60 day FRN

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Federal Register / Vol. 80, No. 228 / Friday, November 27, 2015 / Notices

services for those diagnosed with
established HIV infection; 7. STD
screening and treatment; 8. Partner
services for patients with STDs; 9.
Behavioral risk reduction interventions;
10. Screening for behavioral health and
social services’ needs; 11. Linkage to
behavioral health and social services;
12. Navigators to assist accessing HIV
prevention and behavioral health and
social services; 13. Navigators to assist
enrollment in a health plan. The
following are the eleven HIV care
services: 1. HIV primary care, including

antiretroviral (ARV) treatment; 2.
Retention interventions; 3. Reengagement interventions; 4. Adherence
interventions; 5. STD screening and
treatment; 6. Partner services; 7.
Behavioral risk reduction interventions;
8. Screening patients for behavioral
health and social services’ needs; 9.
Linkage to behavioral health and social
services; 10. Navigators to assist linking
to care and accessing behavioral health
and social services; 11. Navigators to
assist enrollment in a health plan.

CDC HIV program grantees will
collect, enter or upload, and report
agency-identifying information, budget
data, information on the HIV prevention
and care services, and client
demographic characteristics with an
estimate of 2,466 burden hours. It is
estimated that the 37 respondents will
see approximately 200 patients per year.
The respondents will take about 20
minutes to enter the data for each of the
200 patients using the monitoring and
evaluation form.

ESTIMATED ANNUALIZED BURDEN HOURS
Type of
respondents

Form name

Number of
respondents

Number of
responses per
respondent

Average
burden per
response
(in hours)

Total burden
hours

Health jurisdictions ............................

Health Department Collaborative .....

37

200

20/60

2,466

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. 2015–30130 Filed 11–25–15; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–16–16FE; Docket No. CDC–2015–
0108]

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:

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 and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection entitled ‘‘Monitoring and
Reporting System for Rape Prevention
and Education (RPE) Awardees.’’ CDC
will use the information collected to
monitor cooperative agreement
awardees and to identify challenges to

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SUMMARY:

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program implementation and
achievement of outcomes.
DATES: Written comments must be
received on or before January 26, 2016.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0108 by any of the following methods:
Federal eRulemaking Portal:
Regulation.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. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.
Please note: All public comment should be
submitted 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 the Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE., MS—D74, Atlanta,
Georgia 30329; phone: 404–639–7570;
Email: [email protected].
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
FOR FURTHER INFORMATION CONTACT:

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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 OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
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; (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; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and

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Federal Register / Vol. 80, No. 228 / Friday, November 27, 2015 / Notices
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information.
Proposed Project
Monitoring and Reporting System for
Rape Prevention and Education (RPE)
Awardees—New—National Center for
Injury Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
According to CDC’s National Intimate
Partner and Sexual Violence Survey
(NISVS), in the United States, nearly 1
in 5 women and 1 in 71 men have been
raped in their lifetime, while 1 in 2
women and 1 in 5 men have
experienced severe sexual violence
victimization other than rape at some
point in their lives. Sexual violence is
a major public health problem, but it is
preventable. The majority of
victimization starts early in life with
approximately 80% of female victims
experiencing their first rape before the
age of 25 and almost half experiencing
their first rape before age 18. CDC’s
Rape Prevention and Education
Initiative is a national program which
funds, through a cooperative agreement,

Awardees will report progress and
activity information to CDC on an
annual schedule using an Excel-based
fillable electronic templates, prepopulated to the extent possible by CDC
staff, to be submitted via Grant
Solutions. Each awardee will submit an
Annual reporting Progress Report Tool
and an Annual reporting Evaluation
Plan Tool. In Year 1, each awardee will
have additional burden related to initial
collection of the reporting tools. Initial
population of the tools is a one-time
activity, after completing the initial
population of the tools, pertinent
information only needs to be updated
for each annual report. The same
instruments will be used for all
information collection and reporting.
CDC will use the information to
monitor each awardee’s progress and to
identify facilitators and challenges to
program implementation and
achievement of outcomes. Monitoring
allows CDC to determine whether an
awardee is meeting performance and
budget goals and to make adjustments in
the type and level of technical
assistance provided to them, as needed,
to support attainment of their
performance measures.
OMB approval is requested for three
years. Participation in the information
collection is required as a condition of
funding. There are no costs to
respondents other than their time.

all 50 state health departments, the
District of Columbia, Puerto Rico, and
territories (e.g., Guam, U.S. Virgin
Islands, and the Commonwealth of
Northern Mariana Islands) to conduct
state- and territorial-wide sexual
violence prevention activities.
The current Rape Prevention and
Education (RPE) Cooperative Agreement
builds on a decade long (2002–2012)
investment in the infrastructure and
capacity for sexual violence prevention
within state health departments, state
sexual assault coalitions, rape crisis
centers and other community based
organizations. Support and guidance for
these programs have been provided
through cooperative agreement funding
and technical assistance administered
by CDC’s National Center for Injury
Prevention and Control (NCIPC).
The goal of this information collection
is to receive the needed data to monitor
cooperative agreement programs funded
under the Rape Prevention Education
program (CDC–RFA–CE14–1401), for
program monitoring and improvement
among funded state health departments.
Data to be collected will provide
crucial information for program
performance monitoring and budget
tracking, and provide CDC with the
capacity to respond in a timely manner
to requests for information about the
program from the Department of Health
and Human Services (HHS), the White
House, Congress, and other sources.

ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden per
response
(in hours)

Number of
responses per
respondent

Total burden
(in hours)

Form name

State and Territorial Health Departments or Sexual Assault Coalition
Designee.

Program Report Tool (initial collection—Year 1).

55

1

7

385

Work Plan Tool (initial collection—
Year 1).
Program Report Tool (annual reporting collection—Years 2–3).
Work Plan Tool (annual reporting
collection—Years 2–3).

55

1

10

550

55

2

3

330

55

2

3

330

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

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

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

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

1,595

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

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Number of
respondents

Type of respondents

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. 2015–30131 Filed 11–25–15; 8:45 am]
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