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APPROVED AS MODIFIED July 2, 2015, BHC IRB Portland Psychotherapy Clinic, Research, and Training Center RESEARCH CONSENT FORM TITLE OF STUDY: Exposure and Response Prevention with Acceptance and Commitment
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How to fill out a research consent form:

01
Start by reading the instructions: Carefully review the entire consent form to understand its purpose and what is being asked of you.
02
Provide personal information: Fill in your full name, date of birth, address, and any other details requested by the form. This information helps the researchers identify and contact you if necessary.
03
Understand the study: Read through the description of the research project, including its objectives, procedures, potential risks, benefits, and any compensation or incentives that may be offered.
04
Ask questions: If you have any doubts or concerns about the study, don't hesitate to ask the researchers for clarification before signing the consent form. They should be able to provide you with answers or direct you to additional resources.
05
Give voluntary consent: Consent to participate in the research study is typically given voluntarily. This means that you have the right to refuse or withdraw your participation at any time without consequences.
06
Signature and date: Sign and date the consent form, indicating that you understand and agree to participate in the research study.
07
Keep a copy: Before submitting the consent form to the researchers, make sure to keep a copy for your records. This can be useful in case you need to refer back to the details of the study or your consent in the future.

Who needs a research consent form?

01
Participants: Individuals who are invited or recruited to take part in a research study are typically required to sign a research consent form. This ensures that they have been informed about the study and have voluntarily agreed to participate.
02
Researchers: Research consent forms are also essential for researchers as they provide legal and ethical documentation of participants' informed consent. Having signed consent forms helps protect researchers in case any ethical concerns or legal issues arise during or after the study.
03
Ethics committees or review boards: Institutional review boards or ethics committees often require researchers to submit consent forms as part of the research protocol review process. These committees ensure that the rights, welfare, and privacy of research participants are protected. The consent form helps them assess the ethical aspects of the research before giving approval for the study to proceed.
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Research consent form is a document that explains the study to potential participants and obtains their voluntary agreement to participate.
Researchers conducting studies involving human subjects are required to file research consent form.
The research consent form should be filled out by providing detailed information about the study, risks and benefits, confidentiality, and participant rights.
The purpose of research consent form is to ensure that participants understand the study, voluntarily agree to participate, and protect their rights.
The research consent form must include details about the study objectives, procedures, risks, benefits, confidentiality, and participant rights.
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