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Center Number: Study Number: HTA Project 09/06/01 (MERIDIAN) Patient Identification Number for this trial (if known): Ethics reference: 11/OH/0006 Form U STUDY CONSENT FORM 28 March 2012, Version
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How to fill out study consent form

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How to fill out a study consent form:

01
Read the entire study consent form carefully to understand the purpose, procedures, risks, and benefits involved in the study. Make sure you fully comprehend the information provided.
02
Provide your personal information accurately, including your name, contact details, and any other required details such as age, gender, or occupation.
03
Agree to participate in the study by signing and dating the consent form. This indicates your voluntary consent to be involved in the research.
04
If you have any questions or concerns regarding the study, seek clarification from the researcher or study coordinator before signing the form. It is essential to have a clear understanding of what you are agreeing to.
05
If you are filling out the consent form on behalf of a minor or someone who is unable to provide informed consent, ensure that you have the legal authority to do so. Follow any specific instructions provided for obtaining consent on behalf of others.
06
If you have any additional information or comments that you think might be relevant to the study, write them in the designated section or communicate them to the researcher.
07
Keep a copy of the signed consent form for your records. It is important to have a record of your consent and the details of the study in case you need to reference them in the future.

Who needs a study consent form?

01
Individuals participating in research studies or trials are required to sign a study consent form. This includes both adults and minors.
02
The purpose of the study consent form is to ensure that participants are fully informed about the study's nature, purpose, risks, benefits, and their rights as participants before they agree to participate.
03
Researchers and institutions conducting the study have an ethical and legal obligation to obtain informed consent from participants. This helps protect the rights and well-being of participants and ensures that they are aware of what they are entering into.
Note: It is essential to consult with the specific rules and regulations of the country or institution conducting the study as requirements may vary.
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Study consent form is a document that outlines the rights of participants in a research study, as well as the risks and benefits involved.
Researchers conducting a study involving human subjects are required to file a study consent form.
Study consent forms should be filled out by providing detailed information about the study, including the purpose, procedures, risks, benefits, and contact information for the researchers.
The purpose of a study consent form is to ensure that participants are fully informed about the research study they are participating in and that they voluntarily agree to take part.
Information reported on study consent forms typically includes details about the study procedures, risks, benefits, confidentiality, compensation (if any), and contact information for the researchers.
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