Proposed Data Collections Submitted for Public Comment and Recommendations, 71432-71433 [2014-28233]

Download as PDF 71432 Federal Register / Vol. 79, No. 231 / Tuesday, December 2, 2014 / Notices 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. 2014–28232 Filed 12–1–14; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day–15–0214] Proposed Data Collections Submitted for Public Comment and Recommendations rljohnson on DSK3VPTVN1PROD with NOTICES The Centers for Disease Control and Prevention (CDC), as part of its continuing effort to reduce public burden, 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. To request more information on the below proposed project or to obtain a copy of the information collection plan and instruments, call 404–639–7570 or send comments to LeRoy Richardson, 1600 Clifton Road, MS–D74, Atlanta, GA 30333 or send an email to omb@cdc.gov. Comments submitted in response to this notice will be summarized and/or included in the request for Office of Management and Budget (OMB) approval. 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. Written comments should be received within 30 days of this notice. Proposed Project National Health Interview Survey (NHIS) (OMB No. 0920–0214, expires 03/31/2016)—Revision—National Center for Health Statistics (NCHS), Centers for Disease Control and Prevention (CDC). Background and Brief Description Section 306 of the Public Health Service (PHS) Act (42 U.S.C. 242k), as amended, authorizes that the Secretary of Health and Human Services (DHHS), acting through NCHS, shall collect data on the extent and nature of illness and disability of the population of the United States. The annual National Health Interview Survey is a major source of general statistics on the health of the U.S. population and has been in the field continuously since 1957. Clearance is sought for three years, to collect data for 2015, 2016, and 2017. This voluntary and confidential household-based survey collects demographic and health-related information on a nationally representative sample of persons and households throughout the country. Personal identification information is requested from survey respondents to facilitate linkage of survey data with health-related administrative and other records. Each year we collect information from approximately 55,000 households, which contain about 137,500 individuals. Information is collected using computer assisted personal interviews (CAPI). A core set of data is collected each year that remains largely unchanged while sponsored supplements vary from year to year. The core set includes socio-demographic characteristics, health status, health care services, and health behaviors. For 2015, supplemental questions will be cycled in pertaining to cancer control, epilepsy, and inflammatory bowel disease and occupational health. Supplemental topics that continue or are enhanced from 2014 will be related to food security, heart disease and stroke, children’s mental health, disability and functioning, sexual orientation, smokeless tobacco and ecigarettes, immunizations, and computer use. Questions on the Affordable Care Act from 2014 have been reduced in number in 2015. In addition, a follow-back survey will be conducted on previous NHIS respondents. The follow-back survey will focus on topics related to the Affordable Care Act including health care access and use, and health insurance coverage and will include multiple modes of contacting respondents. To improve the analytic utility of NHIS data, minority populations are oversampled annually. In 2015, sample augmentation procedures used in previous years will continue to increase the number of African American, Hispanic, and Asian American persons. In accordance with the 1995 initiative to increase the integration of surveys within the DHHS, respondents to the NHIS serve as the sampling frame for the Medical Expenditure Panel Survey conducted by the Agency for Healthcare Research and Quality. The NHIS has long been used by government, academic, and private researchers to evaluate both general health and specific issues, such as cancer, diabetes, and access to health care. It is a leading source of data for the Congressionally mandated ‘‘Health US’’ and related publications, as well as the single most important source of statistics to track progress toward the National Health Promotion and Disease Prevention Objectives, ‘‘Healthy People 2020.’’ The total annualized burden hours have increased by 3,333 hours to 48,833 hours. There is no cost to the respondents other than their time. ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Type of respondent Form name Adult Family Member ...................................... Screener Questionnaire ................................. VerDate Sep<11>2014 15:30 Dec 01, 2014 Jkt 235001 PO 00000 Frm 00057 Fmt 4703 Sfmt 4703 10,000 E:\FR\FM\02DEN1.SGM 02DEN1 Number of responses per respondent 1 Average burden per response (in hours) 5/60 71433 Federal Register / Vol. 79, No. 231 / Tuesday, December 2, 2014 / Notices ESTIMATED ANNUALIZED BURDEN HOURS—Continued Number of respondents Type of respondent Form name Adult Family Member ...................................... Sample Adult ................................................... Adult Family Member ...................................... Adult Family Member ...................................... Adult Family Member ...................................... Adult Family Member ...................................... Family Core .................................................... Adult Core ...................................................... Child Core ...................................................... Supplements .................................................. Followback ..................................................... Reinterview Survey ........................................ 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. 2014–28233 Filed 12–1–14; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [Docket No. CDC–2014–0012] Recommendations for Providers Counseling Male Patients and Parents Regarding Male Circumcision and the Prevention of HIV Infection, STIs, and Other Health Outcomes 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), located within the Department of Health and Human Services (HHS), is seeking public comment on draft recommendations for health care providers who deliver information and counseling about elective male circumcision and the prevention of HIV and other adverse health outcomes to male patients and parents in the United States. The draft recommendations include information about the health benefits and risks of elective male circumcision performed by health care providers. DATES: Written comments must be received on or before January 16, 2015. ADDRESSES: You may submit comments identified by Docket Number CDC– 2014–0012 by any of the following methods: • Federal eRulemaking Portal: https:// www.regulations.gov. Follow the instructions for submitting comments. • Mail: Division of HIV/AIDS Prevention, National Center for HIV/ rljohnson on DSK3VPTVN1PROD with NOTICES SUMMARY: VerDate Sep<11>2014 15:30 Dec 01, 2014 Jkt 235001 AIDS, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, 1600 Clifton Road NE., Mailstop D–21, Atlanta, Georgia 30333. Attn: Male Circumcision Recommendations. Instructions: All submissions received must include the agency name and docket number or RIN. All relevant comments received will be posted without change to https:// regulations.gov, including any personal information provided. CDC will not consider or post any comments that contain vulgar or offensive language, threats, personal accusations, and/or statements intended to promote commercial products or services, or images. Additionally, CDC will not post any pictures that are submitted. For access to the docket to read the recommendations, background document, or comments received, go to https://www.regulations.gov. FOR FURTHER INFORMATION CONTACT: Division of HIV/AIDS, National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, 1600 Clifton Road NE., MS D–21, Atlanta, Georgia 30329, phone: 404–639–5200. Email: circumcision@cdc.gov. SUPPLEMENTARY INFORMATION: These recommendations are intended to assist health care providers in the United States who are counseling men and parents of male infants, children and adolescents in decision making about male circumcision. Such decision making is made in the context of not only health considerations, but also other social, cultural, ethical, and religious factors. Although data have been accumulating about infant male circumcision for many years, clinical trials conducted between 2005–2010 have demonstrated safety and significant efficacy of voluntary adult male circumcision performed by clinicians for reducing the risk of acquisition of human immunodeficiency virus (HIV) by a male during penile-vaginal sex (‘‘heterosexual sex’’). Three randomized PO 00000 Frm 00058 Fmt 4703 Sfmt 9990 Number of responses per respondent 45,000 36,000 14,000 45,000 12,000 5,000 1 1 1 1 1 1 Average burden per response (in hours) 23/60 15/60 10/60 20/60 20/60 5/60 clinical trials showed that adult male circumcision reduced HIV infection risk by 50–60% over time. These trials also found that adult circumcision reduced the risk of men acquiring two common sexually transmitted infections (STIs), herpes simplex virus type-2 (HSV–2) and types of human papilloma virus (HPV) that can cause penile and other anogenital cancers, by 30%. Since the release of these trial data, various organizations have updated their recommendations about adult male and infant male circumcision. In addition to obtaining public comment on the draft Recommendations, CDC considers this document to be important information as defined by the Office of Management and Budget’s (OMB) 2004 Information Quality Bulletin for Peer Review and, therefore, subject to peer review. CDC will share the summary of public comments with external experts who conduct a peer review of the evidence on this topic. Their review will include an evaluation of completeness, accuracy, interpretation, and generalizability of the evidence to the United States and whether the evidence is sufficient to support the draft counseling recommendations. After considering all public comment and the results of the peer review, CDC will publish a notice in the Federal Register announcing the final recommendations. Dated: November 19, 2014. Ron A. Otten, Acting Deputy Associate Director for Science, Centers for Disease Control and Prevention. [FR Doc. 2014–27814 Filed 11–28–14; 4:15 pm] BILLING CODE 4163–18–P E:\FR\FM\02DEN1.SGM 02DEN1

Agencies

[Federal Register Volume 79, Number 231 (Tuesday, December 2, 2014)]
[Notices]
[Pages 71432-71433]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-28233]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30Day-15-0214]


Proposed Data Collections Submitted for Public Comment and 
Recommendations

    The Centers for Disease Control and Prevention (CDC), as part of 
its continuing effort to reduce public burden, 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. To request more information on the 
below proposed project or to obtain a copy of the information 
collection plan and instruments, call 404-639-7570 or send comments to 
LeRoy Richardson, 1600 Clifton Road, MS-D74, Atlanta, GA 30333 or send 
an email to omb@cdc.gov.
    Comments submitted in response to this notice will be summarized 
and/or included in the request for Office of Management and Budget 
(OMB) approval. 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. Written comments should be received within 30 
days of this notice.

Proposed Project

    National Health Interview Survey (NHIS) (OMB No. 0920-0214, expires 
03/31/2016)--Revision--National Center for Health Statistics (NCHS), 
Centers for Disease Control and Prevention (CDC).

Background and Brief Description

    Section 306 of the Public Health Service (PHS) Act (42 U.S.C. 
242k), as amended, authorizes that the Secretary of Health and Human 
Services (DHHS), acting through NCHS, shall collect data on the extent 
and nature of illness and disability of the population of the United 
States. The annual National Health Interview Survey is a major source 
of general statistics on the health of the U.S. population and has been 
in the field continuously since 1957. Clearance is sought for three 
years, to collect data for 2015, 2016, and 2017.
    This voluntary and confidential household-based survey collects 
demographic and health-related information on a nationally 
representative sample of persons and households throughout the country. 
Personal identification information is requested from survey 
respondents to facilitate linkage of survey data with health-related 
administrative and other records. Each year we collect information from 
approximately 55,000 households, which contain about 137,500 
individuals.
    Information is collected using computer assisted personal 
interviews (CAPI). A core set of data is collected each year that 
remains largely unchanged while sponsored supplements vary from year to 
year. The core set includes socio-demographic characteristics, health 
status, health care services, and health behaviors. For 2015, 
supplemental questions will be cycled in pertaining to cancer control, 
epilepsy, and inflammatory bowel disease and occupational health.
    Supplemental topics that continue or are enhanced from 2014 will be 
related to food security, heart disease and stroke, children's mental 
health, disability and functioning, sexual orientation, smokeless 
tobacco and e-cigarettes, immunizations, and computer use. Questions on 
the Affordable Care Act from 2014 have been reduced in number in 2015. 
In addition, a follow-back survey will be conducted on previous NHIS 
respondents. The follow-back survey will focus on topics related to the 
Affordable Care Act including health care access and use, and health 
insurance coverage and will include multiple modes of contacting 
respondents.
    To improve the analytic utility of NHIS data, minority populations 
are oversampled annually. In 2015, sample augmentation procedures used 
in previous years will continue to increase the number of African 
American, Hispanic, and Asian American persons.
    In accordance with the 1995 initiative to increase the integration 
of surveys within the DHHS, respondents to the NHIS serve as the 
sampling frame for the Medical Expenditure Panel Survey conducted by 
the Agency for Healthcare Research and Quality. The NHIS has long been 
used by government, academic, and private researchers to evaluate both 
general health and specific issues, such as cancer, diabetes, and 
access to health care. It is a leading source of data for the 
Congressionally mandated ``Health US'' and related publications, as 
well as the single most important source of statistics to track 
progress toward the National Health Promotion and Disease Prevention 
Objectives, ``Healthy People 2020.''
    The total annualized burden hours have increased by 3,333 hours to 
48,833 hours. There is no cost to the respondents other than their 
time.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                                      Average
                                                                     Number of       Number of      burden per
          Type of respondent                    Form name           respondents    responses per   response  (in
                                                                                    respondent        hours)
----------------------------------------------------------------------------------------------------------------
Adult Family Member...................  Screener Questionnaire..          10,000               1            5/60

[[Page 71433]]

 
Adult Family Member...................  Family Core.............          45,000               1           23/60
Sample Adult..........................  Adult Core..............          36,000               1           15/60
Adult Family Member...................  Child Core..............          14,000               1           10/60
Adult Family Member...................  Supplements.............          45,000               1           20/60
Adult Family Member...................  Followback..............          12,000               1           20/60
Adult Family Member...................  Reinterview Survey......           5,000               1            5/60
----------------------------------------------------------------------------------------------------------------


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. 2014-28233 Filed 12-1-14; 8:45 am]
BILLING CODE 4163-18-P
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