Aggregate Reports for Tuberculosis Program Evaluation

Forms and Documents

Document Name	Status
Form 0920-0457 Follow-up and Treatment of Contacts to Tuberculosis Case Form - Electronic (Data Clerks and Program Managers) Form and Instruction	Modified
Form 0920-0457 Targeted Testing and Treatment for Latent Tuberculosis Infection Form and Instruction	Modified
Att 1_Legislative Authority.pdf Supplementary Document	2022-07-26
Att 4_NCHHSTP Project Determination Form.pdf Supplementary Document	2022-07-26
60 Day Required Combined Request_2022.docx Supplementary Document	2022-07-26
Att 5 arpes_manual.pdf Supplementary Document	2022-07-26
Att 6_PIA_ARPE approved 10 Jun 2019.pdf Supplementary Document	2022-07-26
Att 7 Awardees_2022.docx Supplementary Document	2022-07-26
ARPE TT 2020109 Att3b Compared with OMB Version.docx Supplementary Document	2020-01-16
ARPE CI 20200109 Att3a Compared to OMB Version.docx Supplementary Document	2020-01-16
Justification for Non_Substantive Change Request (0920-0457).docx Justification for No Material/Nonsubstantive Change	2020-01-16
SS B_2022.docx Supporting Statement B	2022-07-26
SSA_2022.docx Supporting Statement A	2022-07-26
Att 7 Awardees.docx Supplementary Document	2019-07-25
Att 6_PIA_ARPE approved 10 Jun 2019.pdf Supplementary Document	2019-07-25
Att 5_Aggregate Reports for Program Evaluation Training Manual and Users Guide.pdf Supplementary Document	2019-07-25
Att 4_NCHHSTP Project Determination Form.pdf Supplementary Document	2019-07-25
Att 2_60-Day FRN_0920-0457.pdf Supplementary Document	2019-07-25
Att 1_Legislative Authority.pdf Supplementary Document	2019-07-25

IC Document Collections

IC ID	Document Title	Status
6884	Follow-up and Treatment of Contacts to Tuberculosis Case Form - Electronic (Data Clerks and Program Managers) Form and Instruction	Modified
178818	Targeted Testing and Treatment for Latent Tuberculosis Infection Form and Instruction	Modified

ICR Details

OMB Control No: 0920-0457	ICR Reference No: 202207-0920-009
Status: Received in OIRA	Previous ICR Reference No: 202001-0920-008
Agency/Subagency: HHS/CDC	Agency Tracking No: 0920-0457
Title: Aggregate Reports for Tuberculosis Program Evaluation
Type of Information Collection: Extension without change of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular	Date Submitted to OIRA: 07/26/2022

	Requested	Previously Approved
Expiration Date	36 Months From Approved	12/31/2022
Responses	134	134
Time Burden (Hours)	268	268
Cost Burden (Dollars)	7,234	7,234

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Abstract: This collection is an extension of a currently approved under OMB Control No. 0920-0457. The purpose of this data collection is to continue to address the change in the national strategies for TB control and prevention, emphasizing the treatment of individuals with latent TB infection (LTBI). The data collection allows programs to continue to assess high-risk populations served and evaluate the adaptation and effectiveness of new diagnostic tests and drug regimens used in treating LTBI.CDC is requesting approval for 268 burden hours.

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Authorizing Statute(s): US Code: 42 USC 241 Name of Law: Public Health Service - Research and Investigations generally
  

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:
	87 FR 14270	03/14/2022
30-day Notice:	Federal Register Citation:	Citation Date:
	87 FR 41319	07/12/2022
Did the Agency receive public comments on this ICR? No

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

IC Title	Form No.	Form Name
Follow-up and Treatment of Contacts to Tuberculosis Case Form - Electronic (Data Clerks and Program Managers)	0920-0457	Follow-up and Treatment of Contacts to Tuberculosis Cases Form
Targeted Testing and Treatment for Latent Tuberculosis Infection	0920-0457	Targeted Testing and Treatment for Latent Tuberculosis Infection

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ICR Summary 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	134	134	0	0	0	0
Annual Time Burden (Hours)	268	268	0	0	0	0
Annual Cost Burden (Dollars)	7,234	7,234	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: $106,721

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: 07/26/2022

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