Phase 1 Consent Consumer

Assessment of Terms and Phrases Commonly Used in Prescription Drug Promotion

Phase 1 Consent Consumer

OMB: 0910-0895

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Terms and Phrases: Meaning Elicitation Survey
Interview Consent Form: Consumers
Introduction and Purpose
You have been invited to take part in a research study. The purpose of the study is to
understand how consumers understand terms and phrases that are commonly used in
prescription drug advertising materials. RTI International, a non-profit research organization
in North Carolina, is conducting this study sponsored by the US Food and Drug
Administration (FDA).
Procedures
You are one of 30 people being asked to participate in this phase of the study based on your
answers to our screening questions. If you agree to participate, you will take part in a
telephone interview. The interview will last up to 60 minutes. We will audio-record and
transcribe your answers to the questions so that we can refer to them later when we write
our report. All identifying information will be removed from the transcripts. Other members
of the project team, including FDA staff, may be listening to the interviews as they are
taking place. All aspects of the study may not be revealed until the end.
Benefits
There is no direct benefit to you for participating. Your responses are very important
because they will help researchers understand how people understand information included
in prescription drug advertising materials.
Risks
There are no known risks to participating in this study. While the interview questions we ask
are not meant to be sensitive, there is always a chance that you may feel uncomfortable
with some of the questions. You do not have to answer any question that you don’t want to
answer. While we have taken steps to ensure your confidentiality, there is still a small risk
that your privacy could be broken.
Confidentiality
The privacy and confidentiality of your information is of the highest importance, and we are
committed to maintaining a secure environment in which you can participate. All
information you share in this study will be kept confidential to the extent provided by law.
The study team will not disclose your name or any of your responses, and your personal
information (name, address, phone number) will not be linked to any of your responses.
The information you share with us will be combined into a summary report so that details of
individual interviews cannot be linked to a specific participant. The audio recordings and
transcripts from the interviews will be destroyed at the end of the project. You will not be
re-contacted about this research study in the future.
Reimbursement
After the interview has been completed, you will receive a check by mail for $75 within 4-6
weeks in appreciation for your time.

Right to Refuse or Withdraw
Your participation in this study is completely voluntary, and you can withdraw from the
study for any reason at any time without penalty.
Persons to Contact
If you have questions about the study, you can call the project director, Dr. Bridget Kelly, at
1-800-334-8571, ext. 22098. She can be reached between 9:00 AM and 5:00 PM Eastern
Time Monday to Friday. If you have questions about your rights as a participant, you can
call RTI’s Office of Research Protection toll-free at 1-866-214-2043.
[CONSENT1.] If you have read the previous screens and agree to participate, please click the
Yes button. If not, click the No button.
1. Yes, I agree to participate. [Continue to interview appointment schedule]
2. No, I do not agree to participate. [Go on to next question]
[IF CONSENT1=NO OR SKIP]
[CONSENT2.] Are you sure you don't want to participate? Your opinions are important to us.
Please select the Yes button if you’d like to schedule an interview. Select the No button to
exit.
1. Yes, I agree to participate. [Continue to interview appointment schedule]
2. No, I do not agree to participate. [Exit]


File Typeapplication/pdf
AuthorDavis, Christine
File Modified2020-07-30
File Created2020-07-30

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