Proposed Data Collection Submitted for Public Comment and Recommendations, 20165-20166 [2021-07836]
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20165
Federal Register / Vol. 86, No. 72 / Friday, April 16, 2021 / Notices
• Calculate percent positivity for testing
continuously
SimpleReport will allow the user,
after the administration of a test, to load
in patient data, data about the facility,
and data about the testing device. The
user can then use the application as a
part of their testing workflow to manage
their work. Information submitted to the
application will be sent to the
tests are reported on paper, on fax, or
are not reported at all.
SimpleReport will help public health
departments get faster, better data and
help them:
• Do contact tracing and case
investigation faster with positive
cases
• Identify outbreaks in the community
faster
appropriate State, Local, Territorial, or
Tribal Public Health Department. The
Health Department, as appropriate, may
share the anonymized data with CDC for
public health purposes.
CDC requests OMB approval for an
estimated 379,600 annual burden hours.
There is no cost to respondents other
than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
Testing Facility Users ....
Testing Facility Users ....
SimpleReport Use—User Training ......................
SimpleReport Use—Inputting Patient Data and
Test Result Reporting.
SimpleReport Use—Repeated Tests on Existing
Users.
Long-Term Program—User Training ...................
Long-Term Program—Inputting Patient Data and
Test Result Reporting.
Long-Term Program—Repeated Tests on Existing Users.
Testing Facility Users ....
Testing Facility Users ....
Testing Facility Users ....
Testing Facility Users ....
Total .......................
..............................................................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–07839 Filed 4–15–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60 Day–21–1265; Docket No. CDC–2021–
0040]
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 proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled the Chronic Disease SelfManagement Questionnaire. The
SUMMARY:
jbell on DSKJLSW7X2PROD with NOTICES
Number of
respondents
Type of respondent
VerDate Sep<11>2014
19:57 Apr 15, 2021
Jkt 253001
Frm 00052
Fmt 4703
Average
burden per
response
(hours)
Total burden
(hours)
10,000
10,000
1
1
10/60
6/60
1,600
1,000
10,000
12
6/60
12,000
250,000
250,000
1
1
10/60
6/60
40,000
25,000
250,000
12
6/60
300,000
........................
........................
........................
379,600
questionnaire used for this study will
assess Chronic Disease SelfManagement participant health
behaviors and overall health before and
after a six-week workshop.
DATES: CDC must receive written
comments on or before June 15, 2021.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2021–
0040 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. 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 M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS–
D74, Atlanta, Georgia 30329; phone:
404–639–7118; Email: omb@cdc.gov.
PO 00000
Average
number of
responses per
respondent
Sfmt 4703
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;
4. Minimize the burden of the
collection of information on those who
SUPPLEMENTARY INFORMATION:
E:\FR\FM\16APN1.SGM
16APN1
20166
Federal Register / Vol. 86, No. 72 / Friday, April 16, 2021 / Notices
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; and
5. Assess information collection costs.
Proposed Project
Evaluation of the Chronic Disease
Self-Management Program in the US
Affiliated Pacific Islands (OMB Control
No. 0920–1265, Exp. 06/30/2021)—
Extension—National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
reported effects of the program on
program participants. Because this is the
first time CDSMP is being implemented
in the USAPI, we do not know if the
intervention, which has proven to
improve health outcomes in many
ethnic groups within the United States,
will lead to improved health outcomes
for these communities.
Collecting this data helps us assess
fidelity to and adaptations to the
intervention and to understand if
CDSMP, an evidence-based
intervention, has the same effect in the
US Affiliated Pacific Islands as it has in
multiple ethnic groups within the
United States. CDC requests OMB
approval for an estimated 95 annual
burden hours. There are no costs to
respondents other than their time.
Background and Brief Description
NCCDPHP is evaluating the
implementation of Stanford University’s
Chronic Disease Self-Management
Program (CDSMP) in the US Affiliated
Pacific Islands (USAPI). These
jurisdictions include American Samoa,
Guam, the Commonwealth of the
Northern Mariana Islands, the Republic
of Palau, the Republic of the Marshall
Islands, and the Federated States of
Micronesia.
The purpose of the evaluation is to
understand how CDSMP is being
implemented in the region, to identify
barriers and facilitators to
implementation, to monitor fidelity to
Stanford University’s model and
document adaptations to the
curriculum, and to understand the self-
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Average
burden per
response
(in hr)
Total burden
(in hr)
Form name
Program Participant ......
Chronic Disease Self-Management Workshop
Evaluation.
Chronic Disease Self-Management Questionnaire (Pre-Post Test).
190
1
10/60
32
190
2
10/60
63
..............................................................................
........................
........................
........................
95
Program Participant ......
Total .......................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–07836 Filed 4–15–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review; OPRE
Data Collection for Supporting Youth
To Be Successful in Life (SYSIL) (New
Collection)
Office of Planning, Research,
and Evaluation, Administration for
Children and Families, HHS.
ACTION: Request for public comment.
AGENCY:
The Administration for
Children and Families (ACF) is
requesting approval from the Office of
Management and Budget (OMB) for a
new data collection. The Supporting
Youth to be Successful in Life study
(SYSIL) will build evidence on how to
end homelessness among youth and
young adults with experience in the
child welfare system by continuing
work with an organization who
SUMMARY:
jbell on DSKJLSW7X2PROD with NOTICES
Number of
respondents
Type of respondent
VerDate Sep<11>2014
19:57 Apr 15, 2021
Jkt 253001
conducted foundational work as part of
the Youth At-Risk of Homelessness
project (OMB Control Number: 0970–
0445). SYSIL will provide important
information to the field by designing
and conducting a federally led
evaluation of a comprehensive service
model for youth at risk of homelessness.
DATES: Comments due within 30 days of
publication. OMB must make a decision
about the collection of 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 SYSIL evaluation
includes an implementation study and
an impact study, which will use a
rigorous quasi-experimental design that
includes a comparison group. This new
PO 00000
Frm 00053
Fmt 4703
Sfmt 4703
information collection request includes
the baseline and follow-up survey
instruments for the impact study (a
single instrument administered four
times), and discussion guides for
interviews and focus groups for the
implementation study. The data
collected from the baseline and followup surveys will be used to describe the
characteristics of the study sample of
youth, develop models for estimating
program impacts, and determine
program effectiveness by comparing
outcomes between youth in the
treatment (youth receiving the Pathways
program) and control groups. Data from
the interviews and focus groups will
provide a detailed understanding of
program implementation. We will also
conduct brief check-ins with program
directors using a subset of questions
from the interview guides to collect
information on services provided at two
additional points in time. The study
will also use administrative data from
the child welfare system, homelessness
management information system, and
program providers. Administrative data
will be used in its existing format and
does not impose any new information
collection or recordkeeping
requirements on respondents.
E:\FR\FM\16APN1.SGM
16APN1
]]>Agencies
[Federal Register Volume 86, Number 72 (Friday, April 16, 2021)]
[Notices]
[Pages 20165-20166]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-07836]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60 Day-21-1265; Docket No. CDC-2021-0040]
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 proposed and/or
continuing information collection, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on a proposed
information collection project titled the Chronic Disease Self-
Management Questionnaire. The questionnaire used for this study will
assess Chronic Disease Self-Management participant health behaviors and
overall health before and after a six-week workshop.
DATES: CDC must receive written comments on or before June 15, 2021.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2021-
0040 by any of the following methods:
Federal eRulemaking Portal: Regulations.gov. Follow the
instructions for submitting comments.
Mail: Jeffrey M. 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 M. Zirger, Information Collection
Review Office, Centers for Disease Control and Prevention, 1600 Clifton
Road NE, MS-D74, Atlanta, Georgia 30329; phone: 404-639-7118; 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;
4. Minimize the burden of the collection of information on those
who
[[Page 20166]]
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; and
5. Assess information collection costs.
Proposed Project
Evaluation of the Chronic Disease Self-Management Program in the US
Affiliated Pacific Islands (OMB Control No. 0920-1265, Exp. 06/30/
2021)--Extension--National Center for Chronic Disease Prevention and
Health Promotion (NCCDPHP), Centers for Disease Control and Prevention
(CDC).
Background and Brief Description
NCCDPHP is evaluating the implementation of Stanford University's
Chronic Disease Self-Management Program (CDSMP) in the US Affiliated
Pacific Islands (USAPI). These jurisdictions include American Samoa,
Guam, the Commonwealth of the Northern Mariana Islands, the Republic of
Palau, the Republic of the Marshall Islands, and the Federated States
of Micronesia.
The purpose of the evaluation is to understand how CDSMP is being
implemented in the region, to identify barriers and facilitators to
implementation, to monitor fidelity to Stanford University's model and
document adaptations to the curriculum, and to understand the self-
reported effects of the program on program participants. Because this
is the first time CDSMP is being implemented in the USAPI, we do not
know if the intervention, which has proven to improve health outcomes
in many ethnic groups within the United States, will lead to improved
health outcomes for these communities.
Collecting this data helps us assess fidelity to and adaptations to
the intervention and to understand if CDSMP, an evidence-based
intervention, has the same effect in the US Affiliated Pacific Islands
as it has in multiple ethnic groups within the United States. CDC
requests OMB approval for an estimated 95 annual burden hours. There
are no costs to respondents other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondent Form name respondents responses per response (in (in hr)
respondent hr)
----------------------------------------------------------------------------------------------------------------
Program Participant........... Chronic Disease 190 1 10/60 32
Self-Management
Workshop
Evaluation.
Program Participant........... Chronic Disease 190 2 10/60 63
Self-Management
Questionnaire
(Pre-Post Test).
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 95
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2021-07836 Filed 4-15-21; 8:45 am]
BILLING CODE 4163-18-P
