2696 Federal Register / Vol. 72, No.

13 / Monday, January 22, 2007 / Notices

ESTIMATED ANNUALIZED BURDEN HOURS

Number of re- Average burden
Number of re- Total burden
Respondents sponses per re- per response
spondents (hours)
spondent (in hrs.)

Clerical ............................................................................................. 33 2 2.75 182

Directors ........................................................................................... 33 2 1.5 99

Total .......................................................................................... ............................ ............................ ............................ 281

Dated: January 11, 2007. Acting Reports Clearance Officer, 1600 Infectious Diseases (CCID), Centers for
Joan F. Karr, Clifton Road, MS–D74, Atlanta, GA Disease Control and Prevention (CDC).
Acting Reports Clearance Officer, Centers for 30333 or send an e-mail to
Background and Brief Description
Disease Control and Prevention. omb@cdc.gov.
[FR Doc. E7–770 Filed 1–19–07; 8:45 am] Comments are invited on: (a) Whether This project involves formative
BILLING CODE 4163–18–P the proposed collection of information research to elicit consumer opinions on
is necessary for the proper performance HIV counseling, testing, and referral
of the functions of the agency, including (CTR) in non-health care settings. The
DEPARTMENT OF HEALTH AND whether the information shall have study entails conducting focus groups
HUMAN SERVICES practical utility; (b) the accuracy of the with persons who are either HIV
agency’s estimate of the burden of the positive or at risk for HIV because of
Centers for Disease Control and proposed collection of information; (c) their drug injection or sexual behavior.
Prevention ways to enhance the quality, utility, and The purpose of the focus groups is to
clarity of the information to be explore: (1) Facilitators and barriers to
[60Day-07–07AH] using CTR services in non-health care
collected; and (d) ways to minimize the
Proposed Data Collections Submitted burden of the collection of information settings; (2) ideal service components to
for Public Comment and on respondents, including through the decrease barriers to early diagnosis,
Recommendations use of automated collection techniques decrease risk behaviors, link clients
or other forms of information with follow-up care, and ensure client
In compliance with the requirement technology. Written comments should rights; (3) perceived risks and benefits of
of Section 3506(c)(2)(A) of the be received within 60 days of this CTR; and (4) preferences for providing
Paperwork Reduction Act of 1995 for notice. informed consent.
opportunity for public comment on CDC will use study findings to inform
proposed data collection projects, the Proposed Project the development of new
Centers for Disease Control and Formative Research to inform the recommendations for HIV CTR in non-
Prevention (CDC) will publish periodic development of new recommendations health care settings. We expect a total of
summaries of proposed projects. To for Human Immunodeficiency Virus 450 participants to be screened for
request more information on the (HIV), Counseling, Testing, and Referral eligibility. Of the 450 participants who
proposed projects or to obtain a copy of in non-health care settings—New- are screened, we expect that 180 people
the data collection plans and National Center for HIV/AIDS, Viral will participate in a focus group. There
instruments, call 404–639–5960 and Hepatitis, STD, and TB Prevention are no costs to the respondents other
send comments to Joan Karr, CDC (NCHHSTP), Coordinating Center for than their time.

ESTIMATED ANNUALIZED BURDEN HOURS

Average burden
Number of re- Responses per Total burden
Respondents per response
spondents respondent hours
(In hours)

Screener .......................................................................................... 450 1 20/60 150

Focus Group .................................................................................... 180 1 2 360

Total .......................................................................................... ............................ ............................ ............................ 510

Dated: January 11, 2007. DEPARTMENT OF HEALTH AND Paperwork Reduction Act of 1995 for
Joan F. Karr, HUMAN SERVICES opportunity for public comment on
Acting Reports Clearance Officer, Centers for proposed data collection projects, the
Disease Control and Prevention. Centers for Disease Control and Centers for Disease Control and
[FR Doc. E7–771 Filed 1–19–07; 8:45 am]
Prevention Prevention (CDC) will publish periodic
BILLING CODE 4163–18–P
summaries of proposed projects. To
[60Day–07–07AI] request more information on the
proposed projects or to obtain a copy of
rmajette on PROD1PC67 with NOTICES

Proposed Data Collections Submitted

for Public Comment and the data collection plans and
Recommendations instruments, call 404–639–5960 and
send comments to Joan F. Karr, CDC
In compliance with the requirement Acting Reports Clearance Officer, 1600
of Section 3506(c)(2)(A) of the Clifton Road, MS–D74, Atlanta, GA

VerDate Aug<31>2005 15:20 Jan 19, 2007 Jkt 211001 PO 00000 Frm 00050 Fmt 4703 Sfmt 4703 E:\FR\FM\22JAN1.SGM 22JAN1
 Federal Register / Vol. 72, No. 13 / Monday, January 22, 2007 / Notices
30333 or send an e-mail 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.
Proposed Project
Medical Monitoring Project Provider
Survey-New-National Center for HIV,
STD, and TB Prevention (NCHSTP),
Respondents
HIV Care Providers ..........................................................................
Dated: January 11, 2007.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E7–772 Filed 1–19–07; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–07–07AF]
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
rmajette on PROD1PC67 with NOTICES
the data collection plans and
instruments, call 404–639–5960 and
send comments to Joan F. Karr, CDC
Acting Reports Clearance Officer, 1600
Clifton Road, MS–D74, Atlanta, GA
VerDate Aug<31>2005 15:20 Jan 19, 2007 Jkt 211001
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
CDC is requesting a 3-year approval
from the Office of Management and
Budget (OMB) to survey randomly
selected HIV care providers (e.g.,
physicians, nurse practitioners and
physician’s assistants) in the United
States regarding their training history,
areas of specialization, ongoing sources
of training and continuing education
about HIV care, and awareness of HIV
treatment guidelines and resources.
Results from this survey will be used in
conjunction with data from CDC’s
Medical Monitoring Project (MMP) to
assess who is providing HIV care, to
examine the impact of provider
characteristics on the quality and
standard of care being provided to
patients with HIV, to determine
opportunities to improve resources
available to HIV care providers, and to
ESTIMATED ANNUALIZED BURDEN HOURS
Number of re-
spondents
2,500
30333 or send an e-mail 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.
Proposed Project
Evaluation of the Safe Dates Project—
New—National Center for Injury
Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The specific aims of this study are to
describe the implementation and drivers
of implementation of the Safe Dates
program (implementation evaluation); to
evaluate its impact on desired
outcomes, including prevention of and
PO 00000 Frm 00051 Fmt 4703 Sfmt 4703
2697
evaluate the reasons for sampled
providers’ participation and non-
participation in MMP. Participation in
the survey is not contingent upon a
provider’s involvement with the MMP.
All selected HIV care providers will
be asked to participate in the survey,
regardless of their participation in the
MMP.
For this proposed data collection,
MMP project areas have identified all
HIV care providers in their jurisdictions
and selected a sample of 40–60
providers in each jurisdiction to
participate in MMP, including those
providers who may not be participating
in the MMP. CDC plans to survey these
sampled providers. Respondents will
have the option to use either a Web-
based application or paper survey to
participate in the survey. There is no
cost to respondents to participate in this
survey other than their time.
Number of re- Average burden
Total burden
sponses per re- per response
(Hours)
spondent (In hours)
1 30/60 1,250
reduction in dating violence
victimization and perpetration
(including psychological abuse,
stalking, physical violence, and sexual
violence) among ninth-grade students
(experimental effectiveness evaluation);
and to evaluate its cost-effectiveness,
including cost-utility (cost evaluation).
The evaluation will require
participation from staff and students at
54 schools (18 treatment schools
receiving the Safe Dates program with
teacher training and observation, 18
treatment schools receiving the Safe
Dates program without teacher training
and observation, and 18 control schools
not receiving the Safe Dates program).
Implementation evaluation data will
be collected primarily through Web
questionnaires completed by principals,
school prevention coordinators, and
teachers delivering the program;
effectiveness evaluation data will be
collected via classroom scannable forms
with ninth-graders who attend treatment
or control schools; and cost evaluation
data will be collected via a Web survey
of teachers delivering the program who
receive training and observation. High
schools that agree to participation will
be matched into sets of three.
Characteristics that will be considered
in the matching process include
demographics and urban/rural county
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