[Federal Register: June 1, 2009 (Volume 74, Number 103)]
[Notices]
[Page 26248]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr01jn09-50]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-09-05CS]
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 omb@cdc.gov. Send written comments to CDC Desk Officer, Office of
Management and Budget, Washington, DC or by fax to (202) 395-6974.
Written comments should be received within 30 days of this notice.
Proposed Project
Nurse Delivered Risk Reduction Intervention for HIV-Positive
Women--New--National Center for HIV/AIDS, Viral Hepatitis, STD, and TB
Prevention, Centers for Disease Control and Prevention (CDC).
Background and Brief Description
During the past two decades, HIV surveillance data indicates an
increase in HIV/AIDS cases among women in the non-urban Southeastern
United States. In 2006, the majority of HIV/AIDS cases (80%) among
women were attributed to high-risk heterosexual contact with an
infected partner. Black women in particular have been
disproportionately impacted by HIV/AIDS. Factors shown to be associated
with HIV in the South include poverty, lack of access to medical care,
poor education, lack of awareness of the disease, and exposure to other
sexually transmitted diseases. Presently, there is an urgent need for
enhanced HIV transmission prevention interventions for HIV positive
women in the southeastern United States.
The purpose of this project is to adapt and test the efficacy of an
HIV transmission prevention intervention for reducing sexual risk among
330 HIV-positive women in North Carolina and to identify factors
associated with risk among women. The study will be conducted in two
parts (intervention trial and individual in-depth interviews). The
intervention trial will evaluate a brief, nurse delivered, single
session intervention. The trial will use a randomized wait-list
comparison design with a three-month follow-up assessment. To determine
eligibility for participation in the study, a brief, in-person,
screening will be used. Eligible participants will complete baseline
and follow-up behavioral assessments. The assessments contain questions
about participants' background, health and health care, sexual
activity, substance use, and other psychosocial issues. The in-depth
interviews will be conducted with a subgroup of 25-30 women. The
purpose of the in-depth interviews is to assess experiences with the
intervention, elicit recommendations for developing risk reduction
intervention strategies, and to better understand the factors that
place women at risk for HIV. Study participants will be recruited from
health departments and clinics providing healthcare to HIV-positive
women and AIDS Service Organizations. There is no cost to the
participants other than their time. The total estimated annual burden
hours are 635.
Estimated Annualized Burden Hours
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Number of Avg. burden
Type of respondents Form name Number of responses per per response
respondents respondent (in hours)
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Potential Participants................ Screener Contact Form... 550 1 10/60
Intervention Participants--and Locator Form............ 330 1 3/60
Comparison Group).
Intervention Participants--and Assessment Baseline..... 330 1 45/60
Comparison Group.
Intervention Participants--and Assessment Follow-up.... 330 1 45/60
Comparison Group.
Subset of Intervention Group.......... In-depth Interview...... 30 1 1
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Dated: May 26, 2009.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E9-12622 Filed 5-29-09; 8:45 am]
BILLING CODE 4163-18-P