Proposed Data Collection Submitted for Public Comment and Recommendations, 9320-9321 [2018-04330]

Download as PDF 9320 Federal Register / Vol. 83, No. 43 / Monday, March 5, 2018 / Notices ESTIMATED ANNUALIZED BURDEN HOURS—Continued Average burden per response (in hours) Number of responses per respondent Number of respondents Total burden hours Type of respondent Form name Site data manager ............................ Study participant ............................... Study participant ............................... Form 1—Questionnaire .................... Form 1—Questionnaire .................... Smartphone survey .......................... 3 720 720 5 5 52 10 1.5 2/60 150 5,400 1,248 Total ........................................... ........................................................... ........................ ........................ ........................ 6,828 Leroy A. Richardson, Chief, Information Collection Review Office, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2018–04329 Filed 3–2–18; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES To request more information on the proposed project or to obtain a copy of the information collection plan and instruments, contact Leroy A. Richardson, 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. FOR FURTHER INFORMATION CONTACT: Centers for Disease Control and Prevention [60Day–18–0571; Docket No. CDC–2018– 0017] 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 ‘‘Minimum Data Elements (MDEs) for the National Breast and Cervical Cancer Early Detection Program (NBCCEDP).’’ DATES: CDC must receive written comments on or before May 4, 2018. ADDRESSES: You may submit comments, identified by Docket No. CDC–2018– 0017 by any of the following methods: • Federal eRulemaking Portal: Regulations.gov. Follow the instructions for submitting comments. • Mail: Leroy A. Richardson, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS– D74, Atlanta, Georgia 30329. sradovich on DSK3GMQ082PROD with NOTICES SUMMARY: VerDate Sep<11>2014 19:25 Mar 02, 2018 Jkt 244001 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. 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; SUPPLEMENTARY INFORMATION: PO 00000 Frm 00062 Fmt 4703 Sfmt 4703 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 Minimum Data Elements (MDEs) for the National Breast and Cervical Cancer Early Detection Program (NBCCEDP)— (OMB Control Number 0920–0571, exp. 12/31/2018)—Revision—National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC) Background and Brief Description CDC seeks to request a three-year OMB approval to revise the information collection project approved under OMB Control number 0920–0571. Based on feedback from grantees and internal subject matter experts, CDC proposes use of revised minimum data elements (MDEs), which decrease the estimated annualized time burden. Both breast and cervical cancers are prevalent among U.S. women. In 2014, more than 236,000 women were diagnosed with breast cancer, and more than 12,000 women were diagnosed with cervical cancer. Evidence shows that deaths from both breast and cervical cancers can be avoided by increasing women screening services (mammography and Pap tests). However, women who are under- or uninsured, have no regular source of healthcare, and/or have recently immigrated to the U.S. typically underutilize screening services. Congress passed the Breast and Cervical Cancer Mortality Prevention Act of 1990, which directed CDC to establish the National Breast and Cervical Cancer Early Detection Program (NBCCEDP). The purpose of E:\FR\FM\05MRN1.SGM 05MRN1 9321 Federal Register / Vol. 83, No. 43 / Monday, March 5, 2018 / Notices the NBCCEDP is to increase breast and cervical cancer screening rates among priority populations by funding grantees to provide breast and cervical cancer screening services to eligible women. The NBCCEDP funds 70 grantees including state health departments and the District of Columbia, universities, and tribes or tribal organizations. Priority populations for the NBCCEDP include women residing within defined geographical locations (as determined by the funded program) who are (1) at or below 250% of the federal poverty level, (2) aged 40–64 years for breast cancer services, and aged 21–64 years for cervical cancer services, and (3) under- or uninsured. CDC issued a new funding opportunity announcement to support a (6) timeliness of services; and (7) patient navigation. Redesigned data elements will enable CDC to better gauge progress in meeting clinical service delivery processes and patient-level outcomes. Findings will allow CDC to assess program progress in meeting goals and monitor implementation activities, evaluate outcomes, and identify grantee technical assistance needs. In addition, data collected will inform program improvement and help identify successful activities that need to be maintained, replicated, or expanded. The total estimated annualized burden hours will decrease from 536 to 350 hours. There are no costs to respondents other than their time. 5-year cooperative agreement under CDC–RFA–DP17–1701. The number of grantees will increase from 67 grantees to 70 grantees. The current program includes a stronger focus on grantees partnering with health systems to increase breast and cervical cancer screening rates. CDC proposes a revision to the MDEs to include removal of several data variables that are no longer relevant for CDC analyses, as well as collapsing/ revising several data variables to reduce burden and increase clarity for respondents. The MDEs focus on the following areas: (1) Patient demographics; (2) breast cancer screening; (3) cervical cancer screening; (4) breast and cervical cancer diagnoses; (5) breast and cervical cancer treatment; ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Average burden per response (in hours) Number of responses per respondent Total burden (in hours) Type of respondent Form name NBCCEDP Grantees ......................... MDEs ................................................ 70 2 2.50 350 Total ........................................... ........................................................... ........................ ........................ ........................ 350 Leroy A. Richardson, Chief, Information Collection Review Office, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2018–04330 Filed 3–2–18; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Comment Request Title: Study of We Grow Together: The Q–CCIIT Professional Development System. OMB No.: New Collection. Description: The Administration for Children and Families (ACF) at the U.S. Department of Health and Human Services (HHS) seeks approval to conduct a field test of We Grow Together, a system of professional development supports including webbased resources and exercises to be used by caregivers/teachers, with the help of professional development providers, to improve the quality of infant and toddler care. The study team has developed We Grow Together: The Q–CCIIT Professional Development System based on the research literature to support caregiver-child interactions in care settings serving infants and toddlers. This field test is designed to (1) examine changes associated with use of the We Grow Together system and (2) examine implementation and participant experiences with the We Grow Together system. As a secondary goal, ACF will also further evaluate the properties of the Q–CCIIT observational measure. Ultimately, findings from the field test will provide information about the experiences of professional development providers (PD providers) and caregivers with the We Grow Together system so that ACF can improve the system to make the resources as accessible as possible for infant-toddler caregivers. Prior to using the We Grow Together system, PD providers will complete a web-based training survey and all participants will complete a web-based background survey. Periodically during the field test, website users will be asked at log-on to respond to a series of web-based questions. After system implementation, participants will complete a web-based feedback survey. The study team will also collect classroom rosters from caregivers before and after the field test. Respondents: Early care and education (ECE) setting representatives (e.g., directors or owners), caregivers (center-based and family child care settings), and professional development providers (e.g., coaches). sradovich on DSK3GMQ082PROD with NOTICES ANNUAL BURDEN ESTIMATES Total/annual number of respondents Instrument ECE setting eligibility screener ........................................................................ Caregiver background survey .......................................................................... PD provider background survey ...................................................................... Caregiver We Grow Together website user data pop-up questions ............... PD provider We Grow Together website user pop-up questions ................... Caregiver feedback survey .............................................................................. VerDate Sep<11>2014 19:25 Mar 02, 2018 Jkt 244001 PO 00000 Frm 00063 Fmt 4703 Sfmt 4703 Number of responses per respondent 745 300 175 300 175 300 E:\FR\FM\05MRN1.SGM 1 1 1 6 5 1 05MRN1 Average burden hours per response .25 .75 .50 .17 .10 1.0 Annual burden hours 186 225 88 306 88 300

Agencies

[Federal Register Volume 83, Number 43 (Monday, March 5, 2018)]
[Notices]
[Pages 9320-9321]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-04330]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[60Day-18-0571; Docket No. CDC-2018-0017]


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 ``Minimum Data Elements (MDEs) 
for the National Breast and Cervical Cancer Early Detection Program 
(NBCCEDP).''

DATES: CDC must receive written comments on or before May 4, 2018.

ADDRESSES: You may submit comments, identified by Docket No. CDC-2018-
0017 by any of the following methods:
     Federal eRulemaking Portal: Regulations.gov. Follow the 
instructions for submitting comments.
     Mail: Leroy A. Richardson, 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.

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 Leroy A. Richardson, Information Collection 
Review Office, Centers for Disease Control and Prevention, 1600 Clifton 
Road NE, MS-D74, Atlanta, Georgia 30329; phone: 404-639-7570; 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

    Minimum Data Elements (MDEs) for the National Breast and Cervical 
Cancer Early Detection Program (NBCCEDP)--(OMB Control Number 0920-
0571, exp. 12/31/2018)--Revision--National Center for Chronic Disease 
Prevention and Health Promotion (NCCDPHP), Centers for Disease Control 
and Prevention (CDC)

Background and Brief Description

    CDC seeks to request a three-year OMB approval to revise the 
information collection project approved under OMB Control number 0920-
0571. Based on feedback from grantees and internal subject matter 
experts, CDC proposes use of revised minimum data elements (MDEs), 
which decrease the estimated annualized time burden.
    Both breast and cervical cancers are prevalent among U.S. women. In 
2014, more than 236,000 women were diagnosed with breast cancer, and 
more than 12,000 women were diagnosed with cervical cancer. Evidence 
shows that deaths from both breast and cervical cancers can be avoided 
by increasing women screening services (mammography and Pap tests). 
However, women who are under- or uninsured, have no regular source of 
healthcare, and/or have recently immigrated to the U.S. typically 
underutilize screening services.
    Congress passed the Breast and Cervical Cancer Mortality Prevention 
Act of 1990, which directed CDC to establish the National Breast and 
Cervical Cancer Early Detection Program (NBCCEDP). The purpose of

[[Page 9321]]

the NBCCEDP is to increase breast and cervical cancer screening rates 
among priority populations by funding grantees to provide breast and 
cervical cancer screening services to eligible women. The NBCCEDP funds 
70 grantees including state health departments and the District of 
Columbia, universities, and tribes or tribal organizations.
    Priority populations for the NBCCEDP include women residing within 
defined geographical locations (as determined by the funded program) 
who are (1) at or below 250% of the federal poverty level, (2) aged 40-
64 years for breast cancer services, and aged 21-64 years for cervical 
cancer services, and (3) under- or uninsured.
    CDC issued a new funding opportunity announcement to support a 5-
year cooperative agreement under CDC-RFA-DP17-1701. The number of 
grantees will increase from 67 grantees to 70 grantees. The current 
program includes a stronger focus on grantees partnering with health 
systems to increase breast and cervical cancer screening rates.
    CDC proposes a revision to the MDEs to include removal of several 
data variables that are no longer relevant for CDC analyses, as well as 
collapsing/revising several data variables to reduce burden and 
increase clarity for respondents. The MDEs focus on the following 
areas: (1) Patient demographics; (2) breast cancer screening; (3) 
cervical cancer screening; (4) breast and cervical cancer diagnoses; 
(5) breast and cervical cancer treatment; (6) timeliness of services; 
and (7) patient navigation.
    Redesigned data elements will enable CDC to better gauge progress 
in meeting clinical service delivery processes and patient-level 
outcomes. Findings will allow CDC to assess program progress in meeting 
goals and monitor implementation activities, evaluate outcomes, and 
identify grantee technical assistance needs. In addition, data 
collected will inform program improvement and help identify successful 
activities that need to be maintained, replicated, or expanded.
    The total estimated annualized burden hours will decrease from 536 
to 350 hours. There are no costs to respondents other than their time.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                     Number of    Average burden
      Type of respondent            Form name        Number of     responses per   per response    Total burden
                                                    respondents     respondent      (in hours)      (in hours)
----------------------------------------------------------------------------------------------------------------
NBCCEDP Grantees..............  MDEs............              70               2            2.50             350
                                                 ---------------------------------------------------------------
    Total.....................  ................  ..............  ..............  ..............             350
----------------------------------------------------------------------------------------------------------------


Leroy A. Richardson,
Chief, Information Collection Review Office, Office of Scientific 
Integrity, Office of the Associate Director for Science, Office of the 
Director, Centers for Disease Control and Prevention.
[FR Doc. 2018-04330 Filed 3-2-18; 8:45 am]
 BILLING CODE 4163-18-P


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