Agency Information Collection Activities: Proposed Collection: Public Comment Request; Information Collection Request Title: Evaluation of the Maternal and Child Health Bureau Pediatric Mental Health Care Access (PMHCA) Program and the Maternal and Child Health Bureau Screening and Treatment for Maternal Depression and Related Behavioral Disorders Program, OMB No. 0906-xxxx, New, 55579-55580 [2019-22636]
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55579
Federal Register / Vol. 84, No. 201 / Thursday, October 17, 2019 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection: Public
Comment Request; Information
Collection Request Title: Evaluation of
the Maternal and Child Health Bureau
Pediatric Mental Health Care Access
(PMHCA) Program and the Maternal
and Child Health Bureau Screening
and Treatment for Maternal Depression
and Related Behavioral Disorders
Program, OMB No. 0906–xxxx, New
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services.
ACTION: Notice.
AGENCY:
In compliance with the
requirement of the Paperwork
Reduction Act of 1995 for opportunity
for public comment on proposed data
collection projects, HRSA announces
plans to submit an Information
Collection Request (ICR), described
below, to the Office of Management and
Budget (OMB). Prior to submitting the
ICR to OMB, HRSA seeks comments
from the public regarding the burden
estimate, below, or any other aspect of
the ICR.
DATES: Comments on this ICR should be
received no later than December 16,
2019.
ADDRESSES: Submit your comments to
paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance
Officer, Room 14N136B, 5600 Fishers
Lane, Rockville, Maryland 20857.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and draft
instruments, email paperwork@hrsa.gov
or call Lisa Wright-Solomon, the HRSA
Information Collection Clearance Officer
at (301) 443–1984.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the
information request collection title for
reference.
Information Collection Request Title:
Evaluation of Maternal and Child Health
SUMMARY:
Bureau Pediatric Mental Health Care
Access Program and the Maternal and
Child Health Bureau Screening and
Treatment for Maternal Depression and
Related Behavioral Disorders Program,
OMB No. 0906–xxxx—New.
Abstract: HRSA’s Maternal and Child
Health Bureau Pediatric Mental Health
Care Access (PMHCA) and Maternal
Depression and Related Behavioral
Disorders (MDRBD) programs aim to
increase identification of behavioral
health conditions by screening specified
populations (e.g., children, adolescents,
young adults, and pregnant and
postpartum women, especially those
living in rural, isolated, and
underserved areas); providing clinical
behavioral health consultation; care
coordination support (e.g.,
communication/collaboration, accessing
resources, referral services) and training
to health care providers; and increasing
access to clinical interventions
including by telehealth. Provider
education and training will support the
knowledge and skills acquisition
needed to accomplish this goal. PMHCA
program is authorized by the Public
Health Service Act, § 330M (42 U.S.C.
254c–19), as amended. The MDRBD
program is authorized by the Public
Health Service Act, § 317L–1 (42 U.S.C.
247b–13a), as amended. In order to
evaluate progress made toward the
programs’ goals, this data collection will
use four instruments: Health Care
Provider (HCP) Survey, Practice-Level
Survey, Program Implementation
Survey, and Program Implementation
Semi-Structured Interview.
Need and Proposed Use of the
Information: This information is needed
to evaluate the PMHCA and MDRBD
Programs by providing HRSA with the
necessary information to guide future
policy decisions regarding increasing
health care providers capacity to
address patient’s behavioral health and
access to behavioral health services.
Specifically, data collected for the
evaluation will be used to study the
efforts of awardee programs to achieve
key awardee outcomes (e.g., increase in
access to behavioral health services;
providers trained; available communitybased resources, including counselors or
family service providers) and to
measure whether and to what extent
awardee programs are associated with
changes in these key awardee outcomes.
The evaluation will also examine
changes over time, within a state and/
or across the PMCHA and MDRBD
programs, with regard to (1) enrolled
providers/practices related to screening,
referral, and care coordination for
behavioral health conditions; (2)
provision of behavioral health services
for mental health conditions in primary
care settings by enrolled health care
providers; (3) use of consultative
services; and (4) facilitation of access to
behavioral health services for mental
health conditions.
Likely Respondents: Both HCP and
Practice-Level Survey responses will be
collected from health care providers and
practices that are participating in the
PMCHA and MDRBD programs. Likely
respondents include:
• HCP Surveys: Physicians, nurse
practitioners, physician assistants,
nurse midwives (for MDBRD), other
health care professionals (e.g.,
behavioral health providers, case
coordinators, nurses, social workers)
• Practice-Level Surveys: Practice
managers (e.g., office managers, office
leadership, nurse champions)
• Program Implementation Surveys and
Semi-Structured Interviews: PMHCA
and MDRBD cooperative agreementfunded Project Directors/Principal
Investigators
Burden Statement: Burden in this
context means the time expended by
persons to generate, maintain, retain,
disclose or provide the information
requested. This includes the time
needed to review instructions; to
develop, acquire, install, and utilize
technology and systems for the purpose
of collecting, validating, and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information; to search
data sources; to complete and review
the collection of information; and to
transmit or otherwise disclose the
information. The total annual burden
hours estimated for this ICR are
summarized in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form name
Health Care Provider Survey ...............................................
Practice-Level Survey ..........................................................
Program Implementation Survey .........................................
VerDate Sep<11>2014
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Number of
responses per
respondent
13,035
4,165
28
Fmt 4703
Sfmt 4703
3
3
3
Total
responses
39,105
12,495
84
E:\FR\FM\17OCN1.SGM
17OCN1
Average
burden per
response
(in hours)
0.17
0.25
0.50
Tota
burden
hours
6,648
3,124
42
55580
Federal Register / Vol. 84, No. 201 / Thursday, October 17, 2019 / Notices
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Number of
respondents
Form name
Number of
responses per
respondent
Total
responses
Average
burden per
response
(in hours)
Tota
burden
hours
Program Implementation Semi-Structured Interview ...........
28
1
28
1.00
28
Total ..............................................................................
17,256
........................
51,712
........................
9,842
HRSA specifically requests comments
on (1) the necessity and utility of the
proposed information collection for the
proper performance of the agency’s
functions, (2) the accuracy of the
estimated burden, (3) ways to enhance
the quality, utility, and clarity of the
information to be collected, and (4) the
use of automated collection techniques
or other forms of information
technology to minimize the information
collection burden.
Maria G. Button,
Director, Executive Secretariat.
Contact Person: Jing Chen, Ph.D., Scientific
Review Officer, Office of Scientific Review,
National Center for Advancing Translational
Sciences (NCATS), National Institutes of
Health, 6701 Democracy Blvd., Democracy 1,
Room 1080, Bethesda, MD 20892–4874,
chenjing@mail.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.859, Pharmacology,
Physiology, and Biological Chemistry
Research; 93.350, B—Cooperative
Agreements; 93.859, Biomedical Research
and Research Training, National Institutes of
Health, HHS)
Dated: October 10, 2019.
[FR Doc. 2019–22636 Filed 10–16–19; 8:45 am]
Melanie J. Pantoja,
BILLING CODE 4165–15–P
Program Analyst, Office of Federal Advisory
Committee Policy.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2019–22572 Filed 10–16–19; 8:45 am]
BILLING CODE 4140–01–P
National Institutes of Health
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Center for Advancing
Translational Sciences; Notice of
Closed Meeting
National Institutes of Health
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Center for
Advancing Translational Sciences Special
Emphasis Panel; Platform Delivery
Technologies for Nucleic Acid Therapeutics.
Date: November 13–14, 2019.
Time: 8:30 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, One
Democracy Plaza, 6701 Democracy
Boulevard, Bethesda, MD 20892, (Virtual
Meeting).
VerDate Sep<11>2014
17:26 Oct 16, 2019
Jkt 250001
Office of the Director, National
Institutes of Health; Amended Notice
of Meeting
Notice is hereby given of a change in
the meeting of the Office of AIDS
Research Advisory Council, November
7, 2019 from 8:30 a.m. to 4:30 p.m.,
National Institutes of Health, 5601
Fishers Lane, Room 1D13, Rockville,
MD 20852 which was published in the
Federal Register on February 15, 2019,
84 FR 4495.
This meeting notice is amended to
change the meeting date from November
7, 2019 to October 28, 2019 at the
National Institutes of Health, 5601
Fishers Lane, Room 1D13, Rockville,
MD 20852. The meeting is open to the
public.
Dated: October 10, 2019.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Eye Institute; Notice of Closed
Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Eye Institute
Special Emphasis Panel; NEI Genetic
Epidemiology and Secondary Data Analysis
Applications.
Date: November 4–5, 2019.
Time: 8:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Eye Institute, National
Institutes of Health, 6700 B Rockledge Drive,
Suite 3400, Bethesda, MD 20892 (Virtual
Meeting).
Contact Person: Brian Hoshaw, Ph.D.,
Acting Review Chief, National Eye Institute,
National Institutes of Health, Division of
Extramural Research, 6700 B Rockledge
Drive, Suite 3400, Rockville, MD 20892, (301)
451–2020, hoshawb@mail.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.867, Vision Research,
National Institutes of Health, HHS)
Dated: October 10, 2019.
Miguelina Perez,
Tyeshia M. Roberson,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2019–22571 Filed 10–16–19; 8:45 am]
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2019–22573 Filed 10–16–19; 8:45 am]
BILLING CODE 4140–01–P
BILLING CODE 4140–01–P
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]]>Agencies
[Federal Register Volume 84, Number 201 (Thursday, October 17, 2019)]
[Notices]
[Pages 55579-55580]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-22636]
[[Page 55579]]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Proposed Collection:
Public Comment Request; Information Collection Request Title:
Evaluation of the Maternal and Child Health Bureau Pediatric Mental
Health Care Access (PMHCA) Program and the Maternal and Child Health
Bureau Screening and Treatment for Maternal Depression and Related
Behavioral Disorders Program, OMB No. 0906-xxxx, New
AGENCY: Health Resources and Services Administration (HRSA), Department
of Health and Human Services.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the requirement of the Paperwork Reduction
Act of 1995 for opportunity for public comment on proposed data
collection projects, HRSA announces plans to submit an Information
Collection Request (ICR), described below, to the Office of Management
and Budget (OMB). Prior to submitting the ICR to OMB, HRSA seeks
comments from the public regarding the burden estimate, below, or any
other aspect of the ICR.
DATES: Comments on this ICR should be received no later than December
16, 2019.
ADDRESSES: Submit your comments to [email protected] or mail the HRSA
Information Collection Clearance Officer, Room 14N136B, 5600 Fishers
Lane, Rockville, Maryland 20857.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the data collection plans and
draft instruments, email [email protected] or call Lisa Wright-
Solomon, the HRSA Information Collection Clearance Officer at (301)
443-1984.
SUPPLEMENTARY INFORMATION: When submitting comments or requesting
information, please include the information request collection title
for reference.
Information Collection Request Title: Evaluation of Maternal and
Child Health Bureau Pediatric Mental Health Care Access Program and the
Maternal and Child Health Bureau Screening and Treatment for Maternal
Depression and Related Behavioral Disorders Program, OMB No. 0906-
xxxx--New.
Abstract: HRSA's Maternal and Child Health Bureau Pediatric Mental
Health Care Access (PMHCA) and Maternal Depression and Related
Behavioral Disorders (MDRBD) programs aim to increase identification of
behavioral health conditions by screening specified populations (e.g.,
children, adolescents, young adults, and pregnant and postpartum women,
especially those living in rural, isolated, and underserved areas);
providing clinical behavioral health consultation; care coordination
support (e.g., communication/collaboration, accessing resources,
referral services) and training to health care providers; and
increasing access to clinical interventions including by telehealth.
Provider education and training will support the knowledge and skills
acquisition needed to accomplish this goal. PMHCA program is authorized
by the Public Health Service Act, Sec. 330M (42 U.S.C. 254c-19), as
amended. The MDRBD program is authorized by the Public Health Service
Act, Sec. 317L-1 (42 U.S.C. 247b-13a), as amended. In order to
evaluate progress made toward the programs' goals, this data collection
will use four instruments: Health Care Provider (HCP) Survey, Practice-
Level Survey, Program Implementation Survey, and Program Implementation
Semi-Structured Interview.
Need and Proposed Use of the Information: This information is
needed to evaluate the PMHCA and MDRBD Programs by providing HRSA with
the necessary information to guide future policy decisions regarding
increasing health care providers capacity to address patient's
behavioral health and access to behavioral health services.
Specifically, data collected for the evaluation will be used to study
the efforts of awardee programs to achieve key awardee outcomes (e.g.,
increase in access to behavioral health services; providers trained;
available community-based resources, including counselors or family
service providers) and to measure whether and to what extent awardee
programs are associated with changes in these key awardee outcomes. The
evaluation will also examine changes over time, within a state and/or
across the PMCHA and MDRBD programs, with regard to (1) enrolled
providers/practices related to screening, referral, and care
coordination for behavioral health conditions; (2) provision of
behavioral health services for mental health conditions in primary care
settings by enrolled health care providers; (3) use of consultative
services; and (4) facilitation of access to behavioral health services
for mental health conditions.
Likely Respondents: Both HCP and Practice-Level Survey responses
will be collected from health care providers and practices that are
participating in the PMCHA and MDRBD programs. Likely respondents
include:
HCP Surveys: Physicians, nurse practitioners, physician
assistants, nurse midwives (for MDBRD), other health care professionals
(e.g., behavioral health providers, case coordinators, nurses, social
workers)
Practice-Level Surveys: Practice managers (e.g., office
managers, office leadership, nurse champions)
Program Implementation Surveys and Semi-Structured Interviews:
PMHCA and MDRBD cooperative agreement-funded Project Directors/
Principal Investigators
Burden Statement: Burden in this context means the time expended by
persons to generate, maintain, retain, disclose or provide the
information requested. This includes the time needed to review
instructions; to develop, acquire, install, and utilize technology and
systems for the purpose of collecting, validating, and verifying
information, processing and maintaining information, and disclosing and
providing information; to train personnel and to be able to respond to
a collection of information; to search data sources; to complete and
review the collection of information; and to transmit or otherwise
disclose the information. The total annual burden hours estimated for
this ICR are summarized in the table below.
Total Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Form name Number of responses per Total per response Tota burden
respondents respondent responses (in hours) hours
----------------------------------------------------------------------------------------------------------------
Health Care Provider Survey..... 13,035 3 39,105 0.17 6,648
Practice-Level Survey........... 4,165 3 12,495 0.25 3,124
Program Implementation Survey... 28 3 84 0.50 42
[[Page 55580]]
Program Implementation Semi- 28 1 28 1.00 28
Structured Interview...........
-------------------------------------------------------------------------------
Total....................... 17,256 .............. 51,712 .............. 9,842
----------------------------------------------------------------------------------------------------------------
HRSA specifically requests comments on (1) the necessity and
utility of the proposed information collection for the proper
performance of the agency's functions, (2) the accuracy of the
estimated burden, (3) ways to enhance the quality, utility, and clarity
of the information to be collected, and (4) the use of automated
collection techniques or other forms of information technology to
minimize the information collection burden.
Maria G. Button,
Director, Executive Secretariat.
[FR Doc. 2019-22636 Filed 10-16-19; 8:45 am]
BILLING CODE 4165-15-P
