Use of Smartphones to Collect Information about Health Behaviors: Feasibility Study

Forms and Documents

Document Name	Status
SS B_051712.doc Supporting Statement B	2012-06-08
Appx B_Published 60d FRN.pdf Supplementary Document	2012-06-08
Appx B2_Comts in Resp to FRN.doc Supplementary Document	2012-06-08
Appx A_Authorizing Legislation.doc Supplementary Document	2012-06-08
Appx C2_CATI Informed Consent.doc Supplementary Document	2012-06-14
Supporting Statement_A_061912_Admin_Review.docx Supporting Statement A	2012-06-20

IC Document Collections

IC ID	Document Title	Status
202850	Pre-Test for Smartphone Feasibility Study Other-Word	New
202849	Second Text Message Survey Follow-up for non-Smartphone Users Other-WORD	New
202848	First Text Message Survey Follow-up for non-Smartphone Users Other-WORD	New
202847	Second Web Survey Follow up for Smartphone Users Other-WORD	New
202846	First Web Survey Follow-up for Smartphone Users Other-WORD	New
202845	CATI Recruitment Other-WORD	New
202844	CATI Screener Other-WORD	New

ICR Details

OMB Control No:	ICR Reference No: 201206-0920-006
Status: Historical Inactive	Previous ICR Reference No:
Agency/Subagency: HHS/CDC	Agency Tracking No:
Title: Use of Smartphones to Collect Information about Health Behaviors: Feasibility Study
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OIRA Conclusion Action: Withdrawn	Conclusion Date: 10/05/2012
	Date Received in OIRA: 06/22/2012
Terms of Clearance: Withdrawn with the understanding that the Program will modify the supporting statements to describe both the goals and the methods of the collection in greater detail. Once revisions have been made, the ICR may be resubmitted for review.

	Inventory as of this Action	Requested	Previously Approved
Expiration Date		12 Months From Approved
Responses	0	0	0
Time Burden (Hours)	0	0	0
Cost Burden (Dollars)	0	0	0

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Abstract: CdC is conducting a feasibility study to evaluate the utility of smartphones for collecting information from adults in the U.S. related to tobacco use and other health behavior. The goals of this study is to help CDC better prepare for public health surveillance, by determining the use of smartphones in collecting data and utilizing advance technology as a potential tool.

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Authorizing Statute(s): US Code: 3 USC 301 Name of Law: Research and Investigation
  

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:
	77 FR 11545	02/27/2012
30-day Notice:	Federal Register Citation:	Citation Date:
	77 FR 35404	06/13/2012
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 7

IC Title	Form No.	Form Name
First Text Message Survey Follow-up for non-Smartphone Users
Second Text Message Survey Follow-up for non-Smartphone Users
Pre-Test for Smartphone Feasibility Study
CATI Recruitment
First Web Survey Follow-up for Smartphone Users
CATI Screener
Second Web Survey Follow up for Smartphone Users

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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 collection (one time study).

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Annual Cost to Federal Government: $117,154

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? 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: 06/22/2012

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