Proposed Data Collection Submitted for Public Comment and Recommendations, 34631-34633 [2020-12244]

Download as PDF Federal Register / Vol. 85, No. 109 / Friday, June 5, 2020 / Notices period following the payment of the fee. Section 1102.403 clarified that States may align a one-year period with any 12-month period, which may, or may not, be based on the calendar year. The registration cycle is left to the individual States to determine. Current Action: There are no changes being made to this regulation. Type of Review: Extension of a currently approved collection. Affected Public: States; businesses or other for-profit and not-for-profit organizations. Estimated Number of Respondents: 500 AMCs, 55 States. Estimated Total Annual Burden Hours: 500 hours. Frequency of Response: Event generated. By the Appraisal Subcommittee. James R. Park, Executive Director. [FR Doc. 2020–12174 Filed 6–4–20; 8:45 am] BILLING CODE 6700–01–P GENERAL SERVICES ADMINISTRATION [OMB Control No. 3090–0118; Docket No. 2020–0001; Sequence No. 4] Information Collection; Federal Management Regulation; Standard Form 94, Statement of Witness Office of Government-Wide Policy (OGP), General Services Administration (GSA). ACTION: Notice; request for comments. AGENCY: Under the provisions of the Paperwork Reduction Act, the Regulatory Secretariat Division will be submitting to the Office of Management and Budget (OMB) a request to review and approve an existing information collection requirement regarding OMB Control No: 3090–0118; Standard Form 94, Statement of Witness. DATES: Submit comments on or before August 3, 2020. ADDRESSES: Submit comments identified by Information Collection 3090–0118; Standard Form 94, Statement of Witness via https:// www.regulations.gov. Submit comments via the Federal eRulemaking portal by searching for ‘‘Information Collection 3090–0118; Standard Form 94, Statement of Witness’’. Select the link ‘‘Submit a Comment’’ that corresponds with ‘‘Information Collection 3090– 0118; Standard Form 94, Statement of Witness.’’ Follow the instructions provided at the ‘‘Submit a Comment’’ screen. Please include your name, company name (if any), and lotter on DSK9F5VC42PROD with NOTICES SUMMARY: VerDate Sep<11>2014 18:21 Jun 04, 2020 Jkt 250001 ‘‘Information Collection 3090–0118; Standard Form 94, Statement of Witness’’ on your attached document. If your comment cannot be submitted using https://www.regulations.gov, call or email the points of contact in the FOR FURTHER INFORMATION CONTACT section of this document for alternate instructions. Instructions: Please submit comments only and cite Information Collection 3090–0118; Standard Form 94, Statement of Witness, in all correspondence related to this collection. Comments received generally will be posted without change to https:// www.regulations.gov, including any personal and/or business confidential information provided. To confirm receipt of your comment(s), please check www.regulations.gov, approximately two-to-three days after submission to verify posting. FOR FURTHER INFORMATION CONTACT: Mr. Ray Wynter, GSA, Office of Government-wide Policy (MAG), Office of Asset and Transportation Management, at telephone 202–501– 3802 or via email to ray.wynter@gsa.gov. SUPPLEMENTARY INFORMATION: A. Purpose GSA’s Office of Government-wide Policy is announcing the availability of Standard Form 94, Statement of Witness that is publicly available on https:// www.gsa.gov/forms. This updated Standard Form 94, Statement of Witness is a renewal of a currently approved information collection requirement regarding statement from witnesses. This form will be used to collect information from witnesses reporting accidents and/or damage to Federal Fleet Vehicles. B. Annual Reporting Burden Respondents: 290. Responses per Respondent: 1. Total Annual Responses: 290. Hours per Response: 0.333. Total Burden Hours: 97. C. Public Comments Public comments are particularly invited on: Whether this collection of information is necessary, whether it will have practical utility; whether our estimate of the public burden of this collection of information is accurate, and based on valid assumptions and methodology; ways to enhance the quality, utility, and clarity of the information to be collected; and ways in which we can minimize the burden of the collection of information on those who are to respond, through the use of appropriate technological collection techniques or other forms of information technology. PO 00000 Frm 00043 Fmt 4703 Sfmt 4703 34631 Obtaining Copies of Proposals: Requesters may obtain a copy of the information collection documents from the Regulatory Secretariat Division, at GSARegSec@gsa.gov. Please cite OMB Control No. 3090–0118, Standard Form 94, Statement of Witness, in all correspondence. Beth Anne Killoran, Deputy Chief Information Officer. [FR Doc. 2020–12181 Filed 6–4–20; 8:45 am] BILLING CODE 6820–14–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60Day–20–1074; Docket No. CDC–2020– 0064] Proposed Data Collection Submitted for Public Comment and Recommendations Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). ACTION: Notice with comment period. AGENCY: The Centers for Disease Control and Prevention (CDC), as part of its continuing effort to reduce public burden and maximize the utility of government information, invites the general public and other Federal agencies the opportunity to comment on a proposed and/or continuing information collection, as required by the Paperwork Reduction Act of 1995. This notice invites comment on a proposed information collection project titled Colorectal Cancer Control Program (CRCCP) Monitoring Activities. CDC is requesting a revision to OMB No. 0920– 1074 to include a redesigned survey, a redesigned clinic-level data collection instrument, and a new quarterly awardee-level program update survey. DATES: CDC must receive written comments on or before August 4, 2020. ADDRESSES: You may submit comments, identified by Docket No. CDC–2020– 0064 by any of the following methods: • Federal eRulemaking Portal: Regulations.gov. Follow the instructions for submitting comments. • Mail: Jeffrey M. Zirger, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS–D74, Atlanta, Georgia 30329. Instructions: All submissions received must include the agency name and Docket Number. CDC will post, without change, all relevant comments to Regulations.gov. SUMMARY: E:\FR\FM\05JNN1.SGM 05JNN1 34632 Federal Register / Vol. 85, No. 109 / Friday, June 5, 2020 / Notices Please note: Submit all comments through the Federal eRulemaking portal (regulations.gov) or by U.S. mail to the address listed above. To request more information on the proposed project or to obtain a copy of the information collection plan and instruments, contact Jeffrey M. Zirger, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS– D74, Atlanta, Georgia 30329; phone: 404–639–7118; Email: omb@cdc.gov. FOR FURTHER INFORMATION CONTACT: lotter on DSK9F5VC42PROD with NOTICES SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3501–3520), Federal agencies must obtain approval from the Office of Management and Budget (OMB) for each collection of information they conduct or sponsor. In addition, the PRA also requires Federal agencies to provide a 60-day notice in the Federal Register concerning each proposed collection of information, including each new proposed collection, each proposed extension of existing collection of information, and each reinstatement of previously approved information collection before submitting the collection to the OMB for approval. To comply with this requirement, we are publishing this notice of a proposed data collection as described below. The OMB is particularly interested in comments that will help: 1. Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; 2. Evaluate the accuracy of the agency’s estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; 3. Enhance the quality, utility, and clarity of the information to be collected; and 4. Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submissions of responses. 5. Assess information collection costs. VerDate Sep<11>2014 18:21 Jun 04, 2020 Jkt 250001 Proposed Project Colorectal Cancer Control Program (CRCCP) Monitoring Activities (OMB Control No. 0920–1074, Exp. 7/31/ 2020)—Revision—National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC) Background and Brief Description CDC is requesting a revision to Colorectal Cancer Control Program (CRCCP) Monitoring Activities (OMB Control No. 0920–1074). Based on feedback from awardees and internal subject matter experts, CDC proposes use of a revised annual grantee survey instrument (renamed, Annual Awardee Survey), a revised clinic-level data collection instrument, and a new awardee-level quarterly program update. The number of respondents will also increase from 30 to 35 awardees. Total estimated annualized burden will increase. OMB approval is requested for three years. Colorectal cancer (CRC) is the second leading cause of death from cancer in the United States among cancers that affect both men and women. There is substantial evidence that CRC screening reduces the incidence of and death from the disease. Screening for CRC can detect disease early when treatment is more effective, and prevent cancer by finding and removing precancerous polyps. Of individuals diagnosed with early stage CRC, more than 90% live five or more years. Despite strong evidence supporting screening, only 68.8% of adults currently report being up-to-date with CRC screening as recommended by the U.S. Preventive Services Task Force, with more than 22 million age-eligible adults estimated to be untested. To reduce CRC morbidity, mortality, and associated costs, use of CRC screening tests must be increased among age-eligible adults with the lowest CRC screening rates. The purpose of the Colorectal Cancer Control Program (CRCCP) is to partner with health systems and their individual primary care clinics to implement EBIs to increase CRC screening among defined populations of adults ages 50–75 that have CRC screening rates lower than the national, regional, or local rate. The previous cooperative agreement supporting the CRCCP (DP15–1502) funded 30 awardees that are state governments or bona-fide agents, universities, and tribal organizations. All 30 recipients received Component 1 funding, which required recipients to partner with health systems and their primary care clinics to implement at least two of four priority PO 00000 Frm 00044 Fmt 4703 Sfmt 4703 evidence-based interventions (EBIs) described in The Guide to Community Preventive Services as well as other supporting strategies. In addition, six recipients received Component 2 funding to provide clinical screening and follow-up services for a limited number of individuals aged 50–64 in the program’s priority population who are asymptomatic, at average risk for CRC, have inadequate or no health insurance for CRC screening, and are low income. In 2020, CDC issued a new funding opportunity, Public Health and Health System Partnerships to Increase Colorectal Cancer Screening in Clinical Settings (DP20–2002), a five-year cooperative agreement to increase CRC screening among defined populations of adults ages 50–75 that have CRC screening rates lower than the national, regional, or local rate. Similar to DP15– 1502, DP20–2002 funds recipients to partner with health systems and their primary care clinics to implement multiple EBIs, partner with organizations to support implementation of EBIs in those clinics, and collect high-quality clinic-level data when a clinic is recruited to participate (baseline) and annually thereafter to monitor EBI implementation and assess screening rate changes. DP20–2002 eliminates Component 2 funding to provide direct clinical service delivery. However, DP20–2002 requires recipients to conduct a formal capacity/ readiness assessment of potential clinics to implement EBIs, use assessment findings to select appropriate EBIs for implementation, and provide clinics with limited financial resources to support follow-up colonoscopies for under- and uninsured patients after an abnormal CRC screening test. CDC proposes three information collections—a revised Annual Awardee Survey, a revised Clinic-Level Data Collection Instrument, and a new awardee-level Quarterly Program Update—to reflect the strategies and objectives detailed in DP20–2002. The previous Annual Awardee Survey assessed: (1) Program management, (2) health information technology, (3) partnerships, (4) data use, (5) training and technical assistance (TA), (6) clinic service delivery. The revised instrument no longer includes questions related to clinic service delivery since these pertained solely to Component 2, which is no longer funded under DP20–2002. In addition, many program management questions were eliminated and will now be gathered via the Quarterly Program Update on a quarterly basis to better inform CDC TA. Several data use questions were eliminated as they did not yield meaningful data to inform E:\FR\FM\05JNN1.SGM 05JNN1 34633 Federal Register / Vol. 85, No. 109 / Friday, June 5, 2020 / Notices CDC TA during the previous funding cycle. The previous Clinic-level Data Collection instrument assessed: (1) Health system and clinic characteristics, (2) EBI and supporting activities implementation within clinics; (3) monitoring and quality improvement activities, and (4)CRC screening rates. The revised instrument was reorganized (e.g., sections merged, variables moved to new sections) for increased efficiency and to improve overall data quality. In addition, wording and responses for many variables and their response options have undergone minor revisions to better capture awardees’ partnerships with both health systems and clinics, and appropriate capture of baseline and annual variables. The revised Redesigned data elements will enable CDC to better gauge progress in meeting CRCCP program goals and monitor implementation activities, evaluate outcomes, and identify awardee TA needs. In addition, data collected will inform program improvement and help identify successful activities that need to be maintained, replicated, or expanded. OMB approval is requested for three years. The number of awardees will increase from 30 awardees in DP15– 1502 to 35 awardees in DP20–2002, and the number of clinic partners is expected to increase from 12 to 24 per awardee. Therefore, the total estimated annualized burden hours have increased from 204 to 663 hours. instrument gathers information to assess health system and clinic characteristics; program reach; CRC screening practices and outcomes; clinics’ quality improvement and monitoring activities; EBI implementation, and additional factors that affect EBI implementation over time. The new Quarterly Program Update will collect standardized awardee-level information on aspects of program management, including (1) quarterly program expenditures, (2) current staff vacancies, (3) program successes and challenges, and (4) current TA needs. This information collection will provide CDC staff rapid reporting of programmatic information to inform their efforts to provide awardees with tailored TA. ESTIMATED ANNUALIZED BURDEN HOURS Average burden per response (in hr) Total burden (in hr) Form name CRCCP Awardees ......... CRCCP Annual Awardee Survey ........................ CRCCP Clinic-level Information Collection Instrument. CRCCP Quarterly Program Update .................... 35 35 1 24 15/60 43/60 9 602 35 4 22/60 52 .............................................................................. ........................ ........................ ........................ 663 Total ........................ Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Scientific Integrity, Office of Science, Centers for Disease Control and Prevention. [FR Doc. 2020–12244 Filed 6–4–20; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60Day–20–20OS; Docket No. CDC–2020– 0062] Proposed Data Collection Submitted for Public Comment and Recommendations Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). ACTION: Notice with comment period. AGENCY: The Centers for Disease Control and Prevention (CDC), as part of its continuing effort to reduce public burden and maximize the utility of government information, invites the general public and other Federal agencies the opportunity to comment on a proposed and/or continuing information collection, as required by the Paperwork Reduction Act of 1995. SUMMARY: lotter on DSK9F5VC42PROD with NOTICES Number of responses per respondent Number of respondents Type of respondent VerDate Sep<11>2014 18:21 Jun 04, 2020 Jkt 250001 This notice invites comment on a proposed information collection project titled COVID–19 Pandemic Response, Laboratory Data Reporting. The collection will be used to gather comprehensive laboratory testing data to ensure a rapid and thorough federal response to the COVID–19 pandemic. DATES: CDC must receive written comments on or before August 4, 2020. ADDRESSES: You may submit comments, identified by Docket No. CDC–2020– 0062 by any of the following methods: • Federal eRulemaking Portal: Regulations.gov. Follow the instructions for submitting comments. • Mail: Jeffrey M. Zirger, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS–D74, Atlanta, Georgia 30329. Instructions: All submissions received must include the agency name and Docket Number. CDC will post, without change, all relevant comments to Regulations.gov. Please note: Submit all comments through the Federal eRulemaking portal (regulations.gov) or by U.S. mail to the address listed above. To request more information on the proposed project or to obtain a copy of FOR FURTHER INFORMATION CONTACT: PO 00000 Frm 00045 Fmt 4703 Sfmt 4703 the information collection plan and instruments, contact Jeffrey M. Zirger, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS– D74, Atlanta, Georgia 30329; phone: 404–639–7570; Email: omb@cdc.gov. Under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3501–3520), Federal agencies must obtain approval from the Office of Management and Budget (OMB) for each collection of information they conduct or sponsor. In addition, the PRA also requires Federal agencies to provide a 60-day notice in the Federal Register concerning each proposed collection of information, including each new proposed collection, each proposed extension of existing collection of information, and each reinstatement of previously approved information collection before submitting the collection to the OMB for approval. To comply with this requirement, we are publishing this notice of a proposed data collection as described below. The OMB is particularly interested in comments that will help: 1. Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including SUPPLEMENTARY INFORMATION: E:\FR\FM\05JNN1.SGM 05JNN1

Agencies

[Federal Register Volume 85, Number 109 (Friday, June 5, 2020)]
[Notices]
[Pages 34631-34633]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-12244]


=======================================================================
-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[60Day-20-1074; Docket No. CDC-2020-0064]


Proposed Data Collection Submitted for Public Comment and 
Recommendations

AGENCY: Centers for Disease Control and Prevention (CDC), Department of 
Health and Human Services (HHS).

ACTION: Notice with comment period.

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

SUMMARY: The Centers for Disease Control and Prevention (CDC), as part 
of its continuing effort to reduce public burden and maximize the 
utility of government information, invites the general public and other 
Federal agencies the opportunity to comment on a proposed and/or 
continuing information collection, as required by the Paperwork 
Reduction Act of 1995. This notice invites comment on a proposed 
information collection project titled Colorectal Cancer Control Program 
(CRCCP) Monitoring Activities. CDC is requesting a revision to OMB No. 
0920-1074 to include a redesigned survey, a redesigned clinic-level 
data collection instrument, and a new quarterly awardee-level program 
update survey.

DATES: CDC must receive written comments on or before August 4, 2020.

ADDRESSES: You may submit comments, identified by Docket No. CDC-2020-
0064 by any of the following methods:
     Federal eRulemaking Portal: Regulations.gov. Follow the 
instructions for submitting comments.
     Mail: Jeffrey M. Zirger, Information Collection Review 
Office, Centers for Disease Control and Prevention, 1600 Clifton Road 
NE, MS-D74, Atlanta, Georgia 30329.
    Instructions: All submissions received must include the agency name 
and Docket Number. CDC will post, without change, all relevant comments 
to Regulations.gov.


[[Page 34632]]


    Please note:  Submit all comments through the Federal 
eRulemaking portal (regulations.gov) or by U.S. mail to the address 
listed above.


FOR FURTHER INFORMATION CONTACT: To request more information on the 
proposed project or to obtain a copy of the information collection plan 
and instruments, contact Jeffrey M. Zirger, Information Collection 
Review Office, Centers for Disease Control and Prevention, 1600 Clifton 
Road NE, MS-D74, Atlanta, Georgia 30329; phone: 404-639-7118; Email: 
[email protected].

SUPPLEMENTARY INFORMATION: 
    Under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3501-
3520), Federal agencies must obtain approval from the Office of 
Management and Budget (OMB) for each collection of information they 
conduct or sponsor. In addition, the PRA also requires Federal agencies 
to provide a 60-day notice in the Federal Register concerning each 
proposed collection of information, including each new proposed 
collection, each proposed extension of existing collection of 
information, and each reinstatement of previously approved information 
collection before submitting the collection to the OMB for approval. To 
comply with this requirement, we are publishing this notice of a 
proposed data collection as described below.
    The OMB is particularly interested in comments that will help:
    1. Evaluate whether the proposed collection of information is 
necessary for the proper performance of the functions of the agency, 
including whether the information will have practical utility;
    2. Evaluate the accuracy of the agency's estimate of the burden of 
the proposed collection of information, including the validity of the 
methodology and assumptions used;
    3. Enhance the quality, utility, and clarity of the information to 
be collected; and
    4. Minimize the burden of the collection of information on those 
who are to respond, including through the use of appropriate automated, 
electronic, mechanical, or other technological collection techniques or 
other forms of information technology, e.g., permitting electronic 
submissions of responses.
    5. Assess information collection costs.

Proposed Project

Colorectal Cancer Control Program (CRCCP) Monitoring Activities (OMB 
Control No. 0920-1074, Exp. 7/31/2020)--Revision--National Center for 
Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for 
Disease Control and Prevention (CDC)

Background and Brief Description

    CDC is requesting a revision to Colorectal Cancer Control Program 
(CRCCP) Monitoring Activities (OMB Control No. 0920-1074). Based on 
feedback from awardees and internal subject matter experts, CDC 
proposes use of a revised annual grantee survey instrument (renamed, 
Annual Awardee Survey), a revised clinic-level data collection 
instrument, and a new awardee-level quarterly program update. The 
number of respondents will also increase from 30 to 35 awardees. Total 
estimated annualized burden will increase. OMB approval is requested 
for three years.
    Colorectal cancer (CRC) is the second leading cause of death from 
cancer in the United States among cancers that affect both men and 
women. There is substantial evidence that CRC screening reduces the 
incidence of and death from the disease. Screening for CRC can detect 
disease early when treatment is more effective, and prevent cancer by 
finding and removing precancerous polyps. Of individuals diagnosed with 
early stage CRC, more than 90% live five or more years. Despite strong 
evidence supporting screening, only 68.8% of adults currently report 
being up-to-date with CRC screening as recommended by the U.S. 
Preventive Services Task Force, with more than 22 million age-eligible 
adults estimated to be untested. To reduce CRC morbidity, mortality, 
and associated costs, use of CRC screening tests must be increased 
among age-eligible adults with the lowest CRC screening rates.
    The purpose of the Colorectal Cancer Control Program (CRCCP) is to 
partner with health systems and their individual primary care clinics 
to implement EBIs to increase CRC screening among defined populations 
of adults ages 50-75 that have CRC screening rates lower than the 
national, regional, or local rate. The previous cooperative agreement 
supporting the CRCCP (DP15-1502) funded 30 awardees that are state 
governments or bona-fide agents, universities, and tribal 
organizations. All 30 recipients received Component 1 funding, which 
required recipients to partner with health systems and their primary 
care clinics to implement at least two of four priority evidence-based 
interventions (EBIs) described in The Guide to Community Preventive 
Services as well as other supporting strategies. In addition, six 
recipients received Component 2 funding to provide clinical screening 
and follow-up services for a limited number of individuals aged 50-64 
in the program's priority population who are asymptomatic, at average 
risk for CRC, have inadequate or no health insurance for CRC screening, 
and are low income.
    In 2020, CDC issued a new funding opportunity, Public Health and 
Health System Partnerships to Increase Colorectal Cancer Screening in 
Clinical Settings (DP20-2002), a five-year cooperative agreement to 
increase CRC screening among defined populations of adults ages 50-75 
that have CRC screening rates lower than the national, regional, or 
local rate. Similar to DP15-1502, DP20-2002 funds recipients to partner 
with health systems and their primary care clinics to implement 
multiple EBIs, partner with organizations to support implementation of 
EBIs in those clinics, and collect high-quality clinic-level data when 
a clinic is recruited to participate (baseline) and annually thereafter 
to monitor EBI implementation and assess screening rate changes. DP20-
2002 eliminates Component 2 funding to provide direct clinical service 
delivery. However, DP20-2002 requires recipients to conduct a formal 
capacity/readiness assessment of potential clinics to implement EBIs, 
use assessment findings to select appropriate EBIs for implementation, 
and provide clinics with limited financial resources to support follow-
up colonoscopies for under- and uninsured patients after an abnormal 
CRC screening test.
    CDC proposes three information collections--a revised Annual 
Awardee Survey, a revised Clinic-Level Data Collection Instrument, and 
a new awardee-level Quarterly Program Update--to reflect the strategies 
and objectives detailed in DP20-2002.
    The previous Annual Awardee Survey assessed: (1) Program 
management, (2) health information technology, (3) partnerships, (4) 
data use, (5) training and technical assistance (TA), (6) clinic 
service delivery. The revised instrument no longer includes questions 
related to clinic service delivery since these pertained solely to 
Component 2, which is no longer funded under DP20-2002. In addition, 
many program management questions were eliminated and will now be 
gathered via the Quarterly Program Update on a quarterly basis to 
better inform CDC TA. Several data use questions were eliminated as 
they did not yield meaningful data to inform

[[Page 34633]]

CDC TA during the previous funding cycle.
    The previous Clinic-level Data Collection instrument assessed: (1) 
Health system and clinic characteristics, (2) EBI and supporting 
activities implementation within clinics; (3) monitoring and quality 
improvement activities, and (4)CRC screening rates. The revised 
instrument was reorganized (e.g., sections merged, variables moved to 
new sections) for increased efficiency and to improve overall data 
quality. In addition, wording and responses for many variables and 
their response options have undergone minor revisions to better capture 
awardees' partnerships with both health systems and clinics, and 
appropriate capture of baseline and annual variables. The revised 
instrument gathers information to assess health system and clinic 
characteristics; program reach; CRC screening practices and outcomes; 
clinics' quality improvement and monitoring activities; EBI 
implementation, and additional factors that affect EBI implementation 
over time.
    The new Quarterly Program Update will collect standardized awardee-
level information on aspects of program management, including (1) 
quarterly program expenditures, (2) current staff vacancies, (3) 
program successes and challenges, and (4) current TA needs. This 
information collection will provide CDC staff rapid reporting of 
programmatic information to inform their efforts to provide awardees 
with tailored TA.
    Redesigned data elements will enable CDC to better gauge progress 
in meeting CRCCP program goals and monitor implementation activities, 
evaluate outcomes, and identify awardee TA needs. In addition, data 
collected will inform program improvement and help identify successful 
activities that need to be maintained, replicated, or expanded.
    OMB approval is requested for three years. The number of awardees 
will increase from 30 awardees in DP15-1502 to 35 awardees in DP20-
2002, and the number of clinic partners is expected to increase from 12 
to 24 per awardee. Therefore, the total estimated annualized burden 
hours have increased from 204 to 663 hours.

                                                            Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
                                                                                                             Number of    Average burden
               Type of respondent                               Form name                    Number of     responses per   per  response   Total burden
                                                                                            respondents     respondent        (in hr)         (in hr)
--------------------------------------------------------------------------------------------------------------------------------------------------------
CRCCP Awardees.................................  CRCCP Annual Awardee Survey............              35               1           15/60               9
                                                 CRCCP Clinic-level Information                       35              24           43/60             602
                                                  Collection Instrument.
                                                 CRCCP Quarterly Program Update.........              35               4           22/60              52
                                                                                         ---------------------------------------------------------------
    Total......................................  .......................................  ..............  ..............  ..............             663
--------------------------------------------------------------------------------------------------------------------------------------------------------


Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific 
Integrity, Office of Science, Centers for Disease Control and 
Prevention.
[FR Doc. 2020-12244 Filed 6-4-20; 8:45 am]
 BILLING CODE 4163-18-P


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