INFORMED CONSENT

Informed Consent to Participate in a Research Study

[Insert Unit Name and Address]

Title of Research Project:

Name of Principal Investigator:
Email of Principal Investigator:
Phone # of Principal Investigator:

A. PURPOSE AND BACKGROUND

[Insert researcher’s name and affiliation] is conducting research on [insert what the research is about
in terms understandable to the potential participant]. The purpose of your participation in this
research is to help the researcher [insert why you are doing this research.] You were selected as a
possible participant in this study because [state why the subject was selected]. NOTE: If Researcher is
not the Principal Investigator, add information regarding supervision of researcher.

B. PROCEDURES
If you agree to participate in this research study, the following will occur: [State your process step by
step with detail and include the approximate amount of time the process will take. You should include
information on interview or questionnaire topics, any personal information requested, data collection
methods (audio, video, written) and frequency (if more than one collection).]

C. RISKS
[If there are risks you must state what they are. NOTE: Being uncomfortable, embarrassed and/or
inconvenienced are risks]

D. CONFIDENTIALITY
The records from this study will be kept as confidential as possible. No individual identities will be
used in any reports or publications resulting from the study. All [insert data collection and retention
method i.e. questionnaires, tapes, transcripts, summaries] will be given codes and stored separately
from any names or other direct identification of participants. Research information will be kept in
locked files at all times. Only research personnel will have access to the files and [insert data
collection and retention method] and only those with an essential need to see names or other
identifying information will have access to that particular file. After the study is completed [state time
frame for retaining collect data and whether it will be destroyed].
NOTE: All informed consent forms must have an explanation of the procedures by which
participant confidentiality will be protected and/or the extent that information will be disclosed and
to whom.

E. BENEFITS OF PARTICIPATION
There will be no direct benefit to you from participating in this research study. The anticipated benefit
of your participation in this study is [insert the objective you are trying to achieve with this study].
NOTE: “direct benefit” is something that benefits the individual participant such as free medical
care or compensation. If the participant is being given something for participating, state that here in
substitute for the first sentence.
 INFORMED CONSENT
Informed Consent to Participate in a Research Study

[Insert Unit Name and Address]

Title of Research Project:

Name of Principal Investigator:
Phone Number of Principal Investigator:

F. VOLUNTARY PARTICIPATION
Your decision whether or not to participate in this study is voluntary and will not affect your
relationship with the Smithsonian Institution or [insert name of any cooperating organization]. If you
choose to participate in this study, you can withdraw your consent and discontinue participation at any
time without prejudice.

G. QUESTIONS
If you have any questions about the study, please contact [insert name of PI] by calling [insert
phone number with area code]. You can also contact [insert IRB contact information] with any
questions about the rights of research participants or research related concerns.

CONSENT

YOU ARE MAKING A DECISION WHETHER OR NOT TO PARTICIPATE IN A RESEARCH

STUDY. YOUR SIGNATURE BELOW INDICATES THAT YOU HAVE DECIDED TO
PARTICIPATE IN THE STUDY AFTER READING ALL OF THE INFORMATION ABOVE AND
YOU UNDERSTAND THE INFORMATION IN THIS FORM, HAVE HAD ANY QUESTIONS
ANSWERED AND HAVE RECEIVED A COPY OF THIS FORM FOR YOU TO KEEP.

Signature Date
Research Participant
Date
Signature

Interviewer