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Stimulants and HIV: Addressing Contemporary and Recurring Epidemics (R61/R33 - Clinical Trial Required)

Stimulants and HIV: Addressing Contemporary and Recurring Epidemics (R61/R33 - Clinical Trial Required) 

Required Information for Application:

1. Applicant Information:

   - Full name and contact information of the principal investigator

   - Affiliation and position/title of the principal investigator

   - Brief description of the qualifications and experience of the principal investigator

   

2. Project Title:

   - Title that accurately reflects the focus of the proposed research

   

3. Project Summary:

   - A concise summary of the proposed research project, including its objectives, methods, and expected outcomes

   

4. Background and Significance:

   - Explanation of the significance of stimulant use in the context of the opioid epidemic and the impact on HIV cases among gay men and other MSM

   - Discussion of the clinical issues faced by providers when dealing with stimulant/opioid users

   - Description of the limited tools available for stimulant treatment and addressing non-SUD or mild SUD stimulant use

   

5. Specific Aims:

   - Clear and specific objectives of the proposed research project

   

6. Research Strategy:

   - Detailed description of the methods and approaches that will be used to achieve the stated aims

   - Discussion of any innovative aspects or new treatments that will be incorporated

   

7. Expected Results:

   - Anticipated outcomes of the research project and their potential impact

   

8. Resources and Facilities:

   - Information about the research facilities, equipment, or resources that will be utilized for the project

   

9. Budget:

   - Detailed breakdown of the estimated costs for the proposed research, including personnel, supplies, equipment, and other expenses

   

10. Timeline:

    - A proposed timeline or schedule for the completion of the research project

    

11. References:

    - List of relevant references and literature that support the proposed research

    

12. Compliance and Ethics:

    - Description of how the research will comply with ethical guidelines and regulations, especially when dealing with human subjects

    

13. Institutional Support:

    - Confirmation of institutional support for the proposed research, including any letters of support or collaboration from relevant departments or organizations

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88%

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93%

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