APPENDIX 1: 60 Day Federal Register Notice

APPENDIX 1. 60 Day FRN - AMCS_2.5.19.pdf

OPRE Study: Assessing Models of Coordinated Services for Low-Income Children and Their Families (AMCS) Site Visits [Descriptive Case Studies]

APPENDIX 1: 60 Day Federal Register Notice

OMB: 0970-0535

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Federal Register / Vol. 84, No. 24 / Tuesday, February 5, 2019 / Notices

agencies to electronically exchange
child support and spousal support case
information with other state child
support agencies. Using the EDE
benefits state child support agencies by
reducing delays, costs, and barriers
associated with interstate case
processing; increasing state collections;
improving document security;
standardizing data sharing; increasing
state participation; and improving case

processing and overall child and
spousal support outcomes.
The activities associated with the EDE
are authorized by (1) 42 U.S.C. 652(a)(7),
which requires OCSE to provide
technical assistance to the states to help
them establish effective systems for
collecting child support and spousal
support; (2) 42 U.S.C. 666(c)(1), which
requires state child support agencies to
have expedited procedures to obtain
and promptly share information with

other state child support agencies; and
(3) 45 CFR 303.7(a)(5), provides the
mechanism for state child support
agencies to fulfill the federal
requirement to transmit requests for
child support case information and
provide requested information
electronically to the greatest extent
possible as required by the regulation.
Respondents: State Child Support
Agencies.

ANNUAL BURDEN ESTIMATES
Number of
respondents

Information collection instrument
Online Data Entry Screens ........................................................................

Estimated Total Annual Burden
Hours: 1,147.94.
In compliance with the requirements
of the Paperwork Reduction Act of 1995
(Pub. L. 104–13, 44 U.S.C. Chap 35), the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded by writing
to the Administration for Children and
Families, Office of Planning, Research
and Evaluation, 330 C Street SW,
Washington, DC 20201. Attn: ACF
Reports Clearance Officer. Email
address: infocollection@acf.hhs.gov. All
requests should be identified by the title
of the information collection.
The Department specifically requests
comments on: (a) Whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
the quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2019–01059 Filed 2–4–19; 8:45 am]
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Number of
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38

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Assessing Models of
Coordinated Services for Low-Income
Children and Their Families (AMCS)
(New Collection)
Office of Planning, Research,
and Evaluation; Administration for
Children and Families; HHS.
ACTION: Request for Public Comment.
AGENCY:

The Office of Planning,
Research, and Evaluation (OPRE),
Administration for Children and
Families (ACF), U.S. Department of
Health and Human Services (HHS), is
proposing to collect data for a new
study, Assessing Models of Coordinated
Services for Low-Income Children and
Their Families (AMCS).
DATES: Comments due within 60 days of
publication. In compliance with the
requirements of Section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995,
the Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
ADDRESSES: Copies of the proposed
collection of information can be
obtained and comments may be
forwarded by writing to the
Administration for Children and
Families, Office of Planning, Research,
and Evaluation, 330 C Street SW,
Washington, DC 20201, Attn: OPRE
Reports Clearance Officer. Email
address: OPREinfocollection@
acf.hhs.gov. All requests should be
identified by the title of the information
collection.
SUPPLEMENTARY INFORMATION:
SUMMARY:

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1,777

Average burden
hours per
response
.017 (60 seconds)

Total
burden
hours
1,147.94

Description: Through AMCS, ACF
seeks to learn more about how states
and communities coordinate early care
and education, family economic
security, and/or other health and human
services to most efficiently and
effectively serve the needs of lowincome children and their families. ACF
aims to understand strategies used to
support partnerships, including the
federal barriers to agency collaboration.
In support of achieving these goals, the
study team will conduct site visits to six
programs that offer coordinated
services. The study team will gather
information through interviews with
program staff members, such as agency
leaders or frontline staff, and focus
groups with parents.
Data collection activities will include
up to six program site visits. Programs
will be identified through a scan of
publicly available information about
programs, recommendations from
stakeholders, and proposed telephone
interviews (the information collection
request for these interviews will be
submitted under the generic clearance:
Formative Data Collections for ACF
Research, OMB #0970–0356). Once
potential programs are identified,
agency leaders will be invited to
participate in the site visit. Site visits
will include semi-structured interviews
with up to 30 total staff at each site.
Staff invited will include lead program
and partner staff to include agency
leaders (including program directors,
executive directors, or CEOs), directors
of programs within the site, frontline
staff (including service navigators or
coordinators), and focus groups with 8–
10 parents at each site. Semi-structured
interviews with program and partner
staff will obtain in-depth information
about the goals and objectives of
programs, the services provided, how

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the coordinated services are
implemented, how staffing is managed,
data use, and any facilitators and
barriers to coordination. Focus groups
with parents participating in the
program will provide the opportunity to
learn about how parents perceive the
program, how it meets their needs, what
benefits they gain from the program, and

how they enroll, participate, and
progress through the program.
Respondents: Lead program and
partner program staff members working
in six programs across the United States
that coordinate early care and education
services with family economic security
services and/or other health and human
services, as well as parents receiving

services from these programs. Staff
respondents will be selected with the
goal of having staff represent each level
of the organization. Parents who have
participated in the program for at least
six months and who have received early
childhood services and at least one
other program service will be invited to
participate in focus groups.

ANNUAL BURDEN ESTIMATES
Total/annual
number of
respondents

Instrument
Master Interview Protocol ................................................................................
Parent Focus Group Protocol ..........................................................................

Estimated Total Annual Burden
Hours: 420.
Comments: The Department
specifically requests comments on (a)
whether the proposed collection of
information is necessary for the proper
performance of the functions of the
agency, including whether the
information shall have practical utility;
(b) the accuracy of the agency’s estimate
of the burden of the proposed collection
of information; (c) the quality, utility,
and clarity of the information to be
collected; and (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology. Consideration will be given
to comments and suggestions submitted
within 60 days of this publication.
Authority: 42 U.S.C. 9858(a)(5).
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2019–00942 Filed 2–4–19; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Administration on Intellectual and
Developmental Disabilities, President’s
Committee for People With Intellectual
Disabilities
Administration for Community
Living, HHS.
ACTION: Notice.
AGENCY:

The President’s Committee
for People with Intellectual Disabilities
(PCPID) will host a face to face meeting
for its members to discuss the potential
topics of the Committee’s 2019 Report to
the President. All the PCPID meetings,
in any format, are open to the public.

SUMMARY:

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Thursday, March 21, 2019 from
9:00 a.m. to 4:30 p.m.; and Friday,
March 22, 2019 from 9:00 a.m. to 4:30
p.m. (EST).
ADDRESSES: This meeting will be held in
U.S. Department of Health and Human
Services/Hubert H. Humphrey Building
located at 200 Independence Avenue
SW, Room 800, Washington, DC 20201.
Individuals who would like to
participate via conference call may do
so by dialing toll-free #: 1–888–949–
2790, when prompted enter pass code:
1989852. Individuals whose full
participation in the meeting will require
special accommodations (e.g., sign
language interpreting services, assistive
listening devices, materials in
alternative format such as large print or
Braille) should notify Ms. Allison Cruz,
Director, Office of Innovation, via email
at Allison.Cruz@acl.hhs.gov, or via
telephone at 202–795–7334, no later
than Monday, February 28, 2019. The
PCPID will attempt to accommodate
requests made after this date, but cannot
guarantee the ability to grant requests
received after the deadline. All meeting
sites are barrier free, consistent with the
Americans with Disabilities Act (ADA)
and the Federal Advisory Committee
Act (FACA).
Agenda: The Committee will discuss
the preparation of the PCPID 2019
Report to the President.
SUPPLEMENTARY INFORMATION: The
purpose of this meeting is to discuss the
Committee’s preparation of the 2019
Report to the President, including its
content and format, and related data
collection and analysis required to
complete the writing of the Report.
Background Information on the
Committee: The PCPID acts in an
advisory capacity to the President and
the Secretary of Health and Human
Services on a broad range of topics
relating to programs, services and
support for individuals with intellectual
DATES:

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Number of
responses per
respondent

Average
burden hours
per response

1
1

Annual burden
hours

2
1

360
60

disabilities. The PCPID executive order
stipulates that the Committee shall: (1)
Provide such advice concerning
intellectual disabilities as the President
or the Secretary of Health and Human
Services may request; and (2) provide
advice to the President concerning the
following for people with intellectual
disabilities: (A) Expanding employment
opportunities; (B) connecting people to
services; (C) supporting families and
caregivers; (D) strengthening the
networks; and (E) protecting rights and
preventing abuse.
Dated: January 29, 2019.
Julie Hocker,
Commissioner, Administration on Disabilities
(AoD).
[FR Doc. 2019–01122 Filed 2–4–19; 8:45 am]
BILLING CODE 4154–01–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Single-Source Supplement; Advancing
Person-Centered, Trauma-Informed
Supportive Services for Holocaust
Survivors Program
Administration for Community
Living, HHS.
ACTION: Announcing the Intent To
Award a Single-Source Supplement for
the Advancing Person-Centered,
Trauma-Informed Supportive Services
for Holocaust Survivors Program
AGENCY:

The Administration for Community
Living (ACL) announces the intent to
award a single-source supplement to the
current cooperative agreement held by
the Jewish Federations of North
America for the project Advancing
Person-Centered, Trauma-Informed
Supportive Services for Holocaust
Survivors. The purpose of this project is
to, (1) advance the development and

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