Proposed Data Collections Submitted for Public Comment and Recommendations, 19362-19363 [2011-8271]

Download as PDF 19362 Federal Register / Vol. 76, No. 67 / Thursday, April 7, 2011 / Notices dissemination. The Division is the focal point for policy development and analysis related to financing, access/ delivery, organization and quality of Intellectual Disabilities and Serious and Persistent Mental Illnesses services, including those financed by Medicaid, Medicare, SAMHSA, Administration on Developmental Disabilities and HRSA. The Division works closely with other offices in ASPE because the two vulnerable populations that are its focus are users of both human services and health services. II. Delegations of Authority: All delegations and redelegations of authority made to officials and employees of affected organizational components will continue in them or their successors pending further redelegation, provided they are consistent with this reorganization. Dated: March 30, 2011. E.J. Holland, Jr., Assistant Secretary for Administration. [FR Doc. 2011–8357 Filed 4–6–11; 8:45 am] BILLING CODE 4150–04–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60Day–11–11EC] mstockstill on DSKH9S0YB1PROD 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 Daniel Holcomb, 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 VerDate Mar<15>2010 19:53 Apr 06, 2011 Jkt 223001 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 Epidemiologic Study of Health Effects Associated With Low Pressure Events in Drinking Water Distribution Systems —New—National Center for Emerging and Zoonotic Infectious Diseases— Office of Infectious Diseases—CDC. Background and Brief Description In the United States, drinking water distribution systems are designed to deliver safe, pressurized drinking water to our homes, hospitals, schools and businesses. However, the water distribution infrastructure is 50–100 years old in much of the U.S. and an estimated 240,000 water main breaks occur each year. Failures in the distribution system such as water main breaks, cross-connections, back-flow, and pressure fluctuations can result in potential intrusion of microbes and other contaminants that can cause health effects, including acute gastrointestinal and respiratory illness. Approximately 200 million cases of acute gastrointestinal illness occur in the U.S. each year, but we don’t have reliable data to assess how many of these cases are associated with drinking water. Further, data are even more limited on the human health risks associated with exposure to drinking water during and after the occurrence of low pressure events (such as water main breaks) in drinking water distribution systems. A study conducted in Norway from 2003–2004 found that people exposed to low pressure events in the water distribution system had a higher risk for gastrointestinal illness. A similar study is needed in the United States. The purpose of this data collection is to conduct an epidemiologic study in the U.S. to assess whether individuals exposed to low pressure events in the water distribution system are at an increased risk for acute gastrointestinal or respiratory illness. This study would be, to our knowledge, the first U.S. study to systematically examine the PO 00000 Frm 00056 Fmt 4703 Sfmt 4703 association between low pressure events and acute gastrointestinal and respiratory illnesses. Study findings will inform the Environmental Protection Agency (EPA), CDC, and other drinking water stakeholders of the potential health risks associated with low pressure events in drinking water distribution systems and whether additional measures (e.g., new standards, additional research, or policy development) are needed to reduce the risk for health effects associated with low pressure events in the drinking water distribution system. We will conduct a cohort study among households that receive water from five water utilities across the U.S. The water systems will be geographically diverse and will include both chlorinated and chloraminated systems. These water utilities will provide information about low pressure events that occur during the study period. Households in areas exposed to the low pressure event and an equal number of households in an unexposed area will be randomly selected and sent a survey questionnaire. After consenting to participate, households will be asked about symptoms and duration of any recent gastrointestinal or respiratory illness, tap water consumption, and other factors including international travel, daycare attendance or employment, and exposure to undercooked or unpasteurized food, pets and other animal contact, and recreational water. Study participants will be able to choose their method of survey response from a variety of options including a paper survey, telephone-administered survey, or Web-based survey. A Spanish language version of the survey for all response options will also be available. Participation in this study will be voluntary. No financial compensation will be provided to study participants. The study duration is anticipated to last 12 months. An estimated 5,200 individuals will be contacted and we anticipate 2,080 adults (18 years of age or older) will consent to participate in this study. We will conduct a pilot study (duration 3 months) prior to launching the full epidemiologic study. An estimated 1,000 individuals will be contacted and we anticipate 400 adults (18 years of age or older) will consent to participate in the pilot study. The total estimated annualized hours associated with this study, including the pilot, is expected to be 601. E:\FR\FM\07APN1.SGM 07APN1 19363 Federal Register / Vol. 76, No. 67 / Thursday, April 7, 2011 / Notices ESTIMATE OF ANNUALIZED BURDEN HOURS Type of respondents Full Study: Households Households Households Households Number of respondents Form name Number of responses per respondent Average burden per response (hours) Total burden (hours) ......................... ......................... ......................... ......................... Introductory letter and consent form ....... Web-based questionnaire ....................... Paper-based questionnaire ..................... Telephone-based questionnaire ............. 5,200 1,248 624 208 1 1 1 1 1/60 12/60 12/60 12/60 87 250 125 42 Total (full study): .......... ................................................................. ........................ ........................ ........................ 504 ......................... ......................... ......................... ......................... Introductory letter and consent form ....... Web-based questionnaire ....................... Paper-based questionnaire ..................... Telephone-based questionnaire ............. 1000 240 120 40 1 1 1 1 1/60 12/60 12/60 12/60 17 48 24 8 Total (pilot study) ......... ................................................................. ........................ ........................ ........................ 97 Total (Full & Pilot) ........ ................................................................. ........................ ........................ ........................ 601 Pilot Study: Households Households Households Households Daniel Holcomb, Reports Clearance Officer, Centers for Disease Control and Prevention. [FR Doc. 2011–8271 Filed 4–6–11; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day–11–0672] Agency Forms Undergoing Paperwork Reduction Act Review mstockstill on DSKH9S0YB1PROD with NOTICES 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 Indicators of the Performance of Local, State, Territorial, and Tribal Education Agencies in HIV Prevention, Coordinated School Health Program, and Asthma Management Activities for Adolescent and School Health Programs (OMB No. 0920–0672, exp. 6/30/2011)— Revision—National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC). VerDate Mar<15>2010 19:53 Apr 06, 2011 Jkt 223001 Background and Brief Description CDC is requesting OMB approval for three years to continue annual information collection for the Indicators for School Health programs. The Indicators assess programmatic activities among local education agencies (LEA) and State, territorial, and Tribal government education agencies (SEAs, TEAs, and TGs) funded by the Division of Adolescent and School Health (DASH), Centers for Disease Control and Prevention. Currently, the Indicators for School Health Programs are the only standardized annual reporting process for HIV prevention activities or coordinated school health program (CSHP) activities among LEAs and SEAs/TEAs/TGs funded by DASH. The questionnaires correspond to the specific funding source from the Division of Adolescent and School Health: two questionnaires pertain to HIV-prevention program activities among LEAs and SEAs/TEAs/TGs; one pertains to CSHP/PANT activities among SEAs/TGs; and one pertains to asthma management activities among LEAs. All information is collected electronically on a Web site managed by DASH. Two HIV prevention questionnaires include questions on project planning, materials distribution, professional development activities, provision of technical assistance, collaboration with external partners, and reducing health disparities among populations at disproportionate risk. The CSHP/PANT questionnaire focuses on the activities above as well as on physical activity, healthy eating, and tobacco-use prevention activities. The asthma management questionnaire includes PO 00000 Frm 00057 Fmt 4703 Sfmt 4703 questions on project planning, materials distribution, professional development activities, provision of technical assistance, collaboration with external partners, reducing health disparities among populations at disproportionate risk, and health services. The information collected by CDC is used to: (1) Provide standardized information about how LEAs and SEAs/ TEAs/TGs use funds for programs in HIV prevention, asthma management, and coordinated school health/physical activity, nutrition, and tobacco-use prevention (CSHP/PANT); (2) assess the extent to which programmatic adjustments are indicated; (3) provide descriptive and process information about program activities; and (4) provide greater accountability for use of public funds. The questionnaires previously approved for collecting FY2009 data will be used to collect FY2010 data. Minor changes to the questionnaires will be implemented for the FY2011 and FY2012 data collections, however, the proposed changes will not alter the estimated burden per response. An increase in the average number of funded programs over the three years of this clearance will result in a net increase in burden hours. A minor change to the title of the clearance is being requested to more accurately reflect the participation of Territorial and Tribal Education Agencies. There are no costs to respondents other than their time. The total estimated annualized burden hours are 811. E:\FR\FM\07APN1.SGM 07APN1

Agencies

[Federal Register Volume 76, Number 67 (Thursday, April 7, 2011)]
[Notices]
[Pages 19362-19363]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-8271]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[60Day-11-11EC]


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 Daniel Holcomb, 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

    Epidemiologic Study of Health Effects Associated With Low Pressure 
Events in Drinking Water Distribution Systems --New--National Center 
for Emerging and Zoonotic Infectious Diseases--Office of Infectious 
Diseases--CDC.

Background and Brief Description

    In the United States, drinking water distribution systems are 
designed to deliver safe, pressurized drinking water to our homes, 
hospitals, schools and businesses. However, the water distribution 
infrastructure is 50-100 years old in much of the U.S. and an estimated 
240,000 water main breaks occur each year. Failures in the distribution 
system such as water main breaks, cross-connections, back-flow, and 
pressure fluctuations can result in potential intrusion of microbes and 
other contaminants that can cause health effects, including acute 
gastrointestinal and respiratory illness.
    Approximately 200 million cases of acute gastrointestinal illness 
occur in the U.S. each year, but we don't have reliable data to assess 
how many of these cases are associated with drinking water. Further, 
data are even more limited on the human health risks associated with 
exposure to drinking water during and after the occurrence of low 
pressure events (such as water main breaks) in drinking water 
distribution systems. A study conducted in Norway from 2003-2004 found 
that people exposed to low pressure events in the water distribution 
system had a higher risk for gastrointestinal illness. A similar study 
is needed in the United States.
    The purpose of this data collection is to conduct an epidemiologic 
study in the U.S. to assess whether individuals exposed to low pressure 
events in the water distribution system are at an increased risk for 
acute gastrointestinal or respiratory illness. This study would be, to 
our knowledge, the first U.S. study to systematically examine the 
association between low pressure events and acute gastrointestinal and 
respiratory illnesses. Study findings will inform the Environmental 
Protection Agency (EPA), CDC, and other drinking water stakeholders of 
the potential health risks associated with low pressure events in 
drinking water distribution systems and whether additional measures 
(e.g., new standards, additional research, or policy development) are 
needed to reduce the risk for health effects associated with low 
pressure events in the drinking water distribution system.
    We will conduct a cohort study among households that receive water 
from five water utilities across the U.S. The water systems will be 
geographically diverse and will include both chlorinated and 
chloraminated systems. These water utilities will provide information 
about low pressure events that occur during the study period. 
Households in areas exposed to the low pressure event and an equal 
number of households in an unexposed area will be randomly selected and 
sent a survey questionnaire. After consenting to participate, 
households will be asked about symptoms and duration of any recent 
gastrointestinal or respiratory illness, tap water consumption, and 
other factors including international travel, daycare attendance or 
employment, and exposure to under-cooked or unpasteurized food, pets 
and other animal contact, and recreational water. Study participants 
will be able to choose their method of survey response from a variety 
of options including a paper survey, telephone-administered survey, or 
Web-based survey. A Spanish language version of the survey for all 
response options will also be available. Participation in this study 
will be voluntary. No financial compensation will be provided to study 
participants. The study duration is anticipated to last 12 months. An 
estimated 5,200 individuals will be contacted and we anticipate 2,080 
adults (18 years of age or older) will consent to participate in this 
study. We will conduct a pilot study (duration 3 months) prior to 
launching the full epidemiologic study. An estimated 1,000 individuals 
will be contacted and we anticipate 400 adults (18 years of age or 
older) will consent to participate in the pilot study. The total 
estimated annualized hours associated with this study, including the 
pilot, is expected to be 601.

[[Page 19363]]



                                       Estimate of Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                      Average
                                                     Number of       Number of      burden per     Total burden
      Type of respondents           Form name       respondents    responses per     response         (hours)
                                                                    respondent        (hours)
----------------------------------------------------------------------------------------------------------------
Full Study:
    Households................  Introductory               5,200               1            1/60              87
                                 letter and
                                 consent form.
    Households................  Web-based                  1,248               1           12/60             250
                                 questionnaire.
    Households................  Paper-based                  624               1           12/60             125
                                 questionnaire.
    Households................  Telephone-based              208               1           12/60              42
                                 questionnaire.
                                                 ---------------------------------------------------------------
        Total (full study):...  ................  ..............  ..............  ..............             504
----------------------------------------------------------------------------------------------------------------
Pilot Study:
    Households................  Introductory                1000               1            1/60              17
                                 letter and
                                 consent form.
    Households................  Web-based                    240               1           12/60              48
                                 questionnaire.
    Households................  Paper-based                  120               1           12/60              24
                                 questionnaire.
    Households................  Telephone-based               40               1           12/60               8
                                 questionnaire.
                                                 ---------------------------------------------------------------
        Total (pilot study)...  ................  ..............  ..............  ..............              97
                                                 ---------------------------------------------------------------
        Total (Full & Pilot)..  ................  ..............  ..............  ..............             601
----------------------------------------------------------------------------------------------------------------


Daniel Holcomb,
Reports Clearance Officer, Centers for Disease Control and Prevention.
[FR Doc. 2011-8271 Filed 4-6-11; 8:45 am]
BILLING CODE 4163-18-P
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