Formative Research to Develop HIV Social Marketing Campaigns for Healthcare Providers

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Project Determination Approval #6838.pdf	Supplementary Document	Uploaded 2021-08-13	Repair queued
Att11 PIA_DevelopHIVSocial-Signed.pdf	Supplementary Document	Uploaded 2021-07-15	Repair queued
Att10-Recruitment Firm Privacy Agreement.docx	Supplementary Document	Uploaded 2021-08-03	Repair queued
Att8-Informed Consent.docx	Supplementary Document	Uploaded 2021-07-15	Repair queued
Att2-60 Day FRN Published 3-6-2021 1182.pdf	Supplementary Document	Uploaded 2021-07-15	Missing upstream
Att1-Legislation.pdf	Supplementary Document	Uploaded 2021-08-03	Repair queued
SSB_04-23-21.docx	Supporting Statement B	Uploaded 2021-08-13	Repair queued
SSA(0920-1182)_rev2.docx	Supporting Statement A	Uploaded 2021-08-13	Repair queued

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
223937	Att 9_Provider Screener	Other-WORD	Modified
223936	Att 7_Materials Testing Guide	Other-WORD	Modified
223935	Att 6_Concept Testing Guide	Other-WORD	Modified
223934	Att 5_Message Testing Guide	Other-WORD	Modified
223933	Att 4c_Exploratory Testing Guide_HIV Prevention: HIV Testing & PrEP	Other-WORD	Modified
223932	Att 4b_Exploratory Testing Guide_ Patient Centered Care	Other-WORD	Modified
223931	Att 4a_Exploratory Testing Guide_Prevention with Positives & Retentiuon in Care	Other-WORD	Modified
223930	Att 3_Web-Based Survey	Other-WORD	Modified

ICR Details

OMB Control No: 0920-1182	ICR Reference No: 202106-0920-013
Status: Received in OIRA	Previous ICR Reference No: 201610-0920-007
Agency/Subagency: HHS/CDC	Agency Tracking No: 0920-1182
Title: Formative Research to Develop HIV Social Marketing Campaigns for Healthcare Providers
Type of Information Collection: Reinstatement with change of a previously approved collection	Common Form ICR:  No
Type of Review Request: Regular	Date Submitted to OIRA: 08/31/2021

table that charts list comparision

	Requested	Previously Approved
Expiration Date	36 Months From Approved
Responses	2,277	0
Time Burden (Hours)	902	0
Cost Burden (Dollars)	0	0

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Abstract: The purpose of this study is to conduct in-depth interviews with healthcare providers to inform the development and/or refinement of provider-focused message, concepts, and materials for CDC's Let's Stop HIV Together social marketing campaign. The results will be used to develop and/or revise timely, relevant, clear, and engaging messages, concepts, and materials for the campaign in support of HHS' Ending the HIV Epidemic plan.

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Authorizing Statute(s): US Code: 42 USC 301 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:
	86 FR 13388	03/08/2021
30-day Notice:	Federal Register Citation:	Citation Date:
	86 FR 48145	08/27/2021
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 8

table that charts list of burden

IC Title	Form No.	Form Name
Att 3_Web-Based Survey
Att 4a_Exploratory Testing Guide_Prevention with Positives & Retentiuon in Care
Att 4b_Exploratory Testing Guide_ Patient Centered Care
Att 4c_Exploratory Testing Guide_HIV Prevention: HIV Testing & PrEP
Att 5_Message Testing Guide
Att 6_Concept Testing Guide
Att 7_Materials Testing Guide
Att 9_Provider Screener

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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	2,277	0	0	2,277	0	0
Annual Time Burden (Hours)	902	0	0	902	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 reinstatement request for ICR 0920-1182. We are requesting changes to reduce the burden by 48 hours, which is the differences of the hours that were used in the original ICR, and replace the “Transgender Health” exploratory interview guide with the “Patient-Centered Care” exploratory interview guide. The changes will not have a negative impact on the data collection nor CDC’s ability to answer key research questions. Section A.2 discusses the rationale for these changes.

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Annual Cost to Federal Government: $484,033

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: 08/31/2021

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