Audience Analysis for Biomonitoring

Forms and Documents

Document Name	Status
Form Attachment 5 Message Testing Focus Groups with Selected Women Form and Instruction	New
Form Attachment 4 Exploratory Focus Group with Selected Women Form and Instruction	New
Form Attachment 3 Screener Interviews for Selected Women to Participate in Focus Group Study Form	New
Supporting Statement_PART AB_Biomonitoring_FINAL.docx Supporting Statement A	2011-02-11

IC Document Collections

IC ID	Document Title	Status
195476	Message Testing Focus Groups with Selected Women Form and Instruction	New
195475	Exploratory Focus Group with Selected Women Form and Instruction	New
195474	Screener Interviews for Selected Women to Participate in Focus Group Study Form	New

ICR Details

OMB Control No: 0920-0878	ICR Reference No: 201011-0920-009
Status: Historical Active	Previous ICR Reference No:
Agency/Subagency: HHS/CDC	Agency Tracking No:
Title: Audience Analysis for Biomonitoring
Type of Information Collection: New collection (Request for a new OMB Control Number)	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved with change	Conclusion Date: 02/25/2011
	Date Received in OIRA: 11/30/2010
Terms of Clearance:

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	07/31/2011	05/31/2011
Responses	378	0	0
Time Burden (Hours)	273	0	0
Cost Burden (Dollars)	2,646	0	0

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Abstract: The CDC is interested in developing a framework for communicating health risk messages, particularly about emerging environmental chemicals, to the attentive public audience such as selected women who are pregnant or have very young children. The three environmental chemicals, Bisphenol A (BPA), phthalates, and mercury have been selected for this study. They are of particular interest to these selected women as the risks of exposure are higher for very young children because of their hand-to-mouth behaviors and direct oral (mouth) contact with materials containing these chemicals. Furthermore, young children eat and drink more per pound of body weight than adults. The proposed qualitative study (involving focus groups) is designed to inform the development of messages that will be most attractive and compelling in terms of communicating health risk information about emerging chemicals. This information is not available from any other source. The information gathered in this research will be used internally by CDC staff and its contractor Westat to develop messages for communicating with intended audiences. No personal identifiers will be linked to data or provided to CDC. However, information in identifiable form (IIF) will be used by the focus group facility to screen participants for the focus groups. The IIF includes respondent name and phone number. Participants will only provide their first name during the focus group discussions. The audio-tapes of the focus groups will be stored in a locked file cabinet, and accessible only to Westat project staff. The recording will be destroyed at the end of the study, which is currently May, 2011.

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Authorizing Statute(s): US Code: 42 USC 241 Name of Law: The Public Health and Welfare
  

Citations for New Statutory Requirements: US Code: 42 USC 241 Name of Law: Research and Investigation

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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:
	75 FR 35041	06/21/2010
30-day Notice:	Federal Register Citation:	Citation Date:
	75 FR 65489	10/25/2010
Did the Agency receive public comments on this ICR? Yes

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Number of Information Collection (IC) in this ICR: 3

IC Title	Form No.	Form Name
Screener Interviews for Selected Women to Participate in Focus Group Study	Attachment 3, Attachment 3	Screener Interviews for Selected Women to Participate in Focus Group Study
Exploratory Focus Group with Selected Women	Attachment 4	Exploratory Focus Group with Women Selected
Message Testing Focus Groups with Selected Women	Attachment 5	Message Testing Focus Group Discussion Guide

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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	378	0	54	324	0	0
Annual Time Burden (Hours)	273	0	108	165	0	0
Annual Cost Burden (Dollars)	2,646	0	1,134	1,512	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 new Information Collection Request.

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Annual Cost to Federal Government: $144,000

Does this IC contain surveys, censuses, or employ statistical methods? No

Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002? Yes

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: 11/30/2010

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