Agency Forms Undergoing Paperwork Reduction Act Review, 11101-11102 [2019-05554]
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11101
Federal Register / Vol. 84, No. 57 / Monday, March 25, 2019 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Form name
Caller who contacts the Quitline on behalf of
someone else.
NQDW Intake Questionnaire (English-subset).
ASQ Intake Questionnaire (Chinese, Korean,
or Vietnamese-subset).
Submission of NQDW Intake Questionnaire
Electronic Data File to CDC.
Submission of NQDW (ASQ) Seven-Month
Follow-up Electronic Data File to CDC.
NQDW Quitline Services Survey ...................
Tobacco Control Manager or their Designee/
Quitline Service Provider.
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–05555 Filed 3–22–19; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–19–18AWP]
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 ‘‘Using social
media for recruitment in cancer
prevention and control survey-based
research (SMFR Study)’’ 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 18, 2018 to obtain comments
from the public and affected agencies.
CDC received five 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,
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18:13 Mar 22, 2019
Jkt 247001
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 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, Washington, DC 20503 or by fax
to (202) 395–5806. Written comments
should be received within 30 days of
notice publication.
Proposed Project
Using Social Media for Recruitment in
Cancer Prevention and Control SurveyBased Research—New—National Center
for Chronic Disease Prevention and
Health Promotion (NCCDPHP), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
This project involves formative
research to assess the feasibility of using
social media to conduct survey-based
cancer prevention and control research
for study recruitment. To achieve this
goal, the project will field four online
surveys for three distinct populations
using Facebook, Twitter, and Google ads
as tools for recruitment. Sampling bias
and ability to use weights, among other
statistical methods, to correct for
PO 00000
Frm 00057
Fmt 4703
Sfmt 4703
Number of
responses
per
respondent
Number of
respondents
Type of respondent
Average
burden per
respondent
(in hours)
12,217
1
1/60
86
1
1/60
54
4
1
1
1
1
54
4
20/60
potential bias will be assessed at the
conclusion of the study.
This project has two aims:
Aim 1: To develop and launch
surveys with three populations of
interest to cancer prevention and
control research using social media
platforms for study recruitment. This
will consist of using Facebook, Twitter,
and Google ads to recruit participants
from three groups: Cancer survivors,
those at high risk for cancer, and the
general population (for cancer
screening). Survey questions will be
taken from previously administered
national surveys, such as NHIS, HINTS,
and MEPS, in addition to questions
specially developed for this study.
Aim 2: To assess the extent of
sampling bias associated with surveys
using social media platforms and the
internet as frames for non-proportional
sampling and the ability to use weights
or other statistical methods to correct for
potential biases. Content for the social
media surveys will include questions
from nationally representative surveys
(such as the National Health Interview
Survey) to enable socio-demographic
and health history comparisons with
nationally representative populations.
In addition we will explore the ability
to use post-stratification weights,
propensity scores, or other statistical
methods to address issues of potential
sampling bias.
The first survey will target cancer
survivors and focus on general health
and well-being post-treatment. The
second survey will target the general
population, focusing on cancer
screening and access to care. The third
and fourth surveys will target those at
high risk for cancer focusing on
communication of genetic risk among
family members and the tools and
resources needed for risk
communication.
Individuals will be recruited to
participate in the web survey through
ads posted on social media sites
including Facebook, Twitter, and
E:\FR\FM\25MRN1.SGM
25MRN1
11102
Federal Register / Vol. 84, No. 57 / Monday, March 25, 2019 / Notices
Google Analytics. Self-reported data
provided on users’ profile pages may be
applied for targeting to maximize the
value of each ad.
• Ads for the survivorship survey will
be targeted toward users who ‘like’,
search, and/or visit web pages geared
toward survivors, such as the National
Cancer Survivors Day Facebook page.
Individuals will be screened for
eligibility until the target of up to 1,000
completes is met. It is expected that to
reach 1,000 eligible respondents for the
survivorship survey, 3,000 individuals
will need to be screened.
• Ads for the general population
survey will be targeted toward users
whose profiles indicate they are 40 or
older. Individuals will be screened for
eligibility until the target of up to 1,000
completes is met. It is expected that to
reach 1,000 eligible respondents for the
general population survey, 1,500
individuals will need to be screened.
• Ads for the high-risk survey will be
targeted toward users who ‘like’, visit,
or search for terms related to cancer and
genetic testing. Individuals will be
screened for eligibility until the target of
up to 1,000 completes is met. It is
expected that to reach 1,000 eligible
respondents for the high-risk survey,
2,000 individuals will need to be
screened.
• Eligible high-risk participants will
be invited via email to participate in the
follow-up high-risk survey. Additional
social media ads may also be placed,
using the targeting methods described
above. In order to survey 1,000 high-risk
adults, it is expected that an additional
4,000 individuals will be screened.
Participation in this project is
completely voluntary. There are no
costs to the respondents other than their
time. The total estimated annualized
burden is 1,567 hours.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondents
Form name
Adults at High Risk for Cancer .......................
Adults over 40 .................................................
Cancer Survivors ............................................
Adults at High Risk for Cancer .......................
Adults at High Risk for Cancer .......................
Adults over 40 .................................................
Cancer Survivors ............................................
Adults at High Risk for Cancer .......................
Survey Screener ............................................
Survey Screener ............................................
Survey Screener ............................................
Follow-Up Screener .......................................
High-Risk Survey ...........................................
General Population Survey ............................
Survivorship Survey .......................................
High-Risk Follow-Up Survey ..........................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–05554 Filed 3–22–19; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Clifton Road, NE, Mailstop: E–07,
Atlanta, Georgia, 30329–4027,
Telephone 404/639–8000; hdd0@
cdc.gov.
The Chief Operating Officer, Centers
for Disease Control and Prevention, has
been delegated the authority to sign
Federal Register notices pertaining to
announcements of meetings and other
committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Advisory Council for the Elimination of
Tuberculosis (ACET); Notice of Charter
Renewal
Sherri Berger,
Chief Operating Officer, Centers for Disease
Control and Prevention.
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice of charter renewal.
[FR Doc. 2019–05592 Filed 3–22–19; 8:45 am]
AGENCY:
This gives notice under the
Federal Advisory Committee Act of
October 6, 1972, that the Advisory
Council for the Elimination of
Tuberculosis Meeting (ACET), Centers
for Disease Control and Prevention,
Department of Health and Human
Services, has been renewed for a 2-year
period through March 15, 2021.
FOR FURTHER INFORMATION CONTACT:
Hazel Dean, ScD, DrPH (Hon), FACE,
Designated Federal Officer, Advisory
Council for the Elimination of
Tuberculosis (ACET), CDC, HHS, 1600
SUMMARY:
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BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Agency Information Collection
Activities; Submission for OMB
Review; the State Plan for Independent
Living (SPIL) (0985–0044)
Administration for Community
Living (ACL), HHS.
ACTION: Notice.
AGENCY:
The Administration for
Community Living (ACL) is announcing
SUMMARY:
PO 00000
Frm 00058
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
2,000
1,500
3,000
4,000
1,000
1,000
1,000
1,000
1
1
1
1
1
1
1
1
Average
burden per
response
(in hrs.)
2/60
2/60
2/60
2/60
19/60
22/60
15/60
17/60
that the proposed collection of
information listed above has been
submitted to the Office of Management
and Budget (OMB) for review and
clearance as required under the
Paperwork Reduction Act of 1995. This
30-Day notice collects comments on the
information collection requirements
related to State Plan for Independent
Living (SPIL) (Information Collection
Request Ext (ICR Ext)).
DATES: Comments on the information
collection request must be submitted
electronically by 11:59 p.m. (EST) or
postmarked by April 24, 2019.
ADDRESSES: Submit written comments
on the collection of information by:
(a) Email to: OIRA_submission@
omb.eop.gov, Attn: OMB Desk Officer
for ACL;
(b) fax to 202.395.5806, Attn: OMB
Desk Officer for ACL; or
(c) by mail to the Office of
Information and Regulatory Affairs,
OMB, New Executive Office Bldg., 725
17th St. NW, Rm. 10235, Washington,
DC 20503, Attn: OMB Desk Officer for
ACL.
FOR FURTHER INFORMATION CONTACT:
Peter Nye, Administration for
Community Living, Washington, DC
20201, (202) 795–7606 or peter.nye@
acl.hhs.gov.
In
compliance with 44 U.S.C. 3507, ACL
SUPPLEMENTARY INFORMATION:
E:\FR\FM\25MRN1.SGM
25MRN1
Agencies
[Federal Register Volume 84, Number 57 (Monday, March 25, 2019)]
[Notices]
[Pages 11101-11102]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-05554]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-19-18AWP]
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 ``Using social media for recruitment in
cancer prevention and control survey-based research (SMFR Study)'' 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 18, 2018 to obtain
comments from the public and affected agencies. CDC received five
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 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,
Washington, DC 20503 or by fax to (202) 395-5806. Written comments
should be received within 30 days of notice publication.
Proposed Project
Using Social Media for Recruitment in Cancer Prevention and Control
Survey-Based Research--New--National Center for Chronic Disease
Prevention and Health Promotion (NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
This project involves formative research to assess the feasibility
of using social media to conduct survey-based cancer prevention and
control research for study recruitment. To achieve this goal, the
project will field four online surveys for three distinct populations
using Facebook, Twitter, and Google ads as tools for recruitment.
Sampling bias and ability to use weights, among other statistical
methods, to correct for potential bias will be assessed at the
conclusion of the study.
This project has two aims:
Aim 1: To develop and launch surveys with three populations of
interest to cancer prevention and control research using social media
platforms for study recruitment. This will consist of using Facebook,
Twitter, and Google ads to recruit participants from three groups:
Cancer survivors, those at high risk for cancer, and the general
population (for cancer screening). Survey questions will be taken from
previously administered national surveys, such as NHIS, HINTS, and
MEPS, in addition to questions specially developed for this study.
Aim 2: To assess the extent of sampling bias associated with
surveys using social media platforms and the internet as frames for
non-proportional sampling and the ability to use weights or other
statistical methods to correct for potential biases. Content for the
social media surveys will include questions from nationally
representative surveys (such as the National Health Interview Survey)
to enable socio-demographic and health history comparisons with
nationally representative populations. In addition we will explore the
ability to use post-stratification weights, propensity scores, or other
statistical methods to address issues of potential sampling bias.
The first survey will target cancer survivors and focus on general
health and well-being post-treatment. The second survey will target the
general population, focusing on cancer screening and access to care.
The third and fourth surveys will target those at high risk for cancer
focusing on communication of genetic risk among family members and the
tools and resources needed for risk communication.
Individuals will be recruited to participate in the web survey
through ads posted on social media sites including Facebook, Twitter,
and
[[Page 11102]]
Google Analytics. Self-reported data provided on users' profile pages
may be applied for targeting to maximize the value of each ad.
Ads for the survivorship survey will be targeted toward
users who `like', search, and/or visit web pages geared toward
survivors, such as the National Cancer Survivors Day Facebook page.
Individuals will be screened for eligibility until the target of up to
1,000 completes is met. It is expected that to reach 1,000 eligible
respondents for the survivorship survey, 3,000 individuals will need to
be screened.
Ads for the general population survey will be targeted
toward users whose profiles indicate they are 40 or older. Individuals
will be screened for eligibility until the target of up to 1,000
completes is met. It is expected that to reach 1,000 eligible
respondents for the general population survey, 1,500 individuals will
need to be screened.
Ads for the high-risk survey will be targeted toward users
who `like', visit, or search for terms related to cancer and genetic
testing. Individuals will be screened for eligibility until the target
of up to 1,000 completes is met. It is expected that to reach 1,000
eligible respondents for the high-risk survey, 2,000 individuals will
need to be screened.
Eligible high-risk participants will be invited via email
to participate in the follow-up high-risk survey. Additional social
media ads may also be placed, using the targeting methods described
above. In order to survey 1,000 high-risk adults, it is expected that
an additional 4,000 individuals will be screened.
Participation in this project is completely voluntary. There are no
costs to the respondents other than their time. The total estimated
annualized burden is 1,567 hours.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response
respondents respondent (in hrs.)
----------------------------------------------------------------------------------------------------------------
Adults at High Risk for Cancer........ Survey Screener......... 2,000 1 2/60
Adults over 40........................ Survey Screener......... 1,500 1 2/60
Cancer Survivors...................... Survey Screener......... 3,000 1 2/60
Adults at High Risk for Cancer........ Follow-Up Screener...... 4,000 1 2/60
Adults at High Risk for Cancer........ High-Risk Survey........ 1,000 1 19/60
Adults over 40........................ General Population 1,000 1 22/60
Survey.
Cancer Survivors...................... Survivorship Survey..... 1,000 1 15/60
Adults at High Risk for Cancer........ High-Risk Follow-Up 1,000 1 17/60
Survey.
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2019-05554 Filed 3-22-19; 8:45 am]
BILLING CODE 4163-18-P