Agency Information Collection Activities; Submission to OMB for Review and Approval; Public Comment Request, 93945-93946 [2016-30786]
Download as PDF
<![CDATA[
93945
Federal Register / Vol. 81, No. 246 / Thursday, December 22, 2016 / Notices
abuse by allowing for targeted
communication.
Likely Respondents: Medical
Prescribers.
The total annual burden hours
estimated for this ICR are summarized
in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS
Number of
responses
per
respondent
Number of
respondents
Form name
Average
burden per
response
(in hours)
Total
burden hours
Opioid Pledge Form .........................................................................................
5,000
1
5/60
416.67
Total ..........................................................................................................
5,000
1
5/60
416.67
Terry S. Clark,
Asst Information Collection Clearance
Officer.
[FR Doc. 2016–30787 Filed 12–21–16; 8:45 am]
BILLING CODE 4150–28–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
[Document Identifier: 0990–New–30D]
Agency Information Collection
Activities; Submission to OMB for
Review and Approval; Public Comment
Request
Office of the Secretary, HHS.
Notice.
AGENCY:
ACTION:
In compliance with section
3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the Office of the
Secretary (OS), Department of Health
and Human Services, has submitted an
Information Collection Request (ICR),
described below, to the Office of
Management and Budget (OMB) for
review and approval. The ICR is for a
new collection. Comments submitted
during the first public review of this ICR
will be provided to OMB. OMB will
accept further comments from the
SUMMARY:
public on this ICR during the review
and approval period.
DATES: Comments on the ICR must be
received on or before January 23, 2017.
ADDRESSES: Submit your comments to
OIRA_submission@omb.eop.gov or via
facsimile to (202) 395–5806.
FOR FURTHER INFORMATION CONTACT:
Information Collection Clearance staff,
Information.CollectionClearance@
hhs.gov or (202) 690–5683.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the
Information Collection Request Title
and document identifier 0990–New–
30D for reference.
Information Collection Request Title:
National Tissue Recovery through
Utilization Survey (NTRUS).
Abstract: The Office of the Assistant
Secretary for Health, Department of
Health and Human Services, is
requesting OMB approval on a new ICR.
This survey is being conducted to
generate national estimates of recovery
through utilization activity; of donated
human tissue for calendar years 2012
and 2015, and to compare metrics across
three data collection periods that
includes results from a 2007 survey, the
most recent year these data were
collected. The survey and data
collection and analysis methods will be
similar to the 2007 survey. The general
categories of information to be collected
are listed under the Survey Section of
the Annualized Burden Hour table
below.
Need and Proposed Use of the
Information: Policy advice provided by
the HHS Advisory Committee on Blood
and Tissue Safety and Availability to
the HHS Secretary and Assistant
Secretary for Health is used to direct
departmental efforts to address
transfusion and transplantation issues,
such as emergency preparedness and
infectious disease transmission related
to donated human tissue. The advice
provided is partly dependent on
analysis of relevant information, such as
tissue collection through utilizations
data.
Likely Respondents: Respondents for
this survey would be U.S. tissue banks
that screen and recover tissue from
living and deceased donors, and
process, store, and/or distribute tissues
grafts for transplantation from these
donors.
The total annual burden hours
estimated for this ICR are summarized
in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden per
response
(in hours)
Survey section
All tissue banks .................................
Tissue bank activities, tissue types
handled, and inspections.
Referrals, authorization, and informed consent; Tissue recovery
and acquisition.
Tissue processing ............................
Tissue storage ..................................
Tissue distribution ............................
Communicable disease testing and
adverse outcome reports.
110
1
10/60
18.33
80
1
1
80
35
65
58
35
1
1
1
1
1
20/60
30/60
1
35
21.67
29
35
...........................................................
........................
........................
........................
219
sradovich on DSK3GMQ082PROD with NOTICES
Tissue banks that handle referrals,
Recover/acquire tissue.
Tissue banks that process tissue .....
Tissue banks that store tissue ..........
Tissue banks that distribute tissue ...
Tissue banks that have donor infectious disease testing performed
and may handle adverse outcome
reports.
Total ...........................................
VerDate Sep<11>2014
17:40 Dec 21, 2016
Jkt 241001
PO 00000
Frm 00065
Fmt 4703
Number of
respondents
Number
responses
per
respondent
Type of
respondent
Sfmt 4703
E:\FR\FM\22DEN1.SGM
22DEN1
Total burden
hours
93946
Federal Register / Vol. 81, No. 246 / Thursday, December 22, 2016 / Notices
Terry S. Clark,
Asst Information Collection Clearance
Officer.
[FR Doc. 2016–30786 Filed 12–21–16; 8:45 am]
BILLING CODE 4150–28–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Substance Abuse and Mental Health
Services Administration
Agency Information Collection
Activities: Proposed Collection;
Comment Request
sradovich on DSK3GMQ082PROD with NOTICES
In compliance with Section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 concerning
opportunity for public comment on
proposed collections of information, the
Substance Abuse and Mental Health
Services Administration (SAMHSA)
will publish periodic summaries of
proposed projects. To request more
information on the proposed projects or
to obtain a copy of the information
collection plans, call the SAMHSA
Reports Clearance Officer on (240) 276–
1243.
Comments are invited on: (a) Whether
the proposed collections of information
are 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) ways to enhance 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.
Proposed Project: Children’s Mental
Health Initiative National Evaluation—
NEW
The Substance Abuse and Mental
Health Services Administration
(SAMHSA), Center for Mental Health
Services (CMHS) is requesting approval
from the Office of Management and
Budget (OMB) for the new collection of
data for the Children’s Mental Health
Initiative (CMHI) National Evaluation.
Evaluation Plan and Data Collection
Activities. The purpose of the Children’s
Mental Health Initiative (CMHI)
National Evaluation is to assess the
success of the CMHI grants in
expanding and sustaining the reach of
SOC values, principles, and practices.
These include maximizing system-level
coordination and planning, offering a
comprehensive array of services, and
prioritizing family and youth
VerDate Sep<11>2014
17:40 Dec 21, 2016
Jkt 241001
involvement. In order to obtain a clear
picture of CMHI grant activities, this
longitudinal, multi-level evaluation will
measure activities and performance of
grantees essential to building and
sustaining effective Systems of Care
(SOC)’s.
Data collection activities will occur
through four evaluation components.
Each component includes data
collection activities and analyses
involving similar topics. Each
component has one or more instruments
that will be used to address various
aspects. The four components with their
corresponding data collection activities
are as follows:
(1) The Implementation Assessment is
designed using a strategic framework
that provides five analytic dimensions:
(1) Policies, (2) services/supports, (3)
financing, (4) training/workforce, and
(5) strategic communications. These
dimensions cut across the State System,
Local System and Service Delivery
levels and together link to a range of
proximal and distal outcomes. The
evaluation will identify and assess the
mechanisms and strategies employed to
implement and expand systems of care,
and explore the impact on system
performance and child and family
outcomes. Evaluation activities are
framed by the five strategic areas to
examine whether specific mechanisms
and strategies lead to proximal and
distal outcomes. System of care
principles are woven throughout the
framework at both the State and Local
levels. Data collection activities include:
(A) Key Partner Interviews with highlevel administrators, youth and family
representatives, and child agencies to
organize qualitative data collection into
these five areas and to allow within and
across grantee evaluation of the
implementation and impact of activities
in these areas; and (B) the System of
Care Expansion and Sustainability
Survey (SOCESS), a self-report survey
administered to representatives from
grantee organizations, family and youth
organizations, child-serving sectors,
advocacy organizations for diverse
populations, provider organizations,
and financial officers, among others.
The SOCESS is designed to capture selfreport implementation data in the five
analytic dimensions adopted by the
2015 CMHI National Evaluation.
(2) The Network and Geographic
Analysis Component will use Network
Analysis Surveys to determine the depth
and breadth of the SOC collaboration
across agencies and organization.
Geographic Information Systems (GIS)
will measure the geographic coverage
and spread of the SOC, including
reaching underserved areas and
PO 00000
Frm 00066
Fmt 4703
Sfmt 4703
populations. At the child/youth and
family level, Census block groups
(derived from home addresses) will be
used to depict the geographic spread of
populations served by SOCs.
(3) The Financial Component involves
the review of implementation grantees’
progress in developing financial
sustainability and expansion plans. The
Financial Mapping Interview and
Financing Plan Survey and Interviews
will be conducted with financial
administrators of Medicaid Agencies,
Mental Health Authorities, mental
health provider trade associations, and
family organizations. The Financial Plan
Interview will focus on how the
financial planning process supported or
hindered attainment of sustainable
financing. The Benchmarking Analysis
will compare relative rates of access,
utilization, and costs for children’s
mental health services using the
Benchmarking Tool and administrative
data requested from financial
administrators and personnel working
with Medicaid Agency and Mental
Health Authority reporting and payment
systems.
(4) The Child and Family Outcome
Component will collect longitudinal
data on child clinical and functional
outcomes, family outcomes, and child
and family background. Data will be
collected at intake, 6-months, and 12months post service entry (as long as the
child/youth is still receiving services).
Data will also be collected at discharge
if the child/youth leaves services before
the 12-month data collection point. Data
will be collected using the following
scales for youth age five and older: (A)
A shortened version of the Caregiver
Strain Questionnaire, (B) the Columbia
Impairment Scale, (C) the Pediatric
Symptom Checklist-17, and (D)
background information gathered
through SAMHSA National Outcomes
Measures (NOMS). Data for youth age 0–
4 will be collected using the: (A) Baby
Pediatric Symptom Checklist; (B) Brief
Infant and Toddler Emotional
Assessment; (C) Pre-School Pediatric
Symptom Checklist and d) background
information from the NOMS.
Estimated Burden. Data will be
collected from 69 grantee sites. Data
collection for this evaluation will be
conducted over a 4-year period. The
average annual respondent burden
estimate reflects the average number of
respondents in each respondent
category, the average number of
responses per respondent per year, the
average length of time it will take to
complete each response, and the total
average annual burden for each category
of respondent for all categories of
respondents combined. Table 1 shows
E:\FR\FM\22DEN1.SGM
22DEN1
]]>Agencies
[Federal Register Volume 81, Number 246 (Thursday, December 22, 2016)]
[Notices]
[Pages 93945-93946]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-30786]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
[Document Identifier: 0990-New-30D]
Agency Information Collection Activities; Submission to OMB for
Review and Approval; Public Comment Request
AGENCY: Office of the Secretary, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the Office of the Secretary (OS), Department of
Health and Human Services, has submitted an Information Collection
Request (ICR), described below, to the Office of Management and Budget
(OMB) for review and approval. The ICR is for a new collection.
Comments submitted during the first public review of this ICR will be
provided to OMB. OMB will accept further comments from the public on
this ICR during the review and approval period.
DATES: Comments on the ICR must be received on or before January 23,
2017.
ADDRESSES: Submit your comments to OIRA_submission@omb.eop.gov or via
facsimile to (202) 395-5806.
FOR FURTHER INFORMATION CONTACT: Information Collection Clearance
staff, Information.CollectionClearance@hhs.gov or (202) 690-5683.
SUPPLEMENTARY INFORMATION: When submitting comments or requesting
information, please include the Information Collection Request Title
and document identifier 0990-New-30D for reference.
Information Collection Request Title: National Tissue Recovery
through Utilization Survey (NTRUS).
Abstract: The Office of the Assistant Secretary for Health,
Department of Health and Human Services, is requesting OMB approval on
a new ICR. This survey is being conducted to generate national
estimates of recovery through utilization activity; of donated human
tissue for calendar years 2012 and 2015, and to compare metrics across
three data collection periods that includes results from a 2007 survey,
the most recent year these data were collected. The survey and data
collection and analysis methods will be similar to the 2007 survey. The
general categories of information to be collected are listed under the
Survey Section of the Annualized Burden Hour table below.
Need and Proposed Use of the Information: Policy advice provided by
the HHS Advisory Committee on Blood and Tissue Safety and Availability
to the HHS Secretary and Assistant Secretary for Health is used to
direct departmental efforts to address transfusion and transplantation
issues, such as emergency preparedness and infectious disease
transmission related to donated human tissue. The advice provided is
partly dependent on analysis of relevant information, such as tissue
collection through utilizations data.
Likely Respondents: Respondents for this survey would be U.S.
tissue banks that screen and recover tissue from living and deceased
donors, and process, store, and/or distribute tissues grafts for
transplantation from these donors.
The total annual burden hours estimated for this ICR are summarized
in the table below.
Total Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number burden per Total burden
Type of respondent Survey section respondents responses per response (in hours
respondent hours)
----------------------------------------------------------------------------------------------------------------
All tissue banks.............. Tissue bank 110 1 10/60 18.33
activities,
tissue types
handled, and
inspections.
Tissue banks that handle Referrals, 80 1 1 80
referrals, Recover/acquire authorization,
tissue. and informed
consent; Tissue
recovery and
acquisition.
Tissue banks that process Tissue 35 1 1 35
tissue. processing.
Tissue banks that store tissue Tissue storage.. 65 1 20/60 21.67
Tissue banks that distribute Tissue 58 1 30/60 29
tissue. distribution.
Tissue banks that have donor Communicable 35 1 1 35
infectious disease testing disease testing
performed and may handle and adverse
adverse outcome reports. outcome reports.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 219
----------------------------------------------------------------------------------------------------------------
[[Page 93946]]
Terry S. Clark,
Asst Information Collection Clearance Officer.
[FR Doc. 2016-30786 Filed 12-21-16; 8:45 am]
BILLING CODE 4150-28-P
