Proposed Data Collection Submitted for Public Comment and Recommendations, 52301-52302 [2017-24523]
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52301
Federal Register / Vol. 82, No. 217 / Monday, November 13, 2017 / Notices
test the updated Scorecard in year one
and create a finalized version of the
instrument based on respondent
feedback gathered during the pilot. After
the completion of the pilot test, CDC
will submit a finalized instrument as a
revision request for a three-year
clearance.
Participation in the CDC Worksite
Health Scorecard is voluntary and there
are no costs to respondents other than
their time. The total estimated
annualized burden hours are 303.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of
respondent
Employer pilot .........................
CDC
CDC
CDC
CDC
Worksite
Worksite
Worksite
Worksite
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. 2017–24472 Filed 11–9–17; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–18–18AG; Docket No. CDC–2017–
0095]
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.
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed work and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on the Evaluation of the
Cancer Survivorship Demonstration
Project. This information collection
aims to help CDC better understand
strategies and best practices to identify
and address current cancer survivorship
needs and gaps.
DATES: CDC must receive written
comments on or before January 12,
2018.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2017–
0095 by any of the following methods:
asabaliauskas on DSKBBXCHB2PROD with NOTICES
SUMMARY:
18:38 Nov 09, 2017
Jkt 244001
Health
Health
Health
Health
Scorecard
Scorecard
Scorecard
Scorecard
Registration Application ....
...........................................
Cognitive interview ............
Pilot evaluation ..................
• 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.
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.
FOR FURTHER INFORMATION CONTACT:
AGENCY:
VerDate Sep<11>2014
Number of
respondents
Form name
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.
PO 00000
Frm 00038
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
200
200
32
200
1
1
1
1
Average
burden per
response
(in hours)
2/60
1.25
1
5/60
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 Cancer Survivorship
Demonstration Project—New—National
Center for Chronic Disease Prevention
and Health Promotion (NCCDPHP),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Under CDC’s National Comprehensive
Cancer Control Program (NCCCP)
Request for Applications DP5–1501, the
Division of Cancer Prevention and
Control (DCPC) funded six grantees to
implement evidence-based and
promising strategies to increase
knowledge of cancer survivor needs,
increase survivor knowledge of
treatment and follow-up care, and
increase provider knowledge of
guidelines pertaining to treatment of
cancer. Specifically, this initiative
employs strategies that relate to
increasing surveillance and community-
E:\FR\FM\13NON1.SGM
13NON1
52302
Federal Register / Vol. 82, No. 217 / Monday, November 13, 2017 / Notices
clinical linkages. Through this
initiative, DCPC intends to help address
the public health needs of cancer
survivors. To facilitate evidenceinformed policymaking and quality
improvement of federal programs, CDC
needs a comprehensive evaluation to
characterize survivorship interventions
and document outcomes.
CDC seeks to request OMB approval
to collect information needed for this
evaluation. The proposed information
collection will focus on how each
grantee has expanded their knowledge
of cancer survivor needs, increased
utilization of surveillance data to inform
program planning by providers and
coalition members, and enhanced
partnerships to facilitate and broaden
program reach. CDC will also collect
data on challenges encountered and
addressed, factors that facilitated
implementation, and lessons learned
along the way. The requested
information does not currently exist for
organizations and entities working to
improve cancer survivorship needs.
With this data, CDC will gain critical
insights for improving achieving
immediate strategic efforts and goals to
improve the public health needs of
cancer survivors.
CDC plans to collect information
during two cycles of the program using
a Web-based Grantee survey of NCCCP
DP15–1501 grantee program directors
and program managers, a Web-based
Partner Survey of grantees’ self-
CDC intends to also seek OMB
approval to conduct semi-structured
interviews by telephone with a
purposive sample of one program
director and one program manager for
each of the six grantee sites (12
respondents total). CDC will conduct
the semi-structured interviews with the
same respondents at two time points for
a total estimated burden of 36 hours.
CDC will ask the respondents to
provide information on the following:
(1) Administration of the Behavioral
Risk Factor Surveillance System Cancer
Survivorship Module; (2)
communication, education, and training
activities to support the implementation
of cancer survivorship interventions; (3)
community clinical linkage strategies to
support cancer survivors, knowledge
regarding best practices for survivorship
care; partnership engagement; (4)
dissemination of evidence-based
survivorship interventions; and (5)
recommendations for improving the
implementation of evidence-based
survivorship interventions.
CDC will analyze the collected
information and use in aggregate to
inform future efforts to support cancer
survivors and to initiate evidenceinformed program decisions when
rolling this initiative out to all NCCCP
grantees. Without this data collection,
CDC will not be able to provide tailored
technical assistance to its grantees and
communicate program efforts.
identified key partners (e.g., coalition
members, providers, patient navigators),
and semi-structured telephone
interviews with NCCCP DP15–1501
grantee program directors and program
managers. The data from the survey and
semi-structured interviews will provide
additional insight into program efforts.
CDC is requesting OMB approval to
conduct a Web-based Grantee survey
using Survey Gizmo to a purposive
sample of one program director and one
program manager for each of the six
grantee sites (12 respondents total) and
to conduct a Web-based Partner Survey
of 10 self-identified key partners in each
of 6 grantees for a total of 60
respondents. CDC will administer the
Web-based surveys to the same
respondents at two time points for a
total estimated burden of 8 hours for the
Web-based Grantee Survey and 40 hours
for the Web-based Partner Survey.
CDC will ask the respondents to
provide information regarding the type
of respondent; their use of surveillance
data to inform survivorship
interventions; communication,
education, and training activities to
support the implementation of
survivorship interventions; partnership
engagement; challenges and facilitators
regarding the implementation of
evidence-based cancer survivorship
strategies; reach of cancer survivorship
interventions; and respondent
background information.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Average
burden per
response
(in hours)
Number of
responses per
respondent
Total burden
(in hours)
Type of respondent
Form name
NCCCP Grantee Program Director ..
NCCCP Grantee Partner ..................
Web-based Grantee survey .............
Semi-structured telephone interview
Web-based Partner survey ..............
12
12
60
2
2
2
20/60
1.50
20/60
8
36
40
Total ...........................................
...........................................................
........................
........................
........................
84
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.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2017–24523 Filed 11–9–17; 8:45 am]
[60Day–17–17AUZ; Docket No. CDC–2017–
0065]
asabaliauskas on DSKBBXCHB2PROD with NOTICES
BILLING CODE 4163–18–P
Centers for Disease Control and
Prevention
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:
VerDate Sep<11>2014
18:38 Nov 09, 2017
Jkt 244001
PO 00000
Frm 00039
Fmt 4703
Sfmt 4703
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 to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on ‘‘Project NICE: Navigating
Insurance Coverage Expansion’’. Project
NICE will evaluate the efficacy of an inperson health insurance enrollment
assistance intervention among Black
and Hispanic men who have sex with
SUMMARY:
E:\FR\FM\13NON1.SGM
13NON1
]]>Agencies
[Federal Register Volume 82, Number 217 (Monday, November 13, 2017)]
[Notices]
[Pages 52301-52302]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-24523]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-18-18AG; Docket No. CDC-2017-0095]
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 efforts to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies to take this opportunity to comment on proposed work
and/or continuing information collections, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on the Evaluation of
the Cancer Survivorship Demonstration Project. This information
collection aims to help CDC better understand strategies and best
practices to identify and address current cancer survivorship needs and
gaps.
DATES: CDC must receive written comments on or before January 12, 2018.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2017-
0095 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:
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 Cancer Survivorship Demonstration Project--New--
National Center for Chronic Disease Prevention and Health Promotion
(NCCDPHP), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
Under CDC's National Comprehensive Cancer Control Program (NCCCP)
Request for Applications DP5-1501, the Division of Cancer Prevention
and Control (DCPC) funded six grantees to implement evidence-based and
promising strategies to increase knowledge of cancer survivor needs,
increase survivor knowledge of treatment and follow-up care, and
increase provider knowledge of guidelines pertaining to treatment of
cancer. Specifically, this initiative employs strategies that relate to
increasing surveillance and community-
[[Page 52302]]
clinical linkages. Through this initiative, DCPC intends to help
address the public health needs of cancer survivors. To facilitate
evidence-informed policymaking and quality improvement of federal
programs, CDC needs a comprehensive evaluation to characterize
survivorship interventions and document outcomes.
CDC seeks to request OMB approval to collect information needed for
this evaluation. The proposed information collection will focus on how
each grantee has expanded their knowledge of cancer survivor needs,
increased utilization of surveillance data to inform program planning
by providers and coalition members, and enhanced partnerships to
facilitate and broaden program reach. CDC will also collect data on
challenges encountered and addressed, factors that facilitated
implementation, and lessons learned along the way. The requested
information does not currently exist for organizations and entities
working to improve cancer survivorship needs. With this data, CDC will
gain critical insights for improving achieving immediate strategic
efforts and goals to improve the public health needs of cancer
survivors.
CDC plans to collect information during two cycles of the program
using a Web-based Grantee survey of NCCCP DP15-1501 grantee program
directors and program managers, a Web-based Partner Survey of grantees'
self-identified key partners (e.g., coalition members, providers,
patient navigators), and semi-structured telephone interviews with
NCCCP DP15-1501 grantee program directors and program managers. The
data from the survey and semi-structured interviews will provide
additional insight into program efforts.
CDC is requesting OMB approval to conduct a Web-based Grantee
survey using Survey Gizmo to a purposive sample of one program director
and one program manager for each of the six grantee sites (12
respondents total) and to conduct a Web-based Partner Survey of 10
self-identified key partners in each of 6 grantees for a total of 60
respondents. CDC will administer the Web-based surveys to the same
respondents at two time points for a total estimated burden of 8 hours
for the Web-based Grantee Survey and 40 hours for the Web-based Partner
Survey.
CDC will ask the respondents to provide information regarding the
type of respondent; their use of surveillance data to inform
survivorship interventions; communication, education, and training
activities to support the implementation of survivorship interventions;
partnership engagement; challenges and facilitators regarding the
implementation of evidence-based cancer survivorship strategies; reach
of cancer survivorship interventions; and respondent background
information.
CDC intends to also seek OMB approval to conduct semi-structured
interviews by telephone with a purposive sample of one program director
and one program manager for each of the six grantee sites (12
respondents total). CDC will conduct the semi-structured interviews
with the same respondents at two time points for a total estimated
burden of 36 hours.
CDC will ask the respondents to provide information on the
following: (1) Administration of the Behavioral Risk Factor
Surveillance System Cancer Survivorship Module; (2) communication,
education, and training activities to support the implementation of
cancer survivorship interventions; (3) community clinical linkage
strategies to support cancer survivors, knowledge regarding best
practices for survivorship care; partnership engagement; (4)
dissemination of evidence-based survivorship interventions; and (5)
recommendations for improving the implementation of evidence-based
survivorship interventions.
CDC will analyze the collected information and use in aggregate to
inform future efforts to support cancer survivors and to initiate
evidence-informed program decisions when rolling this initiative out to
all NCCCP grantees. Without this data collection, CDC will not be able
to provide tailored technical assistance to its grantees and
communicate program efforts.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form name Number of responses per per response Total burden
respondents respondent (in hours) (in hours)
----------------------------------------------------------------------------------------------------------------
NCCCP Grantee Program Director Web-based 12 2 20/60 8
Grantee survey.
Semi-structured 12 2 1.50 36
telephone
interview.
NCCCP Grantee Partner......... Web-based 60 2 20/60 40
Partner survey.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 84
----------------------------------------------------------------------------------------------------------------
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. 2017-24523 Filed 11-9-17; 8:45 am]
BILLING CODE 4163-18-P
