Sample Consent Form - UBC Psychology - University of British ... 2025

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  1. Click ‘Get Form’ to open it in the editor.
  2. Begin by entering your personal information in the designated fields, including your name and contact details. This ensures that your identity is linked to the consent form.
  3. Review the introduction and purpose section carefully. This provides essential context about the study you are consenting to participate in.
  4. In the study procedures section, note the time commitment and tasks involved. Make sure you understand what participation entails before proceeding.
  5. Read through the confidentiality and anonymity assurances. It’s important to know how your data will be handled.
  6. Once you are comfortable with all information, proceed to sign and date the form at the bottom. Ensure that you also print your name as required.

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I have read and I understand the provided information and have had the opportunity to ask questions. I understand that my participation is voluntary and that I am free to withdraw at any time, without giving a reason and without cost. I understand that I will be given a copy of this consent form.
0:24 2:17 Content fill in a description about the consent you're asking for think about your target audience.MoreContent fill in a description about the consent you're asking for think about your target audience. And be specific about why you're collecting the data and what it will be used for. Note.
Informed consent means giving a potential subject time to ask questions and consider whether or not they want to participate in a study. Someone knowledgeable about the research should be available to answer questions and conduct a consent interview. 4.
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People also ask

If the patient provides their informed consent, there is now a clear pathway to treatment. Essentially, informed consent is in place to protect the patient. The consent form is a legal document that ensures ongoing communication between a patient and their health care provider.
The consent form provides potential research subjects sufficient written information to decide whether to participate in a research study or not based on an explanation of the proposed research and the nature of the participation that is requested of them.
By signing below I am indicating my consent to participate in the research. I understand that the data collected from my participation will be used primarily for a PhD thesis, and will also be used in summary form for journal publication, and I consent for it to be used in that manner.
A document with important information about a medical procedure or treatment, a clinical trial, or genetic testing. It also includes information on possible risks and benefits.
The informed consent document should succinctly describe the research as it has been presented in the IRB application. Use the second (you) or third person (he/she) to present the study details. Avoid use of the first person (I). Include a statement of agreement at the conclusion of the informed consent document.

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