[Federal Register Volume 75, Number 38 (Friday, February 26, 2010)]
[Notices]
[Page 8955]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2010-4001]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-10-0761]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) publishes a
list of information collection requests under review by the Office of
Management and Budget (OMB) in compliance with the Paperwork Reduction
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call
the CDC Reports Clearance Officer at (404) 639-5960 or send an e-mail
to [email protected]. Send written comments to CDC Desk Officer, Office of
Management and Budget, Washington, DC or by fax to (202) 395-5806.
Written comments should be received within 30 days of this notice.
Proposed Project
Randomized Controlled Trial of Routine Screening for Intimate
Partner Violence--Revision--National Center for Injury Prevention and
Control (NCIPC), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and Prevention (CDC) requests OMB
approval of revisions to a currently approved collection entitled
``Randomized Controlled Trial of Routine Screening for Intimate Partner
Violence'' (approved 01/24/2008; expiration date 01/29/2011). The
proposed changes are a result of findings from the Pretest that showed
high numbers of Spanish speakers at recruitment clinics, a higher
prevalence of reported exposure to intimate partner violence (IPV), and
redundancy of the 20-item mental health scale with other measures being
used. As a result, we are requesting approval to extend trial inclusion
criteria to Spanish speakers, a reduction in sample size, and deletion
of a 20-question mental health scale. These last two changes will
result in a decrease in burden to respondents. In addition, we are
requesting an extension of three years to complete this information
collection. The overarching purpose of the information collection has
not changed nor are there substantial changes to the study methods.
The revisions requested will reduce annual burden by 410 hours.
Deletion of the mental health scale will reduce the burden response by
2 minutes; the reduction of sample size will reduce number of
respondents; and extension of information collection time will decrease
annualized burden. The Pretest has already been conducted and the
estimates of burden for the interview in the Main Study are based on
results from the Pretest. Based on our new sample size estimates
adjusted as a result of findings in the Pretest, in the Main Study, we
will approach an estimated total of 3340 women to establish eligibility
and recruit about 2675 (total) women. The annualized average response
burden equals 308 hours, which is a reduction of 410 burden hours.
There is no cost to respondents.
Estimated Annualized Burden Hours
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Number of Avg. burden/
Type of respondents Form name Number of responses per response (in
respondents respondent hours)
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Women Seeking Health Care Services. Eligibility Script for 70 1 1/60
Pretest.
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Baseline Questionnaire 65 1 15/60
Pretest.
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Follow-up Questionnaire 59 1 12/60
Pretest.
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Eligibility Script for Main 668 1 1/60
Study.
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Baseline Questionnaire Main 535 1 16/60
Study.
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Follow-up Questionnaire 356 1 21/60
Main Study (estimated 30%
lost to follow-up).
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Dated: February 22, 2010.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. 2010-4001 Filed 2-25-10; 8:45 am]
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