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PARTICIPANT CONSENT FORM Title of Study: The effectiveness of group CognitiveBehaviorTherapy (CBT) and exercise in management of depression: A three arm randomized controlled pilot trial Principal
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Anyone who is conducting a study, research, or any activity that involves participants and requires their consent needs a participant consent form title. This can include academic researchers, medical professionals, employers, event organizers, etc.
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The participant consent form title is the name or title of the document that indicates the participant's consent to take part in a study or research project.
Researchers, study coordinators, or individuals responsible for conducting the study are typically required to file the participant consent form title.
The participant consent form title can be filled out by providing the necessary information about the study, including the study purpose, risks, benefits, and confidentiality details, as well as obtaining the participant's signature and date.
The purpose of the participant consent form title is to ensure that participants are fully informed about the study they are participating in, understand the risks and benefits involved, and voluntarily agree to take part.
The participant consent form title must include information about the study objectives, procedures, risks, benefits, confidentiality measures, contact information for questions, and a statement of voluntary participation.
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