Proposed Data Collections Submitted for Public Comment and Recommendations, 40297-40298 [E7-14282]

Download as PDF 40297 Federal Register / Vol. 72, No. 141 / Tuesday, July 24, 2007 / Notices or other forms of information technology. Written comments should be received within 60 days of this notice. Proposed Project Ingredients Added to, and the Quantity of Nicotine Contained in, Smokeless Tobacco Manufactured, Imported, or Packaged in the U.S.— Reinstatement with Change—National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC). Background and Brief Description The Comprehensive Smokeless Tobacco Health Education Act of 1986 (15 U.S.C. 4401 et seq., Pub. L. 99–252) requires each person who manufactures, packages, or imports smokeless tobacco (SLT) to provide the Secretary of Health and Human Services (HHS) with a list of ingredients added to tobacco in the manufacture of smokeless tobacco products. This legislation also authorizes HHS to undertake research, and submit an annual report to Congress (as deemed appropriate) discussing the health effects of the ingredients in smokeless tobacco products. HHS has delegated responsibility for the implementation of this Act to CDC’s Office on Smoking and Health (OSH). The oral use of SLT represents a significant health risk which can cause cancer and a number of non-cancerous oral conditions, and can lead to nicotine addiction and dependence. Furthermore, SLT use is not a safe substitute for cigarette smoking. Estimated burden for testing and reporting of un-ionized nicotine, total moisture, and pH for smokeless tobacco is one response per year, averaging 1,713 hours to prepare, at a cost of $1,139 per respondent, for 11 companies. The total hourly burden would be 18,843 hours, with a total cost of $12,529. The only cost to respondents is their time to complete the survey. ESTIMATED ANNUALIZED BURDEN HOURS Respondents Number of respondents Number of responses per respondent Average burden per response (in hrs.) Total burden (in hours) Smokeless Tobacco Products Manufacturers ................................................. 11 1 1713 18,843 Dated: July 18, 2007. Maryam I. Daneshvar, Acting Reports Clearance Officer, Centers for Disease Control and Prevention. [FR Doc. E7–14273 Filed 7–23–07; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60Day–07–07BJ] mstockstill on PROD1PC66 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 Maryam I. Daneshvar, 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 VerDate Aug<31>2005 17:50 Jul 23, 2007 Jkt 211001 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 Economic Analysis of the National Program of Cancer Registries—NEW— National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC). Background and Brief Description The National Program of Cancer Registries (NPCR) is a nationwide, comprehensive federally sponsored public health program. Established by Congress through the Cancer Registries Amendment Act in 1992, and administered by the Centers for Disease Control and Prevention (CDC), the NPCR collects data on the occurrence of cancer; the type, extent, and location of the cancer; and the type of initial treatment. Since the establishment of NPCR there has been no published systematic analysis of the true economic costs incurred by the program. As the program matures and gains national PO 00000 Frm 00028 Fmt 4703 Sfmt 4703 attention, and in light of the recent increases in total program funding as well as wide variations in the cost per case collected, there is now a greater need for an economic evaluation of the program. The purpose of this task is to assess the costs, effectiveness, and costeffectiveness of NPCR in collecting high quality data on cancer incidence, and to develop tools for making resource allocation decisions that will meet program priorities. Performing an assessment of the resources expended on NPCR in relation to the value created will provide critical information for improving program efficiency within the various components of the NPCR and potentially identifying economies of scale. This task will involve collection and analysis of cost and effectiveness data from all 45 state registries, funded by NPCR, for three years. A pilot questionnaire was developed and piloted tested with 7 registries and information learn during the pilot testing was incorporated to develop a comprehensive cost collection tool. RTI International, the contractor hired by CDC will build a web based data collection tool to collect annual cost data from the 45 state registries. All data will be submitted electronically by grantees to reduce the respondent burden and errors. The contractor will also develop a user’s manual to assist the grantees with completing their data submission. E:\FR\FM\24JYN1.SGM 24JYN1 40298 Federal Register / Vol. 72, No. 141 / Tuesday, July 24, 2007 / Notices Since certain program level data are already collected as part of NPCR Annual Program Evaluation Instrument (OMB i#0920–0706), the additional burden on grantees will be modest. for their time to complete the questionnaire. All respondents will be using the same cost assessment tool. The only cost to the respondent is their time. Once the infrastructure is established to capture the cost data from the NPCR programs, the response burden is expected to be reduced even further. There are no costs to respondents except ESTIMATED ANNUALIZED BURDEN HOURS Respondents Number of respondents Number of responses per respondent Average burden per response (in hours) Total burden (in hours) State Health Officials—NPCR funded registries ............................................. 45 3 22 2,970 ........................ ........................ ........................ 2,970 Total .......................................................................................................... Dated: July 18, 2007. Maryam I. Daneshvar, Acting Reports Clearance Officer, Centers for Disease Control and Prevention. [FR Doc. E7–14282 Filed 7–23–07; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Proposed Project Centers for Disease Control and Prevention [60Day–07–07BK] mstockstill on PROD1PC66 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 Maryam I. Daneshvar, 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 VerDate Aug<31>2005 19:13 Jul 23, 2007 Jkt 211001 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. Transgender HIV Behavioral Survey (THBS)—New—National Center for HIV, Hepatitis, STD, and TB Prevention (NCHHSTP), Centers for Disease Control and Prevention (CDC). Background and Brief Description The purpose of this data collection is to pilot a survey that will be used to monitor behaviors related to Human Immunodeficiency Virus (HIV) infection among transgender persons who are assigned a male sex at birth. The goal of the survey will be to obtain data from samples of transgender persons to (a) describe the prevalence in risk behaviors; (b) describe the prevalence of HIV testing and HIV infection; (c) describe the prevalence of the use of HIV prevention services; (d) identify met and unmet needs for HIV prevention services in order to inform health departments, community based organizations, community planning groups and other stakeholders. The objectives of the pilot will be to assess the content of the questionnaire as well as the efficiency and feasibility of the methods for sampling and recruiting transgender persons. This project addresses the goals of CDC’s HIV Prevention Strategic Plan, specifically the goal of strengthening the national capacity to monitor the HIV epidemic to PO 00000 Frm 00029 Fmt 4703 Sfmt 4703 better direct and evaluate prevention efforts. Data will be collected through inperson and computer-assisted self interviews conducted in 4 Metropolitan Statistical Areas (MSA) throughout the United States. The MSA chosen will be among those currently participating in the National HIV Behavioral Surveillance system (see Federal Registry dated January 19, 2007: Vol. 72, No. 12, pages 2529–2530). A brief inperson screening interview will be used to determine eligibility for participation in the full survey. Data for the full survey will be collected using computer-assisted self interviews. Besides determining the content of the final survey instrument and the sampling methods, the data from the full survey will provide estimates of behavior related to the risk of HIV and other sexually transmitted diseases, prior testing for HIV, and use of HIV prevention services. No other federal agency systematically collects this type of information from transgender persons at risk for HIV infection. This data will have substantial impact on prevention program development and monitoring at the local, state, and national levels. CDC will request a 2-year clearance for this information collection. CDC estimates that, in each year, THBS will involve eligibility screening of a total of 240 persons and will collect survey information from 200 eligible respondents. Thus, over the two year period 480 persons are estimated to complete the screener and 400 eligible respondents to complete the survey. Participation of respondents is voluntary and there is no cost to the respondents other than their time. E:\FR\FM\24JYN1.SGM 24JYN1

Agencies

[Federal Register Volume 72, Number 141 (Tuesday, July 24, 2007)]
[Notices]
[Pages 40297-40298]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-14282]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[60Day-07-07BJ]


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 Maryam I. Daneshvar, 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

    Economic Analysis of the National Program of Cancer Registries--
NEW--National Center for Chronic Disease Prevention and Health 
Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC).

Background and Brief Description

    The National Program of Cancer Registries (NPCR) is a nationwide, 
comprehensive federally sponsored public health program. Established by 
Congress through the Cancer Registries Amendment Act in 1992, and 
administered by the Centers for Disease Control and Prevention (CDC), 
the NPCR collects data on the occurrence of cancer; the type, extent, 
and location of the cancer; and the type of initial treatment. Since 
the establishment of NPCR there has been no published systematic 
analysis of the true economic costs incurred by the program. As the 
program matures and gains national attention, and in light of the 
recent increases in total program funding as well as wide variations in 
the cost per case collected, there is now a greater need for an 
economic evaluation of the program.
    The purpose of this task is to assess the costs, effectiveness, and 
cost-effectiveness of NPCR in collecting high quality data on cancer 
incidence, and to develop tools for making resource allocation 
decisions that will meet program priorities. Performing an assessment 
of the resources expended on NPCR in relation to the value created will 
provide critical information for improving program efficiency within 
the various components of the NPCR and potentially identifying 
economies of scale.
    This task will involve collection and analysis of cost and 
effectiveness data from all 45 state registries, funded by NPCR, for 
three years. A pilot questionnaire was developed and piloted tested 
with 7 registries and information learn during the pilot testing was 
incorporated to develop a comprehensive cost collection tool. RTI 
International, the contractor hired by CDC will build a web based data 
collection tool to collect annual cost data from the 45 state 
registries. All data will be submitted electronically by grantees to 
reduce the respondent burden and errors. The contractor will also 
develop a user's manual to assist the grantees with completing their 
data submission.

[[Page 40298]]

    Since certain program level data are already collected as part of 
NPCR Annual Program Evaluation Instrument (OMB i0920-0706), 
the additional burden on grantees will be modest. Once the 
infrastructure is established to capture the cost data from the NPCR 
programs, the response burden is expected to be reduced even further. 
There are no costs to respondents except for their time to complete the 
questionnaire. All respondents will be using the same cost assessment 
tool. The only cost to the respondent is their time.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                  Number of     Average  burden
                 Respondents                     Number of      responses per     per response     Total burden
                                                respondents       respondent       (in hours)       (in hours)
----------------------------------------------------------------------------------------------------------------
State Health Officials--NPCR funded                       45                3               22            2,970
 registries.................................
                                             -------------------------------------------------------------------
    Total...................................  ...............  ...............  ...............           2,970
----------------------------------------------------------------------------------------------------------------


    Dated: July 18, 2007.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and 
Prevention.
 [FR Doc. E7-14282 Filed 7-23-07; 8:45 am]
BILLING CODE 4163-18-P
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