Proposed Data Collection Submitted for Public Comment and Recommendations, 79922-79923 [2024-22477]
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79922
Federal Register / Vol. 89, No. 190 / Tuesday, October 1, 2024 / Notices
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. 2024–22476 Filed 9–30–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–24–1046; Docket No. CDC–2024–
0074]
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 National Breast
and Cervical Cancer Early Detection
Program (NBCCEDP) Monitoring
Activities. This data collection is
designed to systematically collect
information about implementation,
including delivery of screening and
follow-up clinical services, and
outcomes of the National Breast and
Cervical Cancer Early Detection Program
(NBCCEDP).
DATES: CDC must receive written
comments on or before December 2,
2024.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2024–
0074 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
khammond on DSKJM1Z7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:42 Sep 30, 2024
Jkt 265001
(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: 404–639–7570; 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
National Breast and Cervical Cancer
Early Detection Program (NBCCEDP)
Monitoring Activities (OMB Control No.
0920–1046, Exp. 03/31/2025)—
Revision—National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
PO 00000
Frm 00038
Fmt 4703
Sfmt 4703
Background and Brief Description
CDC is requesting a Revision of the
information collection titled National
Breast and Cervical Cancer Early
Detection Program (NBCCEDP)
Monitoring Activities (OMB Control No.
0920–1046). The information collection
consists of an annual NBCCEDP survey,
baseline and annual clinic-level data
collection, a quarterly program update
(QPU) tool, a service delivery projection
worksheet, and minimum data elements
(MDEs). CDC proposes revisions to the
Annual NBCCEDP Survey, clinic-level
data collection tool and QPU, and
continued use of the service delivery
projection worksheet and MDEs with no
changes. The number of respondents
will increase from 70 to 71 and the total
estimated annualized burden will
decrease from 1,220 hours to 1,162
hours.
Breast and cervical cancers are
prevalent among U.S. women. In 2021,
the U.S. experienced 272,454 new cases
and 42,211 deaths as a result of breast
cancer, as well as 12,536 new cases and
4,051 deaths as a result of cervical
cancer. Evidence shows that deaths
from both breast and cervical cancers
can be avoided by increasing screening
services—mammography, pap, and
human papillomavirus (HPV) tests—
among women. However, in 2021,
approximately one quarter of adults
were not up to date with breast and/or
cervical cancer screening, and screening
was underutilized among women who
are under- or uninsured, have no regular
source of healthcare, or who recently
immigrated to the U.S. As a
longstanding priority within chronic
disease prevention, CDC focuses on
increasing access to these cancer
screenings, particularly among women
who may be at increased risk.
To improve access to cancer
screening, Congress passed the Breast
and Cervical Cancer Mortality
Prevention Act of 1990 (Pub. L. 106–
354), which directed CDC to create the
National Breast and Cervical Cancer
Early Detection Program (NBCCEDP).
The NBCCEDP currently provides
funding to 71 recipients under ‘‘Cancer
Prevention and Control Programs for
State, Territorial, and Tribal
Organizations (DP22–2202).’’ NBCCEDP
awardees include states or their bona
fide agents; U.S. territories; and tribes or
tribal organizations. The purpose of
NBCCEDP is to increase breast and
cervical cancer screening rates among
women residing within defined
geographical locations (as determined
by the funded program) who are at or
below 250% of the federal poverty level;
aged 50–75 years for breast cancer
E:\FR\FM\01OCN1.SGM
01OCN1
79923
Federal Register / Vol. 89, No. 190 / Tuesday, October 1, 2024 / Notices
services, and aged 21–64 years for
cervical cancer services; and under- or
uninsured.
CDC proposes revisions to three of the
previously approved information
collection instruments:
Annual NBCCEDP Survey—This
instrument collects program-level
information annually to monitor
recipients’ challenges, external funding
sources, partnerships, and EBI
implementation. The survey has been
revised to include new survey questions
to improve data quality for items related
to partnership activities and recipients’
requirements for patients’ payments
towards screening services, as well as
the removal of a COVID–19 related
question.
Clinic-Level Data Collection Tool—
This instrument collects clinic-level
data at baseline and annually to assess
health system, clinic, and patient
population characteristics; monitoring
and quality improvement activities; EBI
implementation; and baseline or annual
current best practices for demographic
questions related to sexual orientation
and gender identity (SOGI) and race and
ethnicity (R/E) at this time. However,
CDC plans to revise information
collections that include demographic
items to align with HHS’ SOGI and R/
E guidelines for the next funding cycle
beginning in 2027.
The proposed information collections
will allow CDC to better gauge progress
in meeting NBCCEDP program goals and
monitor implementation activities,
evaluate outcomes, and identify
awardee technical assistance needs. In
addition, findings will inform program
improvement and help identify
successful activities that need to be
maintained, replicated, or expanded.
OMB approval is requested for three
years. CDC requests OMB approval for
an estimated 1,162 annual burden
hours. Participation is required for
NBCCEDP awardees. There are no costs
to respondents other than their time.
screening rates. This tool has been
revised to remove COVID–19 related
variables and update response options
for the measures used to report breast
and cervical cancer screening rates.
QPU—This instrument collects
program-level data four times per year
to monitor award spending, service
delivery, staff vacancies, program
challenges and successes, and TA
needs. This instrument has been revised
to include two optional open-ended
items to allow recipients to provide
context to reported service delivery and
spending data only if needed.
CDC proposes continued use of the
remaining two information collections;
Service Delivery Project Worksheet and
the MDEs, which have not been
changed. To maximize consistency in
our routine data collections for the
current NBCCEDP funding cycle, CDC
has not revised NBCCEDP information
collections to align with the Department
of Health and Human Services (HHS)’
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
NBCCEDP Awardees .......................
Annual NBCCEDP Survey ...............
NBCCEDP Clinic-level Information
Collection Instrument—Breast.
NBCCEDP Clinic-level Information
Collection Instrument—Cervical.
Quarterly Program Update ...............
Service Delivery Projection Worksheet.
MDEs ................................................
Total ...........................................
...........................................................
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. 2024–22477 Filed 9–30–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
khammond on DSKJM1Z7X2PROD with NOTICES
Number of
respondents
Type of respondents
[60Day—24–24IW; Docket No. CDC–2024–
0070]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
AGENCY:
VerDate Sep<11>2014
17:42 Sep 30, 2024
Jkt 265001
ACTION:
1
6
46/60
40/60
54
284
71
6
40/60
284
71
71
4
1
22/60
29/60
151
34
71
2
150/60
355
........................
........................
........................
1,162
Notice with comment period.
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 proposed information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled Becton
Dickinson BACTECTM Blood Culture
Media Bottles Shortage Impact
Questionnaire, which will assess the
impact of the Becton Dickinson (BD)
BACTECTM blood culture media bottles
supply shortage on individual facilities
and how CDC NHSN bloodstream
infection surveillance might be affected.
Frm 00039
Fmt 4703
Total burden
(in hours)
71
71
SUMMARY:
PO 00000
Average
burden per
response
(in hours)
Number of
responses per
respondent
Sfmt 4703
CDC must receive written
comments on or before December 2,
2024.
DATES:
You may submit comments,
identified by Docket No. CDC–2024–
0070 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.
ADDRESSES:
E:\FR\FM\01OCN1.SGM
01OCN1
Agencies
[Federal Register Volume 89, Number 190 (Tuesday, October 1, 2024)]
[Notices]
[Pages 79922-79923]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-22477]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-24-1046; Docket No. CDC-2024-0074]
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 National Breast and Cervical Cancer Early Detection Program
(NBCCEDP) Monitoring Activities. This data collection is designed to
systematically collect information about implementation, including
delivery of screening and follow-up clinical services, and outcomes of
the National Breast and Cervical Cancer Early Detection Program
(NBCCEDP).
DATES: CDC must receive written comments on or before December 2, 2024.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2024-
0074 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: 404-639-7570;
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
National Breast and Cervical Cancer Early Detection Program
(NBCCEDP) Monitoring Activities (OMB Control No. 0920-1046, Exp. 03/31/
2025)--Revision--National Center for Chronic Disease Prevention and
Health Promotion (NCCDPHP), Centers for Disease Control and Prevention
(CDC).
Background and Brief Description
CDC is requesting a Revision of the information collection titled
National Breast and Cervical Cancer Early Detection Program (NBCCEDP)
Monitoring Activities (OMB Control No. 0920-1046). The information
collection consists of an annual NBCCEDP survey, baseline and annual
clinic-level data collection, a quarterly program update (QPU) tool, a
service delivery projection worksheet, and minimum data elements
(MDEs). CDC proposes revisions to the Annual NBCCEDP Survey, clinic-
level data collection tool and QPU, and continued use of the service
delivery projection worksheet and MDEs with no changes. The number of
respondents will increase from 70 to 71 and the total estimated
annualized burden will decrease from 1,220 hours to 1,162 hours.
Breast and cervical cancers are prevalent among U.S. women. In
2021, the U.S. experienced 272,454 new cases and 42,211 deaths as a
result of breast cancer, as well as 12,536 new cases and 4,051 deaths
as a result of cervical cancer. Evidence shows that deaths from both
breast and cervical cancers can be avoided by increasing screening
services--mammography, pap, and human papillomavirus (HPV) tests--among
women. However, in 2021, approximately one quarter of adults were not
up to date with breast and/or cervical cancer screening, and screening
was underutilized among women who are under- or uninsured, have no
regular source of healthcare, or who recently immigrated to the U.S. As
a longstanding priority within chronic disease prevention, CDC focuses
on increasing access to these cancer screenings, particularly among
women who may be at increased risk.
To improve access to cancer screening, Congress passed the Breast
and Cervical Cancer Mortality Prevention Act of 1990 (Pub. L. 106-354),
which directed CDC to create the National Breast and Cervical Cancer
Early Detection Program (NBCCEDP). The NBCCEDP currently provides
funding to 71 recipients under ``Cancer Prevention and Control Programs
for State, Territorial, and Tribal Organizations (DP22-2202).'' NBCCEDP
awardees include states or their bona fide agents; U.S. territories;
and tribes or tribal organizations. The purpose of NBCCEDP is to
increase breast and cervical cancer screening rates among women
residing within defined geographical locations (as determined by the
funded program) who are at or below 250% of the federal poverty level;
aged 50-75 years for breast cancer
[[Page 79923]]
services, and aged 21-64 years for cervical cancer services; and under-
or uninsured.
CDC proposes revisions to three of the previously approved
information collection instruments:
Annual NBCCEDP Survey--This instrument collects program-level
information annually to monitor recipients' challenges, external
funding sources, partnerships, and EBI implementation. The survey has
been revised to include new survey questions to improve data quality
for items related to partnership activities and recipients'
requirements for patients' payments towards screening services, as well
as the removal of a COVID-19 related question.
Clinic-Level Data Collection Tool--This instrument collects clinic-
level data at baseline and annually to assess health system, clinic,
and patient population characteristics; monitoring and quality
improvement activities; EBI implementation; and baseline or annual
screening rates. This tool has been revised to remove COVID-19 related
variables and update response options for the measures used to report
breast and cervical cancer screening rates.
QPU--This instrument collects program-level data four times per
year to monitor award spending, service delivery, staff vacancies,
program challenges and successes, and TA needs. This instrument has
been revised to include two optional open-ended items to allow
recipients to provide context to reported service delivery and spending
data only if needed.
CDC proposes continued use of the remaining two information
collections; Service Delivery Project Worksheet and the MDEs, which
have not been changed. To maximize consistency in our routine data
collections for the current NBCCEDP funding cycle, CDC has not revised
NBCCEDP information collections to align with the Department of Health
and Human Services (HHS)' current best practices for demographic
questions related to sexual orientation and gender identity (SOGI) and
race and ethnicity (R/E) at this time. However, CDC plans to revise
information collections that include demographic items to align with
HHS' SOGI and R/E guidelines for the next funding cycle beginning in
2027.
The proposed information collections will allow CDC to better gauge
progress in meeting NBCCEDP program goals and monitor implementation
activities, evaluate outcomes, and identify awardee technical
assistance needs. In addition, findings will inform program improvement
and help identify successful activities that need to be maintained,
replicated, or expanded.
OMB approval is requested for three years. CDC requests OMB
approval for an estimated 1,162 annual burden hours. Participation is
required for NBCCEDP awardees. There are no costs to respondents other
than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response Total burden
respondents respondent (in hours) (in hours)
----------------------------------------------------------------------------------------------------------------
NBCCEDP Awardees.............. Annual NBCCEDP 71 1 46/60 54
Survey.
NBCCEDP Clinic- 71 6 40/60 284
level
Information
Collection
Instrument--Bre
ast.
NBCCEDP Clinic- 71 6 40/60 284
level
Information
Collection
Instrument--Cer
vical.
Quarterly 71 4 22/60 151
Program Update.
Service Delivery 71 1 29/60 34
Projection
Worksheet.
MDEs............ 71 2 150/60 355
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 1,162
----------------------------------------------------------------------------------------------------------------
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. 2024-22477 Filed 9-30-24; 8:45 am]
BILLING CODE 4163-18-P