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This document outlines the structure and expectations for a three-week skills workshop hosted by Kansas State University Counseling and Psychological Services. It details the importance of attendance, the focus on skill development and self-esteem, and the responsibilities of participants regarding fees and confidentiality.
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01
Begin with a clear title that states the purpose of the form.
02
Provide a brief explanation of the study or procedure, including its goals.
03
Outline the potential risks and benefits involved in participation.
04
Clearly describe what participation will involve (e.g., time, activities).
05
Include information about confidentiality and data protection measures.
06
Explain that participation is voluntary and that participants can withdraw at any time.
07
Provide contact information for questions or concerns.
08
Include a section for participant signature and date, confirming understanding and consent.

Who needs informed consent - skills?

01
Research participants in clinical trials.
02
Patients involved in medical procedures or studies.
03
Minors, with parent or guardian consent.
04
Individuals participating in surveys or qualitative studies.
05
Employees or volunteers in organizational training programs.
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Informed consent refers to the process of ensuring that a participant is fully aware of the risks, benefits, and alternatives of a procedure or study before agreeing to participate. It requires clear communication and understanding.
Researchers, healthcare providers, or institutions conducting medical procedures, studies, or research involving human participants are required to obtain and file informed consent.
To fill out informed consent, ensure that the document includes the study's purpose, procedures, risks, benefits, confidentiality measures, and space for participant signatures, while providing a clear explanation of each component.
The purpose of informed consent is to protect the autonomy of participants by ensuring they make knowledgeable decisions about their involvement in research or medical procedures.
The information that must be reported includes the study's purpose, procedures, risks, benefits, alternative options, confidentiality, and contact information for questions.
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