Agency Information Collection Activities; Proposed Collection; Public Comment Request, 54662-54663 [2013-21566]

Download as PDF 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. ehiers on DSK2VPTVN1PROD with NOTICES SUMMARY: VerDate Mar<15>2010 14:10 Sep 04, 2013 Jkt 229001 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: PO 00000 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: PO 00000 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]


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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
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