Agency Forms Undergoing Paperwork Reduction Act Review
| Citation | 85 FR 4987 |
| Record Number | 2020-01378 |
| Published date | 28 January 2020 |
| Section | Notices |
| Court | Centers For Disease Control And Prevention |
Federal Register, Volume 85 Issue 18 (Tuesday, January 28, 2020)
[Federal Register Volume 85, Number 18 (Tuesday, January 28, 2020)]
[Notices]
[Pages 4987-4988]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-01378]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-20-0822]
Agency Forms Undergoing Paperwork Reduction Act Review
In accordance with the Paperwork Reduction Act of 1995, the Centers
for Disease Control and Prevention (CDC) has submitted the information
collection request titled ``The National Intimate Partner and Sexual
Violence Survey (NISVS)'' to the Office of Management and Budget (OMB)
for review and approval. CDC previously published a ``Proposed Data
Collection Submitted for Public Comment and Recommendations'' notice on
October 9, 2019 to obtain comments from the public and affected
agencies. CDC received two anonymous non-substantive comments related
to the previous notice. This notice serves to allow an additional 30
days for public and affected agency comments.
CDC will accept all comments for this proposed information
collection project. The Office of Management and Budget is particularly
interested in comments that:
(a) 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;
(b) Evaluate the accuracy of the agencies estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and clarity of the information to
be collected;
(d) 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 submission of responses; and
(e) Assess information collection costs.
To request additional information on the proposed project or to
obtain a copy of the information collection plan and instruments, call
(404) 639-7570 or send an email to [email protected]. Direct written comments
and/or suggestions regarding the items contained in this notice to the
Attention: CDC Desk Officer, Office of Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by fax to (202) 395-5806. Provide
written comments within 30 days of notice publication.
Proposed Project
The National Intimate Partner and Sexual Violence Survey (NISVS)
(OMB Control No. 0920-0822, Exp. 02/29/2020)--Revision--National Center
for Injury Prevention and Control (NCIPC), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
This is a revision request for the currently approved National
Intimate Partner and Sexual Violence Survey (NISVS, OMB# 0920-0822). In
2010, the National Intimate Partner and Sexual Violence Surveillance
System (NISVS) 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 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 describes the planned testing of a redesign
of the National Intimate Partner and Sexual Violence Survey (NISVS) and
the approach for collecting NISVS data using multiple data collection
modes and sampling strategies. More specifically, this revision request
is to; (1) Conduct feasibility testing to assess several alternative
design features, including the sample frame (address-based sample
[ABS], random digit dial [RDD], web panel), mode of response
(telephone, web, paper), and incentive structures that help garner
participation and help reduce nonresponse. (2) Conduct experiments that
inform the development of a protocol for alternative sampling and
weighting methods for multi-modal data collection that will result in
the ability to calculate accurate and reliable national and state-level
estimates of SV, IPV, and stalking, and (3) Conduct a pilot data
collection to ensure that the selected optimal alternative sampling
methods and multi-modal data collection approaches for NISVS are ready
for full-scale implementation.
These data will be used only to inform future NISVS data
collections. Results from the feasibility phase experiments may be
prepared for publication, as the findings related to optimal data
collection modes, sampling frames, and incentive structures are likely
to be useful to other federal agencies currently conducting national
data collections. No national prevalence estimates will be generated
from the data collected during the NISVS redesign project. The
feasibility study involves testing of the CATI, paper, and web versions
of the NISVS survey using a variety of sampling frames and single vs.
multiple modes, all for the purpose of determining a new design for
NISVS, and the pilot test of the new design. Data are analyzed using
appropriate statistical software to account for the complexity of the
survey design to compute weighted counts, percentages, and confidence
intervals using national-level data.
OMB approval is requested for three years. The total estimated
annualized burden hours are 1,189. There is no cost to respondents
other than their time.
[[Page 4988]]
Estimated Annualized Burden Hours
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Number of Average burden
Type of respondent Form name Number of responses per per response
respondents respondent (in hours)
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Individuals and Households...................... Phase 2 Screener--RDD (CATI).......................... 958 1 3/60
Phase 2 Screener--ABS, web............................ 333 1 3/60
Phase 2 Screener--ABS, paper--Roster method........... 389 1 3/60
Phase 2 Screener--ABS, paper--YMOF Method............. 389 1 3/60
Phase 2 Questionnaire--RDD (CATI)..................... 667 1 40/60
Phase 2--Questionnaire--ABS, web...................... 427 1 25/60
Phase 2 Questionnaire--ABS, paper..................... 211 1 25/60
Phase 2 Questionnaire--ABS, in-bound CATI............. 29 1 40/60
Phase 2 Questionnaire--Panel, web..................... 667 1 25/60
Phase 2 Cognitive Testing Protocol--Cognitive testing. 40 1 1
Phase 3 Screener--RDD (CATI).......................... 27 1 3/60
Phase 3 Screener--ABS, web............................ 27 1 3/60
Phase 3 Screener--ABS, paper--Roster method........... 14 1 3/60
Phase 3 Screener ABS, paper--YMOF Method.............. 13 1 3/60
Phase 3 Questionnaire--RDD (CATI)..................... 22 1 40/60
Phase 3 Questionnaire--ABS, web....................... 29 1 25/60
Phase 3 Questionnaire--ABS, paper..................... 14 1 25/60
Phase 3 Questionnaire--ABS, in-bound CATI............. 2 1 40/60
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Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2020-01378 Filed 1-27-20; 8:45 am]
BILLING CODE 4163-18-P
