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CONSENTFORMFORRESEARCHSTUDY(20162017) Mobile CSP:UsingMobileLearningtoTeachComputerSciencePrinciplesinSchools ProjectLeaders: RalphMorelli, ProfessorEmeritusofComputerScience, TrinityCollege ralph.morelli@trincoll.edu,
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The 28 informed consent form may be needed by individuals or organizations involved in medical research, clinical trials, or other healthcare-related activities. It is typically required when participants or patients need to provide their consent for a specific treatment, procedure, or participation in a study. The specific requirements for who needs this form may vary depending on local regulations and institutional policies.
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The 28 informed consent form is a document that outlines the agreement between a participant and a researcher regarding their participation in a study or research project.
Researchers conducting studies or research projects that involve human participants are required to have participants sign the 28 informed consent form.
The 28 informed consent form should be filled out by providing all necessary information about the study, the participant's rights, potential risks and benefits, and obtaining signatures from both the participant and the researcher.
The purpose of the 28 informed consent form is to ensure that participants are fully informed about the study they are participating in, understand their rights, and voluntarily agree to take part.
The 28 informed consent form should include details about the study procedures, any possible risks or benefits, confidentiality measures, the participant's rights, contact information for questions or concerns, and signatures from both the participant and the researcher.
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