SayPro Participant Consent Summary (template provided)

SayPro Participant Consent Summary

SayPro Project Title: SayPro Program

SayPro Principal Investigator: [Name]

SayPro Contact Information: [Email/Phone Number]

SayPro Purpose of the Study: The SayPro program aims to [briefly describe the purpose of the program, e.g., improve communication skills, enhance professional development, etc.]. Participants will engage in various activities designed to [list key activities, e.g., workshops, discussions, assessments].

SayPro Participation Requirements: Participants will be asked to [describe what participation involves, e.g., attend sessions, complete surveys, provide feedback]. The expected duration of participation is [duration, e.g., 6 weeks, 3 months].

SayPro Voluntary Participation: Participation in the SayPro program is entirely voluntary. Participants may withdraw at any time without any consequences.

SayPro Confidentiality: All information collected during the program will be kept confidential. Data will be stored securely and will only be accessible to the research team. Personal identifiers will be removed in any published results.

SayPro Risks and Benefits:

• Risks: [Describe any potential risks, e.g., discomfort in sharing personal experiences, etc.]
• Benefits: Participants may benefit from [list potential benefits, e.g., improved skills, networking opportunities, etc.].

SayPro Informed Consent: By signing this summary, you acknowledge that you have read and understood the information provided. You agree to participate in the SayPro program under the terms outlined above.

Participant Signature: ________________________

Date: ________________________

Researcher Signature: ________________________

Date: ________________________