Healthcare Professional Survey of Prescription Drug Promotion II
[Main Survey]
INFORMED CONSENT FORM
[Consent Screen 1]
[DISPLAY]
The Food and Drug Administration is conducting this study to understand health care providers’ attitudes regarding pharmaceutical promotion as it relates to public health. Your responses, and those of your colleagues nationwide, will provide valuable insight into matters affecting the medical community. This survey will take between 15-20 minutes to complete and your responses will be kept confidential.
This research is authorized by Section 1701(a)(4) of the Public Health Service Act (42 U.S.C. 300u(a)(4)). Confidentiality is protected by 5 U.S.C. 552(a) and (b) and 21 CFR part 20.
OMB Control #0910-xxxx. Expires xx/xx/20xx.
[Consent Screen 2]
[DISPLAY]
This survey is being conducted by Westat, an independent social science research firm, on behalf of the U.S. Department of Health and Human Services. Westat is working with WebMD to conduct this survey but is not affiliated with WebMD in any way. If you have questions about this survey, please contact the project director, Dr. Simani Price, at 301-610-5536. She can be reached between 9 AM and 5 PM Eastern Time Monday to Friday.
Privacy and Confidentiality
This survey will ask you for some general demographic information (for example, age, gender, race/ethnicity). However, no personal information, such as your name, will be collected. Your identity will not be linked to your responses. We will be very careful to only let people working on the study see your responses, which will not be linked back to any personal information that can be used to identify you. Your information will be kept private to the extent allowed by law.
Possible Risks or Discomforts
There are no anticipated risks to participating in the survey. However, you can skip any questions you do not wish to answer and continue with the survey. While we will be very careful to let only members of the research team see your information, there is a small risk that others might find out what you say, despite all our best efforts. In the case of a breach of confidentiality, appropriate steps will be taken to notify participants.
Benefits
Your responses are very important because they will help researchers understand how people make decisions about medications. There is no direct benefit to you for your participation.
Incentive
In appreciation for your time, you will receive $(50/60) for completing this survey.
Rights as a Participant
If you have any questions about your rights as a participant, you may wish to contact Westat Human Subjects Protections office at 1-888-920-7631. You may also contact RIHSC at 301-796-9605 or [email protected]. RIHSC is an institutional review board (IRB), a group of people who are responsible for ensuring that the rights of participants in research are protected.
[Consent Screen 3]
Consent1. If you have read the previous screens and agree to participate, please click the Yes button. If not, click the No button.
Yes, I agree to participate. [CONTINUE WITH NEXT SECTION]
No, I do not agree to participate. [GO TO NEXT QUESTION]
Consent2. Are you sure you don't want to participate? Your opinions are important to us. Please select the Yes button to continue this survey. Select the No button to exit.
Yes, I agree to participate. [CONTINUE WITH NEXT SECTION]
No, I do not agree to participate. [END SURVEY]
[DISPLAY]
INTRODUCTION
Thank you for participating in this survey. The questions ask about your experiences with professionally-directed pharmaceutical marketing materials or activities prepared or conducted by drug companies intended to promote the use of the companies’ drugs. It also asks about other information sources for learning about prescription drugs. Please answer honestly and give us your best guess on answers you do not know.
[PROFESSIONAL MATERIALS AND ACTIVITIES]
Q1. How often do you read professional medical journals?
More than once a week
About once a week
About once a month
A few times a year
Once a year or less
Never [GO TO Q2]
Q1a. When you read through journals, how often do you notice pharmaceutical promotions?
Every time
Most of the time
Some of the time
Rarely
Never [GO TO Q2]
Q1b. When you notice a prescription drug advertisement for a new product, how closely do you usually read it?
Read it thoroughly
Read certain parts thoroughly
Skim it
Glance at it
Don’t read it at all
Q1c. When you notice a prescription drug advertisement related to your practice, how closely do you usually read it?
Read it thoroughly
Read certain parts thoroughly
Skim it
Glance at it
Don’t read it at all
Q2. How often do you visit commercial prescription drug websites (e.g., “name of drug.com”)?
More than once a week
About once a week
About once a month
A few times a year
Once a year or less
Never
Q2a. When you visit a prescription drug website, how closely do you usually read it?
Read it thoroughly
Read certain parts thoroughly
Skim it
Glance at it
Don’t read it at all
Q3. How often do you visit medical reference websites (e.g., Epocrates, Prescribers’ Digital Reference [PDR], UpToDate, or Clinical Key) to get information about prescription drugs?
More than once a week
About once a week
About once a month
A few times a year
Once a year or less
Never [GO TO Q4]
Q3a. When you visit these reference websites, how often do you notice prescription drug promotions?
Every time
Most of the time
Some of the time.
Rarely
Never [GO TO Q4]
Q3b. When you notice a prescription drug promotion on a reference website, how closely do you usually read it?
1. Read it thoroughly
2. Read certain parts thoroughly
3. Skim it
4. Glance at it
5. Don’t read it at all
Q4.When you watch television, how often do you notice ads for prescription drugs?
Every time
Most of the time
Some of the time
Rarely
Never
I do not watch TV
Q5. Does your practice allow visits from pharmaceutical sales representatives?
Yes
No [GO TO Q6]
Q5a. How often do pharmaceutical sales representatives bring promotional materials to your practice?
More than once a week
About once a week
About once a month
A few times a year
Once a year or less
Q5b. In the last six months, which of the following have pharmaceutical sales representatives brought to your practice? [Check all that apply.]
Drug samples
Food or beverages for staff
Posters/diagrams for exam rooms
Three-dimensional displays of organs/systems
Sales aids or electronic visual aids containing product information
Brochures for patients or healthcare providers
Personal use items (e.g., pens, fidget spinners, sunglass cleaner wipes)
Coupons/patient discount cards
Other, please specify _________________
Q6. Approximately, how many pharmaceutical sponsored dinner meetings with medical experts do you attend each year? __ [DROP DOWN: ‘0-20,’ ‘>20’]
Q7. In the last 24 months, approximately how many professional conferences have you attended? ___ [DROP DOWN: ‘0-25’, ‘>25’] [IF ZERO, GO TO Q8)
Q7a. How often do you visit the exhibit hall during professional conferences?
Every time
Most of the time
Some of the time
Rarely
Never [GO TO Q7c]
The conferences I attend do not have exhibit halls [GO TO Q7c]
Q7b. What are your goals for visiting the exhibit hall? [Check all that apply.]
Learn about new treatments and technologies
Ask specific questions about treatments and technologies
Pass time between sessions
To pick up giveaways
To interact with colleagues or exhibitors
To attend mini-presentations
For free meals or snacks
Q7c. How often do you attend sessions sponsored by pharmaceutical companies at professional conferences?
Every time
Most of the time
Some of the time
Rarely
Never
[RANDOMIZE PRESENTATION ORDER OF Q8 AND Q8a]
Q8. How influential are the following information sources to you in informing decisions about prescription drugs?
|
Very influential |
Somewhat influential |
Slightly influential |
Not at all influential |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Q8a. How influential are the following information sources to your colleagues in informing decisions about prescription drugs?
|
Very influential |
Somewhat influential |
Slightly influential |
Not at all influential |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
[RANDOMIZE PRESENTATION ORDER OF Q9 AND Q9a]
Q9. Have you done any of the following activities during the last 24 months?
|
Yes |
No |
|
|
|
|
|
|
|
|
|
Q9a. Are you aware of any colleagues who have done any of the following activities during the last 24 months?
|
Yes |
No |
|
|
|
|
|
|
|
|
|
Q10. In the last year, how often have you interacted with pharmaceutical companies online (e.g., speaking with a sales representative via Skype, viewing a product presentation on a website)?
More than once a week
About once a week
About once a month
A few times a year
Once a year or less
Never
Q11. Do you use online sites to interact with other healthcare professional colleagues?
Yes
No [GO TO Q12]
Q11a. How often do you use these sites for the following activities:
|
Always |
Often |
Sometimes |
Rarely |
Never |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Q11b. Do you participate in these sites to:
|
Yes |
No |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
[CLINICAL TRIAL KNOWLEDGE AND TRAINING]
The next few questions are about clinical trial information.
Q12. What types of clinical trial information would you like to see in professional promotional materials? [Check all that apply.]
Sample (e.g., population inclusion/exclusion criteria, number enrolled and dropouts, etc.)
Study design (e.g., blinded or not, cohort study, length of trial, etc.)
Number of trials conducted
Summary of results
Statistical findings
Subgroup analyses
None [GO TO Q15]
Q13. In general, how much information about the clinical trial methodology (e.g., sample, study design, etc.) should be included in professional promotional materials?
All information
A moderate amount
A minimal amount
None
Q14. In general, how much information about the clinical trial outcome should be included in professional promotional materials?
All information
A moderate amount
A minimal amount
None
Q15. How comfortable are you interpreting clinical trial methodology (e.g., sample, study design, etc.) information?
Very
Somewhat
A little
Not at all
Q16. How comfortable are you interpreting clinical trial outcomes information?
Very
Somewhat
A little
Not at all
Q17. How often do you consider clinical trial data when deciding which drugs to prescribe to your patients?
Every time
Most of the time
Some of the time
Rarely
Never
Q18. How much formal training have you had regarding clinical trial methodology (e.g., sample, study design, etc.)?
A lot
A moderate amount
A minimal amount
None
[FDA APPROVAL OF PRESCRIPTION DRUGS]
The next few questions ask about FDA approval and prescription drugs. FDA knows that the approval process for pharmaceutical products is quite complex and that it sometimes uses terminology unfamiliar to many medical professionals. The following questions ask about your familiarity with certain terms. Please answer using your own words and based on your existing knowledge. We ask that you do not consult other sources before answering. It is important for FDA to understand if terms are unclear or confusing so it can improve the language it uses for medical professionals. Please note that FDA does not regulate the practice of medicine and nothing in this questionnaire should be interpreted in such a way.
Q19. Can you describe your understanding of what FDA approval of prescription drugs means?
_______________________________________________________
Q20. Please check the statement that best describes your understanding of how FDA regulates prescription drug promotion.
FDA does not monitor promotional activities once a prescription drug is approved.
FDA reviews all promotional materials before they are released.
FDA regulates prescription drug promotion, but does not generally require review before release.
I’m not sure how FDA regulates prescription drug promotion.
Q21. When prescribing a drug, how important is it to you that the drug is FDA-approved for that particular indication?
Very important
Somewhat important
A little important
Not at all important
It depends [GO TO Q21a]
Q21a. Please explain your answer.
____________________________________________________________________
Q22. How often do you prescribe a drug for a condition for which it is not approved?
Often
Sometimes
Rarely
Never [GO TO Q25]
Do not know
Q23. When you prescribe a drug for off-label use, how often do you record the reasons for prescribing the drug?
Always
Often
Sometimes
Rarely
Never
Q24. When you prescribe a drug for off-label use, how often do you explain to the patient that you are doing so?
Always
Often
Sometimes
Rarely
Never
Q25. In your own words, what is an accelerated approval drug?
______________________________________________
Q25a. How comfortable are you prescribing an accelerated approval drug?
Very comfortable
Moderately comfortable
Somewhat comfortable
Not at all comfortable
I’m not sure what an accelerated approval drug is
Q26. “Scientific exchange” is a complex concept in FDA regulation of pharmaceutical products. In your own words, how would you explain “scientific exchange” to a colleague?
_______________________________________________
I am not sure what “scientific exchange is.”
Q27. Now we want to understand your perspective on “biosimilar.” In your own words, what is a “biosimilar”?
_________________________________________________
I am not sure what “biosimilar” is. [GO TO Q28]
Q27a. How comfortable are you prescribing “biosimilar” products?
Very comfortable
Moderately comfortable
Somewhat comfortable
Not at all comfortable
I am not sure what “biosimilar” is
Q28. Suppose Drug X is FDA approved for use A. Please mark your agreement with the following statement:
Drug X is safe and effective for use A.
Strongly agree
Somewhat agree
Somewhat disagree
Strongly disagree
Q29. Suppose Drug Y is FDA approved for use B and other products containing the same active ingredient are approved for uses B and C. However, Drug Y is not FDA approved for use C. Please mark your agreement with the following statement:
Drug Y is safe and effective for use C.
Strongly agree
Somewhat agree
Somewhat disagree
Strongly disagree
[OPIOID PRESCRIBING]
The next few questions are about the use of prescription drugs for chronic pain.
Q30. During the last three months, for about how many patients have you prescribed opioids for chronic pain?
None
1-5
6-10
11-20
21 or more
Don’t know or not sure
Q30a. Is the number of patients you prescribed opioids for chronic pain in the last 3 months relative to 12 months ago:
1. The same
2. Less
3. More
Q31. During the last 12 months, have you read or attended an educational event that provided information about opioids from one of the following sources? (Check all that apply.)
Presentation at the hospital or conference (not pharmaceutical-sponsored)
Online presentations or webinars (not pharmaceutical-sponsored)
Pharmaceutical-sponsored dinner, workshop, or conference session
Read articles in medical journals
Read prescribing information (PI) or Risk Evaluation or Mitigation Strategy (REMS) materials
Read pharmaceutical promotional materials [GO TO Q31a AND Q31b]
Other, please specify ____________________
I haven’t read or attended an event related to this topic during the last 12 months
Q31a. How often do these materials or events mention abuse potential?
Always
Often
Sometimes
Rarely
Never
Q31b. Promotional materials for opioid products provide an appropriate balance of benefits and risks.
Strongly agree
Somewhat agree
Neither agree nor disagree
Somewhat disagree
Strongly disagree
Q31c. In your opinion, what resources are most helpful to you as you work to ensure you are prescribing opioids in as safe and effective a manner as possible?
______________________________________________
Q32. Which of the following statements best represents your opinion about abuse deterrent formulations (ADF)?
An ADF of a drug will have a lower addictive potential than a non-ADF of the same drug.
An ADF of a drug will have the same addictive potential as a non-ADF of the same drug.
An ADF of a drug will have a higher addictive potential than a non-ADF of the same drug.
I don’t know.
Q32a. Which of the following do you believe are true about ADFs of opioids? For each question, please say whether you believe it is true, false, or not sure.
|
True |
False |
Not Sure |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Q32b. In your opinion, in the last year has the content of promotional materials for opioid products contained more or less information on abuse potential?
__More
__Less
__No change
Q32c. In the last six months, do you recall seeing prescription drug promotion that included information about:
|
Yes |
No |
Not Sure |
i. Non-opioid analgesics |
|
|
|
ii. Medication-assisted treatment (MAT) for opioid deterrence |
|
|
|
iii. Opioid reversal agents |
|
|
|
[DEMOGRAPHICS]
[Q33-Q35 ARE ONLY TO BE ASKED OF PHYSICIAN RESPONDENTS; ALL OTHERS GO TO Q36]
Q33. Do you consider yourself a primary care physician?
Yes
No
Q34. Please indicate the type of degree you hold:
Doctor of Medicine (M.D.)
Doctor of Osteopathic Medicine (D.O.)
Q35. What year did you graduate from medical school? ___________[DROP DOWN RANGE DESCENDING: 2017 to 1935]
Q36. How many years have you been practicing?
Less than 5
5 to 10
11 to 15
16 to 20
More than 20
Q37. During your last normal week of practice, how many patient visits did you have at all office locations? Number of patient visits ___
Q38. Approximately, how many prescriptions do you write in a typical week? ____
Q39. In the last year, how often have you prescribed a brand-name drug when an equivalent generic was available because the patient asked for the brand-name drug specifically?
Often
Sometimes
Rarely
Never
Q40. In which state is your practice based? [DROP DOWN MENU OF STATES]
Q41. How many physicians (including yourself) are associated with the practice you work in? (Please include all practice locations you work in.)
_____________________
Q42. How many physicians’ assistants and/or nurse practitioners (including yourself) are associated with the practice you work in? (Please include all practice locations you work in.)
_____________________
Q43. Which of the following best describes the practice location you work in most often (i.e., where you spend the most hours per week)?
Private solo or group practice
Freestanding clinic/urgiccenter (not part of a hospital outpatient department)
Non-Federal Government clinic (e.g., state, county, city, maternal and child health, etc.)
Federal Government operated clinic (e.g., Veterans Affairs, military, etc.) [GO TO Q43a]
Health maintenance organization or other prepaid practice (e.g., Kaiser Permanente)
Community Health Center (e.g., Federally Qualified Health Center (FQHC), federally funded clinics or “look alike” clinics)
Other, please specify __________________
Q43a. Is the clinic you work for associated with one of the following?
Veterans Affairs
Indian Health Services
Bureau of Prisons
Other: _______________________________
Thank you for participating in this survey. Your answers will help FDA ensure accurate and non-misleading promotion of prescription drugs.
[RECORD TIME TAKEN TO COMPLETE SURVEY]
[WEB PROBES FOR PRETEST]
We would like your feedback on the survey that you completed. This will help FDA improve the survey for future use with healthcare providers.
P1. Were you able to complete the survey in one session?
Yes
No
P2. Did you rely on other sources (e.g., Google, colleagues, etc.) to answer questions that you found difficult to answer?
Yes, please explain: ___________________________________
No
P3. Did you have any difficulty answering the following question?
How influential are the following information sources (journal advertisements, sales aids with product information from pharmaceutical sales representatives, commercial drug websites, sponsored conference sessions, direct to consumer advertising, dinner talks sponsored by pharmaceutical companies, key experts in the field presenting at conferences, colleagues/peers, online communities of healthcare providers) to your colleagues in informing decisions about prescription drugs?
Yes, please explain: ___________________________________
No
P4. Did you have difficulty selecting your answer from the choices provided (all information, a moderate amount, a minimal amount, none) for the following question?
In general, how much information about the clinical trial methodology (e.g., sample, study design, etc.) should be included in professional promotional materials?
Yes, please explain: _________________________________________
No
P5. Were there other questions that you had difficulty answering?
Yes, please explain: _________________________________________
No
Thank you for your feedback.
File Type | application/vnd.openxmlformats-officedocument.wordprocessingml.document |
Author | O'Donoghue, Amie |
File Modified | 0000-00-00 |
File Created | 2021-01-20 |