Agency Information Collection Activities; Proposed Collection; Public Comment Request, 54662-54663 [2013-21566]
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54662
Federal Register / Vol. 78, No. 172 / Thursday, September 5, 2013 / Notices
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Number of
respondents
Form name
Responses
per
respondent
Total
responses
Average
burden per
response
(in hours)
Total burden
hours
Verification of Disadvantaged Background Form ................
Private Practice Option Form ..............................................
600
300
1
1
600
300
.50
.10
300
30
Total ..............................................................................
........................
........................
9,350
........................
8,555
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.
Dated: August 28, 2013.
Bahar Niakan,
Director, Division of Policy and Information
Coordination.
[FR Doc. 2013–21564 Filed 9–4–13; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities; Proposed Collection; Public
Comment Request
Health Resources and Services
Administration, HHS.
AGENCY:
ACTION:
Notice.
In compliance with the
requirement for opportunity for public
comment on proposed data collection
projects (Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995), the
Health Resources and Services
Administration (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.
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SUMMARY:
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14:10 Sep 04, 2013
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Comments on this Information
Collection Request must be received
within 60 days of this notice.
ADDRESSES: Submit your comments to
paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance
Officer, Room 10–29, Parklawn
Building, 5600 Fishers Lane, Rockville,
MD 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 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 the Frontier Community
Health Care Network Coordination
Grant.
OMB No.: 0915–XXXX—New.
Abstract: In fiscal year (FY) 2012,
ORHP funded an evaluation of the
Frontier Community Health Care
Network Coordination (FCHCNC) Grant.
This 3-year grant program awarded to
the Montana Department of Public
Health and Human Services focuses on
a community-based, patient-centered
clinical service coordination and health
promotion model. The program will be
coordinated by clinically trained Care
Transitions Coordinators (CTC) working
with Community Health Workers (CHW)
in 11 participating network
communities. By developing
intervention with patients, the CTCs
and CHWs will work to improve care
transitions and patient outcomes by
reducing or eliminating avoidable
hospitalizations and re hospitalizations,
ER visits, and nursing home placements.
Need and Proposed Use of the
Information: The program will be
subject to a 3-year independent
evaluation. As part of this 3-year
DATES:
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Frm 00046
Fmt 4703
Sfmt 4703
evaluation, HRSA will be collecting
qualitative and quantitative information.
To support the qualitative analysis,
HRSA will conduct site visits and
telephonic key informant interviews
with the critical access hospitals,
tertiary hospitals, and the support staff
coordinating the program. Data
collection will focus on patient/family
satisfaction, whether goals were
achieved in working with patients, and
the strengths and challenges associated
with implementing the program.
Finally, HRSA will be collecting data
quarterly from the grantee sites in order
to gain a deeper understanding of the
program’s implementation.
Additionally, quantitative data will be
gathered by studying the effectiveness of
each intervention, specifically
identifying differences between pre and
post-intervention health care utilization,
hospital readmissions, and other clientspecific outcomes. Where data are
available, HRSA will assess cost
effectiveness of the program.
Likely Respondents: Frontier
Community Health Care Network
Coordination (FCHCNC) Grantees.
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 Information
Collection Request are summarized in
the table below.
E:\FR\FM\05SEN1.SGM
05SEN1
54663
Federal Register / Vol. 78, No. 172 / Thursday, September 5, 2013 / Notices
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form name
Number of
responses per
respondent
Average burden
per response
(in hours)
Total
responses
Total burden
hours
Patient Satisfaction Survey ..............................................
Hospital Administrator Interview Protocol ........................
Primary care Provider Interview Protocol ........................
Community Health Worker Interview Protocol .................
Care Transitions Coordinator Interview Protocol .............
Grantee Interview Protocol ..............................................
Patient Interview/Focus Group Protocol ..........................
Grantee Data Collection Form .........................................
85
22
22
12
1
2
22
11
1
1
1
1
1
1
1
4
85
22
22
12
1
2
22
44
.1
.5
.5
1.0
1.0
.5
.5
4
8.5
11
11
12
1
1
11
176
Total ..........................................................................
177
........................
........................
..........................
231.5
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.
Dated: August 28, 2013.
Bahar Niakan,
Director, Division of Policy and Information
Coordination.
[FR Doc. 2013–21566 Filed 9–4–13; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
National Vaccine Injury Compensation
Program; List of Petitions Received
Health Resources and Services
Administration, HHS.
ACTION: Notice.
AGENCY:
The Health Resources and
Services Administration (HRSA) is
publishing this notice of petitions
received under the National Vaccine
Injury Compensation Program (the
Program), as required by Section
2112(b)(2) of the Public Health Service
(PHS) Act, as amended. While the
Secretary of Health and Human Services
is named as the respondent in all
proceedings brought by the filing of
petitions for compensation under the
Program, the United States Court of
Federal Claims is charged by statute
with responsibility for considering and
acting upon the petitions.
FOR FURTHER INFORMATION CONTACT: For
information about requirements for
filing petitions, and the Program in
ehiers on DSK2VPTVN1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
14:10 Sep 04, 2013
Jkt 229001
general, contact the Clerk, United States
Court of Federal Claims, 717 Madison
Place NW., Washington, DC 20005,
(202) 357–6400. For information on
HRSA’s role in the Program, contact the
Director, National Vaccine Injury
Compensation Program, 5600 Fishers
Lane, Room 11C–26, Rockville, MD
20857; (301) 443–6593.
The
Program provides a system of no-fault
compensation for certain individuals
who have been injured by specified
childhood vaccines. Subtitle 2 of Title
XXI of the PHS Act, 42 U.S.C. 300aa–
10 et seq., provides that those seeking
compensation are to file a petition with
the U.S. Court of Federal Claims and to
serve a copy of the petition on the
Secretary of Health and Human
Services, who is named as the
respondent in each proceeding. The
Secretary has delegated her
responsibility under the Program to
HRSA. The Court is directed by statute
to appoint special masters who take
evidence, conduct hearings as
appropriate, and make initial decisions
as to eligibility for, and amount of,
compensation.
A petition may be filed with respect
to injuries, disabilities, illnesses,
conditions, and deaths resulting from
vaccines described in the Vaccine Injury
Table (the Table) set forth at Section
2114 of the PHS Act or as set forth at
42 CFR 100.3, as applicable. This Table
lists for each covered childhood vaccine
the conditions which may lead to
compensation and, for each condition,
the time period for occurrence of the
first symptom or manifestation of onset
or of significant aggravation after
vaccine administration. Compensation
may also be awarded for conditions not
listed in the Table and for conditions
that are manifested outside the time
periods specified in the Table, but only
if the petitioner shows that the
condition was caused by one of the
listed vaccines.
SUPPLEMENTARY INFORMATION:
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Frm 00047
Fmt 4703
Sfmt 4703
Section 2112(b)(2) of the PHS Act, 42
U.S.C. 300aa–12(b)(2), requires that
‘‘[w]ithin 30 days after the Secretary
receives service of any petition filed
under section 2111 the Secretary shall
publish notice of such petition in the
Federal Register.’’ Set forth below is a
list of petitions received by HRSA on
July 1, 2013, through July 31, 2013. This
list provides the name of petitioner, city
and state of vaccination (if unknown
then city and state of person or attorney
filing claim), and case number. In cases
where the Court has redacted the name
of a petitioner and/or the case number,
the list reflects such redaction.
Section 2112(b)(2) also provides that
the special master ‘‘shall afford all
interested persons an opportunity to
submit relevant, written information’’
relating to the following:
1. The existence of evidence ‘‘that
there is not a preponderance of the
evidence that the illness, disability,
injury, condition, or death described in
the petition is due to factors unrelated
to the administration of the vaccine
described in the petition,’’ and
2. Any allegation in a petition that the
petitioner either:
(a) ‘‘Sustained, or had significantly
aggravated, any illness, disability,
injury, or condition not set forth in the
Table but which was caused by’’ one of
the vaccines referred to in the Table, or
(b) ‘‘Sustained, or had significantly
aggravated, any illness, disability,
injury, or condition set forth in the
Vaccine Injury Table the first symptom
or manifestation of the onset or
significant aggravation of which did not
occur within the time period set forth in
the Table but which was caused by a
vaccine’’ referred to in the Table.
In accordance with Section
2112(b)(2), all interested persons may
submit written information relevant to
the issues described above in the case of
the petitions listed below. Any person
choosing to do so should file an original
and three (3) copies of the information
with the Clerk of the U.S. Court of
E:\FR\FM\05SEN1.SGM
05SEN1
Agencies
[Federal Register Volume 78, Number 172 (Thursday, September 5, 2013)]
[Notices]
[Pages 54662-54663]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-21566]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities; Proposed Collection;
Public Comment Request
AGENCY: Health Resources and Services Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the requirement for opportunity for public
comment on proposed data collection projects (Section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995), the Health Resources and Services
Administration (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 Information Collection Request must be received
within 60 days of this notice.
ADDRESSES: Submit your comments to paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance Officer, Room 10-29, Parklawn
Building, 5600 Fishers Lane, Rockville, MD 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 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 the Frontier
Community Health Care Network Coordination Grant.
OMB No.: 0915-XXXX--New.
Abstract: In fiscal year (FY) 2012, ORHP funded an evaluation of
the Frontier Community Health Care Network Coordination (FCHCNC) Grant.
This 3-year grant program awarded to the Montana Department of Public
Health and Human Services focuses on a community-based, patient-
centered clinical service coordination and health promotion model. The
program will be coordinated by clinically trained Care Transitions
Coordinators (CTC) working with Community Health Workers (CHW) in 11
participating network communities. By developing intervention with
patients, the CTCs and CHWs will work to improve care transitions and
patient outcomes by reducing or eliminating avoidable hospitalizations
and re hospitalizations, ER visits, and nursing home placements.
Need and Proposed Use of the Information: The program will be
subject to a 3-year independent evaluation. As part of this 3-year
evaluation, HRSA will be collecting qualitative and quantitative
information. To support the qualitative analysis, HRSA will conduct
site visits and telephonic key informant interviews with the critical
access hospitals, tertiary hospitals, and the support staff
coordinating the program. Data collection will focus on patient/family
satisfaction, whether goals were achieved in working with patients, and
the strengths and challenges associated with implementing the program.
Finally, HRSA will be collecting data quarterly from the grantee sites
in order to gain a deeper understanding of the program's
implementation.
Additionally, quantitative data will be gathered by studying the
effectiveness of each intervention, specifically identifying
differences between pre and post-intervention health care utilization,
hospital readmissions, and other client-specific outcomes. Where data
are available, HRSA will assess cost effectiveness of the program.
Likely Respondents: Frontier Community Health Care Network
Coordination (FCHCNC) Grantees.
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 Information Collection Request are summarized in the table below.
[[Page 54663]]
Total Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Form name Number of responses per Total per response Total burden
respondents respondent responses (in hours) hours
----------------------------------------------------------------------------------------------------------------
Patient Satisfaction Survey... 85 1 85 .1 8.5
Hospital Administrator 22 1 22 .5 11
Interview Protocol...........
Primary care Provider 22 1 22 .5 11
Interview Protocol...........
Community Health Worker 12 1 12 1.0 12
Interview Protocol...........
Care Transitions Coordinator 1 1 1 1.0 1
Interview Protocol...........
Grantee Interview Protocol.... 2 1 2 .5 1
Patient Interview/Focus Group 22 1 22 .5 11
Protocol.....................
Grantee Data Collection Form.. 11 4 44 4 176
---------------------------------------------------------------------------------
Total..................... 177 .............. .............. ............... 231.5
----------------------------------------------------------------------------------------------------------------
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.
Dated: August 28, 2013.
Bahar Niakan,
Director, Division of Policy and Information Coordination.
[FR Doc. 2013-21566 Filed 9-4-13; 8:45 am]
BILLING CODE 4165-15-P