OMB Control No: 0910-0697
Expiration Date: 12/31/2023
Paperwork Reduction Act Statement: According to the Paperwork Reduction Act of 1995, an agency may not conduct or sponsor, and a person is not required to respond to a collection of information unless it displays a valid OMB control number. The valid OMB control number for this information collection is 0910-0697. The time required to complete this information collection is estimated to average 90 minutes per response, including the time for completing the screen questions, testing the focus group link, logging onto the online platform, reviewing instructions, searching existing data sources, gathering and maintaining the data needed, and completing and reviewing the collection of information.
Send comments regarding this burden estimate or any other aspects of this collection of information, including suggestions for reducing burden to PRAStaff@fda.hhs.gov.
The study we are conducting is on behalf of the U.S. Food and Drug Administration (FDA).
Protocol Title: Patient and Caregiver Diversity in FDA Patient Engagement Activities
Study No.: HP-00097394
Study Contact: T. Joseph (“Joey”) Mattingly II, PharmD, MBA, PhD; Email: jmattingly@rx.umaryland.edu; Phone: 410-706-8068
Study Sponsor: U.S. Food and Drug Administration (FDA)
Date/Time: _________________________
Interviewee: _________________________
Interviewer: _________________________
Introduction
Hello, my name is…. Thank you for taking the time to meet with me (us). I will let my colleague introduce him/herself (if anyone else on the research team is going to assist). I am helping to lead this interview for the University of Maryland. This interview will take about 90 minutes to complete.
Because this is part of a research project, there are some specific things I need to be sure I let you know. This interview is being conducted by research team members from the University of Maryland, Baltimore. This interview is completely voluntary, and you may ask questions at any time throughout our discussion. This interview is used to increase the U.S. Food and Drug Administration’s (also known as the FDA) understanding of patient and caregiver engagement and the diversity in food allergy drug development.
[Informed consent] If you had a chance to review the consent form and agree to participate, we can move right into the interview. If not, we can go over the consent form together. I am happy to answer any question you might have.
[Begin recording]:
Before we get officially started, I need to ask: Do I have your permission to record the interview? The recording will be for note taking and transcription purposes only so that I can be sure I have been accurate in taking down your answers. Interviews will be audio and video recorded and professionally transcribed. Neither the recordings nor the transcripts will be shared or used for any other purposes. We will also take steps to maintain your privacy, including storing your information securely, referring to you only by your first name, removing your identity from transcripts from the interviews, and destroying the recording when the project is completed. Only members of the research team will have access to this information
Please say, “yes,” if you agree to allow the interview to be recorded. Wait for person to say, “yes.”
Thank you. Today is [Date], my name is [Interviewer] and I’m interviewing [Interviewee] representing the [Name of Organization] for the food-allergy engagement study.
Next, I also need to ask: Do you agree to participate in this interview? Please say “yes” if you agree. Wait for the person to say, “yes.”
Thank you. Wonderful, so let’s begin:
Icebreaker
To start off, could you please introduce yourself and tell me about your personal connection to food allergies? (e.g. patient, Caregiver to child with food allergy, Caregiver to spouse with food allergy, Caregiver to other person with food allergy)
Probe
Can you tell me a bit about your or the person in your care past allergy?
How do you go about knowing about food allergy?
How have you been engaged with food allergy research?
(e.g., joining a clinical trial, joining a patient organization, reading the most recent research, etc.)
Have you ever participated in a public food-allergy-related event or activity?
(e.g., town hall meeting, advocacy event, etc.)
Topic |
Questions |
|
(e.g. informational/educational sessions or meetings, using it as a resource, joined its mailing list, participated in a research …etc.)
(e.g., haven’t given much thought to it, requires too much time, didn’t know about them, etc.) |
|
Experience and reasons for engaging with the FDA
The next set of questions is about the work of the US Food and Drug Administration or FDA for short.
The FDA has many responsibilities. The FDA is the Federal government agency that aims to promote public health and safety by checking the safety of food, drugs, vaccines, and medical devices. The FDA doesn’t conduct clinical trials or develop drugs, its role is to review drugs for safety and efficacy.
For today, we are just going to talk about the FDA’s role in medical product development until approval and how it involves patients in its work. I am going to ask you some questions about that more specifically.
Currently, there are several ways in which patients and caregivers can engage with the FDA, such as attending patient-focused drug development meetings, attending a patient listening session, and/or hosting a meeting with the FDA. Its purpose is to ensure patients’ experiences, perspectives, needs, and priorities are captured and included in drug development and evaluation. Our questions are related to FDA’s efforts engaging patients and caregivers to help us improve the diversity of patients and caregivers that get involved.
Topic |
Questions |
Engagement Experience with FDA |
e.g. meeting with FDA staff on an issue; speaking at an FDA meeting; making public remarks at an FDA meeting; submitting comments to an FDA docket, etc…
If yes,where did they hear about it?
|
Motivation
For this next set of question, I’m interested in learning about what motivates you to be engaged in food-allergy-related activities.
Topic |
Questions |
Motivation |
For those with ORGANIZATION experience:
For those with NO ORGANIZATION experience:
|
For those with FDA experience:
For those with NO FDA experience:
|
Barriers
Topic |
Questions |
Barriers |
|
|
Satisfaction
Topic |
Questions |
Satisfaction |
For those with ORGANIZATION experience:
For those with NO ORGANZIATION experience:
|
For those with FDA experience:
For those with NO FDA experience:
|
Wrap-up and closing
We have reached the end of the interview.
Is there anything you’d like to add? Is there anything you would like to ask me?
If you think of anything else you would like to share with us about food allergy patient and caregiver engagement, please feel free to contact the principal investigator, Joey Mattingly via email: jmattingly@rx.umaryland.edu; or phone: 410-706-8068
Thank you for your time and sharing your experiences with us.
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File Type | application/vnd.openxmlformats-officedocument.wordprocessingml.document |
File Title | Interview Guide |
Subject | <p>REMOVE ALL THE INSTRUCTIONS IN BLUE BEFORE SUBMITTING RESEARCH CONSENT FORM Protocol Title: Study No.: [Please |
Author | Joey Mattingly |
File Modified | 0000-00-00 |
File Created | 2022-07-11 |