Agency Forms Undergoing Paperwork Reduction Act Review, 12346-12347 [2024-03240]

Download as PDF 12346 Federal Register / Vol. 89, No. 33 / Friday, February 16, 2024 / Notices questions from Components 1 and 2 to provide relevant, timely data on new, emerging, and priority health topics to be used for decision making. NCHS will use questions from Components 3 and 4 to weight and evaluate the quality of the estimates coming from questions in Components 1 and 2. Components 1 and 2 will contain different topics in each round of the survey. NCHS submits a 30-day Federal Register Notice with information on the contents of each round of data collection. NCHS calibrates survey weights from the RSS to gold standard surveys. Questions used for calibration in this round of RSS will include marital status, employment, social and work limitations, use of the internet in general and for medical reasons, telephone use, civic engagement, and language used at home and in other settings. All of these questions have injury because of intimate partner violence. In Round 4, the RSS will be used as a methodological study to test the ability to obtain data on intimate partner violence-related topics via web panel survey. In addition, RSS Round 4 offers the opportunity for developmental work to develop questions using a split sample to compare current NISVS questions and modified questions to evaluate different wording and question formats and to develop new questionnaire content related to understudied domains of intimate partner violence. The estimated total annual burden hours for the three-year approval period remains at 28,079 burden hours. The NCHS RSS Round 4 (2024) data collection is based on 13,100 complete surveys (4,367 hours). There are no costs to respondents other than their time. been on the National Health Interview Survey (NHIS) in prior years allowing calibration to these data. Finally, all RSS rounds will include several questions that were previously on NHIS or other NCHS surveys, or other suitable Federal surveys for benchmarking to evaluate data quality. Panelists in the RSS will be asked about health status; chronic conditions; pregnancy; disability and age of disability onset; health insurance through an employer; healthcare access and utilization; mental health; mental health care utilization; and health behaviors. Rapid Surveys System (RSS) will include content on psychological aggression by intimate partners, sexual violence, technology-facilitated sexual violence, emerging coercive control by intimate partners, and traumatic brain ESTIMATED ANNUALIZED BURDEN HOURS Form name Adults 18+ ...................................................... Survey: NCHS RSS Round 4 (2024) ............ Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Public Health Ethics and Regulations, Office of Science, Centers for Disease Control and Prevention. [FR Doc. 2024–03242 Filed 2–15–24; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day–24–0740] Agency Forms Undergoing Paperwork Reduction Act Review lotter on DSK11XQN23PROD with NOTICES1 Number of respondents Type of respondents In accordance with the Paperwork Reduction Act of 1995, the Centers for Disease Control and Prevention (CDC) has submitted the information collection request titled ‘‘Medical Monitoring Project (MMP)’’ 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 April 24, 2023 to obtain comments from the public and affected agencies. CDC received one comment related to the previous notice. This notice serves to allow an additional 30 days for public and affected agency comments. VerDate Sep<11>2014 17:24 Feb 15, 2024 Jkt 262001 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 PO 00000 Frm 00045 Fmt 4703 Sfmt 4703 Number of responses per respondent 13,100 Average burden per response (in hours) 1 20/60 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 Medical Monitoring Project (MMP)— (OMB Control No. 0920–0740 Exp. 05/ 31/2024)—Revision—National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention (NCHHSTP), Centers for Disease Control and Prevention (CDC). Background and Brief Description The Centers for Disease Control and Prevention (CDC), Division of HIV Prevention (DHP) requests a Revision of the currently approved Information Collection Request titled Medical Monitoring Project (MMP) (OMB Control No. 0920–0740, Expiration 5/ 31/2024). This data collection addresses the need for national estimates of access E:\FR\FM\16FEN1.SGM 16FEN1 12347 Federal Register / Vol. 89, No. 33 / Friday, February 16, 2024 / Notices to and utilization of HIV-related medical care and services, the quality of HIVrelated ambulatory care, and HIVrelated behaviors and clinical outcomes. For the proposed project, the same data collection methods will be used as for the currently approved project. Data would be collected from a probability sample of HIV-diagnosed adults in the U.S. who consent to an interview and abstraction of their medical records. As for the currently approved project, deidentified information would also be extracted from HIV case surveillance records for a dataset (referred to as the minimum dataset), which is used to assess non-response bias, for quality control, to improve the ability of MMP to monitor ongoing care and treatment of HIV-infected persons, and to make inferences from the MMP sample to HIV-diagnosed persons nationally. No other Federal agency collects such nationally representative populationbased information from HIV-diagnosed adults. The data are expected to have significant implications for policy, program development, and resource allocation at the State/local and national levels. The changes proposed in this Revision request update the data collection system to meet prevailing information needs and enhance the value of MMP data, while remaining within the scope of the currently approved project purpose. The burden is the same as in the currently approved project. Changes were made that did not affect the burden are listed below: • Revisions to the Interview Questionnaire were made to improve coherence, boost the efficiency of the data collection, and increase the relevance and value of the information. These changes did not affect the average burden per response. • Revisions to the Medical Record Abstraction Data Elements were made to streamline the information collected and add important questions, such as those related to mpox vaccination. Because the medical records are abstracted by MMP staff, these changes do not affect the burden of the project. • The Interview and Medical Record data collection system were integrated to improve project efficiency and enhance data quality. This proposed data collection would supplement the National HIV Surveillance System (NHSS, OMB Control No. 0920–0573, Exp. 02/28/ 2026) in 23 selected State and local health departments, which collect information on persons diagnosed with, living with, and dying from HIV infection and AIDS. Through their participation, respondents will help to improve programs to prevent HIV infection as well as services for those who already have HIV. Participation of respondents is voluntary. Total estimated annual burden requested is 5,707 hours. There is no cost to the respondents other than their time. ESTIMATED ANNUALIZED BURDEN HOURS Form name State and Local Health Departments ............ Interview Questionnaire ................................ Look up contact information .......................... Approach persons for enrollment .................. Pull medical records ...................................... Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Public Health Ethics and Regulations, Office of Science, Centers for Disease Control and Prevention. [FR Doc. 2024–03240 Filed 2–15–24; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day–24–1186] Agency Forms Undergoing Paperwork Reduction Act Review lotter on DSK11XQN23PROD with NOTICES1 Number of respondents Type of respondent In accordance with the Paperwork Reduction Act of 1995, the Centers for Disease Control and Prevention (CDC) has submitted the information collection request titled ‘‘Information Collection for Tuberculosis Data from Referring Entities to CureTB’’ 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’’ VerDate Sep<11>2014 17:24 Feb 15, 2024 Jkt 262001 notice on December 15, 2023 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: (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 PO 00000 Frm 00046 Fmt 4703 Sfmt 4703 7,760 1,940 970 7,760 Number of responses per respondent Average hours per response 1 1 1 1 40/60 2/60 5/60 3/60 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 Information Collection for Tuberculosis Data from Referring E:\FR\FM\16FEN1.SGM 16FEN1

Agencies

[Federal Register Volume 89, Number 33 (Friday, February 16, 2024)]
[Notices]
[Pages 12346-12347]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-03240]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30Day-24-0740]


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 ``Medical Monitoring Project (MMP)'' 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 April 24, 2023 to obtain 
comments from the public and affected agencies. CDC received one 
comment 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

    Medical Monitoring Project (MMP)--(OMB Control No. 0920-0740 Exp. 
05/31/2024)--Revision--National Center for HIV/AIDS, Viral Hepatitis, 
STD, and TB Prevention (NCHHSTP), Centers for Disease Control and 
Prevention (CDC).

Background and Brief Description

    The Centers for Disease Control and Prevention (CDC), Division of 
HIV Prevention (DHP) requests a Revision of the currently approved 
Information Collection Request titled Medical Monitoring Project (MMP) 
(OMB Control No. 0920-0740, Expiration 5/31/2024). This data collection 
addresses the need for national estimates of access

[[Page 12347]]

to and utilization of HIV-related medical care and services, the 
quality of HIV-related ambulatory care, and HIV-related behaviors and 
clinical outcomes.
    For the proposed project, the same data collection methods will be 
used as for the currently approved project. Data would be collected 
from a probability sample of HIV-diagnosed adults in the U.S. who 
consent to an interview and abstraction of their medical records. As 
for the currently approved project, de-identified information would 
also be extracted from HIV case surveillance records for a dataset 
(referred to as the minimum dataset), which is used to assess non-
response bias, for quality control, to improve the ability of MMP to 
monitor ongoing care and treatment of HIV-infected persons, and to make 
inferences from the MMP sample to HIV-diagnosed persons nationally. No 
other Federal agency collects such nationally representative 
population-based information from HIV-diagnosed adults. The data are 
expected to have significant implications for policy, program 
development, and resource allocation at the State/local and national 
levels.
    The changes proposed in this Revision request update the data 
collection system to meet prevailing information needs and enhance the 
value of MMP data, while remaining within the scope of the currently 
approved project purpose. The burden is the same as in the currently 
approved project. Changes were made that did not affect the burden are 
listed below:
     Revisions to the Interview Questionnaire were made to 
improve coherence, boost the efficiency of the data collection, and 
increase the relevance and value of the information. These changes did 
not affect the average burden per response.
     Revisions to the Medical Record Abstraction Data Elements 
were made to streamline the information collected and add important 
questions, such as those related to mpox vaccination. Because the 
medical records are abstracted by MMP staff, these changes do not 
affect the burden of the project.
     The Interview and Medical Record data collection system 
were integrated to improve project efficiency and enhance data quality.
    This proposed data collection would supplement the National HIV 
Surveillance System (NHSS, OMB Control No. 0920-0573, Exp. 02/28/2026) 
in 23 selected State and local health departments, which collect 
information on persons diagnosed with, living with, and dying from HIV 
infection and AIDS. Through their participation, respondents will help 
to improve programs to prevent HIV infection as well as services for 
those who already have HIV. Participation of respondents is voluntary. 
Total estimated annual burden requested is 5,707 hours. There is no 
cost to the respondents other than their time.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                    Number of
          Type of respondent                   Form name            Number of     responses per    Average hours
                                                                   respondents      respondent     per response
----------------------------------------------------------------------------------------------------------------
State and Local Health Departments...  Interview Questionnaire.           7,760                1           40/60
                                       Look up contact                    1,940                1            2/60
                                        information.
                                       Approach persons for                 970                1            5/60
                                        enrollment.
                                       Pull medical records....           7,760                1            3/60
----------------------------------------------------------------------------------------------------------------


Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Public Health 
Ethics and Regulations, Office of Science, Centers for Disease Control 
and Prevention.
[FR Doc. 2024-03240 Filed 2-15-24; 8:45 am]
BILLING CODE 4163-18-P
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