and implement quality indicators for service delivery, access, and outcomes of care for continuous improvement in the field of PMH.
  • Support the uptake of common data approaches and open science practices within and across provinces and territories to strengthen the pan‑Canadian LHS.
  • Create a focal point for collaboration across Canada toward the implementation and evaluation of measurement‑based streamlined pathways of “stepped care” by taking an LHS approach to the integration of local community providers with existing specialised PMH programmes.
  • For an application to be eligible, all the requirements stated below must be met and be clearly identified as such in the Participant Table (See How to Apply section) :

  • The Nominate Principal Applicant (NPA) must be an independent researcher affiliated with a Canadian post‑secondary institution and / or its affiliated institutions (including hospitals, research institutes and other non‑profit organisations with a mandate for health research and / or knowledge mobilisation).
  • While there is no limit on team size, including the NPA, a maximum of 15 individuals can be identified as key participants. Applicants are strongly encouraged to develop a diverse and equitable team. Note that an individual can fulfil multiple key participant roles as indicated.
  • Four separate PWLLE and caregiver / family perspectives
  • who have lived and / or living experience relevant to PMH, as Knowledge Users (KUs) to represent PWLLE and caregiver / family perspectives. These individuals may also fulfil the role of a service provider.
  • two PWLLE and
  • two Caregiver / Family members.
  • Three service providers
  • from three different provinces / territories listed as Principal Knowledge Users (PKUs) or KUs, in the context of PMH. Examples of service providers may include, but are not limited to : physicians, midwives, doulas, nurses, occupational therapists, social workers, physiotherapists, psychologists, peer or family support workers, care navigators, and / or Traditional Counsellors, or other health professionals / providers. These team members may also serve as PWLLE and caregiver / family member (see Eligibility criteria) or as a Champion (see Eligibility criteria) according to their participant type (KUs or PKUs).
  • Five separate champions for each of the roles below listed as PAs or PKUs. These team members are expected to coordinate their work with the NPA / Data to Knowledge Champion .
  • The NPA must also be identified as the Data to Knowledge Champion , given their overall coordinating role in ensuring that data is used to answer questions and generate new and useful knowledge.
  • A Practice to Data Champion with expertise in clinical data management and / or data science.
  • A Knowledge to Practice Champion who has experience developing and implementing integrated knowledge mobilisation plans, and who has expertise in knowledge mobilisation and implementation science.
  • An Equity, Diversity and Inclusion (EDI) Champion with expertise in sound EDI practices and principles, including experience in sex and gender‑based analysis (SGBA) or gender diversity. See Additional Information for wise practices on including an EDI Champion and defining their potential roles in the network.
  • An Indigenous Research Champion who self‑identifies as Indigenous (First Nations, Inuit, or Métis), and / or provides evidence of having meaningful and culturally safe involvement with Indigenous Peoples (see How to Apply) in order to :
  • Prioritise First Nations, Inuit and Métis Peoples and communities, in leading their research agendas;
  • Promote cultural safety of Indigenous Peoples and appropriate engagements by researchers working with Indigenous Peoples in meaningful ways to ensure that respectful relations are established;
  • Add value to the research through the use of Indigenous culturally relevant theoretical and conceptual frameworks, and Indigenous culturally relevant research protocols, including Indigenous methodologies;
  • Promote equity and development of trainees, researchers and knowledge users who are of Indigenous ancestry.
  • 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.
  • Note : Elders and / or Indigenous Knowledge‑Holders may participate on an application in a Collaborator role without the need to secure a CIHR PIN. However, the participant must be listed in the submitted Participant Table (see How to Apply ). Their contributions to the proposed activities and their meaningful engagement must be captured in the research proposal to address the points outlined in the evaluation criteria. Please note, names of Collaborators do not appear in CIHR funding decision databases and documents.

    CIHR is committed to promoting the inclusion and advancement of those who have been historically excluded from science as one of the means to enhance excellence in research, training and knowledge mobilisation. This means recognising and reducing systemic barriers, mitigating biases, as well as including and benefiting from the full pool of talented researchers and trainees. CIHR’s position on equity, diversity and inclusion (EDI) is available in the Tri‑Agency Statement on Equity, Diversity and Inclusion. Beyond efforts to bolster EDI, CIHR recognises that First Nations, Métis and Inuit are rights‑holding as First Peoples of Canada, and initiatives should be developed through distinctions‑based approaches, as found in the strategic plan and the Action Plan : Building a healthier future for First Nations, Inuit, and Métis peoples.

    Research Security

    The Policy on Sensitive Technology Research and Affiliations of Concern (STRAC Policy) is applicable to this funding opportunity. Consult the Tri‑Agency guidance on the STRAC Policy for more information.

    Applicants are advised to consult the Use of Grant Funds section of the Tri‑Agency (CIHR, NSERC and SSHRC) Guide on Financial Administration (TAGFA) to determine if an expenditure is an appropriate use of grant funds.

    To further clarify, the following expenses are examples of appropriate uses of grant funds, provided they satisfy the principles and pertinent directives of the TAGFA :

  • Full‑time or part‑time salaries paid to members of the grant team, as long as : a) they do not conduct research independently, as part of the terms and conditions of their employment (i.e. researchers in academia, hospitals and research institutes); or b) they are not themselves the recipient of an agency grant (i.e. the NPA or equivalent) or; c) they are not receiving compensation from other sources for their time spent on the funded research / activities. For more information consult the Directive on Employment and Compensation Expenditures.
  • Costs related to community mobilisation and engagement, including culturally relevant promotional items such as tobacco, cloth, feasting and gift giving for honouring ceremonies, and cash reimbursements (in a method acceptable to the individual or community being reimbursed) to compensate community participation.
  • Contracts and / or consultant fees for knowledge mobilisation and communication activities for Indigenous Elders, community members, and Indigenous Knowledge Keepers involved in activities related to the Indigenous community.
  • Costs related to the translation and preparation of information / material intended for public consumption, including for the purposes of informing and engaging partners (e.g., website content, information pamphlets, guidelines, promotional and event‑related material, etc.).
  • Use of Personal Information

    All information is shared in accordance with the Privacy Act.

    As per the Privacy Act, personal information means information about an identifiable individual that is recorded in any form.

  • Personal information submitted during the application process, including but not limited to information provided through applicant CVs, the Tri‑Agency Self‑identification Questionnaire and other application documents required by this funding opportunity, will be made available to select CIHR personnel with the appropriate training and security clearance and on a need‑to‑know basis, for the purposes of future program planning and design and evaluation and learning for organisational and programme strengthening. In addition, CIHR may share de‑identified, aggregated self‑identification information with the sponsoring institutes and competition partners, for this purpose. For further information about the Self‑identification Questionnaire and the use of personal information, see the Tri‑Agency Self‑identification Questionnaire Frequently Asked Questions.
  • For this funding opportunity, some sections of the application containing information that directly or indirectly identifies the applicant(s), will be shared with some funding partner(s) and / or CIHR Institute staff, to assist with relevance review.
  • Personal information, including related research security forms, collected as part of the implementation of the research security measures, may be shared with Canada’s national security departments and agencies for the purpose of assessing risks to national security.
  • All progress / final reports will be shared with partners supporting the grant (See Conditions of Funding for report details).
  • Conditions of Funding

    In addition to the general conditions of funding governing CIHR grants, the following are the program specific conditions of funding applicable to this funding opportunity :

  • Data related to First Nations, Inuit or Métis communities whose traditional and ancestral territories are in Canada must be managed in accordance with data management principles developed and approved by those communities, and on the basis of free, prior and informed consent. This includes, but is not limited to, considerations of Indigenous data sovereignty, as well as data collection, ownership, protection, use, and sharing.
  • All information intended for public consumption, including for the purposes of informing and engaging partners (e.g., website content, information pamphlets, guidelines, promotional and event‑related material, etc.), must be provided in both official languages (English and French), accessible to screen readers, and should be developed using plain language practices. See Allowable Costs for more details.
  • CIHR reserves the right to terminate or suspend funding if there is a determination of unacceptable national security risk by the Government of Canada.
  • The Nominated Principal Applicant (NPA) is responsible for the following reporting requirements :
  • The NPA will be required to submit annual reports during the term of the grant (including during the Authority to Use Funds period).

  • In addition to the annual reports, the NPA will be required to submit an electronic Final Report to CIHR. This online report will be made available to the NPA on ResearchNet at the beginning of the grant funding period and can be filled in as the research progresses.
  • The funded team may be required to participate in up to 3 meetings / workshops throughout the 5‑year funding term. These meetings will be hosted and organised by CIHR and will include :
  • Up to 2 progress meetings for the purposes of reporting on the project’s progress, sharing lessons learned, and knowledge mobilisation.

  • An end‑of‑grant workshop held at the end of year 5.
  • The team is required to budget for at least one of these meetings / workshops to be an in‑person event. The team should budget for at least three participants including the NPA to attend the meetings / workshops.
  • The Institute of Neurosciences, Mental Health and Addiction will perform a relevance review on the summary of the application to identify applications that are in alignment with the objectives of this funding opportunity.

    Applications that are not deemed to be relevant will be withdrawn from the competition.

    For information on CIHR’s peer review principles, see the Peer Review : Overview section of CIHR’s website.

    To support the strategic objectives of this funding opportunity, the following evaluation criteria will be used :

  • Approach / Design
  • Clarity, appropriateness, and feasibility of the research approach / design to address the objectives of the funding opportunity and meet the needs identified in the proposal.

  • Quality and appropriateness of the incorporation of the Learning Health System (LHS) concept, and processes (i.e., practice to data, data to knowledge, knowledge to practice), in the research approach / design.
  • Quality and appropriateness of the integration of PWLLE and caregivers / families into the LHS approach, including :
  • The extent to which the PWLLE and caregiver / families engagement plan is clear and robust (see How to Apply).

  • Appropriate plans for engaging and collaborating with other key partners for PMH, including community organisations, policy makers, health and social service providers, researchers, and other relevant knowledge users, as needed.
  • Appropriate plans for engaging and collaborating with Indigenous communities using distinctions‑based approaches, including with First Nations, Inuit, or Métis Peoples.
  • Consideration of open science principles, practices, and / or tools in the network approach / design.
  • Demonstration that the research approach / design will uphold the rights, self‑determination, and self‑governance of First Nations, Inuit and Métis Peoples including by respecting the First Nations Principles of OCAP® Footnote 1 and / or other approaches as appropriate (e.g., CARE Principles for Indigenous Data Governance Additional Information), and show appropriate consideration of the protocols of the partnering Indigenous communities and, as necessary, the Tri‑Council Policy Statement Chapter 9 : Research Involving the First Nations, Inuit, and Metis Peoples in Canada to develop meaningful and culturally safe research designs, practices, plans and activities throughout the research project(s).
  • Concrete commitments to incorporating Best practices in Equity, Diversity and Inclusion, including appropriate incorporation of biological variables (e.g., sex, age), consideration of life stage, and other intersecting social factors (e.g., gender, race, ethnicity, language, income) into the research approach / design, where applicable.
  • Appropriateness of the knowledge mobilisation plan, including strategies for sharing knowledge and results in a timely and accessible manner and plans to engage diverse groups in outreach and communication (see How to Apply).
  • Quality and appropriateness of the data management plan (DMP) in describing the collection, creation, documentation, storage, protection and preservation of the source data (see How to Apply), including how ethical issues, including those related to data access and ownership; transparency of processes and procedures, and conflict of interest management are to be addressed.
  • Quality and appropriateness, where applicable, of the DMP in describing considerations related to Indigenous research data management and data sovereignty.
  • The extent to which the NPA is a researcher with proven leadership capabilities, scientific expertise in PMH.
  • The extent to which the applicant team, specifically, the PAs, PKUs, and KUs (see Eligibility Criteria) have the necessary expertise to deliver on the project’s objectives.
  • The extent to which the applicants in specific roles of Practice to Data Champion, Data to Knowledge Champion, and Knowledge to Practice Champion have the necessary expertise and experience for their specified role.
  • The extent to which the engagement of team member(s) representing PWLLE and caregivers / families is meaningful and appropriate.
  • The extent to which there is evidence that the EDI Champion is a core member of the team with a track record and relevant expertise to ensure sound EDI practices and principles, including 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 and the Additional Information section for examples of systemic barriers and guidance.
  • The extent to which the Indigenous Research Champion has the necessary knowledge, expertise and experience in Indigenous health research, and to which the research team has complementary expertise and synergistic potential to conduct Indigenous health research.
  • Evidence of the capacity and experience of the research team to work in Indigenous communities in a meaningful and culturally safe way.
  • Impact
  • The extent to which the project will have a substantive and sustainable impact on health outcomes, practice, programmes, and / or policy.

  • Potential to improve outcomes and equitable access to PMH services.
  • Extent of the role(s) and contribution(s) of all applicant partner(s) in advancing research objectives (if applicable).
  • Proactive and meaningful consideration of partnership risks, including the extent of real and / or perceived conflict of interest and appropriateness of its management and mitigation (if applicable).
  • Feasibility
  • Extent to which the requested budget (inclusive of funds allocated for PWLLE / caregiver / family engagement, knowledge mobilisation and dissemination activities) is justified.

  • Extent to which the project is accomplishable in the given timeframe with the resources available / described.
  • Appropriateness of mechanisms to manage anticipated risks and challenges related to the timeframe and budget.
  • Availability and suitability of personnel, facilities and infrastructure required to achieve a pan‑Canadian LHS network.
  • Funding Decision

    The highest ranking application be funded. Applications that receive a rating below 3.5 will not be funded.

    The names of successfully funded applicants will be published on the CIHR website.

    Partner and Internal Collaborator Participation

    The opportunity to add new partners and internal collaborators to this funding opportunity may arise after publication. These partners and internal collaborators may not be listed; however, the principles that govern relevance review, including consent to share information and funding decisions, will still apply.

  • To complete your Full Application, follow the “Specific Instructions” listed below, and where applicable, consult the Grants – Application Guidelines document.
  • Note, this funding opportunity is using the tri‑agency CV.

  • All participants listed, with the exception of collaborators, are required to :
  • Have / obtain a CIHR PIN

  • Complete the Tri‑Agency Self‑identification Questionnaire
  • Keep your information up to date : Regularly review and update your My CIHR Profile , including confirming the correct Primary Affiliation is linked.
  • The Primary Affiliation field of the My CIHR Profile is important for various funding related activities, including eligibility assessments and Research Support Fund calculations (if applicable). Your My CIHR Profile can be accessed by clicking on your name in the top right‑hand corner of the ResearchNet screen. If your Primary Affiliation name is not available in the drop‑down menu, contact the CIHR Contact Centre.

    Note : Elders and / or Indigenous Knowledge Holders may be named as Collaborators on your application, allowing them to participate without securing a CIHR PIN. (Please note, names of Collaborators do not appear in CIHR funding decision databases and documents).

    Specific instructions to complete your ResearchNet application

  • Participant Information
  • List all participants in the “Identify Participants” task. Consult the Eligibility section and ensure that all requirements are met.

  • All key participants (maximum 15) are required to submit a Tri‑Agency CV. Key participants must include all participants required per Eligibility. As we gradually transition to the tri‑agency CV, the system may continue to display references to the CCV. Please note that all participants must follow the tri‑agency CV instructions as specified in the Funding Opportunity and complete and attach the tri‑agency CV. (Updated : )
  • The maximum length of CVs is 5 pages in English and 6 pages in French. Any content in excess of the page limit set for the language in which it is written will be removed without further notice to the CV owners or the NPA.

  • CVs must follow CIHR's formatting guidelines for attachments.
  • Consult the Tri‑Agency CV instructions and the Tri‑Agency CV – Frequently asked questions for assistance with completing the tri‑agency CV template.

  • All participants must also be listed in the Participant Table under the task “Attach Other Materials” (see below).
  • Note : For the purpose of this task in ResearchNet, key participants can only be listed once. For key participants fulfilling multiple roles (see Eligibility), select one participant type in ResearchNet, but ensure these participants are identified for all roles they fulfill within the uploaded Participant Table.

    Note : Elders and / or Indigenous Knowledge‑Keepers identified in ResearchNet as Collaborators for administrative purposes but that fulfil a key participant role must provide their tri‑agency CV through the task “Attach Other Application Materials” (see below).

  • Attachments :
  • Curriculum Vitae (mandatory for key participants)

    The Nominated Principal Applicant and all remaining key participants (maximum 15) must upload their tri‑agency CV. All TCVs must be uploaded as individual PDFs and labelled as “TCV – Last name, First Name”.

  • Submit tri‑agency CVs by uploading the completed documents in the “Attachment” tab and selecting “Curriculum Vitae” as the Document Type in the dropdown menu.
  • Most Significant Contributions – Optional (maximum one (1) page)
  • All applicants (key and other), excluding Collaborators have the option of providing additional information / context regarding their most significant contributions relating to the application. The contributions that are described should be directly relevant to the grant application, and should demonstrate how the applicant will contribute to the application at hand.

    Task : Enter Proposal Information

  • The Research Proposal must outline each of the elements presented in the Evaluation criteria to describe how the proposal addresses the Objectives of this initiative.
  • Research proposals written in French will be allowed to submit additional pages in support of evidence demonstrating that French documents require approximately 20% more space than similar English documents. Therefore, to ensure an equitable amount of space is provided, the following page limits will apply :

    12 pages when the Research proposal is written in English

  • 14.5 pages when the Research proposal is written in French
  • Note : Any additional pages over the above‑mentioned limit will be removed with no further notification to the Nominated Principal Applicant.

  • Elders and / or Indigenous Knowledge‑Holder's contributions to the proposed activities and their meaningful engagement should be captured in the research proposal to address the points outlined in the evaluation criteria.
  • References, charts, tables, figures and photographs can be uploaded under “Attachments – Research Proposal Appendix”.
  • Please note that the Applicant Team must also submit a detailed PWLLE and Family / Caregiver Engagement Plan , a Knowledge Mobilisation Plan and a Data Management Plan in addition to the Research Proposal (see Task : Attach Other Application Materials for more information).
  • Task : Identify Sensitive Technology Research Areas

  • The NPA must combine all attestation forms into one (1) PDF file and upload it under this task.
  • Completed attestation forms will be neither accessible to, nor shared with, peer reviewers.
  • Task : Complete Summary of Research Proposal

  • Summarise your research proposal. The relevance review will be conducted using the Summary of Research Proposal. Note that your summary cannot exceed one page.
  • Task : Enter Budget Information

  • Provide a detailed budget justification in relation to planned activities and clearly justify all budget items (including cash and in‑kind contributions, if relevant). Teams are required to budget for participants to attend in‑person events (see Conditions of Funding ).
  • Task : Attach Other Application Materials

  • Other – Attach the following under “Other” :
  • Label as “SGBA Certificate – Name ” (mandatory for NPA and EDI Champion) After completing the appropriate training module that applies to your research project, you will receive a certificate of completion that you will save and upload here. The training module should take approximately 40 minutes to complete. Upload the certificate as an unsecured PDF.

  • Label as : “Indigenous Health Research Cultural Safety Form – Name” (mandatory) :
  • This funding opportunity seeks applicants who self‑identify as Indigenous (First Nations, Inuit, or Métis) and / or can provide evidence of having meaningful and culturally safe involvement with Indigenous Peoples. This form is mandatory at minimum for the Indigenous Research Champion, but can also be filled for every applicant fulfilling this requirement.

  • Upload the completed Indigenous Health Research Cultural Safety Form ( PDF (681 KB) ) . The form(s) need(s) to be filled by the corresponding applicant and uploaded in the application by the NPA on their behalf.
  • Label as “PWLLE and Family / Caregiver Engagement Plan” (mandatory) : Description of how the research project will engage PWLLE and caregivers / families as meaningful partners throughout the entire research process (maximum 1 page when written in English; 1.5 page when written in French).
  • Label as “Knowledge Mobilisation Plan” (mandatory) : Description of detailed timelines, deliverables, engagement & accessibility strategies, etc. (maximum 2 pages when written in English; 2.5 pages when written in French).
  • Label as “Data Management Plan” (mandatory) – The data management plan (DMP) should describe how the team will manage the source data as part of its activities. (maximum 2 pages when written in English; 2.5 pages when written in French).
  • The DMP should describe the collection, creation, documentation, storage, protection and of the source data. Where applicable, the DMP should also describe considerations related to Indigenous research data management and data sovereignty.

  • Label as “Tri‑Agency CV – Name” (mandatory if applicable) : Elders and / or Indigenous Knowledge‑Keepers fulfilling a key participant role on the application but identified as Collaborators in ResearchNet for administrative purposes must have their tri‑agency CV included in the application.
  • Label as “Applicant Partner COI Document” (mandatory if applicable) : Describe the role of all applicant partners, how / if they will contribute to research and research related activities, and any consideration of risk and / or conflict of interest as appropriate (Maximum one (1) page).
  • Label as “Relationships with private industry (mandatory if applicable) : Should an applicant or any project participant(s) have current or previous relationships with private industry including, but not limited to, financial or in‑kind support for research, the applicant(s) must justify in a one (1) page attachment for peer review consideration how this / these existing or previous relationship(s) will contribute to the research as well as any potential risk, or conflict of interest considerations as appropriate. CIHR recognizes that the range of industries relevant to this field of research is broad and it is expected that all possible relationships be disclosed.
  • Participant Table (mandatory) – Upload under “Participant Table” :
  • Download this table template which will be used for eligibility and peer review assessment. All participants (including Collaborators) should be listed in the Participant Table.

    Key participants must be clearly identified in the Section 1 of the table. If a participant fulfils multiple eligibility requirements, repeat the name of this participant on the appropriate rows. The ‘Expertise and Experience’ box should be used for a brief description of what the participant brings to their role on the application. If a participant holds multiple roles, this description can vary for each role. The participant fulfilling one of these roles must also submit a tri‑agency CV (see Task : Identify Participants ).

  • Other participants should be clearly identified in the Section 2 of the table. No tri‑agency CV is allowed for these participants, but PAs, Co‑apps, PKUs, KUs can provide a most significant contribution (optional) in addition to a brief description of what the participant brings to their role on the application in the participant table.
  • Note : Elders and / or Indigenous Knowledge‑Keepers in any role must be listed on the participant table and assigned the role that best matches their contribution (see CIHR definitions ). Elders and / or Indigenous Knowledge‑Keepers fulfilling a key participant role on the application but identified as Collaborators in ResearchNet for administrative purposes must be listed in Section 1 of the table and indicate the role per eligibility (see Eligibility ).
  • Publication list (optional) : List a maximum five (5) publications from the last five years relevant to the proposal (maximum one (1) page).
  • Letters of Support (optional) : Please refer to the CIHR examples of details to be provided in letters of support.
  • Task : Download Supplemental Application Information

  • This task provides an application checklist to ensure all the material is submitted for the application to be eligible. All applicants must complete the fillable PDF form “Application checklist” available on ResearchNet. Once completed, the form must be saved and uploaded as a PDF onto ResearchNet.
  • This task collects information used for the purpose of peer review administration and aids CIHR in recruiting appropriate expertise. Suggest Canadian and / or international reviewers that you think have the expertise to review your application. You should not suggest reviewers in conflict of interest. Consult the Conflict of Interest and Confidentiality Agreement for Peer Reviewers and Peer Review Observers on the CIHR website for more information.
  • CIHR reserves the right to make the final selection of reviewers.
  • Task : Manage Access (optional)

  • The Nominated Principal Applicant (NPA) can delegate access to a maximum of five individuals to support the completion of the application. NPAs should revoke delegates’ access prior to completing the Consent and Submit tasks if they do not want them to retain access to submitted applications via their Completed Activities tab. For more information, please see the Frequently Asked Questions (FAQ).
  • Task : Print Signature Pages

  • Signature Requirements :
  • Signature of the Nominated Principal Applicant is not required for applications submitted through ResearchNet.

  • Signatures must be included for all other applicants (except Collaborators), and individual(s) with signing authority from the Institution Paid.
  • Original signatures are not required. The scanned signed signature pages and the Routing Slip must be uploaded in the Print / Upload Signature Pages task in ResearchNet prior to submitting your application.
  • Note : Additional partners / internal collaborators, including from industry and the private sector, may join this funding initiative over the coming year.

    Internal Collaborators

    Canadian Institutes of Health Research

    At the Canadian Institutes of Health Research (CIHR), we know that research has the power to change lives. As Canada’s health research investment agency, we collaborate with partners and researchers to support the discoveries and innovations that improve our health and strengthen our health care system.

    CIHR – Institute of Neurosciences, Mental Health and Addiction

    The Institute of Neurosciences, Mental Health and Addiction (INMHA) supports research to enhance mental health, neurological health, vision, hearing, and cognitive functioning and to reduce the burden of related disorders through prevention strategies, screening, diagnosis, treatment, support systems, and palliation.

    Learning Health System

    A Learning Health System (LHS) is a health system in which research, data, and experience generate knowledge and evidence that is embedded in and applied to processes, policies and practices to continuously innovate and improve health equity, service delivery and cost, as well as improve the experience for service providers and people accessing services. The LHS concept has been developed for more than a decade by experts from a wide range of disciplines (e.g., clinical‑scientists, clinicians, healthcare analytics, statisticians, biostatisticians, epidemiologists, healthcare informaticians, research funders, etc.). LHSs aim to ensure services remain flexibly, adaptable, and in the best interest of outcomes for individuals by collecting and applying data and knowledge into practice.

    A in Canada, a conceptual framework has been developed to support the implementation of LHSs grounded in core values such as equity, adaptability, person focused, shared accountability, scientific integrity, etc.

    Data Management Plans

    A data management plan (DMP) is a formal document that details the strategies and tools you will implement to effectively manage your data both during your research project and after its completion. DMPs contribute to :

  • Efficiency - identify strategies and potential challenges in advance; develop sound data practices for your research team; prepare data
  • Research Quality - ensure reliability and accuracy of data through careful documentation of your data collection, handling and stewardship practices.
  • Reusability and Impact - improve discoverability, accessibility, and reusability of your data by planning for sharing in a repository; and increase the potential impact of your research.
  • Implementation Science

    Implementation science is the scientific study of methods and strategies that facilitate the uptake of evidence‑based practice and research into regular use by practitioners and policymakers. The field of implementation science seeks to systematically close the gap between what we know and what we do (often referred to as the know‑do gap) by identifying and addressing the barriers that slow or halt the uptake of proven health interventions and evidence‑based practices.

    Equity, Diversity and Inclusion (EDI) Principles and Guidelines

    Wise Practices for including an Equity, Diversity and Inclusion (EDI) Champion

    The champion can take on roles as an educator, mentor, consultant, facilitator, advocate, co‑investigator or principal applicant. In each role, champions are responsible for promoting and integrating EDI considerations throughout all stages of the research.

    The list below provides examples of the types of activities champions may engage in. This list is not exhaustive or prescriptive; rather, it is intended to provide guidance for the inclusion of champions.

  • Promote the value of EDI, especially as it relates to foster and strengthen training environments.
  • Provide advice and guidance to the team on how best to take EDI into account in planning and procedures.
  • Help develop, evaluate and reflect on advancement of EDI in training, mentorship and funding of current and future scientists.
  • Facilitate discussion of EDI, including providing resources on historical EDI issues and sharing new findings and innovations.
  • Ensure there is education and outreach to promote and sustain an inclusive and diverse research environment within the team.
  • Provide EDI resources (such as a toolbox of strategies for advancing EDI and for responding to resistance to EDI considerations).
  • Identify resources and EDI training opportunities for the team to better understand the needs and realities of members of underrepresented groups.
  • Lead / support the development of an approach for considerations of EDI in training activities.
  • These tips will ensure that both champions and research benefit fully from the role.

  • The roles of the champion are clearly articulated in the research proposal.
  • The specific tasks that the champion will perform are defined.
  • The champions have dedicated and specified resources to execute their defined roles, such as course relief for protected time, administrative assistance, and / or trainees to support their work for the team.
  • Where the champion is not a principal or co‑investigator, they are clearly integrated in the leadership or governance structure, to ensure they have meaningful engagement.
  • The champion is recognised through authorship in publications and presentations when relevant contributions are made.
  • CIHR recognises that First Nations, Métis and Inuit are rights‑holding as Indigenous Peoples of Canada and may not consider themselves to be part of equity‑seeking groups (e.g., women, racialised minorities, persons with disability, and members of 2SLGBTQI+ communities). Taking a rights‑and distinctions‑based approach to Indigenous self‑determination in research is important to reflect this position and to strengthen Indigenous health and well‑being.

    Cultural Safety

    Respectful relationships can be established Footnote 2, Footnote 3, Footnote 4, when the research environment is socially, spiritually, emotionally and physically safe. Cultural safety is a participant‑centred approach that encourages self‑reflexivity among health researchers and practitioners. It requires an examination of how systemic and personal biases, authority, privilege and territorial history can influence these relationships. Cultural safety requires building trust with Indigenous Peoples and communities in the conduct of research.

    Realising cultural safety in health and wellbeing research entails understanding the social, political and historical contexts that have resulted in power imbalances. It requires an individual to have cultural humility, competence, sensitivity and awareness in determining relevant health research policies, programmes, and project approaches with Indigenous Peoples.

    Meaningful and culturally safe practices refer to equity in health research and delivery. In a meaningful and culturally safe research environment, each person’s identity, beliefs, needs and reality are acknowledged. Participants feel safe based on mutual respect, meanings, learning experiences and shared knowledge. Cultural safety empowers people and ensures that the participating community, group or individual is a partner in decision‑making.

    The First Nations Principles of Ownership, Control, Access and Possession (OCAP® Footnote 1) serve as an example of First Nations self‑governance, but are distinct to First Nations and not distinct to Inuit or Métis collectives and organisations. CIHR recognises that a distinctions‑based approach is required to ensure that the unique rights, interests and circumstances of the First Nations, Inuit and Métis Peoples are acknowledged, affirmed, and implemented.

    Open Science

    “Open science” refers to an approach to research that emphasises open sharing of research outputs, resources, methods or tools, at any stage of the research process. Publications, research data and software, notebooks, peer review, educational resources and citizen science all fall within its scope. In the context of this funding opportunity, grant holders are required to make peer‑reviewed publications openly accessible within 12 months of publication, as per the Tri‑Agency Open Access Policy on Publications. Grant holders are also encouraged to provide access to data that support published findings, for example by depositing data in a public repository and providing the digital object identifier (DOI) for the dataset in all publications, so long as providing access to the data does not compromise patient privacy or otherwise conflict with ethical or legal obligations.

    Footnotes

    Footnote 1

    OCAP® is a registered trademark of the First Nations Information Governance Centre (FNIGC).

    Return to footnote 1 referrer

    Footnote 2

    Evidence of the capacity and experience of the research team to work in Indigenous communities in a meaningful and culturally safe way.

    Return to footnote 2 referrer

    Footnote 3

    First Nations Health Authority. (n.d.). Cultural Safety and Humility. Received November 12, 2018.

    Return to footnote 3 referrer

    Footnote 4

    Williams, R. (1999). Cultural safety – what does it mean for our work practice? Australian and New Zealand Journal of Public Health, 23(2), 213-214.

    Return to footnote 4 referrer

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