Formative and Summative Evaluation of the National Diabetes Prevention Program

Forms and Documents

Document Name	Status
Form 0920-1090 Evaluation Form for Grantees Form	Modified
Form 0920-1090 Evaluation Form for Sites Form	Modified
0920 1090 Att 6 Overview of Changes Final.doc Supplementary Document	2019-07-02
0920 1090 Att 5D Annual Assessment Rpt Dashboard FInal.docx Supplementary Document	2019-07-02
0920 1090 Att 4 Data System Screenshots Final.docx Supplementary Document	2019-07-02
0920 1090 Att 8A CDC Non-Research Determination Final.pdf Supplementary Document	2019-07-02
0920 1090 Att 2A 60-Day FRN Final.pdf Supplementary Document	2019-07-02
0920 1090 Att 8B ICF IRB Determination Final.pdf Supplementary Document	2019-07-02
0920 1090 Att 5C Thank you Email Final.doc Supplementary Document	2019-07-02
0920 1090 Att 5B Reminder Email Final.doc Supplementary Document	2019-07-02
0920 1090 Att 5A Invitation Email Final.doc Supplementary Document	2019-07-02
0920 1090 Att 1B Authorizing Legislation for PHSA Final.pdf Supplementary Document	2019-07-02
0920 1090 Att 1A Authorizing Legislation for NDPP Final.pdf Supplementary Document	2019-07-02
0920 1090 Att 7 1705 Evaluation Framework Final.xlsx Supplementary Document	2019-07-02
0920 1090 Supporting Statement B Final.docx Supporting Statement B	2019-07-02
0920 1090 Supporting Statement A Final.docx Supporting Statement A	2019-07-02

IC Document Collections

IC ID	Document Title	Status
218088	Evaluation Form for Grantees Form	Modified
218087	Evaluation Form for Sites Form	Modified

ICR Details

OMB Control No: 0920-1090	ICR Reference No: 201906-0920-014
Status: Active	Previous ICR Reference No: 201509-0920-001
Agency/Subagency: HHS/CDC	Agency Tracking No: 0920-1090
Title: Formative and Summative Evaluation of the National Diabetes Prevention Program
Type of Information Collection: Reinstatement with change of a previously approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 10/24/2019
	Date Received in OIRA: 07/03/2019
Terms of Clearance: CDC should improve their monitoring of expiring information collections to avoid unnecessary reinstatement requests.

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	10/31/2022	36 Months From Approved
Responses	110	0	0
Time Burden (Hours)	640	0	0
Cost Burden (Dollars)	0	0	0

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Abstract: CDC's Division of Diabetes Translation's Revision of the Information Collection Request (OMB No. 0920-1090, exp.12/31/2018) supporting an evaluation of the National Diabetes Prevention Program: Research has shown that an evidence-based lifestyle change program leading to weight loss and increased physical activity prevent or delay type 2 diabetes in persons with prediabetes or those at high risk of developing type 2 diabetes. The Public Health Service Act gives CDC general authority to evaluate programs and translate research findings in

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Authorizing Statute(s): PL: Pub.L. 111 - 148 1 Name of Law: National Diabetes Prevention Program
   US Code: 42 USC 241 Name of Law: PHSA
  

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:
	83 FR 50098	10/04/2018
30-day Notice:	Federal Register Citation:	Citation Date:
	84 FR 10091	03/19/2019
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
Evaluation Form for Sites	0920-1090	Evaluation Form for Sites
Evaluation Form for Grantees	0920-1090	Evaluation Form for Grantees

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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	110	0	0	110	0	0
Annual Time Burden (Hours)	640	0	0	640	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: No

Burden Reduction Due to:

Short Statement: A number of changes to the forms and increased burden estimates are proposed to address public comments and ensure that evaluation requirements are consistent with the new coop. agreement.

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Annual Cost to Federal Government: $162,626

Does this IC contain surveys, censuses, or employ statistical methods? Yes Part B of Supporting Statement

Does this ICR request any personally identifiable information (see OMB Circular No. A-130 for an explanation of this term)? Please consult with your agency's privacy program when making this determination.     No

Does this ICR include a form that requires a Privacy Act Statement (see 5 U.S.C. §552a(e)(3))? Please consult with your agency's privacy program when making this determination.     Yes

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? Yes

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: 07/03/2019

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