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SayPro Research Ethics Form

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SayPro Research Ethics Form


1.SayPro Project Information

FieldDetails
Project Title:Enter full project or study title
Principal Investigator:Name of lead researcher/facilitator
Affiliation/Organization:SayPro or partner organization
Contact Information:Email, phone number
Project Start Date:DD/MM/YYYY
Expected End Date:DD/MM/YYYY

2.SayPro Project Description

Provide a clear and concise summary of the research project including:

  • Purpose and objectives
  • Target population and sample size
  • Research methods (surveys, interviews, observation, etc.)
  • Geographic location(s) of data collection

3.SayPro Ethical Considerations

3.1 Informed Consent

  • How will informed consent be obtained? (Written, verbal, electronic)
  • Will participants receive information sheets detailing the study purpose, risks, benefits, and confidentiality?
  • How will consent be documented?
  • For minors or vulnerable populations, specify guardian/parent consent procedures.

3.2 Confidentiality and Privacy

  • Describe measures to protect participant identity and personal data (e.g., anonymization, secure storage).
  • Who will have access to the data?
  • How long will data be stored and what is the plan for secure disposal?

3.3 Potential Risks and Benefits

  • Identify any physical, psychological, social, or legal risks to participants.
  • Outline how risks will be minimized or managed.
  • Describe any direct benefits to participants or communities.

3.4 Vulnerable Populations

  • Indicate if the research involves vulnerable groups (e.g., children, people with disabilities).
  • Describe additional safeguards to protect these participants.

3.5 Community Engagement and Approval

  • Have community leaders, local authorities, or gatekeepers been consulted and provided approval?
  • Attach any letters of support or approval.

4.SayPro Data Management

ItemDescription
Data Collection Methods:Surveys, interviews, observations, etc.
Data Storage Location:Physical/Cloud storage specifics
Data Access:Who can access the data
Data Retention Period:Specify duration (e.g., 5 years)
Data Disposal Method:Describe how data will be securely destroyed

5.SayPro Declarations

I, the undersigned, declare that:

  • I have read and understood the ethical guidelines set by SayPro.
  • The research described above will be conducted in accordance with these guidelines.
  • I will ensure informed consent is obtained and documented appropriately.
  • I will protect participants’ confidentiality and safety throughout the research.
  • I will report any adverse events or ethical issues to the SayPro Ethics Committee promptly.
  • Any changes to the project affecting ethical considerations will be submitted for review.

Principal Investigator Name:
____________________________________________

Signature:
____________________________________________

Date:
____________________________________________


6.SayPro SayPro Ethics Committee Review

Reviewer NamePositionSignatureDateDecision (Approved / Conditional / Not Approved)Comments/Conditions

7.SayPro Attachments Checklist

  • ☐ Research Proposal
  • ☐ Participant Information Sheet
  • ☐ Consent Forms
  • ☐ Letters of Community Approval
  • ☐ Risk Assessment
  • ☐ Other (please specify): ___________________________

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