Proposed Data Collection Submitted for Public Comment and Recommendations, 4917-4918 [2018-02134]
Download as PDF
Federal Register / Vol. 83, No. 23 / Friday, February 2, 2018 / Notices
must be received not later than February
23, 2018.
A. Federal Reserve Bank of
Minneapolis (Mark A. Rauzi, Vice
President) 90 Hennepin Avenue,
Minneapolis, Minnesota 55480–0291:
1. The Lloyd A. Amundson 1999
Generational Trust, Sioux Falls, South
Dakota, Trustees, Angela R. Mixner,
Worthington, Minnesota & Matt W.
Amundson, Hendricks, Minnesota; the
Barbara A. Amundson 1999
Generational Trust, Sioux Falls, South
Dakota, Trustees, Angela R. Mixner and
Matt W. Amundson; and Jane A.
Harberts, Rochester, Minnesota; to
retain or acquire shares of First Sleepy
Eye Bancorporation, Inc., Sioux Falls,
South Dakota, and thereby acquire/
retain shares of First Security Bank of
Sleepy Eye, Sleepy Eye, Minnesota, and
First Security Bank of Canby, Canby,
Minnesota.
In addition, Philip G. Amundson,
Sheridan, Wyoming, Krista B. Ryan,
Byron, Minnesota; the B.A. Amundson
Generational Trust fbo-Jane A. Harberts,
Sioux Falls, South Dakota, Trustees,
Jane A. Harberts and Krista B. Ryan;
and the B.A. Amundson Generational
Trust fbo-Philip G. Amundson, Sioux
Falls, South Dakota, Trustees, Angela R.
Mixner and Matt W. Amundson, acting
in concert, have applied to acquire
shares of First Sleepy Eye
Bancorporation, Inc.
Board of Governors of the Federal Reserve
System, January 30, 2018.
Ann E. Misback,
Secretary of the Board.
[FR Doc. 2018–02122 Filed 2–1–18; 8:45 am]
BILLING CODE P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–18–18FJ; Docket No. CDC–2018–
0011]
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.
sradovich on DSK3GMQ082PROD with NOTICES
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
SUMMARY:
VerDate Sep<11>2014
18:03 Feb 01, 2018
Jkt 244001
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 Evaluation of the Chronic Disease
Self-Management in the US Affiliated
Pacific Islands. This project will assess
participant satisfaction, health behavior,
and overall health before and after a sixweek Chronic Disease Self-Management
workshop.
DATES: CDC must receive written
comments on or before April 3, 2018.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2018–
00011 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Leroy A. Richardson,
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 Leroy A.
Richardson, 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:
PO 00000
Frm 00024
Fmt 4703
Sfmt 4703
4917
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
Evaluation of the Chronic Disease
Self-Management Program in the US
Affiliated Pacific Islands—New—
National Center for Chronic Disease
Prevention and Health Promotion
(NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
NCCDPHP plans to evaluate the first
ever implementation of Stanford
University’s Chronic Disease SelfManagement Program (CDSMP) in the
US Affiliated Pacific Islands (USAPIs).
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 selfreported effects of the program on
program participants.
Evaluating the implementation of
CDSMP in the Pacific is important
because there is a lack of evidencebased chronic disease prevention and
management programs in the USAPIs.
CDSMP has proven to improve health
outcomes in many ethnic groups within
the United States, however, we are
unsure whether the same health
outcomes will be achieved within the
USAPIs. The data collected for this
evaluation will help the CDC assess the
effect of CDSMP on health outcomes in
E:\FR\FM\02FEN1.SGM
02FEN1
4918
Federal Register / Vol. 83, No. 23 / Friday, February 2, 2018 / Notices
the USAPIs and to understand whether
the CDSMP curriculum needs to be
adapted to meet the cultural needs of
the USAPIs and if it is feasible to
expand the CDSMP program in the
USAPIs.
In this evaluation, program
participants (people who are enrolled in
six-week CDSMP workshops) will be
asked to fill out the following voluntary
surveys:
• Chronic Disease Self-Management
Workshop Evaluation Form: This is a
survey to assess program participant
satisfaction with CDSMP. The survey
will be administered once at the end of
the six-week CDSMP workshop.
• Chronic Disease Self-Management
Questionnaire: This is a pre- and posttest for program participants to assess
chronic disease related symptoms and
health behaviors before CDSMP and at
the end of the six-week workshop. The
survey will be administered once at the
start of the six-week workshop and once
at the end of the six-week workshop.
coordinator, and the program assistant.
The server will have a firewall. Data
will be aggregated and the aggregated
data will be used and shared with
stakeholders.
Data will not be collected from
participants electronically because
computers and other electronic data
collection methods will not be available
at the six-week workshops.
The information collection will
involve approximately 190 respondents
for a total cost of $19,501. The estimated
cost to participants is $570. There are a
total of three responses, or three
surveys, per respondent. Each response
will take 10 minutes to complete. The
estimated time burden is 95 hours. We
do not anticipate capital and start-up
costs to respondents and record keepers.
We expect an operation and
maintenance cost for record keepers,
who will print surveys and provide
pens for program participants to fill out
the survey, which will cost $11.40 for
paper and $25 for pens.
The pre-test surveys and the post-test
survey results will be compared.
Program participants will voluntarily
complete three surveys over the course
of the six-week CDSMP workshop. We
anticipate collecting surveys over a
three-year period, or 36 months.
The CDC will provide CDSMP leaders
in the USAPIs with surveys. CDSMP
leaders will administer the voluntary
paper-based surveys to participants
during the workshops, collect the
surveys, and submit the surveys to the
CDC.
CDSMP leaders will store surveys in
a locked cabinet only accessible to
them. They will scan the survey in a
secure location on a dedicated server
only accessible to the CDSMP leader.
The server will have a firewall. CDSMP
leaders will encrypt and submit
electronic copies of the survey to the
CDC.
CDC will maintain the surveys and
abstracted data in secure location on a
dedicated server only accessible by the
evaluation staff, the program
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
(in hours)
Type of respondents
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 ........................
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2018–02134 Filed 2–1–18; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Substance Abuse and Mental Health
Services Administration
sradovich on DSK3GMQ082PROD with NOTICES
Agency Information Collection
Activities: Proposed Collection;
Comment Request
In compliance with Section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 concerning
opportunity for public comment on
proposed collections of information, the
Substance Abuse and Mental Health
Services Administration (SAMHSA)
will publish periodic summaries of
VerDate Sep<11>2014
18:03 Feb 01, 2018
Jkt 244001
proposed projects. To request more
information on the proposed projects or
to obtain a copy of the information
collection plans, call the SAMHSA
Reports Clearance Officer on (240) 276–
1243.
Comments are invited on: (a) Whether
the proposed collections of information
are necessary for the proper
performance of the functions of the
agency, including whether the
information shall have practical utility;
(b) the accuracy of the agency’s estimate
of the burden of the proposed collection
of information; (c) ways to enhance the
quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
PO 00000
Frm 00025
Fmt 4703
Sfmt 4703
Proposed Project: Networking Suicide
Prevention Hotlines—Evaluation of
Imminent Risk (OMB No. 0930–0333)—
Revision
The Substance Abuse and Mental
Health Services Administration’s
(SAMHSA), Center for Mental Health
Services (CMHS) funds a National
Suicide Prevention Lifeline Network
(‘‘Lifeline’’), consisting of a toll–free
telephone number that routes calls from
anywhere in the United States to a
network of local crisis centers. In turn,
the local centers link callers to local
emergency, mental health, and social
service resources. This project is a
revision of the Evaluation of Imminent
Risk and builds on previously approved
data collection activities [Evaluation of
Networking Suicide Prevention Hotlines
Follow–Up Assessment (OMB No.
0930–0274) and Call Monitoring of
National Suicide Prevention Lifeline
Form (OMB No. 0930–0275)]. The
extension data collection is an effort to
advance the understanding of crisis
hotline utilization and its impact.
E:\FR\FM\02FEN1.SGM
02FEN1
Agencies
[Federal Register Volume 83, Number 23 (Friday, February 2, 2018)]
[Notices]
[Pages 4917-4918]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-02134]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-18-18FJ; Docket No. CDC-2018-0011]
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 Evaluation of the Chronic Disease
Self-Management in the US Affiliated Pacific Islands. This project will
assess participant satisfaction, health behavior, and overall health
before and after a six-week Chronic Disease Self-Management workshop.
DATES: CDC must receive written comments on or before April 3, 2018.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2018-
00011 by any of the following methods:
Federal eRulemaking Portal: Regulations.gov. Follow the
instructions for submitting comments.
Mail: Leroy A. Richardson, 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 Leroy A. Richardson, 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
Evaluation of the Chronic Disease Self-Management Program in the US
Affiliated Pacific Islands--New--National Center for Chronic Disease
Prevention and Health Promotion (NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
NCCDPHP plans to evaluate the first ever implementation of Stanford
University's Chronic Disease Self-Management Program (CDSMP) in the US
Affiliated Pacific Islands (USAPIs). 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.
Evaluating the implementation of CDSMP in the Pacific is important
because there is a lack of evidence-based chronic disease prevention
and management programs in the USAPIs. CDSMP has proven to improve
health outcomes in many ethnic groups within the United States,
however, we are unsure whether the same health outcomes will be
achieved within the USAPIs. The data collected for this evaluation will
help the CDC assess the effect of CDSMP on health outcomes in
[[Page 4918]]
the USAPIs and to understand whether the CDSMP curriculum needs to be
adapted to meet the cultural needs of the USAPIs and if it is feasible
to expand the CDSMP program in the USAPIs.
In this evaluation, program participants (people who are enrolled
in six-week CDSMP workshops) will be asked to fill out the following
voluntary surveys:
Chronic Disease Self-Management Workshop Evaluation Form:
This is a survey to assess program participant satisfaction with CDSMP.
The survey will be administered once at the end of the six-week CDSMP
workshop.
Chronic Disease Self-Management Questionnaire: This is a
pre- and post-test for program participants to assess chronic disease
related symptoms and health behaviors before CDSMP and at the end of
the six-week workshop. The survey will be administered once at the
start of the six-week workshop and once at the end of the six-week
workshop. The pre-test surveys and the post-test survey results will be
compared.
Program participants will voluntarily complete three surveys over
the course of the six-week CDSMP workshop. We anticipate collecting
surveys over a three-year period, or 36 months.
The CDC will provide CDSMP leaders in the USAPIs with surveys.
CDSMP leaders will administer the voluntary paper-based surveys to
participants during the workshops, collect the surveys, and submit the
surveys to the CDC.
CDSMP leaders will store surveys in a locked cabinet only
accessible to them. They will scan the survey in a secure location on a
dedicated server only accessible to the CDSMP leader. The server will
have a firewall. CDSMP leaders will encrypt and submit electronic
copies of the survey to the CDC.
CDC will maintain the surveys and abstracted data in secure
location on a dedicated server only accessible by the evaluation staff,
the program coordinator, and the program assistant. The server will
have a firewall. Data will be aggregated and the aggregated data will
be used and shared with stakeholders.
Data will not be collected from participants electronically because
computers and other electronic data collection methods will not be
available at the six-week workshops.
The information collection will involve approximately 190
respondents for a total cost of $19,501. The estimated cost to
participants is $570. There are a total of three responses, or three
surveys, per respondent. Each response will take 10 minutes to
complete. The estimated time burden is 95 hours. We do not anticipate
capital and start-up costs to respondents and record keepers. We expect
an operation and maintenance cost for record keepers, who will print
surveys and provide pens for program participants to fill out the
survey, which will cost $11.40 for paper and $25 for pens.
Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response Total burden
respondents respondent (in hours) (in hours)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Program Participant............................ Chronic Disease Self-Management 190 1 10/60 32
Workshop Evaluation.
Program Participant............................ Chronic Disease Self-Management 190 2 10/60 63
Questionnaire (Pre-Post Test).
--------------------------------------------------------------------------------------------------------
Total...................................... ....................................... .............. .............. .............. 95
--------------------------------------------------------------------------------------------------------------------------------------------------------
Leroy A. Richardson,
Chief, Information Collection Review Office, Office of Scientific
Integrity, Office of the Associate Director for Science, Office of the
Director, Centers for Disease Control and Prevention.
[FR Doc. 2018-02134 Filed 2-1-18; 8:45 am]
BILLING CODE 4163-18-P