[NCCDPHP] Division of Diabetes Translation Programmatic & Participant User Experience Data Collection

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
SSA.docx	Supporting Statement A	Uploaded 2024-11-12	Repair queued
SSB.docx	Supporting Statement B	Uploaded 2024-11-06	Repair queued
Privacy Narrative_DDT GenIC_100124.pdf	Supplementary Document	Uploaded 2024-11-06	Missing upstream
Attachment 5 Sample Questions.docx	Supplementary Document	Uploaded 2024-11-06	Missing upstream
Attachment 4 Comments.pdf	Supplementary Document	Uploaded 2024-11-06	Repair queued
Attachment 2 GenIC ExpeditedReviewForm.docx	Supplementary Document	Uploaded 2024-11-06	Repair queued
Attachment 1 Authorizing Legislation.pdf	Supplementary Document	Uploaded 2024-11-06	Missing upstream

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form

ICR Details

OMB Control No:	ICR Reference No: 202411-0920-001
Status: Received in OIRA	Previous ICR Reference No:
Agency/Subagency: HHS/CDC	Agency Tracking No: 0920-24HQ
Title: [NCCDPHP] Division of Diabetes Translation Programmatic & Participant User Experience Data Collection
Type of Information Collection: New collection (Request for a new OMB Control Number)	Common Form ICR:  No
Type of Review Request: Regular	Date Submitted to OIRA: 11/25/2024

table that charts list comparision

	Requested	Previously Approved
Expiration Date	36 Months From Approved
Responses	4,000	0
Time Burden (Hours)	2,000	0
Cost Burden (Dollars)	0	0

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Abstract: CDC's Division of Diabetes Translation (DDT) request approval of a new generic clearance to conduct data collection to support the development, refinement, and improvement of DDT's education, training, technical assistance, and communication/marketing activities so that DDT can provide a clear, effective, efficient, appropriate, and timely customer service delivery.

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Authorizing Statute(s): None

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:
	89 FR 60636	07/26/2024
30-day Notice:	Federal Register Citation:	Citation Date:
	89 FR 90703	11/18/2024
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 0

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ICR Summary of Burden

table that charts list of burden

	Total Request	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	4,000	0	0	4,000	0	0
Annual Time Burden (Hours)	2,000	0	0	2,000	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: This is a new (GENERIC) data/information collection.

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Annual Cost to Federal Government: $680,000

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.     Yes

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.     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? No

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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: 11/25/2024

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