MODULE - 1 Flashcards
Participants must be provided with comprehensive information about
the study, including its purpose, procedures, potential risks, and benefits, enabling them
to make an informed decision about their involvement. This consent should be given voluntarily, without any form of coercion
Informed Consent
Researchers often need to obtain approval from their institution’s
IRB, especially when the study involves human subjects. The IRB reviews the research proposal to ensure that ethical standards are upheld and that participants’ rights and
welfare are protected
Institutional Approval:
When research is conducted in specific locations such as schools,
hospitals, or companies, obtaining permission from the relevant authorities at these sites
is essential. This ensures that the research activities are authorized and that the site is aware of and agrees to the study being conducted on their premises
Site Permission
Accessing certain datasets or records may require additional permissions, particularly when dealing with sensitive or confidential information.
Researchers must ensure they comply with data protection regulations and institutional policies governing data access and use
Data Access Permissions
It ensures that participants are treated with respect and that their autonomy is honored, allowing them to make informed choices about their participation
Ethical Considerations
Obtaining the necessary approvals protects researchers from potential legal issues related to data collection, privacy, and the conduct of the study
Legal Compliance
Reach out to the relevant decision-maker, such as a department head, institutional review board (IRB), or ethics committee. These individual or groups are responsible for granting permission to conduct research
Identify the Right Contact
Clearly outline the research question,
methodology, anticipated outcomes, potential benefits, and the measures in place to protect participant privacy and confidentiality. A we l-structured proposal strengthens the
credibility of the research and facilitates approval
Develop a Compelling Research Proposal
Emphasize adherence to ethical research practices, including informed consent, anonymity, and robust data protection measures. Ethical compliance ensures the research respects participants’ rights and mitigates risks
Prioritize Ethical Considerations
Use simple, non-technical language to explain the research purpose, participation requirements, potential risks and benefits, and the participant’s right to withdraw at any time
Craft a Clear Consent Form
Understand the specific requirements for obtaining permission in
the research setting, including approvals from local authorities or regulatory bodies. Tailoring the process to the context ensures smoother implementation
Adapt to the Context:
Explain how participant data will be collected, stored, and anonymized to
protect their privacy. Highlight measures in place to comply with data protection regulations
Data Privacy
Provide a clear strategy for recruiting participants, ensuring inclusivity and fairness in the process
Participant Recruitment:
Outline how research findings will be shared with stakeholders, including publications, presentations, or reports tailored to the audience’s needs
Dissemination Plan
Maintain open communication with gatekeepers and participants throughout the research process to address emerging concerns and provide
updates
Follow-Up Communication
