Agency Forms Undergoing Paperwork Reduction Act Review, 49848-49849 [2022-17360]

Download as PDF 49848 Federal Register / Vol. 87, No. 155 / Friday, August 12, 2022 / Notices DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day–22–0612] Agency Forms Undergoing Paperwork Reduction Act Review In accordance with the Paperwork Reduction Act of 1995, the Centers for Disease Control and Prevention (CDC) has submitted the information collection request titled ‘‘WellIntegrated Screening and Evaluation for Women Across the Nation (WISEWOMAN) Reporting System’’ to the Office of Management and Budget (OMB) for review and approval. CDC previously published a ‘‘Proposed Data Collection Submitted for Public Comment and Recommendations’’ notice on June 2, 2022 to obtain comments from the public and affected agencies. CDC received no comment(s) related to the previous notice. This notice serves to allow an additional 30 days for public and affected agency comments. CDC will accept all comments for this proposed information collection project. The Office of Management and Budget is particularly interested in comments that: (a) Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; (b) Evaluate the accuracy of the agencies estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; (c) Enhance the quality, utility, and clarity of the information to be collected; (d) Minimize the burden of the collection of information on those who are to respond, including, through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submission of responses; and (e) Assess information collection costs. To request additional information on the proposed project or to obtain a copy of the information collection plan and instruments, call (404) 639–7570. Comments and recommendations for the proposed information collection should be sent within 30 days of publication of this notice to www.reginfo.gov/public/ do/PRAMain. Find this particular information collection by selecting ‘‘Currently under 30-day Review—Open for Public Comments’’ or by using the search function. Direct written comments and/or suggestions regarding the items contained in this notice to the Attention: CDC Desk Officer, Office of Management and Budget, 725 17th Street NW, Washington, DC 20503 or by fax to (202) 395–5806. Provide written comments within 30 days of notice publication. Proposed Project Well-Integrated Screening and Evaluation for Women Across the Nation (WISEWOMAN) Reporting System (OMB Control No. 0920–0612, Exp. 08/31/2022)—Extension—National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC). Background and Brief Description The WISEWOMAN program, sponsored by the CDC, provides services to low income, uninsured, or underinsured women aged 40–64. WISEWOMAN is designed to prevent, detect, and control hypertension and other cardiovascular disease (CVD) risk factors through healthy behavior support services which are tailored for individual and group behavior change. The WISEWOMAN program provides services to women who are jointly enrolled in the National Breast and Cervical Cancer Early Detection Program (NBCCEDP), which is also sponsored by CDC. The WISEWOMAN program is administered by state health departments and tribal programs. In 2018, new five-year cooperative agreements were awarded under Funding Opportunity Announcement DP18–1816, subject to the availability of funds. CDC collects two types of information from WISEWOMAN awardees. The WISEWOMAN awardee submits an electronic data file to CDC twice per year. The Minimum Data Elements (MDE) file contains data using a unique identifier with client-level information about cardiovascular disease risk factors and types of healthy behavior support services for participants served by the program. The estimated burden per response for the MDE file is 24 hours. In addition, each WISEWOMAN awardee submits an Annual Progress Report to CDC, which provides a narrative summary of the awardee’s objectives and the activities undertaken to meet program goals. The estimated burden per response for the Annual Progress Report is 16 hours. There are no changes to the information collection. CDC will continue to use the information collected from WISEWOMAN awardees to support program monitoring and improvement activities, evaluation, and assessment of program outcomes. The overall program evaluation helps to demonstrate program accomplishments and strengthen the evidence for implementing strategies that improve engagement of underserved populations. The information reported to CDC can also help to determine whether the identified strategies and associated activities can be implemented at various levels within a state or tribal organization. Evaluation is also designed to demonstrate how WISEWOMAN can obtain cardiovascular disease health outcome data on at-risk populations, promote public education about cardiovascular disease risk-factors, and improve the availability of healthy behavior support services for under-served women. OMB approval is requested for two years. Participation in this information collection is required as a condition of cooperative agreement funding. There are no costs to respondents other than their time. The total estimated annualized burden hours are 2,240. jspears on DSK121TN23PROD with NOTICES ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Type of respondents Form name WISEWOMAN Awardees ................................ Screening and Assessment and Lifestyle Program MDEs. Annual Progress Report ................................. VerDate Sep<11>2014 17:38 Aug 11, 2022 Jkt 256001 PO 00000 Frm 00050 Fmt 4703 Sfmt 4703 E:\FR\FM\12AUN1.SGM Number of responses per respondent Average burden per response (in hrs.) 35 2 24 35 1 16 12AUN1 49849 Federal Register / Vol. 87, No. 155 / Friday, August 12, 2022 / Notices Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Scientific Integrity, Office of Science, Centers for Disease Control and Prevention. [FR Doc. 2022–17360 Filed 8–11–22; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day–22–0770] Agency Forms Undergoing Paperwork Reduction Act Review In accordance with the Paperwork Reduction Act of 1995, the Centers for Disease Control and Prevention (CDC) has submitted the information collection request titled ‘‘National HIV Behavioral Surveillance System (NHBS)’’ to the Office of Management and Budget (OMB) for review and approval. CDC previously published a ‘‘Proposed Data Collection Submitted for Public Comment and Recommendations’’ notice on May 13, 2022 to obtain comments from the public and affected agencies. CDC did not receive comments related to the previous notice. This notice serves to allow an additional 30 days for public and affected agency comments. CDC will accept all comments for this proposed information collection project. The Office of Management and Budget is particularly interested in comments that: jspears on DSK121TN23PROD with NOTICES (a) Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; (b) Evaluate the accuracy of the agencies estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; (c) Enhance the quality, utility, and clarity of the information to be collected; (d) Minimize the burden of the collection of information on those who are to respond, including, through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submission of responses; and (e) Assess information collection costs. To request additional information on the proposed project or to obtain a copy of the information collection plan and instruments, call (404) 639–7570. Comments and recommendations for the proposed information collection should be sent within 30 days of publication of this notice to www.reginfo.gov/public/ do/PRAMain. Find this particular information collection by selecting ‘‘Currently under 30-day Review—Open for Public Comments’’ or by using the search function. Direct written comments and/or suggestions regarding the items contained in this notice to the Attention: CDC Desk Officer, Office of Management and Budget, 725 17th Street NW, Washington, DC 20503 or by fax to (202) 395–5806. Provide written comments within 30 days of notice publication. Proposed Project National HIV Behavioral Surveillance System (NHBS) (OMB Control No. 0920–0770, Exp. 01/31/2023)— Revision—National Center for HIV, Viral Hepatitis, STD, and TB Prevention (NCHHSTP), Centers for Disease Control and Prevention (CDC). Background and Brief Description The purpose of this data collection is to monitor behaviors of persons at high risk for infection that are related to Human Immunodeficiency Virus (HIV) transmission and prevention in the United States. The primary objectives of the NHBS are to obtain data from samples of persons at risk to: (a) describe the prevalence and trends in risk behaviors; (b) describe the prevalence of and trends in HIV testing and HIV infection; (c) describe the prevalence of and trends in use of HIV prevention services; and (d) identify met and unmet needs for HIV prevention services in order to inform health departments, community based organizations, community planning groups and other stakeholders. By describing and monitoring the HIV risk behaviors, HIV seroprevalence and incidence, and HIV prevention experiences of persons at highest risk for HIV infection, NHBS provides an important data source for evaluating progress towards national public health initiatives, such as reducing new infections, increasing the use of condoms, and targeting populations at high risk. The Centers for Disease Control and Prevention requests approval for a threeyear Revision of this information collection. Data are collected through in-person interviews conducted with persons systematically selected from 20 Metropolitan Statistical Areas (MSAs) throughout the United States; these 20 MSAs are chosen based on highest number of HIV infections diagnosed. Persons at risk for HIV infection to be interviewed for NHBS include men who have sex with men (MSM), persons who inject drugs (PWID), and heterosexually active persons at increased risk of HIV infection (HET). A brief screening interview will be used to determine eligibility for participation in the behavioral assessment. The data from the behavioral assessment will provide estimates of: (1) behavior related to the risk of HIV and other sexually transmitted diseases; (2) prior testing for HIV; and (3) use of HIV prevention services. All persons interviewed will also be offered an HIV test and will participate in a pre-test counseling session. No other federal agency systematically collects this type of information from persons at risk for HIV infection. These data have substantial impact on prevention program development and monitoring at the local, state, and national levels. CDC estimates that NHBS will involve, per year, in up to 20 MSAs, eligibility screening for 125 persons and eligibility screening plus the behavioral assessment with 500 eligible respondents, resulting in a total of 30,000 eligible survey respondents and 7,500 ineligible screened persons during a three-year period. Data collection will rotate such that interviews will be conducted among one group per year: MSM in Year 1, PWID in Year 2, and HET in Year 3. The type of data collected for each group will vary slightly due to different sampling methods and risk characteristics of the group. Participation of respondents is voluntary and there is no cost to the respondents other than their time. CDC requests OMB approval for an estimated 6,600 annual burden hours. ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Type of respondents Form name Persons Screened .......................................... Eligible Participants ......................................... Eligibility Screener .......................................... Behavioral Assessment MSM ........................ VerDate Sep<11>2014 17:38 Aug 11, 2022 Jkt 256001 PO 00000 Frm 00051 Fmt 4703 Sfmt 4703 12,500 3,333 E:\FR\FM\12AUN1.SGM 12AUN1 Number of responses per respondent 1 1 Average burden per response (in hours) 5/60 24/60

Agencies

[Federal Register Volume 87, Number 155 (Friday, August 12, 2022)]
[Notices]
[Pages 49848-49849]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-17360]



[[Page 49848]]

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30Day-22-0612]


Agency Forms Undergoing Paperwork Reduction Act Review

    In accordance with the Paperwork Reduction Act of 1995, the Centers 
for Disease Control and Prevention (CDC) has submitted the information 
collection request titled ``Well-Integrated Screening and Evaluation 
for Women Across the Nation (WISEWOMAN) Reporting System'' to the 
Office of Management and Budget (OMB) for review and approval. CDC 
previously published a ``Proposed Data Collection Submitted for Public 
Comment and Recommendations'' notice on June 2, 2022 to obtain comments 
from the public and affected agencies. CDC received no comment(s) 
related to the previous notice. This notice serves to allow an 
additional 30 days for public and affected agency comments.
    CDC will accept all comments for this proposed information 
collection project. The Office of Management and Budget is particularly 
interested in comments that:
    (a) Evaluate whether the proposed collection of information is 
necessary for the proper performance of the functions of the agency, 
including whether the information will have practical utility;
    (b) Evaluate the accuracy of the agencies estimate of the burden of 
the proposed collection of information, including the validity of the 
methodology and assumptions used;
    (c) Enhance the quality, utility, and clarity of the information to 
be collected;
    (d) Minimize the burden of the collection of information on those 
who are to respond, including, through the use of appropriate 
automated, electronic, mechanical, or other technological collection 
techniques or other forms of information technology, e.g., permitting 
electronic submission of responses; and
    (e) Assess information collection costs.
    To request additional information on the proposed project or to 
obtain a copy of the information collection plan and instruments, call 
(404) 639-7570. Comments and recommendations for the proposed 
information collection should be sent within 30 days of publication of 
this notice to www.reginfo.gov/public/do/PRAMain. Find this particular 
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function. Direct 
written comments and/or suggestions regarding the items contained in 
this notice to the Attention: CDC Desk Officer, Office of Management 
and Budget, 725 17th Street NW, Washington, DC 20503 or by fax to (202) 
395-5806. Provide written comments within 30 days of notice 
publication.

Proposed Project

    Well-Integrated Screening and Evaluation for Women Across the 
Nation (WISEWOMAN) Reporting System (OMB Control No. 0920-0612, Exp. 
08/31/2022)--Extension--National Center for Chronic Disease Prevention 
and Health Promotion (NCCDPHP), Centers for Disease Control and 
Prevention (CDC).

Background and Brief Description

    The WISEWOMAN program, sponsored by the CDC, provides services to 
low income, uninsured, or underinsured women aged 40-64. WISEWOMAN is 
designed to prevent, detect, and control hypertension and other 
cardiovascular disease (CVD) risk factors through healthy behavior 
support services which are tailored for individual and group behavior 
change. The WISEWOMAN program provides services to women who are 
jointly enrolled in the National Breast and Cervical Cancer Early 
Detection Program (NBCCEDP), which is also sponsored by CDC.
    The WISEWOMAN program is administered by state health departments 
and tribal programs. In 2018, new five-year cooperative agreements were 
awarded under Funding Opportunity Announcement DP18-1816, subject to 
the availability of funds. CDC collects two types of information from 
WISEWOMAN awardees. The WISEWOMAN awardee submits an electronic data 
file to CDC twice per year. The Minimum Data Elements (MDE) file 
contains data using a unique identifier with client-level information 
about cardiovascular disease risk factors and types of healthy behavior 
support services for participants served by the program. The estimated 
burden per response for the MDE file is 24 hours. In addition, each 
WISEWOMAN awardee submits an Annual Progress Report to CDC, which 
provides a narrative summary of the awardee's objectives and the 
activities undertaken to meet program goals. The estimated burden per 
response for the Annual Progress Report is 16 hours.
    There are no changes to the information collection. CDC will 
continue to use the information collected from WISEWOMAN awardees to 
support program monitoring and improvement activities, evaluation, and 
assessment of program outcomes. The overall program evaluation helps to 
demonstrate program accomplishments and strengthen the evidence for 
implementing strategies that improve engagement of underserved 
populations. The information reported to CDC can also help to determine 
whether the identified strategies and associated activities can be 
implemented at various levels within a state or tribal organization. 
Evaluation is also designed to demonstrate how WISEWOMAN can obtain 
cardiovascular disease health outcome data on at-risk populations, 
promote public education about cardiovascular disease risk-factors, and 
improve the availability of healthy behavior support services for 
under-served women.
    OMB approval is requested for two years. Participation in this 
information collection is required as a condition of cooperative 
agreement funding. There are no costs to respondents other than their 
time. The total estimated annualized burden hours are 2,240.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                     Number of    Average burden
          Type of respondents                   Form name            Number of     responses per   per response
                                                                    respondents     respondent       (in hrs.)
----------------------------------------------------------------------------------------------------------------
WISEWOMAN Awardees....................  Screening and Assessment              35               2              24
                                         and Lifestyle Program
                                         MDEs.
                                        Annual Progress Report..              35               1              16
----------------------------------------------------------------------------------------------------------------



[[Page 49849]]

Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific 
Integrity, Office of Science, Centers for Disease Control and 
Prevention.
[FR Doc. 2022-17360 Filed 8-11-22; 8:45 am]
BILLING CODE 4163-18-P
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