Proposed Data Collections Submitted for Public Comment and Recommendations, 36345-36346 [E6-10025]

Download as PDF 36345 Federal Register / Vol. 71, No. 122 / Monday, June 26, 2006 / Notices 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 Colorectal Cancer Screening Demonstration Program—New— Division of Cancer Prevention and Control (DCPC), National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC). Background and Brief Description The CDC, DCPC is requesting approval to collect individual patientlevel screening, diagnostic, and treatment data in association with a new colorectal cancer screening demonstration program. DCPC is funding 5 cooperative agreements from fiscal year (FY) 2005–2008 for implementation of new colorectal cancer (CRC) demonstration programs. These 3-year demonstration programs are designed to increase populationbased CRC screening among persons 50 years and older with low income and inadequate or no health insurance coverage in a geographically defined area. Colorectal Cancer (CRC) is the second leading cause of cancer-related deaths in the United States, following lung Submitted data must contain no patient identifiers. All programs will additionally submit annual cost data to CDC to be used to monitor cost and cost-effectiveness over the 3-year program period. The additional burden to these respondents will be small, since CDC will only select programs that are already performing some CRC screening, and will therefore already be collecting these types of data. Data collection for both patient-level and cost data will continue over the 3 years of the demonstration programs. In the burden table below, two data collection forms will be used: Patientlevel clinical data collection forms and cost data collection forms. The data will be collected from the 5 cooperative agreement recipients, i.e., the respondents. The estimated number of responses represents the number of patients receiving clinical services per recipient program, one report per patient per quarterly reporting period (estimated at 70 patients per program per quarter). This would result in an estimated annualized burden for the quarterly reports of 583 hours. Additionally, respondents will report annual cost data. For reporting the annual cost data, the respondents will submit only one report each for the entire year. There is no cost to respondents other than their time. cancer. Based on scientific evidence which indicates that regular screening is effective in reducing CRC incidence and mortality, regular CRC screening is now recommended for average-risk persons with one or a combination of the following tests: Fecal occult blood testing (FOBT), flexible sigmoidoscopy, colonoscopy, and/or double-contrast barium enema (DCBE). Fecal immunochemical testing (FIT) is considered an acceptable alternative to FOBT. In the absence of evidence indicating a single most effective test, selected programs will be able to choose which screening test(s) they will use from the above list of recommended tests. All funded programs will be required to submit patient-level data on CRC screening and diagnostic services provided as part of this demonstration project. This information will be used to assess the quality and appropriateness of the services delivered. Programs that receive CDC funding to provide screening and diagnostic services will collect individual patientlevel data to capture demographic information, clinical services and outcomes, and submit these data to CDC on a quarterly basis. While CDC funds will not be used for treatment, programs will need to monitor treatment and document that patients are receiving appropriate treatment services. ESTIMATED ANNUALIZED BURDEN HOURS Form type Number of respondents Number of responses per respondent Average burden per response (in hours) Total burden hours Quarterly patient-level clinical data .................................................................. Annual cost data .............................................................................................. 5 5 280 1 25/60 25/60 583 2 ........................ ........................ ........................ 585 Total .......................................................................................................... Dated: June 20, 2006. Joan F. Karr, Acting Reports Clearance Officer, Centers for Disease Control and Prevention. [FR Doc. E6–10024 Filed 6–23–06; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60Day–06–06BJ] rwilkins on PROD1PC63 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 VerDate Aug<31>2005 17:00 Jun 23, 2006 Jkt 208001 PO 00000 Frm 00032 Fmt 4703 Sfmt 4703 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 Seleda Perryman, CDC Assistant 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) E:\FR\FM\26JNN1.SGM 26JNN1 36346 Federal Register / Vol. 71, No. 122 / Monday, June 26, 2006 / Notices 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 Experiment in Mapping Behavioral Risk Factors Surveillance Survey (BRFSS) Data—NEW—National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC). Background and Brief Description The purpose of this study is to design and implement a Web-based interview examining the differential effectiveness of presenting BRFSS data in two different mapping formats, choropleth versus isopleth maps. Traditionally, geospatial data are presented in categories. To maintain a low survey burden for each participant, the instrument will include only 4 questions for each of 10 maps. The interview will also include additional questions about respondent’s preferences for map types and background characteristics. The survey instrument will be comprised of 50 items, including the 40 map questions, 4 questions about users’ preferences for different map formats, and 6 questions about their educational and professional background and demographic characteristics. Analysis of the data will assess 4 key areas to determine which type of map is ideal for presenting BRFSS data: 1. Rate retrieval 2. Pattern recognition 3. Ease of understanding 4. User preferences The results of these analyses will be presented in a final report to be submitted to the CDC. There are no costs to respondents other than their time. choropleth maps, where defined geographic units, such as county or state boundaries, are filled with a uniform color or pattern. Choropleth maps present data as geographic areas shaded with intensity proportional to the data values associated with those areas. Such maps are appropriate for data that have been scaled or normalized. Alternatively, geospatial data can be displayed using isopleth maps, in which the data are not aggregated to predefined geographic units, but instead are ‘‘smoothed’’ across adjacent geographic boundaries. Such maps may show county or state boundaries, but different categories of data are not defined by these geographic units. Little empirical research has examined the differential effectiveness of choropleth versus isopleth maps. In particular, researchers know little about how the two different mapping techniques affect the user’s ability to extract information from the map. The Web-based interview will present both choropleth and isopleth maps displaying BRFSS data in seven color ESTIMATED ANNUALIZED BURDEN HOURS Respondents Number of respondents Number of responses per respondent Average burden per response (in hrs.) Total burden hours Experiment in Mapping BRFSS Data .............................................................. 400 1 30/60 200 ........................ ........................ ........................ 200 Total .......................................................................................................... Dated: June 19, 2006. Joan F. Karr, Acting Reports Clearance Officer, Centers for Disease Control and Prevention. [FR Doc. E6–10025 Filed 6–23–06; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60Day–06–05BL] rwilkins on PROD1PC63 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 VerDate Aug<31>2005 17:00 Jun 23, 2006 Jkt 208001 the data collection plans and instruments, call 404–639–5960 and send comments to Seleda Perryman, CDC Assistant 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 Worksheet for Medical Conditions among Refugees and Immigrants— PO 00000 Frm 00033 Fmt 4703 Sfmt 4703 New—National Center for Infectious Diseases (NCID), Centers for Disease Control and Prevention (CDC). Background and Brief Description Clearance is being requested for a ‘‘Worksheet for Medical Conditions among Refugees and Immigrants’’ for state and local health refugee coordinators to identify specific medical conditions of public health importance in newly arrived refugees and immigrants. CDC requests notification of specific medical conditions listed on the worksheet, including Class A and B health conditions not recognized overseas, and substantial discrepancies in the overseas and U.S. based medical evaluations. Section 412 of the Immigration and Nationality Act (INA) (8 U.S.C. 1522(b)(4)) authorizes the Secretary of Health and Human Services Department of Health and Human Services (DHHS) to: (A) Assure that an adequate number of trained staff are available at the location at which the refugees enter the United States to assure that all necessary medical E:\FR\FM\26JNN1.SGM 26JNN1

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[Federal Register Volume 71, Number 122 (Monday, June 26, 2006)]
[Notices]
[Pages 36345-36346]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-10025]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[60Day-06-06BJ]


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 Seleda Perryman, CDC Assistant 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)

[[Page 36346]]

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

    Experiment in Mapping Behavioral Risk Factors Surveillance Survey 
(BRFSS) Data--NEW--National Center for Chronic Disease Prevention and 
Health Promotion (NCCDPHP), Centers for Disease Control and Prevention 
(CDC).

Background and Brief Description

    The purpose of this study is to design and implement a Web-based 
interview examining the differential effectiveness of presenting BRFSS 
data in two different mapping formats, choropleth versus isopleth maps. 
Traditionally, geospatial data are presented in choropleth maps, where 
defined geographic units, such as county or state boundaries, are 
filled with a uniform color or pattern. Choropleth maps present data as 
geographic areas shaded with intensity proportional to the data values 
associated with those areas. Such maps are appropriate for data that 
have been scaled or normalized. Alternatively, geospatial data can be 
displayed using isopleth maps, in which the data are not aggregated to 
pre-defined geographic units, but instead are ``smoothed'' across 
adjacent geographic boundaries. Such maps may show county or state 
boundaries, but different categories of data are not defined by these 
geographic units. Little empirical research has examined the 
differential effectiveness of choropleth versus isopleth maps. In 
particular, researchers know little about how the two different mapping 
techniques affect the user's ability to extract information from the 
map.
    The Web-based interview will present both choropleth and isopleth 
maps displaying BRFSS data in seven color categories. To maintain a low 
survey burden for each participant, the instrument will include only 4 
questions for each of 10 maps. The interview will also include 
additional questions about respondent's preferences for map types and 
background characteristics. The survey instrument will be comprised of 
50 items, including the 40 map questions, 4 questions about users' 
preferences for different map formats, and 6 questions about their 
educational and professional background and demographic 
characteristics. Analysis of the data will assess 4 key areas to 
determine which type of map is ideal for presenting BRFSS data:
    1. Rate retrieval
    2. Pattern recognition
    3. Ease of understanding
    4. User preferences
    The results of these analyses will be presented in a final report 
to be submitted to the CDC. There are no costs to respondents other 
than their time.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                  Number of     Average  burden
                 Respondents                     Number of      responses per    per  response     Total burden
                                                respondents       respondent       (in hrs.)          hours
----------------------------------------------------------------------------------------------------------------
Experiment in Mapping BRFSS Data............             400                1            30/60              200
                                             -------------------------------------------------------------------
    Total...................................  ...............  ...............  ...............             200
----------------------------------------------------------------------------------------------------------------


    Dated: June 19, 2006.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for Disease Control and 
Prevention.
[FR Doc. E6-10025 Filed 6-23-06; 8:45 am]
BILLING CODE 4163-18-P
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