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This document provides information about a research study aimed at treating PTSD and alcohol dependence in OEF/OIF veterans using SSRI medication and psychotherapy.
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How to fill out Research Study Participation Form

01
Read the instructions carefully before starting.
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Provide your personal information, including your full name, address, and contact details.
03
Indicate your age and gender in the appropriate sections.
04
Answer any health-related questions honestly and to the best of your ability.
05
Review the consent section and ensure you understand your rights.
06
Sign and date the form to indicate your agreement to participate.

Who needs Research Study Participation Form?

01
Individuals interested in participating in medical or academic research studies.
02
Researchers and institutions conducting studies that require informed consent from participants.
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Instructions for Developing an Informed Consent Document General Information. Describe the purpose(s) of this research study in lay terms. Purpose of the Study. Procedures. Risks. Benefits. Compensation, Costs and Reimbursement. Withdrawal or Termination from Study. Confidentiality.
I understand that I will not benefit directly from participating in this research. I agree to my interview being audio-recorded. I understand that all information I provide for this study will be treated confidentially. I understand that in any report on the results of this research my identity will remain anonymous.
A consent form is a document that someone signs to show that they will allow something to happen. Consent forms are used in psychology to insure that a person is aware of what they are agreeing to do and of any risks or costs that may exist.
Function The nature of the procedure or intervention. The risks and benefits of the procedure or intervention. Reasonable alternatives. The risks and benefits of alternatives. An assessment of the patient's understanding of these elements [10][11]
I consent voluntarily to be a participant in this study and understand that I can refuse to answer questions and I can withdraw from the study at any time, without having to give a reason.
The consent form should describe if/when identifiable data will be destroyed and how such data will be protected and how it will be used or shared. Language - Consent forms should be written in the 2nd person (i.e., "you are") and in a language that is clear, concise, and understandable to the subject population.
The elements needed for the documentation of the informed consent discussion include: The nature of the procedure or intervention. The risks and benefits of the procedure or intervention. Reasonable alternatives. The risks and benefits of alternatives. An assessment of the patient's understanding of these elements [10][11]
Considerations in preparing the informed consent document: Elements of consent present. Complete explanations. Lay language. Protection of confidentiality. No unproven claims of effectiveness. Device studies include a statement that the study includes an evaluation of the safety of the test article.

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The Research Study Participation Form is a document used to collect consent and information from individuals who wish to participate in a research study.
Individuals who intend to participate in a research study, including researchers and volunteers, are required to fill out the Research Study Participation Form.
To fill out the Research Study Participation Form, participants must provide personal details, read the study information, and sign to indicate their consent to participate.
The purpose of the Research Study Participation Form is to ensure that participants are informed about the study and voluntarily agree to take part in it, safeguarding their rights and wellbeing.
The Research Study Participation Form typically requires personal information such as the participant's name, contact information, age, and medical history, as well as acknowledgment of understanding the study's purpose and potential risks.
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