Informed Consent Templates and Guidance

All human subject research requires informed consent except where a waiver is allowed by federal regulations.  Informed consent is one of the basic rights of all participants of human subject research.  Most individuals are familiar with the concept providing their consent.  However, regulations, Good Clinical Practice, and ethical guidelines instruct that participants must be properly informed in order to truly provide their consent.

This site aims to provide information to researchers in order to 1) ensure that the participant is properly informed 2) ensure the consent form contains all required information and 3) explain any special circumstances surrounding the informed consent.

Special considerations are available for consenting patients on COVID-19 studies.  These considerations can be found on the Guidance for COVID-19 Consenting Document

Below is an educational video about Informed Consent. Click the image to view the video.

Introduction to Informed Consent

▼   Informed Consent Process vs. Informed Consent Form 

Informed Consent Process

The informed consent process is a phrase that is used to describe the discussion used to inform the participant about the research study.  Any process is a series of actions rather than a one-time occurrence.  Therefore, an informed consent process needs to allow for the following actions to occur:

  1. All elements of the informed consent form are discussed with the participant  through one or multiple conversations
  2. The participant is given adequate time to consider their decision
  3. The participant is able to have all their questions answered to their satisfaction

At the end of the discussion(s), it is suggested to test the participant’s comprehension of the research study.  A comprehension assessment can be done using the Teach-Back Method. Information regarding the Teach-Back Method can be found on the Agency for Healthcare Research and Quality’s website.

For clinical research, the occurrence of the informed consent process, along with the participant’s comprehension, should be documented in the participant’s chart. It is important to document all steps of the process. Documentation can occur in progress notes, telephone logs, a standardized consent process form, etc.

An example of a standardized consent process form can be found here.

An example of documentation of the Teach-Back Method can be found here.


Informed Consent Form

The informed consent form, often abbreviated as ICF, is the physical document explaining the research study.  The ICF is the form that the participant signs to indicate their agreement to participate. Federal regulations, University of South Alabama policy, and Good Clinical Practice require the ICF to contain specific elements and be written in a specific manner.  The requirements of the ICF is discussed in the next section.

▼   Requirements of the Informed Consent Form 

The specific requirements of the informed consent form can be confusing and lengthy.  While most requirements are needed in all studies, there are some requirements that are only needed when particular circumstances occur as part of the research study.

Please review the below sections carefully.  You can reach out to the Office of Research Compliance for any questions.  The contact information for this department can be found here.


Federal Regulations Requirements

Federal regulations (45 CFR 46.116) provide the framework for the type of information that must be included in the informed consent document.  Several elements are mandated by the regulations to be present in the informed consent document.

A checklist of the federally required elements can be found here.  This document also has tips on how to write some of these elements into the ICF.


University of South Alabama Requirements

The University of South Alabama mandates specific language to be used under certain circumstances.  Such circumstances include, but is not limited to, the use of biological materials, the use of Protected Health Information, research related injury, and a participant’s Bill of Rights.

A guide to USA’s requirements can be found here.


Good Clinical Practice Requirements

Good Clinical Practice (GCP) is a set of international standards created to ensure ethical and high-quality research data. GCP standards are applied to all aspects of human subject research. The elements of GCP that apply to an informed consent are listed below.

1.  Readability- the ICF should be written in plain language at a 6th to 8th grade reading level. This can be achieved by:

  • Tailoring the document to the subject’s population
  • Avoid technical jargon or overly complex terms
  • Use straightforward language that is understandable

A toolkit is available here to offer guidance on how to write an effectively readable informed consent form.

2.  Writing tips

  • Use the second (you) or third person (he/she) to present the study details.
  • Include a statement of agreement at the conclusion of the informed consent document. Avoid using “You understand…” statements.
  • Use wide margins (i.e. 1” margins) and bullet points when possible.
▼   Waiver or Alteration of Obtaining Consent 

The Institutional Review Board (IRB) may approve a waiver to obtain consent or a waiver that alters the required elements of an ICF.  Below list criteria for a waiver of consent:

All four of these requirements must be met

  1. The research involves no more than minimal risk to the subjects
  2. The waiver or alteration will not adversely affect the rights and welfare of the subject
  3. The research could not practicably be carried out without the waiver or alteration
  4. Whenever appropriate, the subjects will be provided with additional pertinent information after participation

The form used to request a waiver of consent can be found on under forms and templates.

▼   Waiver of Documentation of Informed Consent 

The Institutional Review Board (IRB) may approve a waiver to obtaining a signed informed consent form.  Below list criteria for a waiver of documentation of consent:

All two of these requirements must be met

  1. That the only record linking the subject and the research would be the consent document and the principal risk would be potential harm resulting from a breach of confidentiality.
  2. That the research presents no more than minimal risk of harm to subjects and involves no procedures for which written consent is normally required outside of the research context.

Even though a signature maybe be waived, the act of obtaining consent may not be. If this occurs, then an Information Sheet can be used. An Information Sheet contains the information required in a consent form. However, the participant’s signature is not required. The informed consent process must still occur (unless waived by the IRB). This method is commonly used in exempt studies.

An example of an Information Sheet can be found here.

The form used to request a waiver of consent can be found on forms and templates.

▼   Research Involving Children 

A child is considered to be a person under the age of 18 years old.  Special consideration is given to research involving children. One such consideration is obtaining the child’s assent to participate. Assent means the child’s affirmative agreement to participate in research. Mere failure to object should not be construed as assent.


Requirements for obtaining minor assent and parental permission

Minors are not able to consent to research activities for themselves.  Therefore, the parent/legal guardian must give permission to participate in research and the minor may give assent to participate.  A child may not take part in a study if they do not provide their assent.

Younger children have limited capacity to understand what participation in a research study means. Therefore, an assent is only required for children 7 to 18 years of age.  This age range is in line with the standard set forth by the American Academy of Pediatrics.

Federal regulations describe when one or both parents need to provide permission. The below table displays the requirements. 

When your study is... Then this is required...
 Minimal Risk One parent/legal guardian may be sufficient 
Greater than Minimal Risk, Direct Benefit to participant  One parent/legal guardian may be sufficient but the IRB must determine whether one or two is required
Greater than Minimal Risk, No Direct Benefit to participate, but likely to yield generalizable knowledge about the participant's condition Both parents/legal guardians, unless one parent is deceased, unknown, incompetent, not reasonably available, or does not have legal responsibility for the custody of the child
Greater than Minimal Risk, No Direct Benefit to participant, but results may alleviate serious problems of children's health or welfare Both parents/legal guardians, unless one parent is deceased, unknown, incompetent, not reasonably available, or does not have legal responsibility for the custody of the child


Additional requirements regarding children in research can be found here.  

▼   Consenting During COVID-19 Pandemic  

All research is being affected by the COVID-19 pandemic. Challenges such as self-isolation, restrictions at the site, travel constraints, disruption in the supply of the investigational product, etc. can lead to difficulties in providing a sufficient informed consent process.

The Food and Drug Administration (FDA) has issued guidance on how to consent subjects during the COVID-19 pandemic: FDA Guidance on Conduct of Clinical Trials of Medical Products during COVID-19 Public Health Emergency.

The guidance can be overwhelming and is not concentrated on consenting. We have created a flowchart to assist you in deciding the appropriate method of consenting.

Flowchart for Consenting During COVID-19