Proposed Data Collection Submitted for Public Comment and Recommendations, 77835-77836 [2022-27506]

Download as PDF Federal Register / Vol. 87, No. 243 / Tuesday, December 20, 2022 / Notices DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60Day–23–0853; Docket No. CDC–2023– 0141] Proposed Data Collection Submitted for Public Comment and Recommendations Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). ACTION: Notice with comment period. AGENCY: The Centers for Disease Control and Prevention (CDC), as part of its continuing effort to reduce public burden and maximize the utility of government information, invites the general public and other federal agencies the opportunity to comment on a continuing information collection, as required by the Paperwork Reduction Act of 1995. This notice invites comment on a proposed information collection project titled Asthma Information Reporting System (AIRS). The purpose of AIRS is to collect performance measure (PM) and surveillance data designed to increase the efficiency and effectiveness of, and to monitor the impact of, state, local and territorial asthma programs. DATES: CDC must receive written comments on or before February 21, 2023. SUMMARY: You may submit comments, identified by Docket No. CDC–2023– 0141 by either of the following methods: • Federal eRulemaking Portal: www.regulations.gov. Follow the instructions for submitting comments. • Mail: Jeffrey M. Zirger, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS H21–8, Atlanta, Georgia 30329. Instructions: All submissions received must include the agency name and Docket Number. CDC will post, without change, all relevant comments to www.regulations.gov. Please note: Submit all comments through the Federal eRulemaking portal (www.regulations.gov) or by U.S. mail to the address listed above. FOR FURTHER INFORMATION CONTACT: To request more information on the proposed project or to obtain a copy of the information collection plan and instruments, contact Jeffrey M. Zirger, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS H21–8, Atlanta, Georgia 30329; lotter on DSK11XQN23PROD with NOTICES1 ADDRESSES: VerDate Sep<11>2014 18:41 Dec 19, 2022 Jkt 259001 Telephone: 404–639–7118; Email: omb@ cdc.gov. SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3501–3520), federal agencies must obtain approval from the Office of Management and Budget (OMB) for each collection of information they conduct or sponsor. In addition, the PRA also requires federal agencies to provide a 60-day notice in the Federal Register concerning each proposed collection of information, including each new proposed collection, each proposed extension of existing collection of information, and each reinstatement of previously approved information collection before submitting the collection to the OMB for approval. To comply with this requirement, we are publishing this notice of a proposed data collection as described below. The OMB is particularly interested in comments that will help: 1. 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; 2. Evaluate the accuracy of the agency’s estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; 3. Enhance the quality, utility, and clarity of the information to be collected; 4. 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 submissions of responses; and 5. Assess information collection costs. Proposed Project Asthma Information and Reporting System (AIRS) (OMB Control No. 0920– 0853, Exp. 5/31/2023)—Extension— National Center for Environmental Health (NCEH), Centers for Disease Control and Prevention (CDC). Background and Brief Description In 1999, the CDC began its National Asthma Control Program (NACP), a public health approach to address the burden of asthma. The program supports the proposed objectives of ‘‘Healthy People 2030’’ for asthma and is based on the public health principles of surveillance, partnerships, interventions, and evaluation. CDC requests a three-year approval to extend the ‘‘Asthma Information Reporting PO 00000 Frm 00049 Fmt 4703 Sfmt 4703 77835 System (AIRS)’’ (OMB Control No. 0920–0853; Exp. Date 5/31/2023). The three-year Extension will allow CDC to continue to monitor states’ program planning and delivery of public health activities and the programs’ collaboration with health care systems through the end of the five-year cooperative agreement—A Comprehensive Public Health Approach to Asthma Control through EvidenceBased Interventions (CDC–RFA–EH19– 1902). The goal of this data collection is to provide NCEH with routine information about the activities and performance of the state, local and territorial recipients funded under the NACP through an annual reporting system. NACP requires recipients to report activities related to partnerships, infrastructure, evaluation and interventions to monitor the programs’ performance in reducing the burden of asthma. AIRS also includes two forms to collect aggregate emergency department (ED) visits and hospital discharge (HD) data from recipients. AIRS was first approved by OMB in 2010 to collect data in a web-based system to monitor and guide participating state health departments. Since implementation in 2010, AIRS and the technical assistance provided by CDC staff have provided states with uniform data reporting methods and linkages to other states’ asthma program information and resources. Thus, AIRS has saved state resources and staff time when asthma programs embark on asthma activities similar to those conducted elsewhere. In the past three years, AIRS data were used to: • Facilitate communication about interventions across states and enable inquiries regarding interventions by populations with a disproportionate burden, age groups, geographic areas and other variables of interest; • Provide feedback to the grantees about their performance relative to others through the distribution of written reports and several presentations summarizing the results; • Customize and provide technical assistance and support materials to address implementation challenges; • Serve as a resource to the branch, division, and center when addressing congressional, departmental and institutional inquiries. For example, the PMs allow us to report the number and age distribution of people reached with intensive asthma self-management education through the recipients and their partners; • Help the branch align its current interventions with CDC goals and E:\FR\FM\20DEN1.SGM 20DEN1 77836 Federal Register / Vol. 87, No. 243 / Tuesday, December 20, 2022 / Notices allowed the monitoring of progress toward these goals. For example, recipient efforts to establish public health–health care collaboration has been integrated into CDC’s 6|18 initiative which connects healthcare purchasers, payers, and providers with CDC researchers, economists, and policy analysts to find ways to improve health and control costs with the 6|18 interventions; • Allow the NACP and the state asthma programs to make more informed decisions about activities to achieve objectives. For example, PM information identified a problem with enrolling patients most in need of intervention into recipient programs. This led to cross-state discussions and changes in recruitment strategies; • Motivate use of data and evaluation findings. For example, the requirement to report actions taken based on evaluation findings encourages program managers and health departments officials to act on recommendations in evaluation reports. CDC requests OMB approval for an estimated 105 annual burden hours. There is no cost to respondents other than their time to participate. ESTIMATED ANNUALIZED BURDEN HOURS Average burden per response (in hours) Total burden (in hours) Form name Funded Asthma Program Recipients Performance Measures Reporting Tool. Emergency Department Visits Reporting Form. Hospital Discharge Reporting Form 30 1 150/60 75 30 1 30/60 15 30 1 30/60 15 .......................................................... ........................ ........................ ........................ 105 Total ........................................... Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Scientific Integrity, Office of Science, Centers for Disease Control and Prevention. [FR Doc. 2022–27506 Filed 12–19–22; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day–23–1030] Agency Forms Undergoing Paperwork Reduction Act Review lotter on DSK11XQN23PROD with NOTICES1 Number of responses per respondent 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 ‘‘Developmental Studies to Improve the National Health Care Surveys’’ 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 September 30, 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: VerDate Sep<11>2014 18:41 Dec 19, 2022 Jkt 259001 (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 PO 00000 Frm 00050 Fmt 4703 Sfmt 4703 Street NW, Washington, DC 20503 or by fax to (202) 395–5806. Provide written comments within 30 days of notice publication. Proposed Project Developmental Studies to Improve the National Health Care Surveys (OMB Control No. 0920–1030, Exp. 06/30/ 2023)—Extension—National Center for Health Statistics (NCHS), Centers for Disease Control and Prevention (CDC). Background and Brief Description Section 306 of the Public Health Service (PHS) Act (42 U.S.C. 242k), as amended, authorizes the Secretary of Health and Human Services (DHHS), acting through the Division of Health Care Statistics (DHCS) within NCHS, shall collect statistics on the extent and nature of illness and disability of the population of the United States. The DHCS conducts the National Health Care Surveys (NHCS), a family of nationally representative surveys of encounters and health care providers in inpatient, ambulatory, and long-term care settings. This information collection request (ICR) is for the extension of a generic clearance to conduct developmental studies to improve this family of surveys. This three-year clearance period will include studies to evaluate and improve upon existing survey design and operations, as well as to examine the feasibility of, and address challenges that may arise with, future expansions of the National Health Care Surveys. Specifically, this request covers developmental research with the E:\FR\FM\20DEN1.SGM 20DEN1

Agencies

[Federal Register Volume 87, Number 243 (Tuesday, December 20, 2022)]
[Notices]
[Pages 77835-77836]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-27506]



[[Page 77835]]

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[60Day-23-0853; Docket No. CDC-2023-0141]


Proposed Data Collection Submitted for Public Comment and 
Recommendations

AGENCY: Centers for Disease Control and Prevention (CDC), Department of 
Health and Human Services (HHS).

ACTION: Notice with comment period.

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

SUMMARY: The Centers for Disease Control and Prevention (CDC), as part 
of its continuing effort to reduce public burden and maximize the 
utility of government information, invites the general public and other 
federal agencies the opportunity to comment on a continuing information 
collection, as required by the Paperwork Reduction Act of 1995. This 
notice invites comment on a proposed information collection project 
titled Asthma Information Reporting System (AIRS). The purpose of AIRS 
is to collect performance measure (PM) and surveillance data designed 
to increase the efficiency and effectiveness of, and to monitor the 
impact of, state, local and territorial asthma programs.

DATES: CDC must receive written comments on or before February 21, 
2023.

ADDRESSES: You may submit comments, identified by Docket No. CDC-2023-
0141 by either of the following methods:
     Federal eRulemaking Portal: www.regulations.gov. Follow 
the instructions for submitting comments.
     Mail: Jeffrey M. Zirger, Information Collection Review 
Office, Centers for Disease Control and Prevention, 1600 Clifton Road 
NE, MS H21-8, Atlanta, Georgia 30329.
    Instructions: All submissions received must include the agency name 
and Docket Number. CDC will post, without change, all relevant comments 
to www.regulations.gov.
    Please note: Submit all comments through the Federal eRulemaking 
portal (www.regulations.gov) or by U.S. mail to the address listed 
above.

FOR FURTHER INFORMATION CONTACT: To request more information on the 
proposed project or to obtain a copy of the information collection plan 
and instruments, contact Jeffrey M. Zirger, Information Collection 
Review Office, Centers for Disease Control and Prevention, 1600 Clifton 
Road NE, MS H21-8, Atlanta, Georgia 30329; Telephone: 404-639-7118; 
Email: [email protected].

SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995 
(PRA) (44 U.S.C. 3501-3520), federal agencies must obtain approval from 
the Office of Management and Budget (OMB) for each collection of 
information they conduct or sponsor. In addition, the PRA also requires 
federal agencies to provide a 60-day notice in the Federal Register 
concerning each proposed collection of information, including each new 
proposed collection, each proposed extension of existing collection of 
information, and each reinstatement of previously approved information 
collection before submitting the collection to the OMB for approval. To 
comply with this requirement, we are publishing this notice of a 
proposed data collection as described below.
    The OMB is particularly interested in comments that will help:
    1. 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;
    2. Evaluate the accuracy of the agency's estimate of the burden of 
the proposed collection of information, including the validity of the 
methodology and assumptions used;
    3. Enhance the quality, utility, and clarity of the information to 
be collected;
    4. 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 
submissions of responses; and
    5. Assess information collection costs.

Proposed Project

    Asthma Information and Reporting System (AIRS) (OMB Control No. 
0920-0853, Exp. 5/31/2023)--Extension--National Center for 
Environmental Health (NCEH), Centers for Disease Control and Prevention 
(CDC).

Background and Brief Description

    In 1999, the CDC began its National Asthma Control Program (NACP), 
a public health approach to address the burden of asthma. The program 
supports the proposed objectives of ``Healthy People 2030'' for asthma 
and is based on the public health principles of surveillance, 
partnerships, interventions, and evaluation. CDC requests a three-year 
approval to extend the ``Asthma Information Reporting System (AIRS)'' 
(OMB Control No. 0920-0853; Exp. Date 5/31/2023).
    The three-year Extension will allow CDC to continue to monitor 
states' program planning and delivery of public health activities and 
the programs' collaboration with health care systems through the end of 
the five-year cooperative agreement--A Comprehensive Public Health 
Approach to Asthma Control through Evidence-Based Interventions (CDC-
RFA-EH19-1902).
    The goal of this data collection is to provide NCEH with routine 
information about the activities and performance of the state, local 
and territorial recipients funded under the NACP through an annual 
reporting system. NACP requires recipients to report activities related 
to partnerships, infrastructure, evaluation and interventions to 
monitor the programs' performance in reducing the burden of asthma. 
AIRS also includes two forms to collect aggregate emergency department 
(ED) visits and hospital discharge (HD) data from recipients.
    AIRS was first approved by OMB in 2010 to collect data in a web-
based system to monitor and guide participating state health 
departments. Since implementation in 2010, AIRS and the technical 
assistance provided by CDC staff have provided states with uniform data 
reporting methods and linkages to other states' asthma program 
information and resources. Thus, AIRS has saved state resources and 
staff time when asthma programs embark on asthma activities similar to 
those conducted elsewhere.
    In the past three years, AIRS data were used to:
     Facilitate communication about interventions across states 
and enable inquiries regarding interventions by populations with a 
disproportionate burden, age groups, geographic areas and other 
variables of interest;
     Provide feedback to the grantees about their performance 
relative to others through the distribution of written reports and 
several presentations summarizing the results;
     Customize and provide technical assistance and support 
materials to address implementation challenges;
     Serve as a resource to the branch, division, and center 
when addressing congressional, departmental and institutional 
inquiries. For example, the PMs allow us to report the number and age 
distribution of people reached with intensive asthma self-management 
education through the recipients and their partners;
     Help the branch align its current interventions with CDC 
goals and

[[Page 77836]]

allowed the monitoring of progress toward these goals. For example, 
recipient efforts to establish public health-health care collaboration 
has been integrated into CDC's 6[verbar]18 initiative which connects 
healthcare purchasers, payers, and providers with CDC researchers, 
economists, and policy analysts to find ways to improve health and 
control costs with the 6[verbar]18 interventions;
     Allow the NACP and the state asthma programs to make more 
informed decisions about activities to achieve objectives. For example, 
PM information identified a problem with enrolling patients most in 
need of intervention into recipient programs. This led to cross-state 
discussions and changes in recruitment strategies;
     Motivate use of data and evaluation findings. For example, 
the requirement to report actions taken based on evaluation findings 
encourages program managers and health departments officials to act on 
recommendations in evaluation reports.
    CDC requests OMB approval for an estimated 105 annual burden hours. 
There is no cost to respondents other than their time to participate.

                                                            Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
                                                                                                                              Average
                                                                                             Number of       Number of      burden per     Total burden
              Type of respondents                               Form name                   respondents    responses per   response  (in    (in hours)
                                                                                                            respondent        hours)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Funded Asthma Program Recipients...............  Performance Measures Reporting Tool....              30               1          150/60              75
                                                 Emergency Department Visits Reporting                30               1           30/60              15
                                                  Form.
                                                 Hospital Discharge Reporting Form......              30               1           30/60              15
                                                --------------------------------------------------------------------------------------------------------
    Total......................................  .......................................  ..............  ..............  ..............             105
--------------------------------------------------------------------------------------------------------------------------------------------------------


Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific 
Integrity, Office of Science, Centers for Disease Control and 
Prevention.
[FR Doc. 2022-27506 Filed 12-19-22; 8:45 am]
BILLING CODE 4163-18-P


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