Qualitative Information Collection on Emerging Diseases among the Foreign-born in the US

Forms and Documents

Document Name	Status
Att. F - Example Participant Screener (1).docx Supplementary Document	2019-11-13
Att. E - Participant Information Sheet (1).docx Supplementary Document	2019-11-13
Att. D - Example of an Interview Guide (1).docx Supplementary Document	2019-11-13
Att. C - Example of a Focus Group Discussion Guide (1).docx Supplementary Document	2019-11-13
Att. B - Published 60-day FRN.pdf Supplementary Document	2019-11-13
Att. A7 Section 301 of the Public Health Service Act (42 USC 241).pdf Supplementary Document	2019-11-13
Att. A6 - 42 CFR Part 34 (1).pdf Supplementary Document	2019-11-13
Att. A5 - Section 325 of the PHSA (1).pdf Supplementary Document	2019-11-13
Att. A4 - Section 212(a)(1)(A) of the INA (1).pdf Supplementary Document	2019-11-13
Att. A3 - 42 CFR 71 (1).pdf Supplementary Document	2019-11-13
Att. A2 - 42 CFR 70 (1).pdf Supplementary Document	2019-11-13
Att. A1 - Section 361 of the Public Health Service Act (42 USC 264) (1).pdf Supplementary Document	2019-11-13
SSB_Migrant Health Generic_Qualitative Final.docx Supporting Statement B	2019-11-13
SSA_Migrant Health Generic_Qualitative_FINAL v2 HHS edit.docx Supporting Statement A	2019-11-21

IC Document Collections

IC ID	Document Title	Status

ICR Details

OMB Control No: 0920-0987	ICR Reference No: 201911-0920-004
Status: Active	Previous ICR Reference No: 201605-0920-017
Agency/Subagency: HHS/CDC	Agency Tracking No: 0920-0987
Title: Qualitative Information Collection on Emerging Diseases among the Foreign-born in the US
Type of Information Collection: Extension without change of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 01/21/2020
	Date Received in OIRA: 11/21/2019
Terms of Clearance: Previous terms continue: Approved with the understanding that individual GenIC requests will be submitted and the submission will include any instruments to be used in data collection along with a description of the aims, population, and methods of the particular project. All GenIC requests will contain a complete justification for any incentives offered. All individual projects under this Generic will be one-time data collections involving a specific combination of public health topic of concern, geographic area, and targeted group(s) of foreign born.

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	01/31/2023	36 Months From Approved	01/31/2020
Responses	1,650	0	1,650
Time Burden (Hours)	1,350	0	1,350
Cost Burden (Dollars)	0	0	0

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Abstract: The goal of the generic information collection is to enhance the ability to determine knowledge, attitudes, health beliefs and practices related to communicable diseases and other emerging health issues amongst high risk foreign-born populations in the United States.

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Authorizing Statute(s): US Code: 42 USC 264 Name of Law: Public Health Service Act
   US Code: 8 USC 1182 Name of Law: Immigration and Nationality Act
  

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:
	84 FR 38988	08/08/2019
30-day Notice:	Federal Register Citation:	Citation Date:
	84 FR 64077	11/20/2019
Did the Agency receive public comments on this ICR? Yes

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

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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	1,650	1,650	0	0	0	0
Annual Time Burden (Hours)	1,350	1,350	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: CDC DGMQ was limited in the number of information collections it could perform with foreign born populations in the United States during the previous three years due to a combination several factors: emergency responses that prevented key Unit staff from focusing on carrying on these types of GenIC’s, a lack of specific project funding, and a transition of key Unit leadership to another office. These factors have subsided, and with the current Zika outbreak and improved communicating regarding the availability of this generic information collection to select CDC staff, CDC believes that conducting information collections under the burden described above is feasible.

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Annual Cost to Federal Government: $263,914

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? 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: 11/21/2019

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