Att 2_60dy FRN

42076

Federal Register / Vol. 78, No. 135 / Monday, July 15, 2013 / Notices

National Center for Injury Prevention
and Control (NCIPC)—Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Safe, stable, nurturing relationships
and environments set children on a
positive trajectory for optimal child
development and health, provide a
buffer against the effects of adverse
child experiences, are fundamental to
healthy brain development and have a
positive impact on a broad range of
health problems across the life course.
Promoting safe, stable, nurturing
relationships and environments may
also reduce child maltreatment which is
a significant public health problem
affecting physical and emotional health
throughout the lifespan.
NCIPC is funding five state health
departments in Fiscal Year 2012 to
coordinate and manage existing and
new partnerships with other sectors to
promote safe, stable, nurturing
relationships and environments for
children; and work with partners to
identify strategies across sectors that
promote safe, stable, nurturing
relationships and environments. CDC

requests OMB approval for two years to
collect information that will establish
the baseline level of state health
departments’ and partners’ awareness
and commitment to ensuring safe,
stable, and nurturing relationships and
environments for children and
preventing child maltreatment.
This information will be collected
from staff at health departments soon
after receiving their award and from
their partners at the start of each new
partnership. Respondents will be 3 staff
members from 5 health departments
receiving funding and 3 staff members
at approximately 11 organizations or
agencies the health departments choose
to partner with. Information will be
collected once using SurveyMonkey,
an electronic web-based interface which
is a secure Web site that meets the Safe
Harbor and European Union data
protection requirements. This ICR will
only collect data pertaining to
organizations. No individual
identifiable information will be
requested.
Each grantee will receive a
personalized advance notification letter,
followed by an email with a link to the

SurveyMonkey site. In turn, the
grantee will send a personalized
advance notification letter, followed by
an email with a link to the
SurveyMonkey site to each new
partner throughout the funding period.
The goal of the data collection is to
assess awardee awareness and
commitment so that CDC may establish
state health departments’ and partners’
level of commitment at the start of the
funding. This information will be
compared to post-funding awareness
and commitment data which, along with
other data sources (i.e., changes in
public awareness and commitment, and
changes in policies and programs), will
allow CDC to establish the success of
this funding announcement.
Given five health departments with 10
partner organizations each and 3 staff at
each organization responding, the total
number of respondents for this project
is 165 (83 respondents per year). Total
project burden over the two years of
data collection is 78 hours (39 hours per
year).
There are no costs to respondents
other than their time.

ESTIMATED ANNUALIZED BURDEN HOURS
Type of
respondents

Form name

Grantees and their partners ..............

Institutional awareness and commitment survey.

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. 2013–16769 Filed 7–12–13; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention

tkelley on DSK3SPTVN1PROD with NOTICES

[60Day 13–13ZC]

Proposed Data Collections Submitted
for Public Comment and
Recommendations
In compliance with the requirement
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on
proposed data collection projects, the
Centers for Disease Control and

VerDate Mar<15>2010

18:53 Jul 12, 2013

Jkt 229001

Number of
respondents
83

Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the
proposed projects or to obtain a copy of
the data collection plans and
instruments, call 404–639–7570 or send
comments to LeRoy Richardson, 1600
Clifton Road, MS D–74, Atlanta, GA
30333 or send an email to [email protected].
Comments are invited on: (a) Whether
the proposed collection of information
is 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. Written comments should
be received within 60 days of this
notice.

PO 00000

Frm 00040

Fmt 4703

Sfmt 4703

Number of
responses per
respondent

Average
burden per
response
(in hrs.)

1

Total burden
(in hrs.)

28/60

39
39

Proposed Project
Case Studies to Explore Interventions
to Support, Build, and Provide Legacy
Awareness for Young Breast Cancer
Survivors—New—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Young breast cancer survivors (YBCS,
defined as women diagnosed with
breast cancer under 45 years old) may
have a more difficult time coping with
breast cancer treatment and aftercare
when compared to older breast cancer
survivors. For example, breast cancer
can be more serious, treatment is often
multimodal and more toxic, and side
effects can be more severe for YBCS
than for older women. As part of the
Patient Protection and Affordable Care
Act (H.R. 3590, 2010), Congress passed
the Education and Awareness Requires
Learning Young (EARLY) Act, Sec.
10413. The EARLY Act directed CDC to

E:\FR\FM\15JYN1.SGM

15JYN1

42077

Federal Register / Vol. 78, No. 135 / Monday, July 15, 2013 / Notices
develop and implement national
campaigns to educate young women
(particularly those at increased risk) and
health care providers about breast
cancer risk and early diagnosis. As a
result of the EARLY Act, CDC
established the Funding Opportunity
Announcement, DP11–1111, Developing
Support and Educational Awareness for
Young (< 45 years of age) Breast Cancer
Survivors in the United States.
Subsequently, CDC awarded a threeyear cooperative agreement to seven
organizations that demonstrated a
capacity to (1) reach YBCS, health care
providers, and caregivers/families, (2)
implement interventions that seek to
provide support services, and (3)
develop educational communication
and awareness resources to support
YBCS.
Other establishments within the U.S.,
such as local and national not-for-profit
organizations and academic institutions,
implement similar YBCS-focused
interventions without funding from
CDC’s DP11–1111 cooperative
agreement. Although these entities are
not funded through CDC, they plan,
develop, and employ similar tools,
strategies, and interventions to reach or
benefit these targeted young cancersurvivor populations.
CDC proposes to conduct exploratory
case studies of organizations that
provide support services and/or
educational resources to YBCS, health
care providers, and/or caregivers/
families. Each selected organization will
serve as a unique case and the unit of

the DP11–1111 cooperative agreement,
(2) implementation of YBCS
interventions, including barriers and
facilitators to implementation, and (3)
similarities and differences among
organizations serving YBCS. Case study
findings will be compiled and
summarized in site-specific and crosssite reports to CDC. Information
collected will help to enhance existing
efforts to provide educational resources
and support services to YBCS and
inform replication of promising YBCS
interventions in other settings.
Case study selection is based on a
purposeful selection of CDC-funded and
non-CDC funded organizations that
support YBCS populations through
educational or service programs.
Potential organizations for this project
include local or national not-for-profit
organizations and academic institutions.
Information will be collected using onsite observations and in-depth
interviews (IDI) with each organization’s
key informants, such as Principal
Investigators, Program Managers,
Program Staff, and Program Partners.
IDIs will last 1–2 hours each. Case study
findings will be compiled and
summarized in site-specific and crosssite reports to CDC. Information will be
collected approximately two years after
initiation of CDC’s cooperative
agreement, DP11–1111. OMB approval
is requested for 12 months.
There are no costs to respondents
other than their time.

analysis. Information will be collected
from up to 12 organizations: Seven case
studies will be conducted with
organizations that receive funding
through CDC’s DP11–1111 cooperative
agreement, and up to five case studies
will be conducted with other
organizations that are implementing
similar YBCS-focused activities and
interventions but do not receive funding
under DP11–1111. Information will be
collected during a single site visit to
each selected organization to conduct
in-person interviews with key
programmatic staff and to record on-site
observations of program planning and
implementation activities.
Case studies are intended to serve as
an exploration of implementation
activities, as well as to provide the
context for implementation.
Specifically, case study findings will
help CDC to identify areas in which
CDC can build upon existing and
emerging efforts to provide support
services and educational resources to
YBCS, highlight barriers and facilitating
factors to implementing interventions
targeting YBCS, determine the added
value of providing the DP11–1111
cooperative agreement (e.g., funding,
technical assistance) to various entities,
identify lessons learned that can be
applied to future implementation of
YBCS interventions, and better
understand the sustainability of YBCS
interventions following/in the absence
of CDC funding.
CDC will be able to gain a deeper
understanding of (1) implementation of

ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Organizations
Funding.

that

Receive

CDC

Organizations that do not Receive
CDC Funding.

tkelley on DSK3SPTVN1PROD with NOTICES

Total ...........................................

VerDate Mar<15>2010

17:55 Jul 12, 2013

IDI Guide for Program Directors/
Principal Investigators.
IDI Guide for Program Managers .....
IDI Guide for Program Staff Members.
IDI Guide for Program Partners .......
IDI Guide for Program Directors/
Principal Investigators.
IDI Guide for Program Managers .....
IDI Guide for Program Staff Members.
IDI Guide for Program Partners .......
...........................................................

Jkt 229001

PO 00000

Frm 00041

Number of
responses per
respondent

Number of
respondents

Form name

Fmt 4703

Avg. burden
per response

Total
burden
(in hrs)

7

1

2

14

7
35

1
1

1
1

7
35

21
5

1
1

1
2

21
10

5
25

1
1

1
1

5
25

15

1

1

15

........................

........................

........................

132

Sfmt 4703

E:\FR\FM\15JYN1.SGM

15JYN1

42078

Federal Register / Vol. 78, No. 135 / Monday, July 15, 2013 / Notices

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.

0457 Expiration 09/30/2013—
Extension—National Center for HIV/
AIDS, Viral Hepatitis, STD, and TB
Prevention (NCHHSTP), Centers for
Disease Control and Prevention (CDC).

[FR Doc. 2013–16770 Filed 7–12–13; 8:45 am]

Background and Brief Description

BILLING CODE 4163–18–P

CDC, NCHHSTP, Division of
Tuberculosis Elimination (DTBE)
proposes extension of the Aggregate
Reports for Tuberculosis Program
Evaluation, previously approved under
OMB No. 0920–0457. This request is for
a 3-year clearance. There are no
revisions to the report forms, data
definitions, or reporting instructions.
Changes within this information
collection request (ICR) reflect an
increase in the annual cost to the
government. The increased cost is due
to increases in salaries of personnel
conducting data collection and analysis
since the last ICR approval.
DTBE is the lead agency for
tuberculosis elimination in the United
States. To ensure the elimination of
tuberculosis in the United States, CDC
monitors indicators for key program
activities, such as finding tuberculosis
infections in recent contacts of cases
and in other persons likely to be
infected and providing therapy for
latent tuberculosis infection. In 2000,
CDC implemented two program
evaluation reports for annual
submission: Aggregate report of followup for contacts of tuberculosis, and

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–13–0457]

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 (404) 639–7570 or send an
email to [email protected]. 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
Aggregate Reports for Tuberculosis
Program Evaluation (OMB No. 0920–

Aggregate report of screening and
preventive therapy for tuberculosis
infection (OMB No. 0920–0457). The
respondents for these reports are the 68
state and local tuberculosis control
programs receiving federal cooperative
agreement funding through DTBE.
These reports emphasize treatment
outcomes, high-priority target
populations vulnerable to tuberculosis,
and programmed electronic report entry,
which transitioned to the National
Tuberculosis Indicators Project (NTIP), a
secure web-based system for program
evaluation data, in 2010. No other
federal agency collects this type of
national tuberculosis data, and the
Aggregate report of follow-up for
contacts of tuberculosis, and Aggregate
report of screening and preventive
therapy for tuberculosis infection are
the only data source about latent
tuberculosis infection for monitoring
national progress toward tuberculosis
elimination with these activities. CDC
provides ongoing assistance in the
preparation and utilization of these
reports at the local and state levels of
public health jurisdiction. CDC also
provides respondents with technical
support for NTIP access (Electronic—
100%, Use of Electronic Signatures—
No). The annual burden to respondents
is estimated to be 226 hours.

ESTIMATED ANNUALIZED BURDEN HOURS
Form name

Data clerks and Program Managers ..........

Follow-up and Treatment of Contacts to
Tuberculosis Cases Form.
Follow-up and Treatment of Contacts to
Tuberculosis Cases Form.
Follow-up and Treatment of Contacts to
Tuberculosis Cases Form.
Targeted Testing and Treatment for Latent Tuberculosis Infection.
Targeted Testing and Treatment for Latent Tuberculosis Infection.
Targeted Testing and Treatment for Latent Tuberculosis Infection.

Program Managers .....................................
Data clerks ..................................................
Data clerks and Program Managers ..........
Program Managers .....................................
Data clerks ..................................................

tkelley on DSK3SPTVN1PROD with NOTICES

Number of
respondents

Type of respondent

Number of
responses per
respondent

100

1 (electronic) ...........

30/60

18

1 (manual) ...............

30/60

18

1 (manual) ...............

3

100

1 (electronic) ...........

30/60

18

1 (manual) ...............

30/60

18

1 (manual) ...............

3

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. 2013–16824 Filed 7–12–13; 8:45 am]
BILLING CODE 4163–18–P

VerDate Mar<15>2010

17:55 Jul 12, 2013

Jkt 229001

PO 00000

Frm 00042

Fmt 4703

Sfmt 9990

Average
burden per
response
(in hours)

E:\FR\FM\15JYN1.SGM

15JYN1