Submission for Office of Management and Budget Review; Evaluation of Resources To Support the Identification and Care of Children With Prenatal Substance or Alcohol Exposure in the Child Welfare System (New Collection), 1388-1389 [2023-00306]
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Federal Register / Vol. 88, No. 6 / Tuesday, January 10, 2023 / Notices
requirements for enrollees in cases
where a provider leaves the network
and for cases where an enrollee might
be seen by an out of network ancillary
provider in an in-network setting. These
standards will help inform consumers
about his or her health plan coverage to
better make cost effective choices. The
Centers for Medicare and Medicaid
Services (CMS) is updating an
information collection request (ICR) in
connection with these standards. The
burden estimates for this ICR included
in this package reflects the additional
time and effort for QHP issuers to
provide these notifications to enrollees.
Form Number: CMS–10594 (OMB
control number 0938–1302); Frequency:
Annually; Affected Public: Private
Sector (business or other for-profits, notfor-profit institutions); Number of
Respondents: 374; Number of
Responses: 374; Total Annual Hours:
551,276. (For policy questions regarding
this collection contact Nicole Levesque
at nicole.levesque@cms.hhs.gov).
2. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Third Party
Payment of QHP Premiums and
Additional Notices for QHP Issuers Data
Collection; Use: The Patient Protection
and Affordable Care Act (Pub. L. 111–
148) and Health Care and Reconciliation
Act of 2010 (Pub. L. 111–152),
collectively referred to as PPACA,
established new competitive private
health insurance markets called
Marketplaces, or Exchanges, which gave
millions of Americans and small
businesses access to qualified health
plans (QHPs), including stand-alone
dental plans (SADPs)-private health and
private health and dental insurance
plans that have been certified as
meeting certain standards.
In the final rule, the Patient Protection
and Affordable Care Act, HHS Notice of
Benefit and Payment Parameters for
2017 (CMS–9937–F), we finalized 45
CFR 156.1256, which requires QHP
issuers, in the case of a material plan or
benefit display error included in 45 CFR
155.420(d)(12), to notify their enrollees
of the error and the enrollees’ eligibility
for a special enrollment period (SEP)
within 30 calendar days after the issuer
is informed by an Federally-facilitated
Exchange (FFE) that the error is
corrected, if directed to do so by the
FFE. This requirement provides
notification to QHP enrollees of errors
that may have impacted their QHP
selection and enrollment and any
associated monthly or annual costs, as
well as the availability of an SEP under
155.420(d)(12) for the enrollee to select
a different QHP, if desired. The Centers
VerDate Sep<11>2014
17:32 Jan 09, 2023
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for Medicare and Medicaid Services
(CMS) is formally submitting this
renewal information collection request
(ICR) to OMB for 3-year approval in
connection with standards regarding
Plan or Display Errors and SEPs. The
portion of the ICR related to Third Party
Payments has been removed. The
burden estimate for the ICR included in
this package reflects the time and effort
for QHP issuers to provide notifications
to enrollees on the ICRs regarding Plan
or Display Errors and SEPs. Form
number: CMS–10595 (OMB control
number: 0938–1301); Frequency:
Annually; Affected Public: Private
Sector (business or other for-profits, notfor-profit institutions); Number of
Respondents: 374; Number of
Responses: 374; Total Burden Hours:
293. (For questions regarding this
collection contact Samantha Nguyen
Kella at 816–426–6339).
3. Type of Information Collection
Request: Reinstatement of a previously
approved collection; Title of
Information Collection: Initial Request
for State Implemented Moratorium
Form; Use: Congress has enacted section
1866 (j)(7) of the Social Security Act,
which allows for the imposition of
temporary moratorium. CMS
promulgated 42 CFR 424.570 in order to
comply with that statute, which requires
that prior to implementing state
Medicaid moratoria the state Medicaid
agency must notify the Secretary in
writing, including all of the details of
the moratoria, and obtain the Secretary’s
concurrence with the imposition of the
moratoria.
The Initial Request for State Medicaid
Implemented Moratorium, named the
‘‘Initial Request for State Medicaid
Implemented Moratorium’’ has been
created to collect that data, in a uniform
manner, which the states report to CMS
when they request a moratorium.
Currently, CMS is collecting this data on
an ad-hoc basis, however this process
needs to be standardized so that
moratoria decisions are being made
based on the same criteria each time.
The form may be used by states and
territories who wish to impose a
Medicaid or Children’s Health
Insurance Program moratorium. CMS
will use this information as a
standardized method to collect and
track state-imposed moratoria requests.
Form number: CMS–10628 (OMB
control number: 0938–1328); Frequency:
Occasionally; Affected Public: State,
Local, or Tribal Governments; Number
of Respondents: 5; Number of
Responses: 5; Total Burden Hours: 25.
(For questions regarding this collection
contact Alisha Sanders at 410–786–
0671).
PO 00000
Frm 00044
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Sfmt 4703
4. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Bid Pricing Tool
(BPT) for Medicare Advantage (MA)
Plans and Prescription Drug Plans
(PDP); Use: Medicare Advantage
organizations (MAO) and Prescription
Drug Plans (PDP) are required to submit
an actuarial pricing ‘‘bid’’ for each plan
offered to Medicare beneficiaries for
approval by CMS. The MAOs and PDPs
use the Bid Pricing Tool (BPT) software
to develop their actuarial pricing bid.
The competitive bidding process
defined by the ‘‘The Medicare
Prescription Drug, Improvement, and
Modernization Act’’ (MMA) applies to
both the MA and Part D programs. It is
an annual process that encompasses the
release of the MA rate book in April, the
bid’s that plans submit to CMS in June,
and the release of the Part D and RPPO
benchmarks, which typically occurs in
August. Form number: CMS–10142
(OMB control number: 0938–0944);
Frequency: Annually; Affected Public:
Private Sector, Business or other forprofits, Not-for-profit institutions;
Number of Respondents: 555; Number
of Responses: 4,995; Total Burden
Hours: 149,850. (For questions regarding
this collection contact Rachel Shevland
at 410–786–3026).
Dated: January 5, 2023.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2023–00275 Filed 1–9–23; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for Office of Management
and Budget Review; Evaluation of
Resources To Support the
Identification and Care of Children
With Prenatal Substance or Alcohol
Exposure in the Child Welfare System
(New Collection)
Children’s Bureau,
Administration for Children and
Families, Department of Health and
Human Services.
ACTION: Request for public comments.
AGENCY:
The Children’s Bureau,
Administration for Children and
Families (ACF), U.S. Department of
Health and Human Services (HHS), is
proposing to collect data for an
evaluation of a set of resources that are
SUMMARY:
E:\FR\FM\10JAN1.SGM
10JAN1
1389
Federal Register / Vol. 88, No. 6 / Tuesday, January 10, 2023 / Notices
being developed to support the
identification and care of children with
prenatal substance or alcohol exposure
in the child welfare system.
DATES: Comments due within 30 days of
publication. The Office of Management
and Budget (OMB) must make a
decision about the collection of
information between 30 and 60 days
after publication of this document in the
Federal Register. Therefore, a comment
is best assured of having its full effect
if OMB receives it within 30 days of
publication.
Written 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. You can also obtain
copies of the proposed collection of
information by emailing infocollection@
acf.hhs.gov. Identify all emailed
requests by the title of the information
collection.
SUPPLEMENTARY INFORMATION:
ADDRESSES:
Description: The proposed
information collection effort will gather
data from end users of a toolkit of
resources sponsored by the Children’s
Bureau in collaboration with the Centers
for Disease Control and Prevention
under an interagency agreement. The
toolkit is intended to support child
welfare agency staff in the identification
and support of children living with
prenatal exposure to alcohol and other
substances. The data collected will be
used in a formative evaluation of the
toolkit, which will be guided by three
research questions: (1) To what degree
do agency staff find toolkit resource to
be relevant and applicable to their
work?; (2) To what degree do toolkit
resources change agency staff attitudes
and increase staff knowledge?; (3) What
implementation approaches and
organizational supports facilitate toolkit
use by child welfare agencies? Proposed
data sources for this effort include five
surveys: (1) a survey to measure users’
reactions to the toolkit; (2) a survey of
users’ attitudes toward Prenatal Alcohol
Exposure (PAE)-related issues; (3) a
survey of users’ knowledge about PAErelated issues; and (4 and 5) two
versions of a survey of transfer potential
and perceived competence, which
measures users’ sense of competence in
PAE-related knowledge and skills and
the extent to which users believe they
will transfer knowledge/skills to their
work. One version of this instrument
contains the full survey and will be
administered after users have been
exposed to the full toolkit and its
resources. The second version contains
a smaller selection of key items from the
survey, tailored to collect information
from users after their exposure to each
of five key modules of the toolkit. All
data will be collected over the course of
6–9 months in 2023.
Respondents: Child welfare
professionals, including state and/or
county-level directors of child welfare
agencies; supervisors; program staff
(e.g., investigation/intake, case
management, foster care/adoption/
permanency, etc.); staff working in
specialist roles that align with toolkit
resources (e.g., data/quality
improvement specialists); local or state
agency managers involved in
determining agency strategic plans and
practice guidance (e.g., substanceexposed newborn program manager);
training system lead staff.
ANNUAL BURDEN ESTIMATES
Total
number of
respondents
Instrument
Survey of reactions to the toolkit .....................................................................
Survey of attitudes ...........................................................................................
Survey of PAE-related knowledge ...................................................................
Survey of transfer potential and perceived competency .................................
Module-specific transfer potential and perceived competency items ..............
Estimated Total Annual Burden
Hours: 47.
Authority: Child Abuse Prevention
and Treatment Act Reauthorization Act,
42 U.S.C. 5105, (2010).
John M. Sweet Jr.,
ACF/OPRE Certifying Officer.
[FR Doc. 2023–00306 Filed 1–9–23; 8:45 am]
BILLING CODE 4184–29–P
khammond on DSKJM1Z7X2PROD with NOTICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Advisory Council on Alzheimer’s
Research, Care, and Services; Meeting
Assistant Secretary for
Planning and Evaluation, HHS.
ACTION: Notice of meeting.
AGENCY:
This notice announces the
public meeting of the Advisory Council
on Alzheimer’s Research, Care, and
SUMMARY:
VerDate Sep<11>2014
17:32 Jan 09, 2023
Jkt 259001
32
32
32
32
32
Services (Advisory Council). The
Advisory Council provides advice on
how to prevent or reduce the burden of
Alzheimer’s disease and related
dementias (ADRD) on people with the
disease and their caregivers. During the
meeting on January 30 and 31, 2023, the
Advisory Council will hear
presentations on issues related to
clinical practice and plans for advanced
care planning. The second day
presentations will review the impact of
new drug approvals and focus on risk
reduction and social determinants of
health. The National Institute of
Neurological Disorders and Stroke
(NINDS) will present research
milestones from the 2022 ADRD summit
and other Federal agencies will also
provide updates.
The meeting will be held
virtually on January 30th from 12:30
DATES:
PO 00000
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Total
number of
responses per
respondent
1
2
3
1
5
Average
burden hours
per response
.05
.17
.27
.09
.03
Total/annual
burden hours
2
11
26
3
5
p.m. to 4:30 p.m. EST and January 31st
from 12:30 p.m. to 4:30 p.m. EST.
ADDRESSES: The meeting will be virtual.
It will stream live at www.hhs.gov/live.
Comments: Time is allocated on the
agenda to hear public comments from
4:00 p.m. to 4:30 p.m. on Tuesday
January 31st. The time for oral
comments will be limited to two (2)
minutes per individual. In order to
provide a public comment, please
register by emailing your name to
napa@hhs.gov by Thursday, January 26.
Registered commenters will receive both
a dial-in number and a link to join the
meeting virtually; individuals will have
the choice to either join virtually via the
link, or to call in only by using the dialin number. NOTE: There may be a 30–45
second delay in the livestream video
presentation of the conference. For this
reason, if you have pre-registered to
submit a public comment, it is
E:\FR\FM\10JAN1.SGM
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]]>Agencies
[Federal Register Volume 88, Number 6 (Tuesday, January 10, 2023)]
[Notices]
[Pages 1388-1389]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-00306]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for Office of Management and Budget Review; Evaluation
of Resources To Support the Identification and Care of Children With
Prenatal Substance or Alcohol Exposure in the Child Welfare System (New
Collection)
AGENCY: Children's Bureau, Administration for Children and Families,
Department of Health and Human Services.
ACTION: Request for public comments.
-----------------------------------------------------------------------
SUMMARY: The Children's Bureau, Administration for Children and
Families (ACF), U.S. Department of Health and Human Services (HHS), is
proposing to collect data for an evaluation of a set of resources that
are
[[Page 1389]]
being developed to support the identification and care of children with
prenatal substance or alcohol exposure in the child welfare system.
DATES: Comments due within 30 days of publication. The Office of
Management and Budget (OMB) must make a decision about the collection
of information between 30 and 60 days after publication of this
document in the Federal Register. Therefore, a comment is best assured
of having its full effect if OMB receives it within 30 days of
publication.
ADDRESSES: Written 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. You can
also obtain copies of the proposed collection of information by
emailing [email protected]. Identify all emailed requests by
the title of the information collection.
SUPPLEMENTARY INFORMATION:
Description: The proposed information collection effort will gather
data from end users of a toolkit of resources sponsored by the
Children's Bureau in collaboration with the Centers for Disease Control
and Prevention under an interagency agreement. The toolkit is intended
to support child welfare agency staff in the identification and support
of children living with prenatal exposure to alcohol and other
substances. The data collected will be used in a formative evaluation
of the toolkit, which will be guided by three research questions: (1)
To what degree do agency staff find toolkit resource to be relevant and
applicable to their work?; (2) To what degree do toolkit resources
change agency staff attitudes and increase staff knowledge?; (3) What
implementation approaches and organizational supports facilitate
toolkit use by child welfare agencies? Proposed data sources for this
effort include five surveys: (1) a survey to measure users' reactions
to the toolkit; (2) a survey of users' attitudes toward Prenatal
Alcohol Exposure (PAE)-related issues; (3) a survey of users' knowledge
about PAE-related issues; and (4 and 5) two versions of a survey of
transfer potential and perceived competence, which measures users'
sense of competence in PAE-related knowledge and skills and the extent
to which users believe they will transfer knowledge/skills to their
work. One version of this instrument contains the full survey and will
be administered after users have been exposed to the full toolkit and
its resources. The second version contains a smaller selection of key
items from the survey, tailored to collect information from users after
their exposure to each of five key modules of the toolkit. All data
will be collected over the course of 6-9 months in 2023.
Respondents: Child welfare professionals, including state and/or
county-level directors of child welfare agencies; supervisors; program
staff (e.g., investigation/intake, case management, foster care/
adoption/permanency, etc.); staff working in specialist roles that
align with toolkit resources (e.g., data/quality improvement
specialists); local or state agency managers involved in determining
agency strategic plans and practice guidance (e.g., substance-exposed
newborn program manager); training system lead staff.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Total number Average burden
Instrument Total number of responses hours per Total/annual
of respondents per respondent response burden hours
----------------------------------------------------------------------------------------------------------------
Survey of reactions to the toolkit.............. 32 1 .05 2
Survey of attitudes............................. 32 2 .17 11
Survey of PAE-related knowledge................. 32 3 .27 26
Survey of transfer potential and perceived 32 1 .09 3
competency.....................................
Module-specific transfer potential and perceived 32 5 .03 5
competency items...............................
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 47.
Authority: Child Abuse Prevention and Treatment Act Reauthorization
Act, 42 U.S.C. 5105, (2010).
John M. Sweet Jr.,
ACF/OPRE Certifying Officer.
[FR Doc. 2023-00306 Filed 1-9-23; 8:45 am]
BILLING CODE 4184-29-P
