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Este formulario proporciona información importante sobre un estudio de investigación que busca implementar una intervención conductual basada en evidencia para ayudar a niños de 1 a 5 años con
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01
Read the entire informed consent form carefully to understand its contents.
02
Fill in your personal information, such as your name, date of birth, and contact details in the designated areas.
03
Review the purpose of the study or procedure, as well as the risks and benefits outlined in the form.
04
Ensure that you understand the procedures involved and ask any questions if something is unclear.
05
Indicate your willingness to participate by signing and dating the form where required.
06
Keep a copy of the signed informed consent form for your records.

Who needs informed consent form and?

01
Participants in clinical trials or research studies.
02
Patients undergoing medical procedures.
03
Individuals involved in psychological or behavioral research.
04
Those taking part in surveys or any research requiring personal data.
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An informed consent form is a document that provides potential participants with detailed information about a study or procedure, allowing them to make an informed decision about their participation.
Researchers conducting studies involving human participants are required to file informed consent forms to ensure participants understand the nature of the study and their rights.
To fill out an informed consent form, participants must read the document carefully, understand the information provided, ask any questions they have, and sign the form to indicate their consent.
The purpose of an informed consent form is to protect the rights and welfare of participants by ensuring they are fully aware of the study's risks, benefits, and procedures before agreeing to participate.
The informed consent form must include information about the study's purpose, procedures, potential risks and benefits, confidentiality issues, and the participant's right to withdraw at any time.
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