[Federal Register: October 27, 2006 (Volume 71, Number 208)]
[Notices]
[Page 63016-63017]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr27oc06-62]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-07-05CG]
Proposed Data Collections Submitted for Public Comment and
Recommendations
In compliance with the requirement of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for opportunity for public comment on
proposed data collection projects, the Centers for Disease Control and
Prevention (CDC) will publish periodic summaries of proposed projects.
To request more information on the proposed projects or to obtain a
copy of the data collection plans and instruments, call 404-639-5960
and send comments to Seleda Perryman, CDC Assistant Reports Clearance
Officer, 1600 Clifton Road, MS-D74, Atlanta, GA 30333 or send an e-mail
to omb@cdc.gov.
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; and (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. Written comments should be received
within 60 days of this notice.
Proposed Project
Medical Monitoring Project (MMP)--New--National Center for HIV, STD
and TB Prevention (NCHSTP), Centers for Disease Control and Prevention
(CDC).
Background and Brief Description
This proposed data collection supplements the HIV/AIDS surveillance
programs in 26 selected State and local health departments, which
collect information on persons diagnosed with, living with, and dying
from HIV infection and AIDS and will incorporate data elements from two
data collections: Supplement to HIV/AIDS Surveillance (SHAS) project
(0920-0262) and the Adult/Adolescent Spectrum of HIV Disease (ASD).
Both projects stopped data collection in 2004.
Although CDC receives surveillance data from all U.S. States, these
supplemental surveillance data are needed to make estimates of key
indicators, such as quality of HIV-related ambulatory care and the
severity of need for HIV-related care and services. A large number of
cities and States are heavily impacted by the HIV/AIDS epidemic,
resulting in the need for population-based national estimates of HIV-
related behaviors, clinical outcomes, and quality of HIV care.
This project will collect data on behaviors and clinical outcomes
from a probability sample of HIV-infected adults receiving care in the
U.S. Collection of data from interviews with HIV-infected patients will
provide information on patient demographics, and the current levels of
behaviors that may facilitate HIV transmission: Sexual and drug use
behaviors; patients' access to, use of and barriers to HIV-related
secondary prevention services; utilization of HIV-related medical
[[Page 63017]]
services; and adherence to drug regimens. Collection of data from
patient medical records will provide information on: Demographics and
insurance status; the prevalence and incidence of AIDS-defining
opportunistic illnesses and co-morbidities related to HIV disease; the
receipt of prophylactic and antiretroviral medications; and whether
patients are receiving screening and treatment according to Public
Health Service guidelines. No other Federal agency collects national
population-based behavioral and clinical information from HIV-infected
adults in care. The data will have significant implications for policy,
program development, and resource allocation at the State/local and
national levels.
CDC is requesting approval for a 3-year clearance for data
collection. Data will be collected by 26 Reporting Areas (19 States,
Puerto Rico and 6 separately funded cities). CDC estimates an average
of 400 respondents per site with an 80% response rate, resulting in
8,320 respondents for the interview portion. A Short interview will be
used for patients who are too ill to complete the Standard interview or
when the interview must be translated, and a Proxy interview will be
available if the patient consents to having a family member or other
person answer the questions in the case of severe illness or in the
event the selected participant died prior to being interviewed. The
proxy and the short interview, each which will be used on approximately
2% of patients, will take approximately 20 minutes. Participation of
respondents is voluntary and there is no cost to the respondents other
than their time.
Estimated Annualized Burden Hours
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Average
Number of Number of burden per Total
Types of data collection respondents responses per response (in burden
respondent hours) hours
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Standard interview................................... 7,988 1 45/60 5,991
Short interview...................................... 166 1 20/60 55
Proxy interview...................................... 166 1 20/60 55
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Total............................................ .............. .............. .............. 6,101
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Dated: October 23, 2006.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E6-18014 Filed 10-26-06; 8:45 am]
BILLING CODE 4163-18-P