Agency Forms Undergoing Paperwork Reduction Act Review, 17063-17064 [2012-7028]
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17063
Federal Register / Vol. 77, No. 57 / Friday, March 23, 2012 / Notices
of issues related to the provision of
ROPS or the ROPS configuration itself,
as self-selected ranking criteria,
following the maximum difference
scaling methodology.
This information will allow CDC to
compile a systematic, quantifiable
inventory of preference data for a group
that is considered representative of
tractor parts dealers nationwide.
Additionally, this data will allow for
segmentation of response by groups
with particularized interests.
The survey pilot questionnaire will be
administered by the New York Center
for Agricultural Medicine and Health
(NYCAMH). Following the
administration of a pilot test
questionnaire to assess comprehension
and message comprehension, a finalized
questionnaire will be routinely
submitted to NEDA establishments by
electronic mail. The estimated burden
per response is 17 minutes. Each
respondent establishment will receive a
personalized advance notification email,
followed by an email with a link to the
CDC Web site.
CDC anticipates that routine
information collection will begin in
August 2012. Assuming full
participation, the total estimated burden
for the one-time retrospective data
collection is 148 hours which includes
500 respondents for the survey and 20
respondents from the pilot project. At a
reduced response rate of 80%, total
burden would be 450 participants for a
total of 134 hours, assuming
replacement and thus full participation
for pilot participants. There are no costs
to respondents other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Tractor parts dealers .........................
Tractor parts dealers .........................
Total ...........................................
NIOSH/NYCAMH
Survey.
NIOSH/NYCAMH
Pilot.
450
1
17/60
128
Parts
Dealers
20
1
17/60
6
...........................................................
........................
........................
........................
134
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–12–0740]
Agency Forms Undergoing Paperwork
Reduction Act Review
srobinson on DSK4SPTVN1PROD with NOTICES
Total burden
(in hrs)
Dealers
[FR Doc. 2012–7030 Filed 3–22–12; 8:45 am]
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) 639–7570 or send an
email to omb@cdc.gov. 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
Medical Monitoring Project (MMP)—
0920–0740, exp. 5/31/2012—Extension
with change—National Center for HIV,
17:14 Mar 22, 2012
Avg. burden
per response
(in hrs)
Parts
Dated: March 19, 2012.
Ron A. Otten,
Director, Office of Scientific Integrity, Office
of the Associate Director for Science (OADS),
Office of the Director, Centers for Disease
Control and Prevention.
VerDate Mar<15>2010
No. of
responses per
respondent
No. of
respondents
Form name
Jkt 226001
Hepatitis, STD and TB Prevention
(NCHHSTP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
This proposed data collection
supplements the HIV/AIDS surveillance
programs in 23 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 population-based
national estimates of key indicators,
related to the quality of HIV-related
ambulatory care, the severity of need for
HIV-related care and services, and HIVrelated behaviors and clinical outcomes.
This project collects 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
provides 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 receiving HIV-related
secondary prevention services;
utilization of HIV-related medical
PO 00000
Frm 00063
Fmt 4703
Sfmt 4703
services; and adherence to drug
regimens. Collection of data from
patient medical records provides
information on: Demographics and
insurance status; the prevalence and
incidence of AIDS-defining
opportunistic illnesses and comorbidities 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 populationbased behavioral and clinical
information from HIV-infected adults in
care. The data are expected to have
significant implications for policy,
program development, and resource
allocation at the state/local and national
levels.
The Centers for Disease Control and
Prevention requests approval for a
3-year extension with change for the
previously approved Medical
Monitoring Project (MMP) 0920–0740
exp. 5/31/2012). Data will be collected
through in-person and telephoneadministered, computer-assisted
interviews conducted by trained
interviewers in 23 Reporting Areas (16
states, Puerto Rico and 6 separately
funded cities), and through medical
record abstraction by trained
abstractors. The methods for the project
have been updated to include telephone
interviews as an interviewing option.
Otherwise, the project activities and
methods will remain the same as those
E:\FR\FM\23MRN1.SGM
23MRN1
17064
Federal Register / Vol. 77, No. 57 / Friday, March 23, 2012 / Notices
database, the national HIV/AIDS
Reporting System [HARS]. These data
will be used for quality control (to
ensure patients were not sampled for
participation in MMP more than once),
to assess nonresponse bias, to
prospectively monitor respondents’ care
utilization and treatment, and to make
inference to the population of persons
living with HIV in the United States.
The interview and minimum data set
data collection instruments have been
revised based on experience in previous
data collection cycles, but these changes
will not affect the burden per
respondent. The medical record
abstraction forms have not changed.
used in the previously approved data
collection period.
A standard interview will be
conducted with approximately 96% of
patients, and will take 45 minutes. A
short interview will be conducted with
patients who are too ill to complete the
standard interview or when the
interview must be translated. The short
interview, which will be conducted
with approximately 4% of patients, will
take approximately 20 minutes.
Medical record abstractions will be
completed for on all eligible
participants. Minimal data on all
sampled patients will be extracted from
an existing HIV case surveillance
CDC’s current goal is to interview 80%
of 9,400 patients or 7,520, 96% of whom
(a total of 7,219 patients) will complete
the standard interview and 4% of whom
(a total of 301 patients) will complete
the short interview. Because the number
of sampled patients is greater (by 62
patients) than for the previously
approved information collection, the
total burden (in hours) will increase by
37 hours, from 8,500 to 8,537.
Participation of respondents is
voluntary and there is no cost to the
respondents other than their time.
The estimated annualized burden
hours are 8,537.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent
Form name
Sampled, Eligible HIV-Infected Patients ..............................................................
Standard
interview.
Short interview.
...................
...................
...................
...................
Sampled, Eligible
Interview.
Facility office staff
Facility office staff
Facility office staff
Facility office staff
HIV-Infected Patients Unable to Complete the Standard
pulling medical records ..........................................................
providing Estimated Patient Loads ........................................
providing patient lists .............................................................
approaching participants for enrollment .................................
Dated: March 19, 2012.
Ron A. Otten,
Director, Office of Scientific Integrity, Office
of the Associate Director for Science (OADS),
Office of the Director, Centers for Disease
Control and Prevention.
[FR Doc. 2012–7028 Filed 3–22–12; 8:45 am]
BILLING CODE 4163–18–P
Proposed Project
The National Survey of Family
Growth (NSFG)—(0920–0314,
Expiration 05/31/2012)—Revision—
National Center for Health Statistics
(NCHS), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30-Day–12–0314]
Agency Forms Undergoing Paperwork
Reduction Act Review
srobinson on DSK4SPTVN1PROD with NOTICES
Number of
respondents
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 of 44 U.S.C.,
Chapter 35. To request a copy of these
requests, call (404) 639–7570 or send an
email to omb@cdc.gov. 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.
VerDate Mar<15>2010
17:14 Mar 22, 2012
Jkt 226001
Section 306 of the Public Health
Service (PHS) Act (42 U.S.C. 242k), as
amended, authorizes that the Secretary
of Health and Human Services (DHHS),
acting through NCHS, shall collect
statistics on ‘‘family formation, growth,
and dissolution,’’ as well as
‘‘determinants of health’’ and
‘‘utilization of health care’’ in the
United States. This three-year clearance
request includes the data collection in
2012–2015 for the continuous NSFG.
The National Survey of Family
Growth(NSFG) was conducted
periodically between 1973 and 2002,
and continuously since 2006, by the
National Center for Health Statistics,
CDC. Each year, about 14,000
households are screened, with about
5,000 participants interviewed annually.
Participation in the NSFG is completely
voluntary and confidential. Interviews
average 60 minutes for males and 80
minutes for females. The response rate
since 2006 is about 77 percent. This
PO 00000
Frm 00064
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
Average
burden per
response
(in hours)
7,219
1
45/60
301
1
20/60
7,520
936
1,030
3,120
1
1
1
1
3/60
2
30/60
5/60
submission requests approval for three
years.
The NSFG program produces
descriptive statistics which measure
factors associated with birth and
pregnancy rates, including
contraception, infertility, marriage,
divorce, and sexual activity, in the US
population 15–44; and behaviors that
affect the risk of sexually transmitted
diseases (STD), including HIV, and the
medical care associated with
contraception, infertility, and pregnancy
and childbirth.
NSFG data users include the DHHS
programs that fund it, including CDC/
NCHS and nine others (The Eunice
Kennedy Shriver National Institute for
Child Health and Human Development
(NIH/NICHD); the Office of Population
Affairs (DHHS/OPA); the Office of the
Assistant Secretary for Planning and
Evaluation (DHHS/OASPE); the
Children’s Bureau (DHHS/ACF/CB); the
ACF’s Office of Planning, Research, and
Evaluation (OPRE); the CDC’s Division
of HIV/AIDS Prevention (CDC/DHAP);
the CDC’s Division of STD Prevention
(CDC/DSTD); the CDC’s Division of
Cancer Prevention and Control (CDC/
DCPC); and the CDC’s Division of Birth
Defects and Developmental Disabilities.
The NSFG is also used by state and local
governments; private research and
action organizations focused on men’s
E:\FR\FM\23MRN1.SGM
23MRN1
Agencies
[Federal Register Volume 77, Number 57 (Friday, March 23, 2012)]
[Notices]
[Pages 17063-17064]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-7028]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-12-0740]
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) 639-7570 or send an email to
omb@cdc.gov. 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
Medical Monitoring Project (MMP)--0920-0740, exp. 5/31/2012--
Extension with change--National Center for HIV, Hepatitis, STD and TB
Prevention (NCHHSTP), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
This proposed data collection supplements the HIV/AIDS surveillance
programs in 23 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 population-based
national estimates of key indicators, related to the quality of HIV-
related ambulatory care, the severity of need for HIV-related care and
services, and HIV-related behaviors and clinical outcomes.
This project collects 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 provides
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 receiving HIV-
related secondary prevention services; utilization of HIV-related
medical services; and adherence to drug regimens. Collection of data
from patient medical records provides 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 are expected to have significant implications
for policy, program development, and resource allocation at the state/
local and national levels.
The Centers for Disease Control and Prevention requests approval
for a 3-year extension with change for the previously approved Medical
Monitoring Project (MMP) 0920-0740 exp. 5/31/2012). Data will be
collected through in-person and telephone-administered, computer-
assisted interviews conducted by trained interviewers in 23 Reporting
Areas (16 states, Puerto Rico and 6 separately funded cities), and
through medical record abstraction by trained abstractors. The methods
for the project have been updated to include telephone interviews as an
interviewing option. Otherwise, the project activities and methods will
remain the same as those
[[Page 17064]]
used in the previously approved data collection period.
A standard interview will be conducted with approximately 96% of
patients, and will take 45 minutes. A short interview will be conducted
with patients who are too ill to complete the standard interview or
when the interview must be translated. The short interview, which will
be conducted with approximately 4% of patients, will take approximately
20 minutes.
Medical record abstractions will be completed for on all eligible
participants. Minimal data on all sampled patients will be extracted
from an existing HIV case surveillance database, the national HIV/AIDS
Reporting System [HARS]. These data will be used for quality control
(to ensure patients were not sampled for participation in MMP more than
once), to assess nonresponse bias, to prospectively monitor
respondents' care utilization and treatment, and to make inference to
the population of persons living with HIV in the United States.
The interview and minimum data set data collection instruments have
been revised based on experience in previous data collection cycles,
but these changes will not affect the burden per respondent. The
medical record abstraction forms have not changed. CDC's current goal
is to interview 80% of 9,400 patients or 7,520, 96% of whom (a total of
7,219 patients) will complete the standard interview and 4% of whom (a
total of 301 patients) will complete the short interview. Because the
number of sampled patients is greater (by 62 patients) than for the
previously approved information collection, the total burden (in hours)
will increase by 37 hours, from 8,500 to 8,537.
Participation of respondents is voluntary and there is no cost to
the respondents other than their time.
The estimated annualized burden hours are 8,537.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Sampled, Eligible HIV-Infected Standard interview...... 7,219 1 45/60
Patients.
Sampled, Eligible HIV-Infected Short interview......... 301 1 20/60
Patients Unable to Complete the
Standard Interview.
Facility office staff pulling medical ........................ 7,520 1 3/60
records.
Facility office staff providing ........................ 936 1 2
Estimated Patient Loads.
Facility office staff providing ........................ 1,030 1 30/60
patient lists.
Facility office staff approaching ........................ 3,120 1 5/60
participants for enrollment.
----------------------------------------------------------------------------------------------------------------
Dated: March 19, 2012.
Ron A. Otten,
Director, Office of Scientific Integrity, Office of the Associate
Director for Science (OADS), Office of the Director, Centers for
Disease Control and Prevention.
[FR Doc. 2012-7028 Filed 3-22-12; 8:45 am]
BILLING CODE 4163-18-P