[PROGRAMMING NOTE: Consent Screen 1 to be shown before the Screener]
[Consent Screen 1]
Thank you for your interest in this research study. The research involves looking at a television ad for a consumer product and completing an online questionnaire. First, we need to ask you a few screening questions to see if you are eligible to participate. Then, if you are eligible and agree to participate, you will be asked to watch an ad twice. After watching the ad, we will ask you to complete a survey. Viewing the ad and completing the survey will take approximately 20 minutes.
[PROGRAMMING NOTE: Consent Screen 2 to be shown after the Screener]
[Consent Screen 2]
The purpose of the study is to learn more about prescription drug advertisements. You are one of about 1,770 people in the United States who are being asked to take a survey about a new prescription drug.
RTI International, an independent nonprofit research organization, is conducting this study on behalf of, and funded by, a federal agency. RTI is working with Dynata to conduct this survey but is not affiliated with Dynata in any way.
Your participation in this study is completely voluntary, and you have the right to stop at any time or to refuse to answer any question. If you decide to participate and later change your mind, you will not be contacted again or asked for further information.
We do not expect that any of the survey questions will make you uncomfortable, but if they do, you can refuse to answer any question. There is also a potential risk of loss of confidentiality. Every effort will be made to protect your information, but this cannot be guaranteed.
There are no direct benefits to you for participating in this study. However, you will be helping with an important research project.
You will receive $4.00 in points for completing this survey.
Many precautions have been taken to protect your information. All information collected in this survey will be kept confidential to the extent provided by law. You will never be identified by name. The information obtained from all of the surveys will be combined into a summary report so that details of individual questionnaires cannot be linked to a specific participant. When we analyze the results, your responses will be combined with responses from other people taking part in the study. You will not be identified in any published or presented materials. The information collected in this study may be used or shared for future research studies.
You will not be contacted in the future about this research after your participation ends.
If you have questions about this survey, please contact your panel provider through your member website for assistance. You will need to mention the Project # [SurveyNumber], and someone will direct your questions to the appropriate researchers at RTI. 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.
[Consent Screen 3]
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 AND RANDOMLY ASSIGN PARTICIPANT TO EXPERIMENTAL CONDITION]
No, I do not agree to participate. [TERMINATE SURVEY]
File Type | application/vnd.openxmlformats-officedocument.wordprocessingml.document |
Author | Sullivan, Helen W (CDER) |
File Modified | 0000-00-00 |
File Created | 2021-10-04 |