Agency Information Collection Activities: Proposed Collection; Comment Request, 13337-13338 [2012-5439]
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Federal Register / Vol. 77, No. 44 / Tuesday, March 6, 2012 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration on Aging
Centers for Medicare & Medicaid
Services
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Annual Reporting
Requirements for the Older American
Act Title VI Grant Program
AGENCY:
ACTION:
Administration on Aging, HHS.
Notice.
The Administration on Aging
(AoA) is announcing that the proposed
collection of information listed below
has been submitted to the Office of
Management and Budget (OMB) for
review and clearance under the
Paperwork Reduction Act of 1995.
SUMMARY:
Submit written or electronic
comments on the collection of
information by April 5, 2012.
DATES:
Submit electronic
comments on the collection of
information to:
Cynthia.LaCounte@aoa.hhs.gov. Submit
written comments on the collection of
information to Cynthia LaCounte,
Administration on Aging, Washington,
DC 20201 or by fax at 202–357–3560.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Margaret Graves at (202) 357–0148 or
Cynthia.LaCounte@aoa.hhs.gov.
In
compliance with 44 U.S.C 3507, AoA
has submitted the following proposed
collection of information to OMB for
review and clearance.
SUPPLEMENTARY INFORMATION:
pmangrum on DSK3VPTVN1PROD with NOTICES
Describe Collection of Information
AoA estimates the burden of this
collection of information as follows:
Annual submission of the Program
Performance Reports are due 90 days
after the end of the budget period and
final project period.
Respondents: Federally Recognized
Tribes, Tribal and Native Hawaiian
Organizations receiving grants under
Title VI, Part A, Grants for Native
Americans; Title VI, Part B, Native
Hawaiian Program and Title VI, Part C,
Native American Caregiver Support
Program.
Estimated Number of Responses: 256.
Total Estimated Burden Hours: 640.
Dated: February 28, 2012.
Kathy Greenlee,
Assistant Secretary for Aging.
[FR Doc. 2012–5437 Filed 3–5–12; 8:45 am]
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[Document Identifier: CMS–10136, CMS–
10116, CMS–10426 and CMS–10406]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Centers for Medicare & Medicaid
Services (CMS) is publishing the
following summary of proposed
collections for public comment.
Interested persons are invited to send
comments regarding this burden
estimate or any other aspect of this
collection of information, including any
of the following subjects: (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.
1. Type of Information Collection
Request: Reinstatement of a previously
approved collection; Title of
Information Collection: Physician Group
Practice Transition Demonstration
(PGP–TD) Performance Assessment Tool
(‘‘PAT’’); Use: The Physician Group
Practice (PGP) Demonstration was
mandated by section 412 of the
Medicare, Medicaid, and SCHIP
Benefits Improvement and Protection
Act of 2000 and is the precursor to the
Medicare Shared Savings Program.
Section 1899(k) of the Social Security
Act, as added by section 10307(k) of the
Affordable Care Act (as amended by
section 10307 of the Health Care and
Education Reconciliation Act of 2010),
states ‘‘the Secretary may enter into an
agreement with an ACO under the
Demonstration under section 1866A,
subject to rebasing and other
modifications deemed appropriate by
the Secretary.’’ The Demonstration
extension is entitled the PGP Transition
Demonstration (PGP–TD).
We are seeking reinstatement of the
collection of information as it was
erroneously discontinued. Only a
portion of the information collection
requirements previously approved
under 0938–0941 should have been
AGENCY:
PO 00000
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13337
discontinued. The collection of
information is strictly voluntary in
nature and was developed in
conjunction with the industry and
Demonstration participants. Only
organizations that voluntarily respond
and elect to participate in the
Demonstration will be reporting the
measures. Moreover, CMS will not be
using this information to regulate or
sanction but rather to provide financial
incentives for improving the quality of
care. The collection of information to be
used under this extension is being used
to test quality data collection systems
and determine incentive payment levels
to participating physician group
practices participating in the PGP–TD.
In addition, this data will be used to
evaluate the effectiveness of these
payment models and provide insight
into the most appropriate way for the
agency to collect clinical information.
Form Number: CMS–10136 (OCN:
0938–0941); Frequency: Yearly; Affected
Public: Private Sector—Business or
other for-profits and not-for-profit
institutions. Number of Respondents:
10. Number of Responses: 10. Total
Annual Hours: 790. (For policy
questions regarding this collection
contact Heather Grimsley at 410–786–
1048. For all other issues call 410–786–
1326.)
2. Type of Information Collection
Request: Extension of a currently
approved collection;
Title of Information Collection:
Conditions for Payment of Power
Mobility Devices, including Power
Wheelchairs and Power-Operated
Vehicles; Use: CMS is renewing our
request for approval for the collection
requirements associated with the final
rule, CMS–3017–F (71 FR 17021), which
was published on April 5, 2006 and
became effective on June 5, 2006. The
regulation CMS–3017–F finalized
provisions set forth in the interim final
regulation (70 FR 50940) published on
August 26, 2005. This final rule
conforms our regulations to section
302(a)(2)(E)(iv) of the Medicare
Prescription Drug, Improvement, and
Modernization Act of 2003. This rule
defines the term power mobility devices
(PMDs) as power wheelchairs and
power operated vehicles (POVs or
scooters). It sets forth revised conditions
for Medicare payment of PMDs and
defines who may prescribe PMDs. This
rule also requires a face-to-face
examination of the beneficiary by the
physician or treating practitioner, a
written prescription, and receipt of
pertinent parts of the medical record by
the supplier within 45 days after the
face-to-face examination that the
durable medical equipment (DME)
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13338
Federal Register / Vol. 77, No. 44 / Tuesday, March 6, 2012 / Notices
suppliers maintain in their records and
make available to CMS and its agents
upon request. Finally, this rule
discusses CMS’ policy on
documentation that may be requested by
CMS and its agents to support a
Medicare claim for payment. Form
Number: CMS–10116 (OCN: 0938–
0971); Frequency: Yearly; Affected
Public: Private Sector—Business or
other for-profits. Number of
Respondents: 90,521. Number of
Responses: 173,810. Total Annual
Hours: 34,762. (For policy questions
regarding this collection contact Susan
Miller at 410–786–2118. For all other
issues call 410–786–1326.)
3. Type of Information Collection
Request: New collection; Title of
Information Collection: End Stage Renal
Disease (ESRD) System Access Request
Form; Use: Within CMS, the Office of
Clinical Standards and Quality is
developing a new suite of systems to
support the End Stage Renal Disease
(ESRD) program. Due to the sensitivity
of the data being collected and reported,
CMS must ensure that only authorized
personnel have access to data. Personnel
are given access to the ESRD systems
through the creation of user IDs and
passwords within the QualityNet
Identity Management System (QIMS);
however, once within the system, the
system determines the rights and
privileges the personnel has over the
data within the system.
The sole purpose the End Stage Renal
Disease System (ESRD) System Access
Request Form is to identify the
individual’s data access rights once
within the ESRD system. This function
and the associated data collection is
currently being accomplished under
‘‘Part B’’ of the QualityNet Identity
Management System Account Form
(CMS–10267; OCN: 0938–1050). Once
the ESRD System Access Form is
approved, the QualityNet Identity
Management System (QIMS) Account
Form will be revised to remove Part B
from the QIMS data collection. Form
Number: CMS–10426 (OCN: 0938–
New); Frequency: Yearly; Affected
Public: Private Sector—Business or
other for-profits. Number of
Respondents: 25,000. Number of
Responses: 25,000. Total Annual Hours:
6,250. (For policy questions regarding
this collection contact Michelle Tucker
at 410–786–0736. For all other issues
call 410–786–1326.)
4. Type of Information Collection
Request: New collection; Title of
Information Collection: Probable Fraud
Measurement Pilot; Use: The Centers for
Medicare & Medicaid Services (CMS) is
seeking Office of Management and
Budget (OMB) approval of the
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collections required for a probable fraud
measurement pilot. The probable fraud
measurement pilot would establish a
baseline estimate of probable fraud in
payments for home health care services
in the fee-for-service Medicare program.
CMS and its agents will collect
information from home health agencies,
the referring physicians and Medicare
beneficiaries selected in a national
random sample of home health claims.
The pilot will rely on the information
collected along with a summary of the
service history of the HHA, the referring
provider, and the beneficiary to estimate
the percentage of total payments that are
associated with probable fraud and the
percentage of all claims that are
associated with probable fraud for
Medicare fee-for-service home health.
Form Number: CMS–10406 (OCN:
0938–New); Frequency: Yearly; Affected
Public: Individual and Private Sector—
Business or other for-profits. Number of
Respondents: 6,000. Number of
Responses: 6,000. Total Annual Hours:
10,500. (For policy questions regarding
this collection contact Kelly Gent at
410–786–0918. For all other issues call
410–786–1326.)
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access CMS’ Web Site
address at https://www.cms.hhs.gov/
PaperworkReductionActof1995, or Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov, or call the
Reports Clearance Office on (410) 786–
1326.
In commenting on the proposed
information collections please reference
the document identifier or OMB control
number. To be assured consideration,
comments and recommendations must
be submitted in one of the following
ways by May 7, 2012:
1. Electronically. You may submit
your comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) accepting comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number lll, Room C4–26–
05, 7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
PO 00000
Frm 00082
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Dated: March 1, 2012.
Martique Jones,
Director, Regulations Development Group,
Division B, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2012–5439 Filed 3–5–12; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Tribal Consultation Meetings
Office of Head Start (OHS),
Administration for Children and
Families, HHS.
ACTION: Notice of meetings.
AGENCY:
Pursuant to the Improving
Head Start for School Readiness Act of
2007, Public Law 110–134, notice is
hereby given of one-day Tribal
Consultation Sessions to be held
between the Department of Health and
Human Services, Administration for
Children and Families, Office of Head
Start leadership and the leadership of
Tribal Governments operating Head
Start (including Early Head Start)
programs. The purpose of these
Consultation Sessions is to discuss ways
to better meet the needs of American
Indian and Alaska Native children and
their families, taking into consideration
funding allocations, distribution
formulas, and other issues affecting the
delivery of Head Start services in their
geographic locations [42 U.S.C. 9835,
Section 640(l)(4)].
DATES: March 22 and April 3, 2012.
ADDRESSES: 2012 Office of Head Start
Tribal Consultation Sessions will be
held at the following locations:
Thursday, March 22, 2012—Phoenix,
Arizona—Sheraton Crescent Hotel, 2620
West Dunlap Avenue Phoenix, AZ
85021; Tuesday, April 3, 2012—Billings,
Montana—Holiday Inn Grand Montana
5500 Midland Road, Billings, MT 59101.
FOR FURTHER INFORMATION CONTACT:
Camille Loya, Acting Regional Program
Manager Region XI, email
Camille.Loya@acf.hhs.gov or phone
(202) 401–5964. Additional information
and online meeting registration is
available at https://
www.headstartresourcecenter.org.
SUPPLEMENTARY INFORMATION: The
Department of Health and Human
Services (HHS) announces Office of
Head Start (OHS) Tribal Consultations
with leaders of Tribal Governments
operating Head Start (including Early
Head Start) programs for each of the
nine geographic regions of Head Start
SUMMARY:
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Agencies
[Federal Register Volume 77, Number 44 (Tuesday, March 6, 2012)]
[Notices]
[Pages 13337-13338]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-5439]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10136, CMS-10116, CMS-10426 and CMS-10406]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Centers for Medicare & Medicaid Services.
In compliance with the requirement of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Centers for Medicare & Medicaid
Services (CMS) is publishing the following summary of proposed
collections for public comment. Interested persons are invited to send
comments regarding this burden estimate or any other aspect of this
collection of information, including any of the following subjects: (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.
1. Type of Information Collection Request: Reinstatement of a
previously approved collection; Title of Information Collection:
Physician Group Practice Transition Demonstration (PGP-TD) Performance
Assessment Tool (``PAT''); Use: The Physician Group Practice (PGP)
Demonstration was mandated by section 412 of the Medicare, Medicaid,
and SCHIP Benefits Improvement and Protection Act of 2000 and is the
precursor to the Medicare Shared Savings Program. Section 1899(k) of
the Social Security Act, as added by section 10307(k) of the Affordable
Care Act (as amended by section 10307 of the Health Care and Education
Reconciliation Act of 2010), states ``the Secretary may enter into an
agreement with an ACO under the Demonstration under section 1866A,
subject to rebasing and other modifications deemed appropriate by the
Secretary.'' The Demonstration extension is entitled the PGP Transition
Demonstration (PGP-TD).
We are seeking reinstatement of the collection of information as it
was erroneously discontinued. Only a portion of the information
collection requirements previously approved under 0938-0941 should have
been discontinued. The collection of information is strictly voluntary
in nature and was developed in conjunction with the industry and
Demonstration participants. Only organizations that voluntarily respond
and elect to participate in the Demonstration will be reporting the
measures. Moreover, CMS will not be using this information to regulate
or sanction but rather to provide financial incentives for improving
the quality of care. The collection of information to be used under
this extension is being used to test quality data collection systems
and determine incentive payment levels to participating physician group
practices participating in the PGP-TD. In addition, this data will be
used to evaluate the effectiveness of these payment models and provide
insight into the most appropriate way for the agency to collect
clinical information. Form Number: CMS-10136 (OCN: 0938-0941);
Frequency: Yearly; Affected Public: Private Sector--Business or other
for-profits and not-for-profit institutions. Number of Respondents: 10.
Number of Responses: 10. Total Annual Hours: 790. (For policy questions
regarding this collection contact Heather Grimsley at 410-786-1048. For
all other issues call 410-786-1326.)
2. Type of Information Collection Request: Extension of a currently
approved collection;
Title of Information Collection: Conditions for Payment of Power
Mobility Devices, including Power Wheelchairs and Power-Operated
Vehicles; Use: CMS is renewing our request for approval for the
collection requirements associated with the final rule, CMS-3017-F (71
FR 17021), which was published on April 5, 2006 and became effective on
June 5, 2006. The regulation CMS-3017-F finalized provisions set forth
in the interim final regulation (70 FR 50940) published on August 26,
2005. This final rule conforms our regulations to section
302(a)(2)(E)(iv) of the Medicare Prescription Drug, Improvement, and
Modernization Act of 2003. This rule defines the term power mobility
devices (PMDs) as power wheelchairs and power operated vehicles (POVs
or scooters). It sets forth revised conditions for Medicare payment of
PMDs and defines who may prescribe PMDs. This rule also requires a
face-to-face examination of the beneficiary by the physician or
treating practitioner, a written prescription, and receipt of pertinent
parts of the medical record by the supplier within 45 days after the
face-to-face examination that the durable medical equipment (DME)
[[Page 13338]]
suppliers maintain in their records and make available to CMS and its
agents upon request. Finally, this rule discusses CMS' policy on
documentation that may be requested by CMS and its agents to support a
Medicare claim for payment. Form Number: CMS-10116 (OCN: 0938-0971);
Frequency: Yearly; Affected Public: Private Sector--Business or other
for-profits. Number of Respondents: 90,521. Number of Responses:
173,810. Total Annual Hours: 34,762. (For policy questions regarding
this collection contact Susan Miller at 410-786-2118. For all other
issues call 410-786-1326.)
3. Type of Information Collection Request: New collection; Title of
Information Collection: End Stage Renal Disease (ESRD) System Access
Request Form; Use: Within CMS, the Office of Clinical Standards and
Quality is developing a new suite of systems to support the End Stage
Renal Disease (ESRD) program. Due to the sensitivity of the data being
collected and reported, CMS must ensure that only authorized personnel
have access to data. Personnel are given access to the ESRD systems
through the creation of user IDs and passwords within the QualityNet
Identity Management System (QIMS); however, once within the system, the
system determines the rights and privileges the personnel has over the
data within the system.
The sole purpose the End Stage Renal Disease System (ESRD) System
Access Request Form is to identify the individual's data access rights
once within the ESRD system. This function and the associated data
collection is currently being accomplished under ``Part B'' of the
QualityNet Identity Management System Account Form (CMS-10267; OCN:
0938-1050). Once the ESRD System Access Form is approved, the
QualityNet Identity Management System (QIMS) Account Form will be
revised to remove Part B from the QIMS data collection. Form Number:
CMS-10426 (OCN: 0938-New); Frequency: Yearly; Affected Public: Private
Sector--Business or other for-profits. Number of Respondents: 25,000.
Number of Responses: 25,000. Total Annual Hours: 6,250. (For policy
questions regarding this collection contact Michelle Tucker at 410-786-
0736. For all other issues call 410-786-1326.)
4. Type of Information Collection Request: New collection; Title of
Information Collection: Probable Fraud Measurement Pilot; Use: The
Centers for Medicare & Medicaid Services (CMS) is seeking Office of
Management and Budget (OMB) approval of the collections required for a
probable fraud measurement pilot. The probable fraud measurement pilot
would establish a baseline estimate of probable fraud in payments for
home health care services in the fee-for-service Medicare program. CMS
and its agents will collect information from home health agencies, the
referring physicians and Medicare beneficiaries selected in a national
random sample of home health claims. The pilot will rely on the
information collected along with a summary of the service history of
the HHA, the referring provider, and the beneficiary to estimate the
percentage of total payments that are associated with probable fraud
and the percentage of all claims that are associated with probable
fraud for Medicare fee-for-service home health. Form Number: CMS-10406
(OCN: 0938-New); Frequency: Yearly; Affected Public: Individual and
Private Sector--Business or other for-profits. Number of Respondents:
6,000. Number of Responses: 6,000. Total Annual Hours: 10,500. (For
policy questions regarding this collection contact Kelly Gent at 410-
786-0918. For all other issues call 410-786-1326.)
To obtain copies of the supporting statement and any related forms
for the proposed paperwork collections referenced above, access CMS'
Web Site address at https://www.cms.hhs.gov/PaperworkReductionActof1995,
or E-mail your request, including your address, phone number, OMB
number, and CMS document identifier, to Paperwork@cms.hhs.gov, or call
the Reports Clearance Office on (410) 786-1326.
In commenting on the proposed information collections please
reference the document identifier or OMB control number. To be assured
consideration, comments and recommendations must be submitted in one of
the following ways by May 7, 2012:
1. Electronically. You may submit your comments electronically to
https://www.regulations.gov. Follow the instructions for ``Comment or
Submission'' or ``More Search Options'' to find the information
collection document(s) accepting comments.
2. By regular mail. You may mail written comments to the following
address: CMS, Office of Strategic Operations and Regulatory Affairs,
Division of Regulations Development, Attention: Document Identifier/OMB
Control Number ------, Room C4-26-05, 7500 Security Boulevard,
Baltimore, Maryland 21244-1850.
Dated: March 1, 2012.
Martique Jones,
Director, Regulations Development Group, Division B, Office of
Strategic Operations and Regulatory Affairs.
[FR Doc. 2012-5439 Filed 3-5-12; 8:45 am]
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