Evaluation of the Food and Drug Administration's General Market Youth Tobacco Prevention Campaign

Forms and Documents

Document Name	Status
SS Part B Final Evaluation Campaign.doc Supporting Statement B	2014-06-10
SS Part A 0910_New Evaluation of FDA Tobacco Public Education Campaign.docx Supporting Statement A	2014-06-10
SS Part A 0910_New Evaluation of FDA Tobacco Public Education Campaign.docx Supplementary Document	2014-06-10
OMB approval Lead Letter 6 4 14.doc Supplementary Document	2014-06-10
OMB approval Youth Consent 6 4 14.doc Supplementary Document	2014-06-10
Panel Maintenance Letter.docx Supplementary Document	2014-06-10
Parent Permission for Youth Interview_1st Follow-Up.doc Supplementary Document	2014-06-10
Rationale for Items Added to or Removed From the ExPECTT Youth FU Instru....docx Supplementary Document	2014-06-10
Rationale for Increasing Incentives and Measuring Ghost Awareness.docx Supplementary Document	2014-06-10
0910-0753 Evaluation Campaign Non substantive change request 83c 2.6.14.docx Justification for No Material/Nonsubstantive Change	2014-02-06

IC Document Collections

IC ID	Document Title	Status
208714	Media Tracking Questionnaires 1st, 2nd amp; 3rd Other-Survey	Modified
208713	Media Tracking Screener Instruction	Modified
208712	Parent Of Youth Baseline Survey Participants Instruction	Modified
208711	Youth 1st, 2nd, amp; 3rd (Male, Rural Smokeless) fullow up questionnaire Instruction	Modified
208710	Youth Baseline Questionnaire (Male Rural Smokeless) Instruction	Modified
208709	Youth 1st, 2nd, 3rd Follow-Up Questionnaire (Experimenter and Non-Trier) Instruction	Modified
208708	Youth Baseline Questionnaire (Experimenter and Non-Trier) Instruction	Modified
208707	General Population Screener and Consent Process (Youth and Parent) Instruction	Modified

ICR Details

OMB Control No: 0910-0753	ICR Reference No: 201405-0910-021
Status: Historical Inactive	Previous ICR Reference No: 201402-0910-002
Agency/Subagency: HHS/FDA	Agency Tracking No: CTP
Title: Evaluation of the Food and Drug Administration's General Market Youth Tobacco Prevention Campaign
Type of Information Collection: No material or nonsubstantive change to a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Withdrawn and continue	Conclusion Date: 06/26/2014
	Date Received in OIRA: 06/17/2014
Terms of Clearance:

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	10/31/2016	10/31/2016	10/31/2016
Responses	70,618	0	70,618
Time Burden (Hours)	12,612	0	12,612
Cost Burden (Dollars)	0	0	0

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Abstract: The Food and Drug Administration (FDA) requests Office of Management and Budget (OMB) approval to conduct in-person and Web-based surveys of youth in targeted areas in the United States. These surveys will be fielded for purposes of evaluating FDA's general market youth tobacco prevention campaigns. The primary outcome evaluation will consist of an initial baseline survey before the launch of each of three campaigns and three longitudinal follow-up surveys of those participants in 8-month intervals following the baseline data collection. In addition, a tracking survey to assess awareness of the campaigns and receptivity to campaign messages will occur in 8-month intervals throughout the data collection period. As part of the outcome evaluation study, a baseline survey will also be conducted with the parent or legal guardian of each youth baseline survey participant in order to collect data on household characteristics and media use. Data from this evaluation will be used to gauge campaign awareness and examine the statistical relationships between exposure to the campaigns and changes in outcome variables of interest.

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Authorizing Statute(s): PL: Pub.L. 111 - 31 31 Name of Law: Family Smoking Prevention and Tobacco Control 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

Did the Agency receive public comments on this ICR? Yes

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Number of Information Collection (IC) in this ICR: 8

IC Title	Form No.	Form Name
Youth Baseline Questionnaire (Experimenter and Non-Trier)
General Population Screener and Consent Process (Youth and Parent)
Youth 1st, 2nd, 3rd Follow-Up Questionnaire (Experimenter and Non-Trier)
Youth Baseline Questionnaire (Male Rural Smokeless)
Youth 1st, 2nd, amp; 3rd (Male, Rural Smokeless) fullow up questionnaire
Parent Of Youth Baseline Survey Participants
Media Tracking Screener
Media Tracking Questionnaires 1st, 2nd amp; 3rd

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

Burden Increase Due to:

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

Burden Reduction Due to:

Short Statement:

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Annual Cost to Federal Government: $12,148,807

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: 06/17/2014

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