60day FRN

14253

Federal Register / Vol. 79, No. 49 / Thursday, March 13, 2014 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Type of respondent
Enrolled
Enrolled
Enrolled
Enrolled

participant
participant
participant
participant

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

Focus group consent .............................................................
Focus group discussion .........................................................
Individual in-depth interview guide consent ..........................
Individual in-depth interview guide ........................................

LeRoy 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. 2014–05482 Filed 3–12–14; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60-Day–14–0895]

TKELLEY on DSK3SPTVN1PROD with NOTICES

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
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–D74, Atlanta, GA
30333 or send an email to omb@cdc.gov.
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

VerDate Mar<15>2010

17:33 Mar 12, 2014

Number of
respondents

Form name

Jkt 232001

technology. Written comments should
be received within 60 days of this
notice.
Proposed Project
Community-based Organization
Monitoring and Evaluation of Respect
(OMB No.0920–0895 exp. 8/31/2014)—
Revision—National Center for HIV/
AIDS, Viral Hepatitis, STD, and TB
Prevention, Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
CDC began formally partnering with
Community-based Organizations (CBOs)
in the late 1980s to expand the reach of
HIV prevention efforts. CBOs were, and
continue to be, recognized as important
partners in HIV prevention because of
their history and credibility with target
populations and their access to groups
that may not be easily reached. Over
time, CDC’s program for HIV prevention
by CBOs has grown in size, scope, and
complexity to respond to changes in the
epidemic, including the diffusion and
implementation of Effective Behavioral
Interventions (EBIs) for HIV prevention.
CDC’s EBIs have been shown to be
effective under controlled research
environments, but there is limited data
on intervention implementation and
client outcomes in real-world settings
(as implemented by CDC-funded CBOs).
The purpose of Community-based
Organization Monitoring and Evaluation
of Respect (CMEP-Respect) is to: (a)
Assess the fidelity of the
implementation of the selected
intervention at the CBO; and (b)
improve the performance of CDCfunded CBOs delivering the Respect
intervention by monitoring changes in
clients’ self-reported attitudes and
beliefs regarding HIV and HIV
transmission risk behaviors after
participating in Respect.
CDC funded four (4) CBOs to
participate in CMEP-Respect for five (5)
years (September 2010-August 2015).

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Number of
responses per
respondent

216
216
30
30

1
1
1
1

Average hours
per response
10/60
1.5
10/60
1.5

From September 1, 2012 through
January 31, 2014, baseline surveys were
conducted with 684 participants; 90-day
follow up surveys were completed with
459 participants, and 180-day follow up
surveys were completed with 343
participants.
CDC is requesting additional time to
complete follow up surveys at 90- and
180-days for participants completing the
intervention on or before August 31,
2014. Following their participation in
the Respect intervention, participants
will complete an 18 minute, self
administered, computer based interview
at two follow-up time points (90- and
180-days following the Respect
intervention) to assess their HIV-related
attitudes and behavioral risks. CBOs
will be expected to retain 80% of these
participants at both follow-up time
points.
Throughout the project, funded CBOs
will be responsible for managing the
daily procedures of CMEP-Respect to
ensure that all required activities are
performed, all deadlines are met, and
quality assurance plans, policies and
procedures are upheld. CBOs will be
responsible for participating in all CDCsponsored grantee meetings related to
CMEP-Respect.
Findings from this project will be
primarily used by the participating
CBOs. The CBOs may use the findings
to: (a) Better understand if the outcomes
are different across demographic and
behavioral risk groups as well as agency
and program model characteristics; and
(b) improve the future implementation,
management, and quality of Respect.
CDC and other organizations interested
in behavioral outcome monitoring of
Respect or similar HIV prevention
interventions can also benefit from
lessons learned through this project.
In this request, CDC is requesting
approval for approximately 200 burden
hours. There is no cost to respondents
except for their time.

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14254

Federal Register / Vol. 79, No. 49 / Thursday, March 13, 2014 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

Average
burden
response
(in hours)

Number of
responses per
respondent

Total burden
(in hours)

Type of respondent

Form name

General Population ...........................
CMEP-Respect grantees ..................
General population ............................
CMEP-Respect grantees ..................

90-day Follow-up Survey .................
90-day SDN Submission ..................
180-day Follow-up Survey ...............
180-day SDN Submission ................

320
4
320
4

1
12
1
12

18/60
5/60
18/60
5/60

96
4
96
4

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

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

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

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

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

200

LeRoy 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. 2014–05478 Filed 3–12–14; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60 Day–14–0006]

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
Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the

Emerging and Zoonotic Infectious
Diseases (NCEZID), Centers for Disease
Control and Prevention (CDC).

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–D74, Atlanta, GA
30333 or send an email to omb@cdc.gov.
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.

Background and Brief Description
Section 212(a)(1) of the Immigration
and Nationality Act states that aliens
with specific health related conditions
are ineligible for admission into the
United States. The Attorney General
may waive application of this
inadmissibility on health-related
grounds if an application for waiver is
filed and approved by the consular
office considering the application for
visa. CDC uses this application
primarily to collect information to
establish and maintain records of waiver
applicants in order to notify the U.S.
Citizenship and Immigration Services
when terms, conditions and controls
imposed by waiver are not met.
CDC is requesting approval from the
Office of Management and Budget
(OMB) to collect this data
(approximately 100 burden hours) for
another three years.
There are no costs to respondents
except their time to complete the
application.

Proposed Project
Statements in Support of Application
of Waiver of Inadmissibility (OMB No.
0920–0006, Expiration 9/30/2014)—
Extension—National Center for

TKELLEY on DSK3SPTVN1PROD with NOTICES

ESTIMATE OF ANNUALIZED BURDEN HOURS
Number of
respondents

Average
burden per
response
(in hours)

Number of
responses per
respondent

Total
burden
hours

Type of respondent

Form name

Physician ..............................................................
Physician ..............................................................

CDC 4.422–1 ................
CDC 4.422–1a ..............

200
200

1
1

10/60
20/60

33
67

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

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

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

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

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

100

Leroy 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. 2014–05529 Filed 3–12–14; 8:45 am]
BILLING CODE 4163–18–P

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