[Federal Register Volume 75, Number 67 (Thursday, April 8, 2010)]
[Notices]
[Pages 17921-17922]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2010-7916]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30-Day-10-0745]


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 e-mail 
to [email protected]. 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

    Colorectal Cancer Screening Program (OMB No. 0920-0745 7/31/2010)--
Revision--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

    Colorectal Cancer (CRC) is the second leading cause of cancer-
related deaths in the United States, following lung 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.
    In 2005, CDC established a demonstration program to screen low-
income individuals 50 years of age and older who have no health 
insurance or inadequate health insurance for CRC. The five 
demonstration sites have reported information to CDC including de-
identified, patient-level demographic, screening, diagnostic, 
treatment, outcome and cost reimbursement data (Colorectal Cancer 
Screening Demonstration Program, OMB No. 0920-0745, exp. 7/31/2010).
    CDC requests OMB approval to continue the information collection 
for three years, with changes. First, the number of funded sites will 
increase from 5 to 26, and the term ``Demonstration'' will be deleted 
from the title. Second, there will be a reduction in the burden per 
respondent associated with the collection of clinical information. 
Reporting forms for medical complications and medically ineligible 
clients will be discontinued, the level of detail collected from 
endoscopy and pathology reports will be reduced, and the reporting form 
for colorectal cancer clinical data elements (CCDE) will be 
streamlined. As a result, the reporting burden per CCDE form will be 
similar regardless of primary test provided. Third, the collection of 
patient-level reimbursement cost data will be discontinued and will be 
replaced by the collection of program-level activity-based cost data 
using a Cost Assessment Tool (CAT). The information to be collected 
through the CAT will allow CDC to compare activity-based costs across 
multiple sites and programs, and will provide a more effective means of 
monitoring and improving the performance and cost-effectiveness of the 
CRC screening program.
    Each program site will screen an estimated 375 patients per year. 
De-identified CCDE information concerning approximately 187 new 
screening records will be transmitted to CDC electronically twice per 
year. Information collected through the Cost Assessment Tool will be 
transmitted electronically to CDC once per year. Reporting is required 
for all sites funded through the CRC screening program.
    The goals of the expanded CRC screening program are to increase 
population-based screening and to reduce health disparities in CRC 
screening, incidence and mortality. The program will continue to 
provide services to low-income individuals age 50 and older with 
inadequate or no health insurance for CRC.
    The total estimated annualized burden hours are 3,010. The increase 
in the number of funded sites and the proposed changes will result in 
an overall increase in burden to respondents. There are no costs to 
respondents other than their time.

                                        Estimated Annualized Burden Hours
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                                                                                                      Average
                                                                      No. of          No. of        burden per
          Type of respondents                   Form type           respondents    responses per   response (in
                                                                                    respondent        hours)
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Colorectal Cancer Screening Programs..  Clinical Data Elements..              26             375           15/60

[[Page 17922]]

 
                                        Cost Assessment Tool....              26               1              22
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    Dated: March 31, 2010.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and 
Prevention.
[FR Doc. 2010-7916 Filed 4-7-10; 8:45 am]
BILLING CODE 4163-18-P