[OPPE] The Performance Measures Project: Improving Performance Measurement and Monitoring by CDC Programs

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Congenital Syphilis PoC Testing Supplement	Form and Instruction	New	Available
STD PCHD PM Data Collection Tool	Form and Instruction	New	Available
STDPCHD_ChangeReqMemo June 2026_final.docx	Justification for No Material/Nonsubstantive Change	Uploaded 2026-07-21	Available
Att 8 - Completion and Carryover Statement_final.docx	Supplementary Document	Uploaded 2026-07-01	Available
Att 6_project-summary-0900f3eb826b2025-5-21-2026-6_9_31.pdf	Supplementary Document	Uploaded 2026-06-15	Available
Att 4_60 Day FRN_PMP_0920-1282_Feb 2026.pdf	Supplementary Document	Uploaded 2026-06-15	Available
Att 3_GenIC Request Template.docx	Supplementary Document	Uploaded 2026-06-15	Available
Att 2_Tech specs and reporting guide_final.docx	Supplementary Document	Uploaded 2026-07-01	Available
Att 1-authorizing legislation.docx	Supplementary Document	Uploaded 2026-06-15	Available
SSB PMP_0920-1282_final.docx	Supporting Statement B	Uploaded 2026-07-01	Available
SSA PMP_0920-1282_final.docx	Supporting Statement A	Uploaded 2026-07-01	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
281609	[NCHHSTP_OPPE] Performance Measurement for STD PCHD (2026-2028)	Form and Instruction	New	Congenital Syphilis PoC Testing Supplement
281609	[NCHHSTP_OPPE] Performance Measurement for STD PCHD (2026-2028)	Form and Instruction	New	STD PCHD PM Data Collection Tool

ICR Details

OMB Control No: 0920-1282	ICR Reference No: 202607-0920-006
Status: Received in OIRA	Previous ICR Reference No: 202606-0920-005
Agency/Subagency: HHS/CDC	Agency Tracking No: 0920-26-0245
Title: [OPPE] The Performance Measures Project: Improving Performance Measurement and Monitoring by CDC Programs
Type of Information Collection: No material or nonsubstantive change to a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular	Date Submitted to OIRA: 07/22/2026

table that charts list comparision

	Requested	Previously Approved
Expiration Date	07/31/2029	07/31/2029
Responses	14,958	14,958
Time Burden (Hours)	314,847	314,847
Cost Burden (Dollars)	0	0

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Abstract: The purpose of this Generic Data Collection is to: 1) help CDC programs and their recipients develop strong performance measurement systems and practices; 2) define and operationalize priority performance measures; and 3) establish common data collection and reporting expectations. Data will enable the accurate, reliable, uniform and timely submission of recipients' progress. This Change Request relates to the GenIC titled Performance Measurement for STD PCHD (2026-2028) and the changes are related to a supplement addendum with minor burden changes.

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Authorizing Statute(s): US Code: 42 USC 45 CFR 75.342 Name of Law: Monitoring and reporting program performance
  

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:
	91 FR 8882	02/24/2026
30-day Notice:	Federal Register Citation:	Citation Date:
	91 FR 31459	05/27/2026
Did the Agency receive public comments on this ICR? Yes

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

table that charts list of burden

IC Title	Form No.	Form Name
[NCHHSTP_OPPE] Performance Measurement for STD PCHD (2026-2028)	n/a, n/a	STD PCHD PM Data Collection Tool ,   Congenital Syphilis PoC Testing Supplement

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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	14,958	14,958	0	0	0	0
Annual Time Burden (Hours)	314,847	314,847	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: Increase due to additional respondents in the previously approved continuing GenIC collections.

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Annual Cost to Federal Government: $127,731

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.     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: 07/22/2026

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