Previous terms continue: All communications about the evaluation results via these uses of the information, including any and all Congressional testimony, will carefully enumerate and describe any underlying limitations of the data and ensure that evaluation results are interpreted with appropriate care and caution. CDC acknowledges that study design limitations decrease their capacity to draw nationally representative conclusions about either smoking-related knowledge and behavior or the impact of the campaign on long-term quit rates in sub-populations. Also, approval of any future tobacco-related campaign evaluations (including future revisions of this package) will require a coordinated approach among federal partners (including CDC, FDA, NIH, and SAMHSA) on outcome measures and questionnaire items. Future data collection requests related to tobacco will include a section in supporting statement Part A describing this collaboration and what steps have been made to harmonize data elements and outcome measures as well as a description of steps taken to eliminate duplication of effort across the federal government in the area of tobacco information collection. Areas where there may be significant overlap include, but are not limited to, cessation behavior, perceptions of health risk, health status, etc.
Inventory as of this Action
Requested
Previously Approved
03/31/2017
03/31/2017
03/31/2017
28,447
0
28,447
8,777
0
8,777
0
0
0
CDC requests non-substantive changes to portions of this data collection activity due to the rapidly changing landscape of electronic vapor products and their advertising.
PL:
Pub.L. 111 - 148 4004
Name of Law: Patient Protection and Affordable Care Act
PL:
Pub.L. 111 - 31 203
Name of Law: Family Smoking Prevention and Tobacco Control Act
US Code:
42 USC 301
Name of Law: Public Health Service Act
On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
(i) Why the information is being collected;
(ii) Use of information;
(iii) Burden estimate;
(iv) Nature of response (voluntary, required for a benefit, or mandatory);
(v) Nature and extent of confidentiality; and
(vi) Need to display currently valid OMB control number;
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.
Non-smoker Follow-up Survey Wave 4
0920-0923 Change Request Justification_9 04 2014.docx
Attachment G-2 KnowledgePanel Email Invitation Reminders 1-15-14.doc
Attachment E-1 RTI IRB Approval Notice.pdf
Non-smoker Follow-up Survey Wave 4