Agency Information Collection Activities: Submission for OMB Review; Comment Request, 26941-26942 [2017-12090]
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Federal Register / Vol. 82, No. 111 / Monday, June 12, 2017 / Notices
products or services. These collections
will allow for ongoing, collaborative and
actionable communications between the
Agency and its customers and
stakeholders. It will also allow feedback
to contribute directly to the
improvement of program management.
Feedback collected under this generic
clearance will provide useful
information, but it will not yield data
that can be generalized to the overall
population. This type of generic
clearance for qualitative information
will not be used for quantitative
information collections that are
designed to yield reliably actionable
results, such as monitoring trends over
time or documenting program
performance. Such data uses require
more rigorous designs that address: the
target population to which
generalizations will be made, the
sampling frame, the sample design
(including stratification and clustering),
the precision requirements or power
calculations that justify the proposed
sample size, the expected response rate,
methods for assessing potential nonresponse bias, the protocols for data
collection, and any testing procedures
that were or will be undertaken prior
fielding the study. Depending on the
degree of influence the results are likely
to have, such collections may still be
eligible for submission for other generic
mechanisms that are designed to yield
quantitative results.
The Agency received 0 comments
were received in response to the 60-day
notice published in the Federal Register
of March 14, 2017 (79 FR 18692).
Current Actions: New collection of
information.
Type of Review: New Collection.
Affected Public: Individuals,
households, professionals, public/
private sector.
Average Expected Annual Number of
Activities: 600.
Respondents per Activity: 50.
Annual Responses: 30,000.
Frequency of Response: Once per
request.
Average Minutes per Response: 30.
Burden Hours: 500,000 hours
annually.
An agency may not conduct or
sponsor, and a person is not required to
respond to, a collection of information
unless it displays a currently valid
Office of Management and Budget
control number.
Darius Taylor,
Deputy Information Collection Officer.
[FR Doc. 2017–12046 Filed 6–9–17; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Notice of
Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meetings.
The meetings 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: Center for Scientific
Review Special Emphasis Panel; Member
Conflict: Epidemiology.
Date: June 19, 2017.
Time: 1:00 p.m. to 4:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Telephone Conference Call).
Contact Person: Heidi B Friedman, PhD.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 1012A,
MSC 7770, Bethesda, MD 20892, 301–379–
5632, hfriedman@csr.nih.gov.
This notice is being published less than 15
days prior to the meeting due to the timing
limitations imposed by the review and
funding cycle.
Name of Committee: Center for Scientific
Review Special Emphasis Panel;
Experimental and Bioinformatic Approaches
in the Druggable Genome.
Date: June 26, 2017.
Time: 10:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications and/or proposals.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Virtual Meeting).
Contact Person: Luis Dettin, PhD.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 2208,
Bethesda, MD 20892, 301 451 1327,
dettinle@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Mentored
Training in Comparative and Veterinary
Medicine.
Date: June 27, 2017.
Time: 2:00 p.m. to 4:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Telephone Conference Call).
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26941
Contact Person: Amy Kathleen Wernimont,
PhD., Scientific Review Officer, Center for
Scientific Review, 6701 Rockledge Drive,
Bethesda, MD 20892, 301–827–6427,
amy.wernimont@nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Immigrant
Women’s Health.
Date: June 30, 2017.
Time: 8:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: The Dupont Hotel, 1500 New
Hampshire Avenue NW., Washington, DC
20036.
Contact Person: Martha L Hare, RN, PhD.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 3154,
MSC 7770, Bethesda, MD 20892, (301) 451–
8504, harem@mail.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Member
Conflict: Acute Brain Injury and
Regeneration.
Date: July 3, 2017.
Time: 2:00 p.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Telephone Conference Call).
Contact Person: Alexander Yakovlev, PhD.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 5206,
MSC 7846, Bethesda, MD 20892–7846, 301–
435–1254, yakovleva@csr.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.306, Comparative Medicine;
93.333, Clinical Research, 93.306, 93.333,
93.337, 93.393–93.396, 93.837–93.844,
93.846–93.878, 93.892, 93.893, National
Institutes of Health, HHS)
Dated: June 6, 2017.
Sylvia L. Neal,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2017–12030 Filed 6–9–17; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Substance Abuse and Mental Health
Services Administration
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Periodically, the Substance Abuse and
Mental Health Services Administration
(SAMHSA) will publish a summary of
information collection requests under
OMB review, in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
documents, call the SAMHSA Reports
Clearance Officer on (240) 276–1243.
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26942
Federal Register / Vol. 82, No. 111 / Monday, June 12, 2017 / Notices
Project: Project—Division of State
Programs—Management Reporting
Tool (DSP–MRT) (OMB No. 0930–
0354)—Revision
The Substance Abuse and Mental
Health Services Administration
(SAMHSA)’s Center for Substance
Abuse Prevention (CSAP) aims to
address two of SAMHSA’s top
substance abuse prevention priorities:
Underage drinking (UAD; age 12 to 20)
and prescription drug misuse and abuse
(PDM; age 12 to 25) through the
Division of State Program—Monitoring
and Reporting Tool. This data collection
will allow all DSP programs to report
into a standard tool that aligns with the
Strategic Prevention Framework model.
This request for data collection includes
a revision from a previously approved
OMB instrument formally known as
Partnerships for Success-Management
and Reporting Tool.
Monitoring data on SPF model will
allow SAMHSA project officers to
systematically collect data to monitor
their grant program performance and
outcomes along with grantee technical
assistance needs. In addition to
assessing activities related to the SPF
steps, the performance monitoring
instruments covered in this statement
collect data to assess the following
grantee required specific performance
measures:
• Number of training and technical
assistance activities per funded
community provided by the grantee to
support communities;
• Reach of training and technical
assistance activities (numbers served)
provided by the grantee;
• Percentage of subrecipient
communities that submit data to the
grantee data system;
• Number of sub-recipient
communities that improved on one or
more targeted NOMs indicators
(Outcome);
• Number of grantees who integrate
Prescription Drug Monitoring Data into
their program needs assessment.
Changes to this package include the
following:
• Standard language for all DSP–MRT
questions;
• New disparities module to align
with SAMHSA’s monitoring
requirements;
• Updated technical assistance
section;
• Deletion of cost questions specific
to funding amounts and in-kind
resources;
• Deletion of advisory council and
other workgroup sub-committee
questions;
• Addition of Section A specific to
SPF-Rx questions;
• Addition of Section B specific to
PDO questions;
ANNUALIZED DATA COLLECTION BURDEN
Number of
respondents
Instrument
Responses
per
respondent
Total
number of
responses
Hours per
response
Total burden
hours
117
25
23
4
2
4
468
63
100
3
1
1
1,404
42
100
FY2020 Total ................................................................
asabaliauskas on DSKBBXCHB2PROD with NOTICES
Standard DSP Monitoring Tool ............................................
Section A: Rx .......................................................................
Section B: PDO ....................................................................
117
........................
631
........................
1,546
Written comments and
recommendations concerning the
proposed information collection should
be sent by July 12, 2017 to the SAMHSA
Desk Officer at the Office of Information
and Regulatory Affairs, Office of
Management and Budget (OMB). To
ensure timely receipt of comments, and
to avoid potential delays in OMB’s
receipt and processing of mail sent
through the U.S. Postal Service,
commenters are encouraged to submit
their comments to OMB via email to:
OIRA_Submission@omb.eop.gov.
Although commenters are encouraged to
send their comments via email,
commenters may also fax their
comments to: 202–395–7285.
Commenters may also mail them to:
Office of Management and Budget,
Office of Information and Regulatory
Affairs, New Executive Office Building,
Room 10102, Washington, DC 20503.
Summer King,
Statistician.
[FR Doc. 2017–12090 Filed 6–9–17; 8:45 am]
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17:28 Jun 09, 2017
Jkt 241001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Substance Abuse and Mental Health
Services Administration
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Periodically, the Substance Abuse and
Mental Health Services Administration
(SAMHSA) will publish a summary of
information collection requests under
OMB review, in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
documents, call the SAMHSA Reports
Clearance Officer on (240) 276–1243.
Project: Mental Health Block Grant Ten
Percent Set Aside Evaluation of First
Episode Psychosis—NEW
The Substance Abuse and Mental
Health Services Administration
(SAMHSA) is directed by Congress
through its FY 2016 Omnibus bill,
Public Law 114–113, to set aside ten
percent of the Mental Health Block
Grant (MHBG) allocation for each state
to support evidence-based programs that
provide treatment for those with early
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serious mental illness (SMI) and a first
episode psychosis (FEP)—an increase
from the previous five percent set aside.
The purpose of this 3-year evaluation
is to assess the relationship between
fidelity of selected coordinated specialty
care (CSC) programs supported with
Mental Health Block Grant (MHBG) Ten
Percent Set Aside funding and
participant outcomes. There are
approximately 250 sites implementing
CSC programs with MHBG ten percent
set aside funding. All 250 sites will be
asked to report on their implementation
through an online survey. Up to 32 CSC
sites across the nation will be recruited
to participate in a process and outcome
evaluation. The data collection activities
for the Mental Health Block Grant Ten
Percent Set Aside Evaluation will
include the following six data collection
tools:
• Site Survey: This is a one-time
online survey with site directors of all
250 centers using MHBG ten percent set
aside funding (not just those included in
the evaluation). The survey focuses on
how centers across the U.S. are
providing services to individuals with
First Episode Psychosis (FEP) in their
communities.
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[Federal Register Volume 82, Number 111 (Monday, June 12, 2017)]
[Notices]
[Pages 26941-26942]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-12090]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Substance Abuse and Mental Health Services Administration
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
Periodically, the Substance Abuse and Mental Health Services
Administration (SAMHSA) will publish a summary of information
collection requests under OMB review, in compliance with the Paperwork
Reduction Act (44 U.S.C. Chapter 35). To request a copy of these
documents, call the SAMHSA Reports Clearance Officer on (240) 276-1243.
[[Page 26942]]
Project: Project--Division of State Programs--Management Reporting Tool
(DSP-MRT) (OMB No. 0930-0354)--Revision
The Substance Abuse and Mental Health Services Administration
(SAMHSA)'s Center for Substance Abuse Prevention (CSAP) aims to address
two of SAMHSA's top substance abuse prevention priorities: Underage
drinking (UAD; age 12 to 20) and prescription drug misuse and abuse
(PDM; age 12 to 25) through the Division of State Program--Monitoring
and Reporting Tool. This data collection will allow all DSP programs to
report into a standard tool that aligns with the Strategic Prevention
Framework model. This request for data collection includes a revision
from a previously approved OMB instrument formally known as
Partnerships for Success-Management and Reporting Tool.
Monitoring data on SPF model will allow SAMHSA project officers to
systematically collect data to monitor their grant program performance
and outcomes along with grantee technical assistance needs. In addition
to assessing activities related to the SPF steps, the performance
monitoring instruments covered in this statement collect data to assess
the following grantee required specific performance measures:
Number of training and technical assistance activities per
funded community provided by the grantee to support communities;
Reach of training and technical assistance activities
(numbers served) provided by the grantee;
Percentage of subrecipient communities that submit data to
the grantee data system;
Number of sub-recipient communities that improved on one
or more targeted NOMs indicators (Outcome);
Number of grantees who integrate Prescription Drug
Monitoring Data into their program needs assessment.
Changes to this package include the following:
Standard language for all DSP-MRT questions;
New disparities module to align with SAMHSA's monitoring
requirements;
Updated technical assistance section;
Deletion of cost questions specific to funding amounts and
in-kind resources;
Deletion of advisory council and other workgroup sub-
committee questions;
Addition of Section A specific to SPF-Rx questions;
Addition of Section B specific to PDO questions;
Annualized Data Collection Burden
----------------------------------------------------------------------------------------------------------------
Number of Responses per Total number Hours per Total burden
Instrument respondents respondent of responses response hours
----------------------------------------------------------------------------------------------------------------
Standard DSP Monitoring Tool.... 117 4 468 3 1,404
Section A: Rx................... 25 2 63 1 42
Section B: PDO.................. 23 4 100 1 100
-------------------------------------------------------------------------------
FY2020 Total................ 117 .............. 631 .............. 1,546
----------------------------------------------------------------------------------------------------------------
Written comments and recommendations concerning the proposed
information collection should be sent by July 12, 2017 to the SAMHSA
Desk Officer at the Office of Information and Regulatory Affairs,
Office of Management and Budget (OMB). To ensure timely receipt of
comments, and to avoid potential delays in OMB's receipt and processing
of mail sent through the U.S. Postal Service, commenters are encouraged
to submit their comments to OMB via email to:
OIRA_Submission@omb.eop.gov. Although commenters are encouraged to send
their comments via email, commenters may also fax their comments to:
202-395-7285. Commenters may also mail them to: Office of Management
and Budget, Office of Information and Regulatory Affairs, New Executive
Office Building, Room 10102, Washington, DC 20503.
Summer King,
Statistician.
[FR Doc. 2017-12090 Filed 6-9-17; 8:45 am]
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