Agency Forms Undergoing Paperwork Reduction Act Review, 61409-61410 [2012-24766]
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61409
Federal Register / Vol. 77, No. 195 / Tuesday, October 9, 2012 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Number of
respondents
Type of respondent
Form name
Child MUH Residents in LA County ...............
MUH Residents in Minnesota, Maine and
Florida.
Resident Survey—Post Intervention: Core ....
Resident Survey—Post Intervention: Children’s Module.
Protocol for Saliva Collection (Adult) .............
Airborne Particle Monitoring Diary .................
Protocol for Saliva Collection (Child) .............
Resident Focus Group Telephone Screening
Interview Script.
Resident Pre-Focus Group Demographic and
Attitudinal Survey.
MUH Resident Focus Group Guide—Process Oriented.
MUH Resident Focus Group Guide—Outcome Oriented.
Dated: October 2, 2012.
Ron A. Otten,
Director, Office of Scientific Integrity (OSI)
Office of the Associate Director for Science
(OADS), Office of the Director, Centers for
Disease Control and Prevention.
Centers for Disease Control and
Prevention
delivery, the CDC has submitted a
Generic Information Collection Request
(Generic ICR): ‘‘Generic Clearance for
the Collection of Qualitative Feedback
on Agency Service Delivery ’’ to OMB
for approval under the Paperwork
Reduction Act (PRA) (44 U.S.C. 3501 et
seq.).
To request additional information,
please contact Kimberly S. Lane,
Reports Clearance Officer, Centers for
Disease Control and Prevention, 1600
Clifton Road, MS–D74, Atlanta, GA
30333 or send an email to omb@cdc.gov.
[30-Day–13–12SF]
SUPPLEMENTARY INFORMATION:
[FR Doc. 2012–24767 Filed 10–5–12; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency Forms Undergoing Paperwork
Reduction Act Review
wreier-aviles on DSK5TPTVN1PROD with NOTICES
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–7570 or send an
email to omb@cdc.gov. Send written
comments to 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 this notice.
Proposed Project
Generic Clearance for the Collection
of Qualitative Feedback on Agency
Service Delivery—NEW—Centers for
Disease Control and Prevention (CDC),
National Institute for Occupational
Safety and Health (NIOSH).
As part of a Federal Government-wide
effort to streamline the process to seek
feedback from the public on service
VerDate Mar<15>2010
15:28 Oct 05, 2012
Jkt 229001
Title: Generic Clearance for the
Collection of Qualitative Feedback on
Agency Service Delivery.
Abstract: The information collection
activity will garner qualitative customer
and stakeholder feedback in an efficient,
timely manner, in accordance with the
Administration’s commitment to
improving service delivery. By
qualitative feedback we mean
information that provides useful
insights on perceptions and opinions,
but are not statistical surveys that yield
quantitative results that can be
generalized to the population of study.
This feedback will provide insights into
customer or stakeholder perceptions,
experiences and expectations, provide
an early warning of issues with service,
or focus attention on areas where
communication, training or changes in
operations might improve delivery of
products or services. These collections
will allow for ongoing, collaborative and
actionable communications between the
Agency and its customers and
stakeholders. It will also allow feedback
to contribute directly to the
improvement of program management.
PO 00000
Frm 00032
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
Average
burden per
response
(in hr)
500
250
1
........................
45/60
15/60
1,000
200
500
60
1
1
1
1
10/60
90/60
10/60
5/60
60
1
5/60
30
1
1
30
1
1
Feedback collected under this generic
clearance will provide useful
information, but it will not yield data
that can be generalized to the overall
population. This type of generic
clearance for qualitative information
will not be used for quantitative
information collections that are
designed to yield reliably actionable
results, such as monitoring trends over
time or documenting program
performance. Such data uses require
more rigorous designs that address: The
target population to which
generalizations will be made, the
sampling frame, the sample design
(including stratification and clustering),
the precision requirements or power
calculations that justify the proposed
sample size, the expected response rate,
methods for assessing potential nonresponse bias, the protocols for data
collection, and any testing procedures
that were or will be undertaken prior
fielding the study. Depending on the
degree of influence the results are likely
to have, such collections may still be
eligible for submission for other generic
mechanisms that are designed to yield
quantitative results.
The Agency received no comments in
response to the 60-day notice published
in the Federal Register on December 22,
2010 (75 FR 80542).
This is a new collection of
information. Respondents will be
screened and selected from Individuals
and Households, Businesses,
Organizations, and/or State, Local or
Tribal Government. Below we provide
CDC’s projected annualized estimate for
the next three years. There is no cost to
respondents other than their time. The
estimated annualized burden hours for
this data collection activity are 28,750.
E:\FR\FM\09OCN1.SGM
09OCN1
61410
Federal Register / Vol. 77, No. 195 / Tuesday, October 9, 2012 / Notices
Average
number of
respondents
per activity
Type of collection
Online surveys, Telephone Surveys, Focus Groups, In person observation/
testing ...........................................................................................................
Dated: October 2, 2012.
Ron A. Otten,
Director, Office of Scientific Integrity (OSI),
Office of the Associate Director for Science
(OADS), Office of the Director, Centers for
Disease Control and Prevention.
[FR Doc. 2012–24766 Filed 10–5–12; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–13–12MQ]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–7570 or send an
email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
Proposed Project
Evaluation of the Young Sisters
Initiative: A Guide to A Better You!
Program—New—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
In 2010, the Centers for Disease
Control and Prevention (CDC) launched
Annual
frequency per
response
14,350
the three-year Breast Cancer in Young
Women (BCYW) project to raise
awareness about these issues among
young breast cancer survivors (YBCS)
and to provide psychosocial and
reproductive health support to women
who are diagnosed before age 45. A key
component of the BCYW program is the
design, testing, implementation and
evaluation of the Young Sisters
Initiative: A Guide to a Better You (YSI)
program. The YSI program is a webbased intervention designed to provide
African American YBCS with culturally
tailored psychosocial and reproductive
health information to support their
needs as cancer survivors.
CDC plans to conduct a process
evaluation of YSI program
implementation in conjunction with
Sisters Network Inc. (SNI), a partner
organization, and ICF International, an
evaluation contractor. Information will
be collected to assess whether the YSI
program can be implemented with
fidelity; reach its target audience of
African American YBCS; and deliver
effective psychosocial and reproductive
health information and support. The
process evaluation will also collect
information to improve understanding
of facilitators and barriers to YSI
program recruitment and
implementation, and to assess how the
program might be adapted for use with
other audiences.
Primary information collection will
consist of two Web-based surveys of YSI
program users, conducted before and
after exposure to YSI program materials.
The initial five-minute demographic
screener will be conducted when users
encounter the YSI Web site.
Respondents will be asked to provide
demographic and health information
necessary for identifying members of the
1
Average
number of
activities
Average hours
per response
4
30/60
target YSI program audience, and to
indicate their willingness to complete a
brief online post-use survey one to two
weeks after their initial YSI program
Web site visit. The post-use survey will
be conducted after YSI Web site users
have time to review the site and
materials. The estimated burden for the
post-use survey is 20 minutes.
Respondents will be asked questions
about the usefulness of resources posted
on the YSI Web site and satisfaction
with the site. No personally identifiable
information will be collected.
Two secondary sources of information
will be used to supplement the process
evaluation data collection, but will not
impose burden on YSI Web site users.
First, CDC’s evaluation contractor will
use information obtained through
Google Analytics to assess how visitors
(particularly the target audience)
navigate and use the YSI Web site. In
addition, the evaluation contractor will
conduct a limited number of telephone
interviews with SNI staff and SNIidentified recruitment partners before
and after the YSI implementation to
assess fidelity to the YSI program core
components and identify any facilitators
and/or barriers experienced during
program implementation.
CDC will use the results of the process
evaluation to inform future efforts to
support and educate YBCS in
vulnerable/minority populations. OMB
approval is requested for one year.
Participation in the information
collection is voluntary, and there are no
costs to respondents other than their
time. The total estimated annualized
burden hours are 142.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
wreier-aviles on DSK5TPTVN1PROD with NOTICES
Type of respondents
Form name
YSI Web Site Users ........................................
YSI Program Demographic Screener ............
YSI Program Post-Use Survey ......................
VerDate Mar<15>2010
17:20 Oct 05, 2012
Jkt 229001
PO 00000
Frm 00033
Fmt 4703
Sfmt 4703
E:\FR\FM\09OCN1.SGM
500
300
09OCN1
Number of
responses per
respondent
1
1
Average
burden per
response
(in hr)
5/60
20/60
]]>Agencies
[Federal Register Volume 77, Number 195 (Tuesday, October 9, 2012)]
[Notices]
[Pages 61409-61410]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-24766]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30-Day-13-12SF]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) publishes a
list of information collection requests under review by the Office of
Management and Budget (OMB) in compliance with the Paperwork Reduction
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call
the CDC Reports Clearance Officer at (404) 639-7570 or send an email to
omb@cdc.gov. Send written comments to 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 this
notice.
Proposed Project
Generic Clearance for the Collection of Qualitative Feedback on
Agency Service Delivery--NEW--Centers for Disease Control and
Prevention (CDC), National Institute for Occupational Safety and Health
(NIOSH).
As part of a Federal Government-wide effort to streamline the
process to seek feedback from the public on service delivery, the CDC
has submitted a Generic Information Collection Request (Generic ICR):
``Generic Clearance for the Collection of Qualitative Feedback on
Agency Service Delivery '' to OMB for approval under the Paperwork
Reduction Act (PRA) (44 U.S.C. 3501 et seq.).
To request additional information, please contact Kimberly S. Lane,
Reports Clearance Officer, Centers for Disease Control and Prevention,
1600 Clifton Road, MS-D74, Atlanta, GA 30333 or send an email to
omb@cdc.gov.
SUPPLEMENTARY INFORMATION:
Title: Generic Clearance for the Collection of Qualitative Feedback
on Agency Service Delivery.
Abstract: The information collection activity will garner
qualitative customer and stakeholder feedback in an efficient, timely
manner, in accordance with the Administration's commitment to improving
service delivery. By qualitative feedback we mean information that
provides useful insights on perceptions and opinions, but are not
statistical surveys that yield quantitative results that can be
generalized to the population of study. This feedback will provide
insights into customer or stakeholder perceptions, experiences and
expectations, provide an early warning of issues with service, or focus
attention on areas where communication, training or changes in
operations might improve delivery of products or services. These
collections will allow for ongoing, collaborative and actionable
communications between the Agency and its customers and stakeholders.
It will also allow feedback to contribute directly to the improvement
of program management.
Feedback collected under this generic clearance will provide useful
information, but it will not yield data that can be generalized to the
overall population. This type of generic clearance for qualitative
information will not be used for quantitative information collections
that are designed to yield reliably actionable results, such as
monitoring trends over time or documenting program performance. Such
data uses require more rigorous designs that address: The target
population to which generalizations will be made, the sampling frame,
the sample design (including stratification and clustering), the
precision requirements or power calculations that justify the proposed
sample size, the expected response rate, methods for assessing
potential non-response bias, the protocols for data collection, and any
testing procedures that were or will be undertaken prior fielding the
study. Depending on the degree of influence the results are likely to
have, such collections may still be eligible for submission for other
generic mechanisms that are designed to yield quantitative results.
The Agency received no comments in response to the 60-day notice
published in the Federal Register on December 22, 2010 (75 FR 80542).
This is a new collection of information. Respondents will be
screened and selected from Individuals and Households, Businesses,
Organizations, and/or State, Local or Tribal Government. Below we
provide CDC's projected annualized estimate for the next three years.
There is no cost to respondents other than their time. The estimated
annualized burden hours for this data collection activity are 28,750.
[[Page 61410]]
----------------------------------------------------------------------------------------------------------------
Average
number of Annual Average Average hours
Type of collection respondents frequency per number of per response
per activity response activities
----------------------------------------------------------------------------------------------------------------
Online surveys, Telephone Surveys, Focus Groups, 14,350 1 4 30/60
In person observation/testing..................
----------------------------------------------------------------------------------------------------------------
Dated: October 2, 2012.
Ron A. Otten,
Director, Office of Scientific Integrity (OSI), Office of the Associate
Director for Science (OADS), Office of the Director, Centers for
Disease Control and Prevention.
[FR Doc. 2012-24766 Filed 10-5-12; 8:45 am]
BILLING CODE 4163-18-P
