Proposed Data Collection Submitted for Public Comment and Recommendations, 36214-36215 [2020-12810]
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36214
Federal Register / Vol. 85, No. 115 / Monday, June 15, 2020 / Notices
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–12807 Filed 6–12–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–20–0909; Docket No. CDC–2020–
0070]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a continuing information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on CDC Diabetes Prevention
Recognition Program (DPRP). This
collection allows CDC to administer the
Diabetes Prevention Recognition
Program (DPRP) and collects
information needed by the Centers for
Medicare & Medicaid Services (CMS) to
support the Medicare Expanded Model
(Medicare Diabetes Prevention Program
[MDPP]).
DATES: CDC must receive written
comments on or before August 14, 2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2020–
0070 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS–D74, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
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SUMMARY:
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17:04 Jun 12, 2020
Jkt 250001
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS–
D74, Atlanta, Georgia 30329; phone:
404–639–7570; Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
4. Minimize the burden of the
collection of information on those who
are to respond, including through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses.
5. Assess information collection costs.
Proposed Project
CDC Diabetes Prevention Recognition
Program (DPRP)—Revision—National
Center for Chronic Disease Prevention
and Health Promotion (NCCDPHP),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
CDC’s Division of Diabetes
Translation (DDT) established and
administers the National DPP’s Diabetes
Prevention Recognition Program
(DPRP), which recognizes organizations
PO 00000
Frm 00031
Fmt 4703
Sfmt 4703
that deliver diabetes prevention
programs according to evidence-based
requirements set forth in the ‘‘Centers
for Disease Control and Prevention
Diabetes Prevention Recognition
Program Standards and Operating
Procedures’’ (DPRP Standards).
Additionally, the Centers for Medicare
and Medicaid Services (CMS) Medicare
Diabetes Prevention Program (MDPP)
expansion of CDC’s National DPP was
announced in early 2016, when the
Secretary of Health and Human Services
determined that the Diabetes Prevention
Program met the statutory criteria for
inclusion in Medicare’s expanded list of
healthcare services for beneficiaries
(https://innovation.cms.gov/initiatives/
medicare-diabetes-prevention-program/
). This is the first time a preventive
service model from the CMS Innovation
(CMMI) Center has been expanded.
After extensive testing of the DPP model
in 17 sites across the U.S. in 2014–2016,
CMS proposed the MDPP in Sections
1102 and 1871 of the Social Security
Act (42 U.S.C. 1302 and 1395hh
§ 424.59), authorizing CDC-recognized
organizations to prepare for enrollment
as MDPP suppliers beginning in January
2018 in order to bill CMS for these
services. Only organizations in good
standing with the CDC DPRP are eligible
as MDPP suppliers. CDC continues to
work with CMS to support the MDPP.
CDC requests an additional three
years of OMB approval to continue
collecting the information needed to
administer the DPRP and information
needed by CMS to support the MDPP
benefit. Based on experience with the
DPRP from 2011–2020, including data
analysis, and feedback from applicant
organizations and internal and external
partners, CDC plans to revise the DPRP
Standards and the associated
information collection.
Key changes are a direct result of
DPRP data analyses and discussion with
National DPP stakeholders, including
those serving vulnerable populations.
Key changes allow for the optional
collection of Hemoglobin A1C levels,
and for weight/physical activity minutes
to be combined (a new method), to
determine Full recognition; the required
collection of Application Delivery Mode
questions; revised organizational type
information; program enrollment
motivation/enrollment source
information; adding Gender; and the
removal of Session ID.
Three data elements have been
minimally revised and no other data
elements have been added to the onetime application form; and, three
elements have been revised, one has
been deleted, and four have been added
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15JNN1
36215
Federal Register / Vol. 85, No. 115 / Monday, June 15, 2020 / Notices
to the evaluation data elements, as per
below:
Application Form:
(1) Delivery Mode—follow-up questions
(revised)
(2) Class Type (revised)
(3) Organization Type (revised)
Evaluation Data Elements:
(4) Enrollment Motivation (new)
(5) Enrollment Source (new)
(6) Session ID (deleted)
(7) HBA1C Value (new)
(8) Participant’s Gender (new)
During the period of this Revision,
CDC estimates receipt of approximately
300 DPRP application forms per year.
The estimated burden per one-time, up-
for upload into the DPRP Data Portal.
The estimated burden per response is
modest since the information requested
for DPRP recognition is routinely
collected by most organizations that
deliver lifestyle change programs for
their own internal evaluation and
possible insurance reimbursement
purposes, including Medicare under the
MDPP benefit. Participation in the DPRP
is voluntary, data are de-identified, no
Personally Identifiable Information (PII)
is collected by CDC, and there are no
costs to respondents other than their
time. CDC is requesting a three-year
approval.
front application response is one hour
(annualized to 300 hours one-time
across all new organizations). In
addition, CDC estimates receipt of semiannual evaluation data submissions
from the same 300 additional
organizations per year; estimated at two
hours per response. The total estimated
average annualized evaluation burden to
respondents is 6,676 hours. This
includes an estimate of the time needed
to extract and compile the required data
records and fields from an existing
electronic database, review the data,
create or enter a data file in the required
format (i.e., CSV file), and submit the
data file via the National DPP website
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent
Public sector organizations that deliver type 2
diabetes prevention programs.
Private sector organizations that deliver type 2
diabetes prevention programs.
Total ............................................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–12810 Filed 6–12–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review; Income
Withholding Order/Notice for Support
(IWO)
Office of Child Support
Enforcement; Administration for
Children and Families; HHS.
ACTION: Request for Public Comment.
AGENCY:
The Administration for
Children and Families (ACF) is
requesting a three-year extension of the
form Income Withholding Order/Notice
for Support (IWO) (OMB #0970–0154,
expiration 8/31/2020). This request
includes minor revisions to the
approved forms.
DATES: Comments due within 30 days of
publication. OMB is required to make a
decision concerning the collection of
jbell on DSKJLSW7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:04 Jun 12, 2020
Jkt 250001
Number of
respondents
Form name
DPRP
DPRP
DPRP
DPRP
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
(in hours)
Application Form ..
Evaluation Data ....
Application Form ..
Evaluation Data ....
90
290
210
1,304
1
2
1
2
1
2
1
2
90
1,160
210
5,216
..........................................
........................
........................
........................
6,676
information between 30 and 60 days
after publication of this document in the
Federal Register. Therefore, a comment
is best assured of having its full effect
if OMB receives it within 30 days of
publication.
ADDRESSES: Written comments and
recommendations for the proposed
information collection should be sent
within 30 days of publication of this
notice to www.reginfo.gov/public/do/
PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function.
SUPPLEMENTARY INFORMATION:
Description: The IWO is the standard
form that must be used to order and
notify employers and income providers
to withhold child support payments
from an obligor’s income. It also
indicates where employers and other
income providers must remit the
payments and other information needed
to withhold correctly.
Child support agencies, courts,
private attorneys, custodial parties, and
others must use the IWO form to initiate
an income withholding order for
support and give notice of income
withholding. State child support
agencies are required to have automated
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Frm 00032
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Sfmt 4703
data processing systems containing
current order and case information.
State child support agencies providing
services to custodial and/or
noncustodial parties enter the terms of
a child support order established by a
tribunal into the state’s automated
system, which automatically populates
the order information into the IWO
form.
Employers and income providers also
use the form to respond to the order/
notice with termination or income
status information. Employers and other
income providers may choose to receive
the IWO form from child support
agencies on paper or electronically, and
may respond on paper or electronically
to notify the sender of termination of
employment or change in the income
status.
The information collection activities
pertaining to the IWO form are
authorized by 42 U.S.C. 666(a)(1), (a)(8),
and 666(b)(6), which require the use of
the IWO form to order income
withholding for all child support orders.
Respondents: Courts, private
attorneys, custodial parties or their
representatives, employers, and other
parties that provide income to
noncustodial parents.
E:\FR\FM\15JNN1.SGM
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]]>Agencies
[Federal Register Volume 85, Number 115 (Monday, June 15, 2020)]
[Notices]
[Pages 36214-36215]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-12810]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-20-0909; Docket No. CDC-2020-0070]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing effort to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies the opportunity to comment on a continuing information
collection, as required by the Paperwork Reduction Act of 1995. This
notice invites comment on CDC Diabetes Prevention Recognition Program
(DPRP). This collection allows CDC to administer the Diabetes
Prevention Recognition Program (DPRP) and collects information needed
by the Centers for Medicare & Medicaid Services (CMS) to support the
Medicare Expanded Model (Medicare Diabetes Prevention Program [MDPP]).
DATES: CDC must receive written comments on or before August 14, 2020.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2020-
0070 by any of the following methods:
Federal eRulemaking Portal: Regulations.gov. Follow the
instructions for submitting comments.
Mail: Jeffrey Zirger, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road
NE, MS-D74, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. CDC will post, without change, all relevant comments
to Regulations.gov.
Please note: Submit all comments through the Federal eRulemaking
portal (regulations.gov) or by U.S. mail to the address listed above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact Jeffrey Zirger, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road
NE, MS-D74, Atlanta, Georgia 30329; phone: 404-639-7570; Email:
[email protected].
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3520), Federal agencies must obtain approval from
the Office of Management and Budget (OMB) for each collection of
information they conduct or sponsor. In addition, the PRA also requires
Federal agencies to provide a 60-day notice in the Federal Register
concerning each proposed collection of information, including each new
proposed collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to the OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
2. Evaluate the accuracy of the agency's estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and clarity of the information to
be collected; and
4. Minimize the burden of the collection of information on those
who are to respond, including through the use of appropriate automated,
electronic, mechanical, or other technological collection techniques or
other forms of information technology, e.g., permitting electronic
submissions of responses.
5. Assess information collection costs.
Proposed Project
CDC Diabetes Prevention Recognition Program (DPRP)--Revision--
National Center for Chronic Disease Prevention and Health Promotion
(NCCDPHP), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
CDC's Division of Diabetes Translation (DDT) established and
administers the National DPP's Diabetes Prevention Recognition Program
(DPRP), which recognizes organizations that deliver diabetes prevention
programs according to evidence-based requirements set forth in the
``Centers for Disease Control and Prevention Diabetes Prevention
Recognition Program Standards and Operating Procedures'' (DPRP
Standards). Additionally, the Centers for Medicare and Medicaid
Services (CMS) Medicare Diabetes Prevention Program (MDPP) expansion of
CDC's National DPP was announced in early 2016, when the Secretary of
Health and Human Services determined that the Diabetes Prevention
Program met the statutory criteria for inclusion in Medicare's expanded
list of healthcare services for beneficiaries (https://innovation.cms.gov/initiatives/medicare-diabetes-prevention-program/).
This is the first time a preventive service model from the CMS
Innovation (CMMI) Center has been expanded. After extensive testing of
the DPP model in 17 sites across the U.S. in 2014-2016, CMS proposed
the MDPP in Sections 1102 and 1871 of the Social Security Act (42
U.S.C. 1302 and 1395hh Sec. 424.59), authorizing CDC-recognized
organizations to prepare for enrollment as MDPP suppliers beginning in
January 2018 in order to bill CMS for these services. Only
organizations in good standing with the CDC DPRP are eligible as MDPP
suppliers. CDC continues to work with CMS to support the MDPP.
CDC requests an additional three years of OMB approval to continue
collecting the information needed to administer the DPRP and
information needed by CMS to support the MDPP benefit. Based on
experience with the DPRP from 2011-2020, including data analysis, and
feedback from applicant organizations and internal and external
partners, CDC plans to revise the DPRP Standards and the associated
information collection.
Key changes are a direct result of DPRP data analyses and
discussion with National DPP stakeholders, including those serving
vulnerable populations. Key changes allow for the optional collection
of Hemoglobin A1C levels, and for weight/physical activity minutes to
be combined (a new method), to determine Full recognition; the required
collection of Application Delivery Mode questions; revised
organizational type information; program enrollment motivation/
enrollment source information; adding Gender; and the removal of
Session ID.
Three data elements have been minimally revised and no other data
elements have been added to the one-time application form; and, three
elements have been revised, one has been deleted, and four have been
added
[[Page 36215]]
to the evaluation data elements, as per below:
Application Form:
(1) Delivery Mode--follow-up questions (revised)
(2) Class Type (revised)
(3) Organization Type (revised)
Evaluation Data Elements:
(4) Enrollment Motivation (new)
(5) Enrollment Source (new)
(6) Session ID (deleted)
(7) HBA1C Value (new)
(8) Participant's Gender (new)
During the period of this Revision, CDC estimates receipt of
approximately 300 DPRP application forms per year. The estimated burden
per one-time, up-front application response is one hour (annualized to
300 hours one-time across all new organizations). In addition, CDC
estimates receipt of semi-annual evaluation data submissions from the
same 300 additional organizations per year; estimated at two hours per
response. The total estimated average annualized evaluation burden to
respondents is 6,676 hours. This includes an estimate of the time
needed to extract and compile the required data records and fields from
an existing electronic database, review the data, create or enter a
data file in the required format (i.e., CSV file), and submit the data
file via the National DPP website for upload into the DPRP Data Portal.
The estimated burden per response is modest since the information
requested for DPRP recognition is routinely collected by most
organizations that deliver lifestyle change programs for their own
internal evaluation and possible insurance reimbursement purposes,
including Medicare under the MDPP benefit. Participation in the DPRP is
voluntary, data are de-identified, no Personally Identifiable
Information (PII) is collected by CDC, and there are no costs to
respondents other than their time. CDC is requesting a three-year
approval.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondent Form name respondents responses per response (in (in hours)
respondent hours)
----------------------------------------------------------------------------------------------------------------
Public sector organizations DPRP Application 90 1 1 90
that deliver type 2 diabetes Form. 290 2 2 1,160
prevention programs. DPRP Evaluation
Data.
Private sector organizations DPRP Application 210 1 1 210
that deliver type 2 diabetes Form. 1,304 2 2 5,216
prevention programs. DPRP Evaluation
Data.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 6,676
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2020-12810 Filed 6-12-20; 8:45 am]
BILLING CODE 4163-18-P
