[Federal Register Volume 80, Number 96 (Tuesday, May 19, 2015)]
[Notices]
[Pages 28618-28619]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-12095]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-15-0822; Docket No. CDC-2015-0035]
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.
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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 a proposed
revision to the approved information collection project entitled ``The
National Intimate Partner and Sexual Violence Survey (NISVS)''. This
project collects information about individual's experiences of sexual
violence, stalking and intimate partner violence.
DATES: Written comments must be received on or before July 20, 2015.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2015-
0035 by any of the following methods:
Federal eRulemaking Portal: Regulation.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: [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 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
National Intimate Partner and Sexual Violence Survey (NISVS)--
Revision--(OMB Control No. 0920-0822, Expiration--6/30/2016), National
Center for Injury Prevention and Control
[[Page 28619]]
(NCIPC), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
In 2010, the National Intimate Partner and Sexual Violence
Surveillance System (NISVSS) reported that approximately 6.9 million
women and 5.6 million men experienced rape, physical violence and/or
stalking by an intimate partner within the last year. The health care
costs of Intimate Partner Violence (IPV) exceed $5.8 billion each year,
nearly $3.9 billion of which is for direct medical and mental health
care services.
In order to address this important public health problem, CDC
implemented, beginning in 2010, the National Intimate Partner and
Sexual Violence Surveillance System that produces national and state
level estimates of Intimate Partner Violence (IPV), Sexual Violence
(SV) and stalking on an annual basis.
This revision request is multi-faceted. CDC is requesting a
continuation of data collection among non-institutionalized adult men
and women aged 18 years or older in the United States assessing
lifetime experiences of IPV, SV and stalking with a new and improved
data collection tool. The revisions to the survey are aimed at reducing
the time and complexity of the instrument, thus reducing the burden on
the respondent. The simplified structure of the instrument will also
reduce the complexity of the data set, making it more assessable for
public use. Additionally, in collaboration with the Department of
Defense (DoD), NISVS will collect information regarding the experiences
of IPV, SV and stalking among active duty women and men in the military
and wives of active duty men. This data collection will take place
during the first three months of data collection.
To comply with OMB requirements, CDC is in the process of
developing an expert panel to address methodological issues with the
NISVS survey. The panel will meet multiple times over the course of the
next year. The members of this panel will provide guidance on how to
improve both survey design (methods, sampling frame, recruitment, mode
of administration) and content/question wording with the goals of
increasing response rates, reducing non-response bias, and maximizing
the opportunities across Federal surveys for covering populations of
interest. This change request also encompasses the implementation of
the panel's recommendations to improve the survey.
In the bi-annual data collection periods, total of 170,000
households will be screened. After determining eligibility and consent,
25,000 will complete the survey. The average burden per screened
respondent remains at three minutes (total burden in hours equals
8,500) while the average burden per surveyed respondent is 25 minutes
(total burden in hours equals 10,417). The survey will be conducted
among English or Spanish speaking male and female adults (18 years and
older) living in the United States.
There are no costs to respondents other than their time.
Estimated Annualized Burden Hours
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Number of Average burden
Type of respondent Form name Number of responses per per response Total burden
respondents respondent (in hours) hours
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Non-Participating Individuals NISVS Survey 170,000 1 3/60 8,500
(Screened). Instrument.
Eligible Individuals NISVS Survey 25,000 1 25/60 10,417
(Surveyed). Instrument.
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Total..................... ................ .............. .............. .............. 18,917
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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. 2015-12095 Filed 5-18-15; 8:45 am]
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