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.