Monitoring Outcomes of the Enhanced Comprehensive HIV Prevention Plan (ECHPP) Project

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Rev Supporting Statement B - ECHPP_3-13-2012.doc	Supplementary Document	Uploaded 2012-03-20	Available
Rev Attach 7a _Clinic Director Script_3-13-2012.doc	Supplementary Document	Uploaded 2012-03-20	Available
Rev Supporting Statement A - ECHPP_3-13-2012.docx	Justification for No Material/Nonsubstantive Change	Uploaded 2012-03-20	Available
Attach 7b _Venue Owner_Manager Script.doc	Supplementary Document	Uploaded 2012-02-15	Available
Rev Attach 9b Clinic Survey Interviewer Script.docx	Supplementary Document	Uploaded 2012-02-15	Available
Attach 7a _Clinic Director Script.doc	Supplementary Document	Uploaded 2012-02-15	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
200569	Community Survey - Eligible High-Risk Heterosexual Individuals	Instruction	Modified
200568	Community Survey - Eligible Injection Drug Users	Instruction	Modified
200567	Community Screener - Screened Injection Drug Users and High-risk heterosexual individuals	Instruction	Modified
200566	Clinic Survey - Eligible HIV-positive Individuals	Instruction	Modified
200565	Clinic Screener - HIV Positive Screened Individuals	Instruction	Modified
200564	Clinic Staff Script - Approaching Clients	Instruction	Modified
200563	Clinic Staff Provision Patient of Loads	Instruction	Modified
200562	Project Orientation - Clinic Staff	Instruction	Modified

ICR Details

OMB Control No: 0920-0922	ICR Reference No: 201203-0920-006
Status: Historical Inactive	Previous ICR Reference No: 201112-0920-015
Agency/Subagency: HHS/CDC	Agency Tracking No:
Title: Monitoring Outcomes of the Enhanced Comprehensive HIV Prevention Plan (ECHPP) Project
Type of Information Collection: No material or nonsubstantive change to a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Disapproved and continue	Conclusion Date: 03/22/2012
	Date Received in OIRA: 03/21/2012
Terms of Clearance:

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	02/28/2015	02/28/2015	02/28/2015
Responses	7,040	0	7,040
Time Burden (Hours)	1,704	0	1,704
Cost Burden (Dollars)	0	0	0

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Abstract: In September 2010, twelve U.S. metropolitan statistical areas (MSAs) conducted the Enhanced Comprehensive HIV Prevention Plan (ECHPP) project. These twelve MSAs (Atlanta, Baltimore, Chicago, Dallas, District of Columbia, Houston, Los Angeles, Miami, New York City, Philadelphia, San Francisco, and San Juan, Puerto Rico) have the highest AIDS prevalence rates in the U.S. The purpose of ECHPP is to enhance existing HIV prevention services and provide an optimal mix of evidence-based behavioral, biomedical, and structural interventions to have maximum impact on the HIV/AIDS epidemic in high prevalence areas. A new data collection activity is requested through this ICR to assist with the ECHPP evaluation. This data collection activity will occur in six of the 12 ECHPP MSAs (Houston, District of Columbia, Los Angeles, Miami, New York City, and San Francisco). This activity is designed to monitor community-level outcomes of ECHPP in these MSAs and supplement existing HIV surveillance data that are already being collected via CDC data systems in these cities. Information about behavioral risk, access of HIV-related services and programs, and exposure to HIV prevention messages will be collected from three populations at increased risk for HIV infection or transmission: injection drug users, heterosexuals at increased risk of HIV infection, and HIV-positive individuals who access HIV/medical care from clinics that provide HIV services.

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Authorizing Statute(s): US Code: 42 USC 241 Name of Law: Public Health Service 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

Did the Agency receive public comments on this ICR? Yes

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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
Project Orientation - Clinic Staff
Clinic Staff Provision Patient of Loads
Clinic Staff Script - Approaching Clients
Clinic Screener - HIV Positive Screened Individuals
Clinic Survey - Eligible HIV-positive Individuals
Community Screener - Screened Injection Drug Users and High-risk heterosexual individuals
Community Survey - Eligible Injection Drug Users
Community Survey - Eligible High-Risk Heterosexual Individuals

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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: $3,633,362

Does this IC contain surveys, censuses, or employ statistical methods? Yes Part B of Supporting Statement

Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002? Yes

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: 03/21/2012

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