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This consent form provides information regarding a research study aimed at evaluating the effectiveness of the TEACCH School Transition to Employment and Post-Secondary Education (T-STEP) Program for autistic young adults. Participants will be involved in assessments and interventions over the course of approximately nine months, allowing researchers to compare the T-STEP Program with a Counseling Program.
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How to fill out study informed consent

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How to fill out study informed consent

01
Begin by clearly stating the purpose of the study.
02
Explain what participation involves, including activities and duration.
03
Outline any potential risks or discomforts associated with participation.
04
Describe any benefits to participants or others.
05
Explain confidentiality and how personal data will be used.
06
Provide information on voluntary participation and the right to withdraw at any time.
07
Include contact information for questions about the study or rights as a participant.
08
Ensure participants sign and date the consent form before participating.

Who needs study informed consent?

01
Individuals participating in research studies
02
Researchers conducting studies involving human subjects
03
Institutional Review Boards (IRBs) overseeing ethical standards
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Study informed consent is a process in which researchers provide potential participants with comprehensive information about a study, allowing them to make an informed decision about their participation.
Researchers and institutions conducting studies that involve human participants are required to file study informed consent.
To fill out study informed consent, provide clear and concise information regarding the study's purpose, procedures, risks, benefits, and the participant's rights, and ensure that it is signed by the participant.
The purpose of study informed consent is to ensure that participants understand the nature of the research and can voluntarily decide whether or not to participate.
Information that must be reported includes the study's purpose, duration, procedures, risks, benefits, and confidentiality measures, as well as the contact information for the research team.
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