Colorectal Cancer Screening Survey

Forms and Documents

Document Name	Status
CRC Study Participants including Control Group Form	Modified
CRC Pre-Test Participants Including Control Group Form	Modified
Att 2 Overview of Survey and Screen Shots REV 12JAN2015_TC.docx Supplementary Document	2015-01-12
0920-1023 change request 1 07 2015.docx Justification for No Material/Nonsubstantive Change	2015-01-12
Attachment 8 Invitation Email.docx Supplementary Document	2014-05-05
Attachment 7 KN privacy statement.docx Supplementary Document	2014-05-05
Attachment 6 RTI IRB approval.docx Supplementary Document	2014-05-05
Attachment 5 Summary of Public Comments.doc Supplementary Document	2014-05-05
Attachment 4 60-day FRN 9 05 2013.pdf Supplementary Document	2014-05-05
Attachment 1. Authorizing Legislation.docx Supplementary Document	2014-05-05
Supporting Statement B_4 21 2014.doc Supporting Statement B	2014-05-05
Supporting Statement A_5_1_2014.docx Supporting Statement A	2014-05-05

IC Document Collections

IC ID	Document Title	Status
211513	CRC Study Participants including Control Group Form	Modified
211512	CRC Pre-Test Participants Including Control Group Form	Modified

ICR Details

OMB Control No: 0920-1023	ICR Reference No: 201501-0920-013
Status: Historical Active	Previous ICR Reference No: 201405-0920-003
Agency/Subagency: HHS/CDC	Agency Tracking No: 15KK
Title: Colorectal Cancer Screening Survey
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: Approved without change	Conclusion Date: 01/22/2015
	Date Received in OIRA: 01/20/2015
Terms of Clearance:

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	06/30/2015	06/30/2015	06/30/2015
Responses	2,030	0	2,030
Time Burden (Hours)	812	0	812
Cost Burden (Dollars)	0	0	0

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Abstract: CDC requests minor changes to survey instruments to remove selected questions to reduce the burden to the approved burden level.

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Authorizing Statute(s): US Code: 42 USC 301.241 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:
	78 FR 54653	09/05/2013
30-day Notice:	Federal Register Citation:	Citation Date:
	79 FR 27308	05/13/2014
Did the Agency receive public comments on this ICR? Yes

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Number of Information Collection (IC) in this ICR: 2

IC Title	Form No.	Form Name
CRC Pre-Test Participants Including Control Group	none	Overview of CRC Screening Survey
CRC Study Participants including Control Group	none	Overview of Survey and Screenshots

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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	2,030	2,030	0	0	0	0
Annual Time Burden (Hours)	812	812	0	0	0	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

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: $208,681

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: 01/20/2015

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