Proposed Data Collections Submitted for Public Comment and Recommendations, 2696 [E7-771]
Download as PDF
<![CDATA[
2696
Federal Register / Vol. 72, No. 13 / Monday, January 22, 2007 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Number of respondents
Respondents
Number of responses per respondent
Average burden
per response
(in hrs.)
Total burden
(hours)
Clerical .............................................................................................
Directors ...........................................................................................
33
33
2
2
2.75
1.5
182
99
Total ..........................................................................................
............................
............................
............................
281
Dated: January 11, 2007.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E7–770 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-07–07AH]
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 404–639–5960 and
send comments to Joan Karr, CDC
Acting Reports Clearance Officer, 1600
Clifton Road, MS–D74, Atlanta, GA
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
Formative Research to inform the
development of new recommendations
for Human Immunodeficiency Virus
(HIV), Counseling, Testing, and Referral
in non-health care settings—NewNational Center for HIV/AIDS, Viral
Hepatitis, STD, and TB Prevention
(NCHHSTP), Coordinating Center for
Infectious Diseases (CCID), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
This project involves formative
research to elicit consumer opinions on
HIV counseling, testing, and referral
(CTR) in non-health care settings. The
study entails conducting focus groups
with persons who are either HIV
positive or at risk for HIV because of
their drug injection or sexual behavior.
The purpose of the focus groups is to
explore: (1) Facilitators and barriers to
using CTR services in non-health care
settings; (2) ideal service components to
decrease barriers to early diagnosis,
decrease risk behaviors, link clients
with follow-up care, and ensure client
rights; (3) perceived risks and benefits of
CTR; and (4) preferences for providing
informed consent.
CDC will use study findings to inform
the development of new
recommendations for HIV CTR in nonhealth care settings. We expect a total of
450 participants to be screened for
eligibility. Of the 450 participants who
are screened, we expect that 180 people
will participate in a focus group. There
are no costs to the respondents other
than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of respondents
Respondents
Average burden
per response
(In hours)
Responses per
respondent
Total burden
hours
Screener ..........................................................................................
Focus Group ....................................................................................
450
180
1
1
20/60
2
150
360
Total ..........................................................................................
............................
............................
............................
510
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
BILLING CODE 4163–18–P
rmajette on PROD1PC67 with NOTICES
Dated: January 11, 2007.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E7–771 Filed 1–19–07; 8:45 am]
[60Day–07–07AI]
Centers for Disease Control and
Prevention
Proposed Data Collections Submitted
for Public Comment and
Recommendations
In compliance with the requirement
of Section 3506(c)(2)(A) of the
VerDate Aug<31>2005
15:20 Jan 19, 2007
Jkt 211001
PO 00000
Frm 00050
Fmt 4703
Sfmt 4703
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 404–639–5960 and
send comments to Joan F. Karr, CDC
Acting Reports Clearance Officer, 1600
Clifton Road, MS–D74, Atlanta, GA
E:\FR\FM\22JAN1.SGM
22JAN1
]]>Agencies
[Federal Register Volume 72, Number 13 (Monday, January 22, 2007)]
[Notices]
[Page 2696]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-771]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-07-07AH]
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 404-639-5960
and send comments to Joan Karr, CDC Acting Reports Clearance Officer,
1600 Clifton Road, MS-D74, Atlanta, GA 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
Formative Research to inform the development of new recommendations
for Human Immunodeficiency Virus (HIV), Counseling, Testing, and
Referral in non-health care settings--New-National Center for HIV/AIDS,
Viral Hepatitis, STD, and TB Prevention (NCHHSTP), Coordinating Center
for Infectious Diseases (CCID), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
This project involves formative research to elicit consumer
opinions on HIV counseling, testing, and referral (CTR) in non-health
care settings. The study entails conducting focus groups with persons
who are either HIV positive or at risk for HIV because of their drug
injection or sexual behavior. The purpose of the focus groups is to
explore: (1) Facilitators and barriers to using CTR services in non-
health care settings; (2) ideal service components to decrease barriers
to early diagnosis, decrease risk behaviors, link clients with follow-
up care, and ensure client rights; (3) perceived risks and benefits of
CTR; and (4) preferences for providing informed consent.
CDC will use study findings to inform the development of new
recommendations for HIV CTR in non-health care settings. We expect a
total of 450 participants to be screened for eligibility. Of the 450
participants who are screened, we expect that 180 people will
participate in a focus group. There are no costs to the respondents
other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average burden
Respondents Number of Responses per per response (In Total burden
respondents respondent hours) hours
----------------------------------------------------------------------------------------------------------------
Screener................................ 450 1 20/60 150
Focus Group............................. 180 1 2 360
-----------------------------------------------------------------------
Total............................... ................ ................ ................ 510
----------------------------------------------------------------------------------------------------------------
Dated: January 11, 2007.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E7-771 Filed 1-19-07; 8:45 am]
BILLING CODE 4163-18-P
