Proposed Data Collections Submitted for Public Comment and Recommendations, 66069-66070 [2011-27588]

Download as PDF Federal Register / Vol. 76, No. 206 / Tuesday, October 25, 2011 / Notices the BHC Act (12 U.S.C. 1842(c)). If the proposal also involves the acquisition of a nonbanking company, the review also includes whether the acquisition of the nonbanking company complies with the standards in section 4 of the BHC Act (12 U.S.C. 1843). Unless otherwise noted, nonbanking activities will be conducted throughout the United States. Unless otherwise noted, comments regarding each of these applications must be received at the Reserve Bank indicated or the offices of the Board of Governors not later than November 18, 2011. A. Federal Reserve Bank of Atlanta (Chapelle Davis, Assistant Vice President) 1000 Peachtree Street, NE., Atlanta, Georgia 30309: 1. BankUnited, Inc., Miami Lakes, Florida; to become a bank holding company by acquiring 100 percent of the voting shares of BankUnited, National Association, Miami Lakes, Florida, upon the conversion of its subsidiary Bank United, a federal savings bank, to a national bank. Board of Governors of the Federal Reserve System, October 20, 2011. Robert deV. Frierson, Deputy Secretary of the Board. [FR Doc. 2011–27534 Filed 10–24–11; 8:45 am] BILLING CODE 6210–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60-Day–12–12AG] sroberts on DSK5SPTVN1PROD 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 404–639–5960 and send comments to Catina Conner, 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 HIV Prevention Among Latino MSM: Evaluation of a Locally Developed Intervention—New—National Center for HIV/AIDS, Viral Hepatitis, STD, TB Prevention (NCHHSTP), Centers for Disease Control and Prevention (CDC). Background and Brief Description Latinos are the largest and fastest growing ethnic minority group in the U.S. and have the second highest rate of HIV/AIDS diagnoses of all racial/ethnic groups in the country. From the beginning of the epidemic through 2007, Latinos accounted for 17% of all AIDS cases reported to the CDC. Among Latino males, male-to-male sexual contact is the single most important source of HIV infection, accounting for 46% of HIV infections in U.S.-born Latino men from 2001 to 2005, and for more than one-half of HIV infections among South American, Cuban, and Mexican-born Latino men in the U.S. (CDC, 2007a; 2007b). In 2006, male-tomale sex accounted for 72% of new HIV infections among Latino males. Relative to other men who have sex with men (MSM), the rate of HIV infection among Latino MSM is twice the rate recorded among whites (43.1 vs. 19.6 per 100,000). Despite the high levels of infection risk that affect Latino MSM, no efficacious interventions to prevent infection by HIV and other sexually transmitted diseases (STDs) are available for this vulnerable population. CDC’s Prevention Research Synthesis group, whose role is to identify HIV prevention interventions that have met rigorous criteria for demonstrating evidence of efficacy, has not identified Number of respondents Type of respondent Form name Prospective Study Participant ...... Participant Screening Form ........ VerDate Mar<15>2010 18:10 Oct 24, 2011 Jkt 226001 PO 00000 Frm 00038 Fmt 4703 any behavioral interventions for Latino MSM that meet current efficacy criteria, and no such interventions are listed in CDC’s 2011 update of its Compendium of Evidence-Based HIV Behavioral Interventions (https://www.cdc.gov/hiv/ topics/research/prs/compendiumevidence-based-interventions.htm). There is an urgent need for efficacious, culturally congruent HIV/STD prevention interventions for Latino MSM. The purpose of this project is to test the efficacy of an HIV prevention intervention for reducing sexual risk among Latino men who have sex with men in North Carolina. The HOLA en Grupos intervention is a Spanishlanguage, small-group, 4-session intervention that is designed to increase consistent and correct condom use and HIV testing among Latino MSM and to affect other behavioral and psychosocial factors that can increase their vulnerability of HIV/STD infection. This study will use a randomized controlled trial design to assess the efficacy of the HOLA en Grupos intervention compared to a general health comparison intervention. CDC is requesting approval for a 3year clearance for data collection. The data collection system involves screening of potential study participants for eligibility, collection of participants’ contact information, and measures of intervention and comparison participants’ socio-demographic characteristics, health seeking actions, HIV/STD and substance use-related risk behaviors, and psychosocial factors at baseline before intervention delivery and 6 months after intervention delivery. An estimated 350 men will be screened for eligibility in order to enroll the 300 men required for the study. The baseline and the 6-month follow-up assessments will be similar. However, the 6-month assessment will ask study participants fewer questions because there is no need to ask all questions during both assessments. Collection of eligibility information from potential participants will require about 10 minutes; collection of baseline assessment information and participant contact information will require about 1 hour and 45 minutes; and collection of the 6-month follow-up assessment information will require about 1 hour. There is no cost to participants other than their time. Number responses per respondent 350 Sfmt 4703 66069 E:\FR\FM\25OCN1.SGM Average burden per respondent (in hours) 1 25OCN1 10/60 Total annual burden in hours 58 66070 Federal Register / Vol. 76, No. 206 / Tuesday, October 25, 2011 / Notices Number of respondents Number responses per respondent Average burden per respondent (in hours) Total annual burden in hours Type of respondent Form name Enrolled Study Participant ........... Enrolled Study Participant ........... Baseline Assessment .................. 6-month follow-up assessment ... 300 300 1 1 1.75 1 525 300 Total ............................................. ...................................................... .......................... .......................... ............................ 883 Catina Conner, Acting Reports Clearance Officer, Centers for Disease Control and Prevention. [FR Doc. 2011–27588 Filed 10–24–11; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30-Day–12–0800] 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 the CDC Reports Clearance Officer at (404) 639–5960 or send an email to omb@cdc.gov. Send written comments to CDC Desk Officer, Office of Management and Budget, Washington, DC or by fax to (202) 395–5806. Written comments should be received within 30 days of this notice. Proposed Project Focus Group Testing to Effectively Plan and Tailor Cancer Prevention and Control Communication Campaigns (OMB No. 0920–0800, exp. 1/31/2012)— Extension (Generic)—National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC). Background and Brief Description The mission of the CDC’s Division of Cancer Prevention and Control (DCPC) is to reduce the burden of cancer in the United States through cancer prevention, reduction of risk, early detection, better treatment, and improved quality of life for cancer survivors. Toward this end, the DCPC supports the scientific development, implementation, and evaluation of various health communication campaigns with an emphasis on specific cancer burdens. This process requires testing of messages, concepts, and materials prior to their final development and dissemination. Communication campaigns vary according to the type of cancer, the qualitative dimensions of the message described above, and the type of respondents. CDC is requesting OMB approval of a three-year extension to an existing generic clearance that supports cancerrelated communications (OMB No. 0920–0800, exp. 1/31/2012). Information will be collected primarily through focus groups, and will be used to assess numerous qualitative dimensions of cancer prevention and control messages, including, but not limited to, knowledge, attitudes, beliefs, behavioral intentions, information needs and sources, and compliance to recommended screening intervals. Insights gained from the focus groups will assist in the development and/or refinement of future campaign messages and materials. Over a three-year period, DCPC plans to conduct or sponsor up to 72 focus groups per year, with each group involving an average of 12 respondents. Screening will be conducted to recruit respondents for specific target audiences, e.g., health care providers or the general public. Each focus group discussion will be facilitated by a written discussion guide, and will last approximately two hours. CDC will submit an information collection request to OMB for approval of each focus group activity. There are no costs to respondents other than their time. The total estimated annualized burden hours are 1,814. ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Type of respondents Form name Health care providers and general public ....... Screening Form .............................................. Focus Group Discussion Guide ..................... Dated: October 18, 2011. Daniel Holcomb, Reports Clearance Officer, Centers for Disease Control and Prevention. DEPARTMENT OF HEALTH AND HUMAN SERVICES sroberts on DSK5SPTVN1PROD with NOTICES [FR Doc. 2011–27586 Filed 10–24–11; 8:45 am] Centers for Disease Control and Prevention BILLING CODE 4163–18–P [30-Day–12–0278] Agency Forms Undergoing Paperwork Reduction Act Review The Centers for Disease Control and Prevention (CDC) publishes a list of information collection requests under VerDate Mar<15>2010 18:10 Oct 24, 2011 Jkt 226001 PO 00000 Frm 00039 Fmt 4703 Sfmt 4703 1,728 864 Number of responses per respondent Average burden per response (in hours) 1 1 3/60 2 review by the Office of Management and Budget (OMB) in compliance with the requirement of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995. To request a copy of these requirements, call the CDC Reports Clearance Officer at (404) 639–5960 or send an e-mail to omb@cdc.gov. Send written comments to CDC Desk Officer, Office of Management and Budget, Washington, DC or by fax to (202) 395–5806. Written comments should be received within 30 days of this notice. E:\FR\FM\25OCN1.SGM 25OCN1

Agencies

[Federal Register Volume 76, Number 206 (Tuesday, October 25, 2011)]
[Notices]
[Pages 66069-66070]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-27588]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[60-Day-12-12AG]


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 Catina Conner, 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

    HIV Prevention Among Latino MSM: Evaluation of a Locally Developed 
Intervention--New--National Center for HIV/AIDS, Viral Hepatitis, STD, 
TB Prevention (NCHHSTP), Centers for Disease Control and Prevention 
(CDC).

Background and Brief Description

    Latinos are the largest and fastest growing ethnic minority group 
in the U.S. and have the second highest rate of HIV/AIDS diagnoses of 
all racial/ethnic groups in the country. From the beginning of the 
epidemic through 2007, Latinos accounted for 17% of all AIDS cases 
reported to the CDC. Among Latino males, male-to-male sexual contact is 
the single most important source of HIV infection, accounting for 46% 
of HIV infections in U.S.-born Latino men from 2001 to 2005, and for 
more than one-half of HIV infections among South American, Cuban, and 
Mexican-born Latino men in the U.S. (CDC, 2007a; 2007b). In 2006, male-
to-male sex accounted for 72% of new HIV infections among Latino males. 
Relative to other men who have sex with men (MSM), the rate of HIV 
infection among Latino MSM is twice the rate recorded among whites 
(43.1 vs. 19.6 per 100,000).
    Despite the high levels of infection risk that affect Latino MSM, 
no efficacious interventions to prevent infection by HIV and other 
sexually transmitted diseases (STDs) are available for this vulnerable 
population. CDC's Prevention Research Synthesis group, whose role is to 
identify HIV prevention interventions that have met rigorous criteria 
for demonstrating evidence of efficacy, has not identified any 
behavioral interventions for Latino MSM that meet current efficacy 
criteria, and no such interventions are listed in CDC's 2011 update of 
its Compendium of Evidence-Based HIV Behavioral Interventions (https://www.cdc.gov/hiv/topics/research/prs/compendium-evidence-based-interventions.htm). There is an urgent need for efficacious, culturally 
congruent HIV/STD prevention interventions for Latino MSM.
    The purpose of this project is to test the efficacy of an HIV 
prevention intervention for reducing sexual risk among Latino men who 
have sex with men in North Carolina. The HOLA en Grupos intervention is 
a Spanish-language, small-group, 4-session intervention that is 
designed to increase consistent and correct condom use and HIV testing 
among Latino MSM and to affect other behavioral and psychosocial 
factors that can increase their vulnerability of HIV/STD infection. 
This study will use a randomized controlled trial design to assess the 
efficacy of the HOLA en Grupos intervention compared to a general 
health comparison intervention.
    CDC is requesting approval for a 3-year clearance for data 
collection. The data collection system involves screening of potential 
study participants for eligibility, collection of participants' contact 
information, and measures of intervention and comparison participants' 
socio-demographic characteristics, health seeking actions, HIV/STD and 
substance use-related risk behaviors, and psychosocial factors at 
baseline before intervention delivery and 6 months after intervention 
delivery. An estimated 350 men will be screened for eligibility in 
order to enroll the 300 men required for the study. The baseline and 
the 6-month follow-up assessments will be similar. However, the 6-month 
assessment will ask study participants fewer questions because there is 
no need to ask all questions during both assessments. Collection of 
eligibility information from potential participants will require about 
10 minutes; collection of baseline assessment information and 
participant contact information will require about 1 hour and 45 
minutes; and collection of the 6-month follow-up assessment information 
will require about 1 hour.
    There is no cost to participants other than their time.

--------------------------------------------------------------------------------------------------------------------------------------------------------
                                                                                                           Number       Average burden     Total annual
               Type of respondent                             Form name                 Number of      responses per    per respondent      burden in
                                                                                       respondents       respondent       (in hours)          hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Prospective Study Participant..................  Participant Screening Form........              350                1          10/60                  58

[[Page 66070]]

 
Enrolled Study Participant.....................  Baseline Assessment...............              300                1              1.75              525
Enrolled Study Participant.....................  6-month follow-up assessment......              300                1              1                 300
                                                                                    --------------------------------------------------------------------
Total..........................................  ..................................  ...............  ...............  ................              883
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Catina Conner,
Acting Reports Clearance Officer, Centers for Disease Control and 
Prevention.
[FR Doc. 2011-27588 Filed 10-24-11; 8:45 am]
BILLING CODE 4163-18-P
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