Agency Forms Undergoing Paperwork Reduction Act Review, 5666-5667 [2020-01855]
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Federal Register / Vol. 85, No. 21 / Friday, January 31, 2020 / Notices
clearance for an extension of the generic
clearance information collection request
(Generic ICR) titled ‘‘Poison Center
Collaborations for Public Health
Emergencies’’ (OMB Control No. 0920–
1166, expiration date 02/29/2020).
CDC’s key partner, the American
Association of Poison Control Centers
(AAPCC), is a national network of 55
poison centers working to prevent and
treat poison exposures. The goal for this
Generic ICR is to continue to provide a
timely mechanism to allow poison
centers, in collaboration with CDC, to
obtain critical exposure and health
information during public health
emergencies. This information is not
captured during initial poison center
calls about triage and treatment of
potential poison exposures. Additional
data collections are needed quickly to
further characterize exposures, risk
factors, and illnesses.
When a public health emergency of
interest to CDC and AAPCC occurs, the
CDC and AAPCC hold a meeting to
mutually decide whether the incident
needs further investigation. For a public
health emergency to be selected for callback, adverse health effects must have
occurred, and a response is needed to
prevent further morbidity and mortality.
The event must meet the criteria below:
(1) The event is a public health
emergency causing adverse health
effects.
(2) Timely data are urgently needed to
inform rapid public health action to
prevent or reduce injury, disease, or
death.
(3) The event is characterized by a
natural or man-made disaster,
contaminated food or water, a new or
existing consumer product, or an
emerging public health threat.
(4) The event has resulted in calls to
a poison center, and the poison center
agrees to conduct the call-back data
collection.
(5) The event is domestic.
(6) Data collection will be completed
in 60 days or less.
Trained poison center staff will
conduct the call-back telephone survey,
after administering consent.
Respondents will include individuals
who call poison centers about exposures
related to the select public health
emergencies. These respondents include
adults, 18 years and older; adolescents,
15 to less than 18 years; and parents or
guardians on behalf of their children
less than 15 years of age.
The total estimate of 300 annual
respondents is based on poison center
experience which assumes two
incidents per year with approximately
150 respondents per event. The average
burden per respondent is approximately
40 minutes for the call-back
questionnaire. We anticipate a total
annualized burden of 200 hours. There
is no cost to the respondents other than
their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
Adult Poison Center Callers ...........................
Adolescent Poison Center Callers ..................
Parent or Guardian Poison Center Callers ....
Call-back Questionnaire for Self ....................
Call-back Questionnaire for Self ....................
Call-back Questionnaire for Proxy .................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–01861 Filed 1–30–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–20–19BHM]
Agency Forms Undergoing Paperwork
Reduction Act Review
jbell on DSKJLSW7X2PROD with NOTICES
Number of
respondents
Type of respondents
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled Understanding
the Needs of Ovarian Cancer Survivors
to the Office of Management and Budget
(OMB) for review and approval. CDC
previously published a ‘‘Proposed Data
Collection Submitted for Public
Comment and Recommendations’’
notice on July 5, 2019 to obtain
comments from the public and affected
agencies. CDC did not receive comments
VerDate Sep<11>2014
17:16 Jan 30, 2020
Jkt 250001
related to the previous notice. This
notice serves to allow an additional 30
days for public and affected agency
comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) 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;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) 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 submission of
responses; and
PO 00000
Frm 00056
Fmt 4703
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210
30
60
Number of
responses per
respondent
1
1
1
Average
burden per
response
(in hours)
40/60
40/60
40/60
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570 or
send an email to omb@cdc.gov. Direct
written comments and/or suggestions
regarding the items contained in this
notice to the Attention: CDC Desk
Officer, Office of Management and
Budget, 725 17th Street NW,
Washington, DC 20503 or by fax to (202)
395–5806. Provide written comments
within 30 days of notice publication.
Proposed Project
Understanding the Needs of Ovarian
Cancer Survivors—New—National
Center for Chronic Disease Prevention
and Health Promotion (NCCDPHP),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Ovarian cancer is the ninth most
common cancer and the fifth leading
cause of cancer death among women in
the United States. Over 20,000 women
are diagnosed with ovarian cancer each
year. Due to the lack of a recommended
screening test, ovarian cancer is often
E:\FR\FM\31JAN1.SGM
31JAN1
5667
Federal Register / Vol. 85, No. 21 / Friday, January 31, 2020 / Notices
diagnosed at late stages, leading to low
five-year survival rates. While previous
studies are able to identify some of the
needs of ovarian cancer survivors,
particularly related to physical
complications and side effects,
additional research is needed to further
understand the experiences and needs
of survivors.
The National Academies of Sciences,
Engineering, and Medicine released
their report, Ovarian Cancers: Evolving
Paradigms in Research and Care, which
identified key priorities for researchers,
including recommending research on
the ‘‘supportive care needs of ovarian
cancer survivors throughout the disease
trajectory’’. In order to address these
research gaps and supplement current
knowledge of the ongoing needs of
survivors, including how to implement
programs and interventions to improve
their health, CDC has supported a
survey of ovarian cancer survivors.
The goal of this project is to better
understand the needs of ovarian cancer
survivors and how to more effectively
develop interventions targeted to this
population. To achieve this goal,
multiple recruitment methods will be
utilized to recruit this unique
population of women for the study. By
using state cancer registries, social
media advertisements, and respondentdriven sampling (RDS), the study will
ensure recruitment of a diverse
population of women.
This study will focus on the following
research questions:
1. What physical and mental
conditions do ovarian cancer survivors
experience?
2. What kinds of pharmacologic and
non-pharmacologic interventions do
ovarian cancer survivors utilize to
manage their conditions?
3. What barriers to ovarian cancer
survivors have in accessing and
receiving appropriate diagnostic care,
treatment, and follow-up care?
4. What unmet needs do ovarian
cancer survivors have?
The overall sample design targets
1,500 completed interviews. We assume
that approximately 80% of completed
surveys will come from more traditional
sampling utilizing lists from the state
cancer registries (n=1,200). The
remainder of the completed interviews
will come through social media
outreach and respondent-driven
sampling (RDS) methods (n=300).
For the social media recruitment,
individuals will be recruited to
participate in the web survey through
advertisements posted on social media
sites. These ads are targeted toward the
specific population of women we wish
to complete the survey. Interested
respondents who click on an ad will be
routed to the survey landing page which
will explain the purpose of the study
and include consent language. If the
respondent is eligible, she will complete
the same survey as those recruited via
the state cancer registries.
Each recruitment method (registrybased or social media-based) will have
an opportunity to recruit other women
into the study through respondentdriven sampling (RDS). We anticipate
that the majority of completed
interviews will be obtained through
traditional sampling practices, RDS
provides an efficient way to identify
other potentially eligible respondents
through a networked-based recruitment
approach.
Participation is voluntary. There are
no costs to respondents other than their
time. The total estimated annual burden
hours are 1,253.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Average
burden per
response
(in hours)
Form name
Ovarian cancer survivors—state cancer registries.
Ovarian cancer survivors—social media recruitment.
Ovarian cancer survivors—Respondent Driven Sampling.
Ovarian cancer survivors recruited via social
medial and RDS (ineligible).
Mail-in or web-based questionnaire ...............
1,200
1
50/60
Web-based Questionnaire .............................
195
1
50/60
Web-based Questionnaire .............................
105
1
50/60
Web-based Screener Only .............................
100
1
2/60
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–01855 Filed 1–30–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
jbell on DSKJLSW7X2PROD with NOTICES
Number of
respondents
Type of respondents
[30Day–20–1163]
Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
VerDate Sep<11>2014
17:16 Jan 30, 2020
Jkt 250001
has submitted the information
collection request titled CDC Fellowship
Programs Assessments for data
collections associated with quality
improvement of CDC fellowship
programs to the Office of Management
and Budget (OMB) for review and
approval. CDC previously published a
‘‘Proposed Data Collection Submitted
for Public Comment and
Recommendations’’ notice on
September 25, 2019 to obtain comments
from the public and affected agencies.
CDC received two non-substantive
comments related to the previous
notice. This notice serves to allow an
additional 30 days for public and
affected agency comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
PO 00000
Frm 00057
Fmt 4703
Sfmt 4703
is particularly interested in comments
that:
(a) 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;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) 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
E:\FR\FM\31JAN1.SGM
31JAN1
]]>Agencies
[Federal Register Volume 85, Number 21 (Friday, January 31, 2020)]
[Notices]
[Pages 5666-5667]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-01855]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-20-19BHM]
Agency Forms Undergoing Paperwork Reduction Act Review
In accordance with the Paperwork Reduction Act of 1995, the Centers
for Disease Control and Prevention (CDC) has submitted the information
collection request titled Understanding the Needs of Ovarian Cancer
Survivors to the Office of Management and Budget (OMB) for review and
approval. CDC previously published a ``Proposed Data Collection
Submitted for Public Comment and Recommendations'' notice on July 5,
2019 to obtain comments from the public and affected agencies. CDC did
not receive comments related to the previous notice. This notice serves
to allow an additional 30 days for public and affected agency comments.
CDC will accept all comments for this proposed information
collection project. The Office of Management and Budget is particularly
interested in comments that:
(a) 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;
(b) Evaluate the accuracy of the agencies estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and clarity of the information to
be collected;
(d) 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 submission of responses; and
(e) Assess information collection costs.
To request additional information on the proposed project or to
obtain a copy of the information collection plan and instruments, call
(404) 639-7570 or send an email to [email protected]. Direct written comments
and/or suggestions regarding the items contained in this notice to the
Attention: CDC Desk Officer, Office of Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by fax to (202) 395-5806. Provide
written comments within 30 days of notice publication.
Proposed Project
Understanding the Needs of Ovarian Cancer Survivors--New--National
Center for Chronic Disease Prevention and Health Promotion (NCCDPHP),
Centers for Disease Control and Prevention (CDC).
Background and Brief Description
Ovarian cancer is the ninth most common cancer and the fifth
leading cause of cancer death among women in the United States. Over
20,000 women are diagnosed with ovarian cancer each year. Due to the
lack of a recommended screening test, ovarian cancer is often
[[Page 5667]]
diagnosed at late stages, leading to low five-year survival rates.
While previous studies are able to identify some of the needs of
ovarian cancer survivors, particularly related to physical
complications and side effects, additional research is needed to
further understand the experiences and needs of survivors.
The National Academies of Sciences, Engineering, and Medicine
released their report, Ovarian Cancers: Evolving Paradigms in Research
and Care, which identified key priorities for researchers, including
recommending research on the ``supportive care needs of ovarian cancer
survivors throughout the disease trajectory''. In order to address
these research gaps and supplement current knowledge of the ongoing
needs of survivors, including how to implement programs and
interventions to improve their health, CDC has supported a survey of
ovarian cancer survivors.
The goal of this project is to better understand the needs of
ovarian cancer survivors and how to more effectively develop
interventions targeted to this population. To achieve this goal,
multiple recruitment methods will be utilized to recruit this unique
population of women for the study. By using state cancer registries,
social media advertisements, and respondent-driven sampling (RDS), the
study will ensure recruitment of a diverse population of women.
This study will focus on the following research questions:
1. What physical and mental conditions do ovarian cancer survivors
experience?
2. What kinds of pharmacologic and non-pharmacologic interventions
do ovarian cancer survivors utilize to manage their conditions?
3. What barriers to ovarian cancer survivors have in accessing and
receiving appropriate diagnostic care, treatment, and follow-up care?
4. What unmet needs do ovarian cancer survivors have?
The overall sample design targets 1,500 completed interviews. We
assume that approximately 80% of completed surveys will come from more
traditional sampling utilizing lists from the state cancer registries
(n=1,200). The remainder of the completed interviews will come through
social media outreach and respondent-driven sampling (RDS) methods
(n=300).
For the social media recruitment, individuals will be recruited to
participate in the web survey through advertisements posted on social
media sites. These ads are targeted toward the specific population of
women we wish to complete the survey. Interested respondents who click
on an ad will be routed to the survey landing page which will explain
the purpose of the study and include consent language. If the
respondent is eligible, she will complete the same survey as those
recruited via the state cancer registries.
Each recruitment method (registry-based or social media-based) will
have an opportunity to recruit other women into the study through
respondent-driven sampling (RDS). We anticipate that the majority of
completed interviews will be obtained through traditional sampling
practices, RDS provides an efficient way to identify other potentially
eligible respondents through a networked-based recruitment approach.
Participation is voluntary. There are no costs to respondents other
than their time. The total estimated annual burden hours are 1,253.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per
Type of respondents Form name respondents responses per response (in
respondent hours)
----------------------------------------------------------------------------------------------------------------
Ovarian cancer survivors--state cancer Mail-in or web-based 1,200 1 50/60
registries. questionnaire.
Ovarian cancer survivors--social media Web-based Questionnaire. 195 1 50/60
recruitment.
Ovarian cancer survivors--Respondent Web-based Questionnaire. 105 1 50/60
Driven Sampling.
Ovarian cancer survivors recruited via Web-based Screener Only. 100 1 2/60
social medial and RDS (ineligible).
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2020-01855 Filed 1-30-20; 8:45 am]
BILLING CODE 4163-18-P
