National Diabetes Education Program Evaluation Survey of the Public (NIDDK)

Forms and Documents

Document	Type	Status	Availability
Form 1 Adults	Form and Instruction	Modified	Repair queued
Form 1 Eligible Respondents	Form and Instruction	Removed	Available
NDEP Public Survey OMB SUPPORTING STATEMENT A_22Aug2014-2-1.docx	Supporting Statement A	Uploaded 2014-08-27	Available
Att G KN Best Practices for ICR Supporting Documentation 22Aug2014.pdf	Supplementary Document	Uploaded 2014-08-25	Available
Att D GfK KnowledgePanel Recruitment_Empanelment Methodology incl Consent 22Aug2014.pdf	Supplementary Document	Uploaded 2014-08-25	Available
Att C GfK Privacy Procedures for Panelists_GfK SSS Data Mgmt Procedures 22Aug2014.pdf	Supplementary Document	Uploaded 2014-08-25	Available
Att B-1 Roadmap overview of NNDS online survey.pdf	Supplementary Document	Uploaded 2014-08-22	Available
Att A Executive Summary_NDEP_NNDS_Initial Results_Trends.pdf	Supplementary Document	Uploaded 2014-08-22	Available
NDEP Public Survey OMB SUPPORTING STATEMENT B_29Sep2014 (2).docx	Supporting Statement B	Uploaded 2014-10-01	Available

IC Document Collections

IC ID	Collection	Type	Status	Form
7476	Adults	Form and Instruction	Modified
187314	Eligible Respondents	Form and Instruction	Removed

ICR Details

OMB Control No: 0925-0552	ICR Reference No: 201408-0925-005
Status: Historical Active	Previous ICR Reference No: 201208-0925-004
Agency/Subagency: HHS/NIH	Agency Tracking No:
Title: National Diabetes Education Program Evaluation Survey of the Public (NIDDK)
Type of Information Collection: Revision of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved with change	Conclusion Date: 10/03/2014
	Date Received in OIRA: 08/28/2014
Terms of Clearance:

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	10/31/2017	36 Months From Approved	10/31/2015
Responses	2,500	0	5,859
Time Burden (Hours)	833	0	650
Cost Burden (Dollars)	0	0	0

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Abstract: The National Diabetes Education Program (NDEP) is a partnership of the National Institutes of Health (NIH) and the Centers for Disease Control and Prevention (CDC) and more than 200 public and private organizations. The long?term goal of the NDEP is to reduce the burden of diabetes and pre-diabetes in the United States, and its territories, by facilitating the adoption of proven strategies to prevent or delay the onset of diabetes and its complications. The program audiences include the public, people at risk for diabetes, people with diabetes and their families, with special emphasis on racial/ethnic populations; health care providers; and payers and purchasers of health care and health care system policy makers.

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Authorizing Statute(s): US Code: 42 USC 285c Name of Law: Diabetes Mellitus Interagency Coordinating Committee
  

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 15351	03/19/2014
30-day Notice:	Federal Register Citation:	Citation Date:
	79 FR 49784	08/22/2014
Did the Agency receive public comments on this ICR? No

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

IC Title	Form No.	Form Name
Adults	1	NDEP Survey Screenshots
Eligible Respondents	1	NDEP 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	2,500	5,859	0	-3,359	0	0
Annual Time Burden (Hours)	833	650	0	183	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: Yes

Burden Reduction Due to: Using Information Technology

Short Statement: This is a request for a revision to an existing data collection currently approved by OMB, as discussed above. The specific changes are: 1. Use of a probability-based web-based survey rather than the random-digit-dialing (RDD) telephone survey that we previously conducted. 2. Update of the survey questionnaire (some formatting changes and question revisions) which has not been updated since it was first developed in 2006. 3. A modest increase in the burden amount from the previously approved 650 hours to 833 hours, an additional 84 hours overall. This burden reflects an increase of 5 minutes per participant due to survey content changes and an additional 400 participants.

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Annual Cost to Federal Government: $250,000

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: 08/28/2014

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