Proposed Data Collections Submitted for Public Comment and Recommendations, 11984-11985 [05-4684]
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11984
Federal Register / Vol. 70, No. 46 / Thursday, March 10, 2005 / Notices
In addition, we are now planning to
quantify the levels of cytokines in nasal
exudates to assess whether they can be
used to verify exposure and to
demonstrate a biological effect (i.e.,
allergic response) following inhalation
of aerosolized brevetoxins. We plan to
include not only the study subjects who
have been involved in our earlier
studies, but also any new individuals
who are hired to work at the relevant
beaches. As mentioned above, we have
collected part data on occupational
exposure to red tides. However, because
we are dealing with natural phenomena
and are subject literally to the tides, and
because the scientific questions are
evolving as we learn more, we must
extend our data collection time for an
additional three years. There are no
costs to respondents except for their
time.
Annualized Burden Table:
Number of
responses per
respondent
Number of
respondents
Respondents
Average
burden per response
Total burden
Pulmonary History Questionnaire ....................................................................
Spirometry ........................................................................................................
Nasal exudates collection/Nasal wash ............................................................
Symptom Questionnaire ..................................................................................
Hearing test .....................................................................................................
Beach Survey ..................................................................................................
5
25
25
25
25
5
1
6
6
6
6
160
20/60
20/60
10/60
5/60
15/60
5/60
2
50
25
13
38
67
Total ..........................................................................................................
........................
........................
........................
195
Dated: March 3, 2005.
Betsey Dunaway,
Acting Reports Clearance Officer, Office of
the Chief Science Officer, Centers for Disease
Control and Prevention.
[FR Doc. 05–4683 Filed 3–9–05; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–05–04KE]
Proposed Data Collections Submitted
for Public Comment and
Recommendations
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) 371–5976 or send an
email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC via fax to (202) 395–6974. Written
comments should be received within 30
days of this notice.
Proposed Project
Evaluation of the Sexually
Transmitted Disease (STD) Faculty
Expansion Program (FEP)—New—
National Center for HIV, STD, and TB
Prevention (NCHSTP), Centers for
Disease Control and Prevention (CDC).
Background:
Primary care physicians play a
significant role in STD prevention and
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18:28 Mar 09, 2005
Jkt 205001
control. Diagnosing, treating, reporting,
partner notification, and patient
counseling which emphasizes
appropriate prevention messages, are all
important physician contributions to
STD control. In the curricula of most
medical schools and residency
programs, STDs and the public health
role of primary care physicians in their
control and prevention receive little
emphasis.
To address this lack of training, CDC
implemented the STD Faculty
Expansion Program (FEP), which aims
to improve capacity of primary care
physicians to diagnose, treat, and
prevent STDs. The FEP provides
medical schools with funding for an
additional faculty member to develop
and implement curriculum for training
medical students and residents, develop
collaborative relationships with local
health departments, and coordinate STD
clinical experiences for medical
students and residents. The potential
long-tern impact of the STD-related
training includes: Increase physician
awareness of STDs, greater comfort and
confidence in counseling patients,
increased case reporting and partner
management, and ultimately lower STD
incidence.
This project is an evaluation of the
FEP. Because the outcomes of greatest
relevance (increased physician
awareness, increased collaboration with
public health departments, decreased
STD incidence) will occur only after
students and residents who are
currently receiving the enhanced
training go into practice, the evaluation
focuses on intermediate outcomes as a
means of assessing the program’s utility
and effectiveness.
Four medical schools (e.g. Morehouse
School of Medicine, University of
Alabama at Birmingham, Louisiana
PO 00000
Frm 00057
Fmt 4703
Sfmt 4703
State University Medical Center, and the
University of California Los Angeles
School of Medicine) currently receive
support under the FEP. The evaluation
of the FEP consists of a survey of thirdyear medical students at the four
currently funded schools and a sample
of third-year medical students in all
other U.S. medical schools.
A paper-and-pencil survey instrument
will be administered to the students in
the four FEP schools in a classroom or
clinic setting or through the school mail
distribution system. The survey
instrument will be distributed to the
sample of students from all other
medical schools using express mail.
Survey topics will include:
—Hours of clinical and didactic training
received during the first three years of
medical school.
—Knowledge and efficacy with basic
STD clinical diagnosis, treatment, and
prevention.
—Students’ confidence in taking a
sexual history and providing specific
prevention counseling to patients.
—Student familiarity with the role of
the public health department in
control and prevention of STDs.
A total of 850 students will be
surveyed—approximately 425 at the
FEP schools and 425 from all other U.S.
medical schools. Evidence that the
FEP’s enhanced STD training is effective
will include greater knowledge of and
comfort in diagnosis, treatment and
prevention of STDs among FEP
students, recall of more time having
been devoted to STDs during medical
training, and greater awareness of the
primary care physician’s public health
role in STD control and prevention. The
time required to complete the survey
will be approximately 25 minutes. The
total annual burden for this data
collection is 354 hours.
E:\FR\FM\10MRN1.SGM
10MRN1
11985
Federal Register / Vol. 70, No. 46 / Thursday, March 10, 2005 / Notices
Annualized Table:
Respondents
Number of respondents
Number of responses per
respondent
Average burden per response
(in hours)
3rd Year Medical Students ..........................................................................................................
850
1
25/60
Dated: March 3, 2005.
Betsey Dunaway,
Acting Reports Clearance Officer, Office of
the Chief Science Officer, Centers for Disease
Control and Prevention.
[FR Doc. 05–4684 Filed 3–9–05; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–05BK]
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) 371–5976 or
send comments to Sandi Gambescia,
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
National Survey of Ambulatory
Surgery (OMB No. 0920–0334)—
Reinstatement—National Center for
Health Statistics (NCHS), Centers for
Disease Control and Prevention (CDC).
The National Survey of Ambulatory
Surgery (NSAS) was previously
conducted by the CDC National Center
for Health Statistics from 1994 through
1996. It is the principal source of data
on ambulatory surgery center (ASC)
services in the United States. It
complements surgery data obtained in
the NCHS National Hospital Discharge
Survey (NHDS) OMB No. 0920–0212,
which provides annual data concerning
the nation’s use of inpatient medical
and surgical care provided in short-stay,
non-Federal hospitals. The NSAS is a
national probability sample survey of
ambulatory surgery visits in hospitals
and freestanding ambulatory surgery
centers. It has been the benchmark
against which special programmatic
data sources are compared.
Data for the NSAS will be collected
annually beginning in 2006 from a
nationally representative sample of
hospitals and freestanding ambulatory
surgery centers. The hospital universe
includes noninstitutional hospitals
exclusive of Federal, military, and
Department of Veterans Affairs hospitals
located in the 50 States and the District
of Columbia. The universe of
freestanding facilities includes the
freestanding ambulatory surgery centers
licensed by states and/or certified as
ambulatory surgery centers for Medicare
reimbursement. As in the earlier survey,
facilities specializing in dentistry,
podiatry, abortion, family planning or
birthing will be excluded. As with
previous years, the data items which are
abstracted from medical records are the
basic core variables from the Uniform
Hospital Discharge Data Set (UHDDS) as
well as surgery times, total charges and
information on anesthesia. There are no
costs to respondents except for their
time to participate in the survey.
Annualized Burden Table:
Number of respondents
Number of responses/respondent
Induction1 .........................................................................................................
Out-of-scope verification ..................................................................................
Sample Listing Sheet:
ASC Personnel .........................................................................................
Census Personnel ....................................................................................
Medical Abstract:
ASC Personnel .........................................................................................
Census Personnel ....................................................................................
Annual Update .................................................................................................
Quality Control .................................................................................................
227
150
1
1
90/60
4/60
340.5
10
224
264
12
12
30/60
0
1,344
0
324
164
488
245
250
250
1
20
12/60
2/60
5/60
2/60
16,200
1,367
41
163
Total ..........................................................................................................
........................
........................
........................
19,465.5
Respondents
1 The
Avg. burden/
response (in
hrs.)
induction of 600 facilities takes place in the first year and 40 each in subsequent years but is averaged over 3 years.
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PO 00000
Frm 00058
Fmt 4703
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E:\FR\FM\10MRN1.SGM
10MRN1
Total burden
hours
Agencies
[Federal Register Volume 70, Number 46 (Thursday, March 10, 2005)]
[Notices]
[Pages 11984-11985]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-4684]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-05-04KE]
Proposed Data Collections Submitted for Public Comment and
Recommendations
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) 371-5976 or send an email to
omb@cdc.gov. Send written comments to CDC Desk Officer, Office of
Management and Budget, Washington, DC via fax to (202) 395-6974.
Written comments should be received within 30 days of this notice.
Proposed Project
Evaluation of the Sexually Transmitted Disease (STD) Faculty
Expansion Program (FEP)--New--National Center for HIV, STD, and TB
Prevention (NCHSTP), Centers for Disease Control and Prevention (CDC).
Background:
Primary care physicians play a significant role in STD prevention
and control. Diagnosing, treating, reporting, partner notification, and
patient counseling which emphasizes appropriate prevention messages,
are all important physician contributions to STD control. In the
curricula of most medical schools and residency programs, STDs and the
public health role of primary care physicians in their control and
prevention receive little emphasis.
To address this lack of training, CDC implemented the STD Faculty
Expansion Program (FEP), which aims to improve capacity of primary care
physicians to diagnose, treat, and prevent STDs. The FEP provides
medical schools with funding for an additional faculty member to
develop and implement curriculum for training medical students and
residents, develop collaborative relationships with local health
departments, and coordinate STD clinical experiences for medical
students and residents. The potential long-tern impact of the STD-
related training includes: Increase physician awareness of STDs,
greater comfort and confidence in counseling patients, increased case
reporting and partner management, and ultimately lower STD incidence.
This project is an evaluation of the FEP. Because the outcomes of
greatest relevance (increased physician awareness, increased
collaboration with public health departments, decreased STD incidence)
will occur only after students and residents who are currently
receiving the enhanced training go into practice, the evaluation
focuses on intermediate outcomes as a means of assessing the program's
utility and effectiveness.
Four medical schools (e.g. Morehouse School of Medicine, University
of Alabama at Birmingham, Louisiana State University Medical Center,
and the University of California Los Angeles School of Medicine)
currently receive support under the FEP. The evaluation of the FEP
consists of a survey of third-year medical students at the four
currently funded schools and a sample of third-year medical students in
all other U.S. medical schools.
A paper-and-pencil survey instrument will be administered to the
students in the four FEP schools in a classroom or clinic setting or
through the school mail distribution system. The survey instrument will
be distributed to the sample of students from all other medical schools
using express mail.
Survey topics will include:
--Hours of clinical and didactic training received during the first
three years of medical school.
--Knowledge and efficacy with basic STD clinical diagnosis, treatment,
and prevention.
--Students' confidence in taking a sexual history and providing
specific prevention counseling to patients.
--Student familiarity with the role of the public health department in
control and prevention of STDs.
A total of 850 students will be surveyed--approximately 425 at the
FEP schools and 425 from all other U.S. medical schools. Evidence that
the FEP's enhanced STD training is effective will include greater
knowledge of and comfort in diagnosis, treatment and prevention of STDs
among FEP students, recall of more time having been devoted to STDs
during medical training, and greater awareness of the primary care
physician's public health role in STD control and prevention. The time
required to complete the survey will be approximately 25 minutes. The
total annual burden for this data collection is 354 hours.
[[Page 11985]]
Annualized Table:
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Respondents Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
3rd Year Medical Students.................................... 850 1 25/60
----------------------------------------------------------------------------------------------------------------
Dated: March 3, 2005.
Betsey Dunaway,
Acting Reports Clearance Officer, Office of the Chief Science Officer,
Centers for Disease Control and Prevention.
[FR Doc. 05-4684 Filed 3-9-05; 8:45 am]
BILLING CODE 4163-18-P