Proposed Data Collection Submitted for Public Comment and Recommendations, 48806-48808 [2016-17602]

Download as PDF 48806 Federal Register / Vol. 81, No. 143 / Tuesday, July 26, 2016 / Notices work, the focus of their work and the population groups and geographic areas served. The evaluation instruments are used to assess training and capacity-building outcomes (knowledge, confidence, intention to use information, actual changes made as a result of training) immediately after and again 90 days after training events. The evaluation instruments vary based on the type of training offered and take between approximately 16 minutes to complete (for intensive multi-day trainings) to 2 minutes to complete (for short didactic or webinar sessions). The CDC’s Funding Opportunity Announcement PS 14–1407, NNPTC, requires the collection of national demographic information on grantees’ trainees and national evaluation outcomes. There are no costs to respondents other than their time. The estimated annualized burden hours for this data collection are 502 hours. ESTIMATES OF ANNUALIZED BURDEN Number of espondents Number esponses per respondent Average urden per esponse (in hours) Total burden hours Type of respondent Form name Healthcare Professionals .................. 4,500 1 3/60 225 116 1 16/60 31 36 1 10/60 6 166 1 10/60 28 58 1 7/60 7 70 20 40 15 548 1 1 1 1 1 4/60 3/60 3/60 2/60 6/60 5 1 2 1 55 180 1 5/60 15 500 1 3/60 25 160 1 3/60 8 150 50 4,500 1 1 1 2/60 2/60 1/60 5 2 75 Healthcare Professionals .................. NNPTC Abbreviated Health Professional Application for Training (HPAT). Intensive Complete Post-Course Evaluation. Intensive Complete Long-Term Evaluation. Intensive-Didactic Post-Course Evaluation. Intensive-Didactic Long-Term Evaluation. Practicum Post-Course Evaluation .. Practicum Long-Term Evaluation ..... Wet Mount Post-Course Evaluation Wet Mount Long-Term Evaluation ... STD Tx Guidelines Complete PostCourse Evaluation. STD Tx Guidelines Complete LongTerm Evaluation. Short Guidelines Post-Course Evaluation. Short Guidelines Long-Term Evaluation. Basic Post-Course Evaluation ......... Basic Long-Term Evaluation ............ Immediate Post-Course email invitation. 3 Month Long-Term email invitation 660 1 1/60 11 Total ........................................... ........................................................... ........................ ........................ ........................ 502 Healthcare Professionals .................. Healthcare Professionals .................. Healthcare Professionals .................. Healthcare Professionals .................. Healthcare Professionals .................. Healthcare Professionals .................. Healthcare Professionals .................. Healthcare Professionals .................. 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. DEPARTMENT OF HEALTH AND HUMAN SERVICES [FR Doc. 2016–17603 Filed 7–25–16; 8:45 am] [60Day–16–0612; Docket No. CDC–2016– 0070] BILLING CODE 4163–18–P Centers for Disease Control and Prevention 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. srobinson on DSK5SPTVN1PROD with NOTICES AGENCY: The Centers for Disease Control and Prevention (CDC), as part of its continuing efforts to reduce public burden and maximize the utility of government information, invites the general public and other Federal SUMMARY: VerDate Sep<11>2014 20:28 Jul 25, 2016 Jkt 238001 PO 00000 Frm 00071 Fmt 4703 Sfmt 4703 agencies to take this opportunity to comment on proposed and/or continuing information collections, as required by the Paperwork Reduction Act of 1995. This notice invites comment on the Well-Integrated Screening and Evaluation for Women Across the Nation (WISEWOMAN) Reporting System. The WISEWOMAN program aims to reduce cardiovascular disease in women ages 40–64 by providing screening services, referrals to medical care, and lifestyle intervention programs. Written comments must be received on or before September 26, 2016. DATES: You may submit comments, identified by Docket No. CDC–2016– 0070 by any of the following methods: ADDRESSES: E:\FR\FM\26JYN1.SGM 26JYN1 srobinson on DSK5SPTVN1PROD with NOTICES Federal Register / Vol. 81, No. 143 / Tuesday, July 26, 2016 / Notices • 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. All relevant comments received will be posted without change to Regulations.gov, including any personal information provided. For access to the docket to read background documents or comments received, go to Regulations.gov. Please note: All public comment should be submitted 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 the 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. 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 OMB for approval. To comply with this requirement, we are publishing this notice of a proposed data collection as described below. 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 VerDate Sep<11>2014 20:28 Jul 25, 2016 Jkt 238001 collected; (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; and (e) estimates of capital or start-up costs and costs of operation, maintenance, and purchase of services to provide information. Burden means the total time, effort, or financial resources expended by persons to generate, maintain, retain, disclose or provide information to or for a Federal agency. This includes the time needed to review instructions; to develop, acquire, install and utilize technology and systems for the purpose of collecting, validating and verifying information, processing and maintaining information, and disclosing and providing information; to train personnel and to be able to respond to a collection of information, to search data sources, to complete and review the collection of information; and to transmit or otherwise disclose the information. Proposed Project Well-Integrated Screening and Evaluation for Women across the Nation (WISEWOMAN) Reporting System (OMB No. 0920–0612, exp. 12/31/ 2016)—Extension—National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC). Background and Brief Description The WISEWOMAN program (WellIntegrated Screening and Evaluation for Women Across the Nation), sponsored by the CDC, was established to examine ways to improve the delivery of services for women who have limited access to health care and elevated risk factors for cardiovascular disease (CVD). The program focuses on reducing CVD risk factors and provides screening services for selected risk factors such as elevated blood cholesterol, hypertension, and abnormal blood glucose levels. The program also provides women with referrals to lifestyle programs and medical care. The WISEWOMAN program provides services to women who are jointly enrolled in the National Breast and Cervical Cancer Early Detection Program (NBCCEDP), also administered by CDC. The WISEWOMAN program is administered by state health departments and tribal programs. In PO 00000 Frm 00072 Fmt 4703 Sfmt 4703 48807 2013, new cooperative agreements were awarded under Funding Opportunity Announcement DP13–1302. These awards are currently in the final year of funding, but may be extended by CDC for one additional year, subject to the availability of funds. CDC collects two types of information from WISEWOMAN awardees. The hardcopy Annual Progress Report provides a narrative summary of each awardee’s objectives and the activities undertaken to meet program goals. The estimated burden per response is 16 hours. In addition, each WISEWOMAN awardee submits an electronic data file to CDC twice per year. The Minimum Data Elements (MDE) file contains deidentified, client-level information about the cardiovascular disease risk factors of women served by the program, and the number and type of lifestyle program sessions they attend. The estimated burden per response for the MDE file is 24 hours. CDC seeks a one-year extension to enable reporting for the final year of activities funded under the current cooperative agreement and the option year, subject to the availability of funds. There are no changes to the information collected, the burden per response, reporting frequency, the number of awardees, or the total annualized burden hours. CDC will continue to use the information collected from WISEWOMAN awardees to support program monitoring and improvement activities, evaluation, and assessment of program outcomes. The overall program evaluation is designed to demonstrate how WISEWOMAN can obtain more complete health data on vulnerable populations, promote public education about disease incidence, cardiovascular disease risk-factors, health promotion, improve the availability of screening and diagnostic services for under-served women, ensure the quality of services provided to underserved women, and develop strategies for improved interventions. OMB approval is requested for one year. Participation in this information collection is required as a condition of cooperative agreement funding. There are no costs to respondents other than their time. The total annualized burden hours are 1,344. E:\FR\FM\26JYN1.SGM 26JYN1 48808 Federal Register / Vol. 81, No. 143 / Tuesday, July 26, 2016 / Notices ESTIMATED ANNUALIZED BURDEN HOURS Number of responses per respondent Number of respondents Average burden per response (in hrs.) Total burden (in hrs.) Type of respondents Form name WISEWOMAN Awardees .................. Screening and Assessment and Lifestyle Program MDEs. Annual Progress Report ................... 21 2 24 1,008 21 1 16 336 ........................................................... ........................ ........................ ........................ 1,344 Total ........................................... 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. 2016–17602 Filed 7–25–16; 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: Phase II Evaluation Activities for Implementing a Next Generation Evaluation Agenda for the Chafee Foster Care Independence Program. OMB No.: New Collection. Description: The Administration for Children and Families (ACF), Office of Planning Research and Evaluation (OPRE) is proposing an information collection activity as part of the Phase II Evaluation Activities for Implementing a Next Generation Evaluation Agenda for the Chafee Foster Care Independence Program. The proposed information collection consists of site visits by staff from the Urban Institute and Chapin Hall at the University of Chicago to conduct formative evaluations of programs serving transition-age foster youth. The evaluations will include preliminary visits to discuss the evaluation process with program administrators. Then, the research team will conduct site visits to each program to speak with program leaders, partners and key stakeholders, front-line staff, and participants. These formative evaluations will determine programs’ readiness for more rigorous evaluation in the future. The activities and products from this project will help ACF to fulfill their ongoing legislative mandate for program evaluation specified in the Foster Care Independence Act of 1999. Respondents: Program leaders, partners and stakeholders, and frontline staff as well as young adults being served by the programs. ANNUAL BURDEN ESTIMATES Total number of respondents Instrument srobinson on DSK5SPTVN1PROD with NOTICES Outreach email for discussion with program admin and staff ................................................................................... Outreach email for Focus Group Recruiters ....................... Informed Consent and Discussion Guide for program leaders ..................................................................................... Informed Consent and Discussion Guide for program partners and stakeholders ...................................................... Informed Consent and Discussion Guide for program front-line staff .................................................................... Informed Consent and Focus Group Guide for program participants ....................................................................... Compilation and Submission of Administrative Data .......... Estimated Total Annual Burden Hours: 800. Additional Information: Copies of the proposed collection may be obtained by writing to the Administration for Children and Families, Office of Planning, Research and Evaluation, 330 C Street SW., Washington, DC 20201, Attn: OPRE Reports Clearance Officer. All requests should be identified by the title of the information collection. Email address: OPREinfocollection@ acf.hhs.gov. OMB Comment: OMB is required to make a decision concerning the collection of information between 30 VerDate Sep<11>2014 20:28 Jul 25, 2016 Jkt 238001 Annual number of respondents Number of responses per respondent Frm 00073 Annual burden hours 16 16 8 8 1 1 1 8 8 64 48 24 4 1 96 80 40 2 1 80 128 64 1 1 64 200 24 100 12 1 2 2 12 200 288 and 60 days after publication of this document in the Federal Register. Therefore, a comment is best assured of having its full effect if OMB receives it within 30 days of publication. Written comments and recommendations for the proposed information collection should be sent directly to the following: Office of Management and Budget, Paperwork Reduction Project, Email: OIRA_ SUBMISSION@OMB.EOP.GOV, Attn: PO 00000 Average burden hours per response Fmt 4703 Sfmt 9990 Desk Officer for the Administration for Children and Families. Robert Sargis, ACF Certifying Officer. [FR Doc. 2016–17618 Filed 7–25–16; 8:45 am] BILLING CODE 4184–01–P E:\FR\FM\26JYN1.SGM 26JYN1

Agencies

[Federal Register Volume 81, Number 143 (Tuesday, July 26, 2016)]
[Notices]
[Pages 48806-48808]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-17602]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[60Day-16-0612; Docket No. CDC-2016-0070]


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.

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

SUMMARY: The Centers for Disease Control and Prevention (CDC), as part 
of its continuing efforts to reduce public burden and maximize the 
utility of government information, invites the general public and other 
Federal agencies to take this opportunity to comment on proposed and/or 
continuing information collections, as required by the Paperwork 
Reduction Act of 1995. This notice invites comment on the Well-
Integrated Screening and Evaluation for Women Across the Nation 
(WISEWOMAN) Reporting System. The WISEWOMAN program aims to reduce 
cardiovascular disease in women ages 40-64 by providing screening 
services, referrals to medical care, and lifestyle intervention 
programs.

DATES: Written comments must be received on or before September 26, 
2016.

ADDRESSES: You may submit comments, identified by Docket No. CDC-2016-
0070 by any of the following methods:

[[Page 48807]]

     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. All relevant comments received will be posted 
without change to Regulations.gov, including any personal information 
provided. For access to the docket to read background documents or 
comments received, go to Regulations.gov. Please note: All public 
comment should be submitted 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 the 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.

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 OMB for approval. To 
comply with this requirement, we are publishing this notice of a 
proposed data collection as described below.
    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; (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; and (e) estimates of capital or start-
up costs and costs of operation, maintenance, and purchase of services 
to provide information. Burden means the total time, effort, or 
financial resources expended by persons to generate, maintain, retain, 
disclose or provide information to or for a Federal agency. This 
includes the time needed to review instructions; to develop, acquire, 
install and utilize technology and systems for the purpose of 
collecting, validating and verifying information, processing and 
maintaining information, and disclosing and providing information; to 
train personnel and to be able to respond to a collection of 
information, to search data sources, to complete and review the 
collection of information; and to transmit or otherwise disclose the 
information.

Proposed Project

    Well-Integrated Screening and Evaluation for Women across the 
Nation (WISEWOMAN) Reporting System (OMB No. 0920-0612, exp. 12/31/
2016)--Extension--National Center for Chronic Disease Prevention and 
Health Promotion (NCCDPHP), Centers for Disease Control and Prevention 
(CDC).

Background and Brief Description

    The WISEWOMAN program (Well-Integrated Screening and Evaluation for 
Women Across the Nation), sponsored by the CDC, was established to 
examine ways to improve the delivery of services for women who have 
limited access to health care and elevated risk factors for 
cardiovascular disease (CVD). The program focuses on reducing CVD risk 
factors and provides screening services for selected risk factors such 
as elevated blood cholesterol, hypertension, and abnormal blood glucose 
levels. The program also provides women with referrals to lifestyle 
programs and medical care. The WISEWOMAN program provides services to 
women who are jointly enrolled in the National Breast and Cervical 
Cancer Early Detection Program (NBCCEDP), also administered by CDC.
    The WISEWOMAN program is administered by state health departments 
and tribal programs. In 2013, new cooperative agreements were awarded 
under Funding Opportunity Announcement DP13-1302. These awards are 
currently in the final year of funding, but may be extended by CDC for 
one additional year, subject to the availability of funds.
    CDC collects two types of information from WISEWOMAN awardees. The 
hardcopy Annual Progress Report provides a narrative summary of each 
awardee's objectives and the activities undertaken to meet program 
goals. The estimated burden per response is 16 hours.
    In addition, each WISEWOMAN awardee submits an electronic data file 
to CDC twice per year. The Minimum Data Elements (MDE) file contains 
de-identified, client-level information about the cardiovascular 
disease risk factors of women served by the program, and the number and 
type of lifestyle program sessions they attend. The estimated burden 
per response for the MDE file is 24 hours.
    CDC seeks a one-year extension to enable reporting for the final 
year of activities funded under the current cooperative agreement and 
the option year, subject to the availability of funds. There are no 
changes to the information collected, the burden per response, 
reporting frequency, the number of awardees, or the total annualized 
burden hours.
    CDC will continue to use the information collected from WISEWOMAN 
awardees to support program monitoring and improvement activities, 
evaluation, and assessment of program outcomes. The overall program 
evaluation is designed to demonstrate how WISEWOMAN can obtain more 
complete health data on vulnerable populations, promote public 
education about disease incidence, cardiovascular disease risk-factors, 
health promotion, improve the availability of screening and diagnostic 
services for under-served women, ensure the quality of services 
provided to underserved women, and develop strategies for improved 
interventions.
    OMB approval is requested for one year. Participation in this 
information collection is required as a condition of cooperative 
agreement funding. There are no costs to respondents other than their 
time. The total annualized burden hours are 1,344.

[[Page 48808]]



                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                     Number of    Average burden
      Type of respondents           Form name        Number of     responses per   per response    Total burden
                                                    respondents     respondent       (in hrs.)       (in hrs.)
----------------------------------------------------------------------------------------------------------------
WISEWOMAN Awardees............  Screening and                 21               2              24           1,008
                                 Assessment and
                                 Lifestyle
                                 Program MDEs.
                                Annual Progress               21               1              16             336
                                 Report.
                                                 ---------------------------------------------------------------
    Total.....................  ................  ..............  ..............  ..............           1,344
----------------------------------------------------------------------------------------------------------------


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. 2016-17602 Filed 7-25-16; 8:45 am]
 BILLING CODE 4163-18-P