Informed Consent Form Template
If you are performing a clinical research study, this informed consent form template will allow you to collect your participants’ consent in minutes. Our form builder records each person’s yes or no, and then you can utilize those responses to determine how you can use each person’s data in the clinical trial.
Get this Informed Consent Form template and the tool behind it
- Sign up to a powerful form builder
- Create any online form for your clinical study
- Keep track of all informed consents in a secure cloud-based repository
- Connect the consent data to other tools
- Share the informed consent form on any device
Frequently Asked Questions
What is an informed consent form?
Informed consent is a principle in medical treatment and research where the medical staff is obligated to give the patient sufficient information about the treatment’s consequences. An informed consent form is a document that outlines this information and that the patient has to sign to agree. The practice of using informed consent forms is common in many countries regarding medical studies and clinical trials.
How do I create an informed consent form?
You can customize our informed consent form template using our form builder. Duplicate the template in your 123 Form Builder account and edit the form with your knowledgeable consent version and other features you see fit. 123 Form Builder makes it easy to create online forms using a user-friendly designer with drag-and-drop functionality.
What is the purpose of an informed consent?
The purpose of this form is to inform your potential participants what you plan to ask them to do during your study so that they can decide if they want to participate. Your should detail the following areas: participation time requirement, participant tasks, communication, risks, compensation, confidentiality, freedom to withdraw, dissemination of results, and contact information for the Principal Investigator.