Next Series of Tobacco Use Supplements to the Current Population Survey (TUS-CPS) (NCI)

Forms and Documents

Document Name	Status
Form 3 Main 2010-2011 Tobacco Use Supplement Questionnaire (TUS-CPS) Form and Instruction	Removed
Form 1-Rev Individuals Form and Instruction	New
Form 1 2011 Follow-Up Questionnaire (TUS-CPS) Form and Instruction	Removed
TUS-CPS Cover Memo for OMB Final (passbacks).docx Supplementary Document	2014-06-24
ASPE Original Comments Feb 2014.docx Supplementary Document	2014-04-28
ASPE Comments_NCI-Response_4-3-14_2014 TUS.docx Supplementary Document	2014-04-28
Memo For Timely Review_1-6-2014.docx Supplementary Document	2014-04-28
Cover Letter Memo TUS-CPS_4-3-2014.docx Supplementary Document	2014-04-28
SSB_TUS-CPS_4-28-14.doc Supporting Statement B	2014-04-28
REVISED SSA_TUS-CPS Final.docx Supporting Statement A	2014-06-24
A13_TUSBrochure2014.pdf Supplementary Document	2014-04-28
A12_DesignOverview.docx Supplementary Document	2014-04-28
A11_Respondent Universe_REV.doc Supplementary Document	2014-04-28
A10_TabulationPlans.doc Supplementary Document	2014-04-28
A9_OHSRP Review_1stPage.pdf Supplementary Document	2014-04-28
A8.2_PrivacyActMemo.pdf Supplementary Document	2014-04-28
A8.1 _Non-applicability Privacy Act.pdf Supplementary Document	2014-04-28
A7_ConfidentialBrochure.pdf Supplementary Document	2014-04-28
A6_CPS-Advance-Letter.pdf Supplementary Document	2014-04-28
A5_Experts Consulted_12-20_2013.doc Supplementary Document	2014-04-28
A4_Comparison of Key Features_4-2-14.pdf Supplementary Document	2014-04-28
A3_PIA-TUS-CPS.pdf Supplementary Document	2014-04-28
A2_Reports Publications_1-2-14.doc Supplementary Document	2014-04-28

IC Document Collections

IC ID	Document Title	Status
7287	Main 2010-2011 Tobacco Use Supplement Questionnaire (TUS-CPS) Form and Instruction	Removed
211374	Individuals Form and Instruction	New
191981	2011 Follow-Up Questionnaire (TUS-CPS) Form and Instruction	Removed

ICR Details

OMB Control No: 0925-0368	ICR Reference No: 201404-0925-002
Status: Historical Active	Previous ICR Reference No: 201102-0925-007
Agency/Subagency: HHS/NIH	Agency Tracking No:
Title: Next Series of Tobacco Use Supplements to the Current Population Survey (TUS-CPS) (NCI)
Type of Information Collection: Reinstatement with change of a previously approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved with change	Conclusion Date: 06/25/2014
	Date Received in OIRA: 05/02/2014
Terms of Clearance: NCI, CDC, FDA, and ASPE will continue to collaborate on design, content, and analysis of the CPS-TUS survey, consistent with the memorandum that is included in this information collection request (see supplemental documents).

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	06/30/2016	24 Months From Approved
Responses	127,500	0	0
Time Burden (Hours)	12,750	0	0
Cost Burden (Dollars)	0	0	0

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Abstract: The 2014-15 Tobacco Use Supplement-Current Population Survey (TUS-CPS) will be conducted by the Census Bureau and is co-sponsored by the National Cancer Institute (NCI) and the Food and Drug Administration (FDA). Fielded since 1992, most recently in 2010-11, this survey is part of a continuing series of surveys (OMB No. 0925-0368) sponsored by NCI that has been administered triennially as part of the Census Bureau's and the Bureau of Labor Statistics' CPS. For the TUS-CPS, data will be collected from the U.S. civilian non-institutionalized population on smoking, other tobacco use, including switching, flavors, dependence, cessation attempts, and policy and social norms. The TUS-CPS has been a key source of national, state, some local-level, and health disparity data on these topics in U.S. households because it uses a large, nationally representative sample. The 2014-15 TUS-CPS is designed to meet both NCI's and FDA's goals. The NCI and FDA are co-sponsoring the 2014-15 TUS-CPS through parallel, but separate interagency agreements with the Census Bureau. The NCI is particularly focused on policy information such as home and workplace smoking policies, cigarette price, and impact of these on subsequent purchase and use behavior; and changes in smoking norms and attitudes. The FDA aims to support research to aid the development and evaluation of tobacco product regulations. The research findings generated from this program are expected to provide data to inform FDA regulation of the manufacture, distribution, and marketing of tobacco products to protect public health. A unique feature is the ability to link other social and economic Census Bureau and Bureau of Labor Statistics data, other sponsor-supported supplement data, and the National Longitudinal Mortality Study cancer incidence and cause-specific mortality data to the TUS-CPS data. Data will be collected in July 2014, January 2015, and May 2015 from about 255,000 respondents.

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Authorizing Statute(s): US Code: 42 USC 412(285a-1) Name of Law: Public Health Service Act
   US Code: 42 USC 413(285a-2) Name of Law: Public Health Service Act
   US Code: 42 USC 411(285a) Name of Law: Public Health Service Act
  

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
	Not associated with rulemaking

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	79 FR 3598	01/22/2014
30-day Notice:	Federal Register Citation:	Citation Date:
	79 FR 22998	04/25/2014
Did the Agency receive public comments on this ICR? Yes

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Number of Information Collection (IC) in this ICR: 1

IC Title	Form No.	Form Name
Main 2010-2011 Tobacco Use Supplement Questionnaire (TUS-CPS)	3, 2	TUS-CPS Q Spanish ,   TUS-CPS Q
2011 Follow-Up Questionnaire (TUS-CPS)	1, 2	May 2011 Follow Up Q ,   TUS-CPS May 2011 Questionnaire Final
Individuals	1, 1-Rev	Revised 2014-2015 TUS-CPS Form ,   Main 2014-2015 Tobacco Use Supplement Questionnaire

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ICR Summary of Burden

	Total Approved	Previously Approved	Change Due to New Statute	Change Due to Agency Discretion	Change Due to Adjustment in Estimate	Change Due to Potential Violation of the PRA
Annual Number of Responses	127,500	0	0	127,500	0	0
Annual Time Burden (Hours)	12,750	0	0	12,750	0	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

Burden increases because of Program Change due to Agency Discretion: Yes

Burden Increase Due to: Miscellaneous Actions

Burden decreases because of Program Change due to Agency Discretion: No

Burden Reduction Due to:

Short Statement: This is a reinstatement with change which means we are adding burden back to the NIH inventory.

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Annual Cost to Federal Government: $1,570,000

Does this IC contain surveys, censuses, or employ statistical methods? Yes Part B of Supporting Statement

Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002? No

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? No

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? No

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? No

Is this ICR related to the Pandemic Response? Uncollected

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Common Form ICR:  No

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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:

(a) It is necessary for the proper performance of agency functions;

(b) It avoids unnecessary duplication;

(c) It reduces burden on small entities;

(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;

(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;

(f) It indicates the retention periods for recordkeeping requirements;

(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:

(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;

(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.

(i) It uses effective and efficient statistical survey methodology (if applicable); and

(j) It makes appropriate use of information technology.

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.

Certification Date: 05/02/2014

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