Proposed Data Collections Submitted for Public Comment and Recommendations, 41758-41759 [E7-14704]
Download as PDF
<![CDATA[
41758
Federal Register / Vol. 72, No. 146 / Tuesday, July 31, 2007 / Notices
are members of tribes, and have a good
sense of cultural health beliefs.
The healthcare provider group will
consist of nomination by the Indian
Health Service Chief Medical Officer
(IHSCMO), who will nominate 3 MD/
NP’s or PA’s and 3 nurses in each
region. The participating emergency
care providers will each be asked to
nominate 2 providers from a cardiology
clinic (cardiologists or cardiac nurses)
and/or a pre-hospital (EMT/Paramedic)
provider. The 6 original from each
region will subtotal to 18 emergency
care providers plus the 2 individuals
they each nominate will subtotal to 36
from each region, a total of 54 prehospital and cardiology providers
participate in the key informant
interviews will equal a minimum of
approximately 27 health providers, 15
community members or 42 key
informant interview, each contacts 2
individuals, a minimum of 168
respondents to the survey.
After the key informant interviews
have been completed and analyzed
there will be two community focus
groups each comprised of 8 to 10
participants from all three regions held.
The first involving patients who have
had an MI and the second focus group
will involve community members at risk
for MIs.
There are no costs to the respondent
except their time to participate in the
survey.
(medical providers) key informant
interviews covering all three regions.
The community key informants will
consist of 3 tribal health directors who
will nominate 3 community key
informants from each region, who will
then each nominate 2 additional
community members to be interviewed
for a sample of 30 community key
informants.
The individual key informant
interviews of the group of patients who
have had an MI or have a high risk of
MI, nominated by the physicians, nurses
and community members will be asked
to nominate individuals whom they
know have had or are at risk for a heart
attack. The medical providers and
community members asked to
ESTIMATED ANNUALIZED BURDEN HOURS
Respondents
Number of
respondents
No. of
responses per
respondent
Average
burden per
response (in
hrs.)
Healthcare providers ........................................................................................
Community leaders ..........................................................................................
Community members interviews ......................................................................
(2) Community member focus group retreats .................................................
Total ..........................................................................................................
54
30
168
20
........................
1
1
1
1
........................
1
1
1
8
........................
Dated: July 25, 2007.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E7–14703 Filed 7–30–07; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60 Day–07–06BN]
rmajette on PROD1PC64 with NOTICES
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.
VerDate Aug<31>2005
15:11 Jul 30, 2007
Jkt 211001
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
Conduct a Chronic Fatigue Syndrome
Registry Pilot Test (Bibb County,
Georgia)—New—National Center for
Infectious Diseases (NCID) Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
CDC is tasked with establishing a
registry of chronic fatigue syndrome
(CFS) and other fatiguing illnesses. The
objective of the registry is to identify
persons with unexplained fatiguing
illnesses, including CFS, who access the
healthcare system because of their
symptoms. Patients will be between the
ages of 12 and 59, inclusive.
PO 00000
Frm 00057
Fmt 4703
Sfmt 4703
Total burden
(in hours)
54
30
168
160
412
Specific aims of the registry are; (1)
Identify and enroll patients with CFS
and other unexplained fatiguing
illnesses who are receiving medical and
ancillary medical care and describe
their epidemiologic and clinical
characteristics; (2) follow CFS patients
and patients with other fatiguing
illnesses over time to characterize the
natural history of CFS and other
unexplained fatiguing illnesses; (3)
assess and monitor health care
providers’ knowledge, attitudes, and
beliefs concerning CFS; (4) and to
identify well-characterized CFS patients
for clinical studies and intervention
trials. These specific aims require
inclusion of subjects in early stages of
CFS (i.e., ill less than one year duration)
who can be followed longitudinally to
assess changes in their CFS symptoms.
Data on persons with CFS in the general
population has been collected in a
separate study and is not an objective of
this Registry.
In order to determine the most
effective and cost-efficient design for
achieving the objective and specific
aims, CDC will conduct a pilot test of
the Registry of CFS and other fatiguing
illnesses in Bibb County, Georgia. The
CFS Registry Pilot Test will assess two
Registry designs for efficacy and
efficiency in identifying adult and
adolescent subjects with CFS who are
E:\FR\FM\31JYN1.SGM
31JYN1
41759
Federal Register / Vol. 72, No. 146 / Tuesday, July 31, 2007 / Notices
receiving medical and ancillary medical
care. Specifically, the CFS Registry Pilot
Test will evaluate surveillance of
patients with CFS identified through
physician practices and a surveillance
of CFS patients identified by physicians
and other health care providers.
The proposed study will begin when
a provider refers a patient to the
registry. Patients who consent to be
contacted for the registry will be asked
to complete a detailed telephone
interview that screens for medical and
psychiatric eligibility. Eligible subjects
will be invited to have a clinical
evaluation that comprises a physical
examination; collection of blood, urine,
and saliva specimens; a mental health
interview; and self-administered
questionnaires.
There is no cost to respondents other
than their time. Patients who are
clinically evaluated will be reimbursed
for their time and effort. The total
annualized burden hours are 2,557.
ESTIMATE OF ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Number of
respondents
Respondent
Average
burden per
response
(hours)
Total burden
(hours)
Referring Providers ..........................................................................................
Patient Consent to be Contacted ....................................................................
Patient Telephone Interview ............................................................................
Patient Clinical Evaluation ...............................................................................
400
677
541
234
2
1
1
1
5/60
10/60
30/60
540/60
67
113
271
2,106
Total Burden .............................................................................................
........................
........................
........................
2,557
Dated: July 24, 2007.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E7–14704 Filed 7–30–07; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Periodically, the Health Resources
and Services Administration (HRSA)
publishes abstracts of information
collection requests under review by the
Office of Management and Budget
(OMB), in compliance with the
Paperwork Reduction Act of 1995 (44
U.S.C. Chapter 35). To request a copy of
the clearance requests submitted to
OMB for review, call the HRSA Reports
Clearance Office on (301) 443–1129.
The following request has been
submitted to the Office of Management
and Budget for review under the
Paperwork Reduction Act of 1995:
Proposed Project: Bureau of Primary
Health Care (BPHC) Uniform Data
System (OMB No. 0915–0193) Revision
The Uniform Data System (UDS)
contains the annual reporting
requirements for the cluster of primary
care grantees funded by the HRSA. The
UDS includes reporting requirements
for grantees of the following primary
care programs: Community Health
Centers, Migrant Health Centers, Health
Care for the Homeless, Public Housing
Primary Care, and other grantees under
section 330. The authorizing statute is
section 330 of the Public Health Service
Act, as amended.
Number of
respondents
Type of report
Responses
per
respondent
HRSA collects data in the UDS which
is used to ensure compliance with
legislative mandates and to report to
Congress and policy makers on program
accomplishments. To meet these
objectives, BPHC requires a core set of
data collected annually that is
appropriate for monitoring and
evaluating performance and reporting
on annual trends.
The 2008 calendar year UDS will be
revised in several ways. Certain UDS
tables are being proposed for
elimination or modification to
streamline data collection and reporting.
A limited number of clinical measures
will be added for reporting quality of
care, health outcomes, and disparities
data. In addition, the tool used to report
calendar year UDS data will be changed
to a Web based tool.
Estimates of annualized reporting
burden are as follows:
Total
responses
Hours per
response
Total burden
hours
1,076
150
1
1
1,076
150
54
18
32,280
2,700
Total ..............................................................................
rmajette on PROD1PC64 with NOTICES
Universal report ....................................................................
Grant report ..........................................................................
1,076
........................
1,076
........................
34,980
Written comments and
recommendations concerning the
proposed information collection should
be sent within 30 days of this notice to
the desk officer for HRSA, either by email to: OIRA_submission@omb.eop.gov
or by fax to 202–395–6974. Please direct
all correspondence to the ‘‘attention of
the desk officer for HRSA.’’
VerDate Aug<31>2005
15:11 Jul 30, 2007
Jkt 211001
Dated: July 20, 2007.
Alexandra Huttinger,
Acting Director, Division of Policy Review
and Coordination.
[FR Doc. E7–14680 Filed 7–30–07; 8:45 am]
BILLING CODE 4165–15–P
PO 00000
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Cancer Institute; Notice of
Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
Frm 00058
Fmt 4703
Sfmt 4703
E:\FR\FM\31JYN1.SGM
31JYN1
]]>Agencies
[Federal Register Volume 72, Number 146 (Tuesday, July 31, 2007)]
[Notices]
[Pages 41758-41759]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-14704]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60 Day-07-06BN]
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
Conduct a Chronic Fatigue Syndrome Registry Pilot Test (Bibb
County, Georgia)--New--National Center for Infectious Diseases (NCID)
Centers for Disease Control and Prevention (CDC).
Background and Brief Description
CDC is tasked with establishing a registry of chronic fatigue
syndrome (CFS) and other fatiguing illnesses. The objective of the
registry is to identify persons with unexplained fatiguing illnesses,
including CFS, who access the healthcare system because of their
symptoms. Patients will be between the ages of 12 and 59, inclusive.
Specific aims of the registry are; (1) Identify and enroll patients
with CFS and other unexplained fatiguing illnesses who are receiving
medical and ancillary medical care and describe their epidemiologic and
clinical characteristics; (2) follow CFS patients and patients with
other fatiguing illnesses over time to characterize the natural history
of CFS and other unexplained fatiguing illnesses; (3) assess and
monitor health care providers' knowledge, attitudes, and beliefs
concerning CFS; (4) and to identify well-characterized CFS patients for
clinical studies and intervention trials. These specific aims require
inclusion of subjects in early stages of CFS (i.e., ill less than one
year duration) who can be followed longitudinally to assess changes in
their CFS symptoms. Data on persons with CFS in the general population
has been collected in a separate study and is not an objective of this
Registry.
In order to determine the most effective and cost-efficient design
for achieving the objective and specific aims, CDC will conduct a pilot
test of the Registry of CFS and other fatiguing illnesses in Bibb
County, Georgia. The CFS Registry Pilot Test will assess two Registry
designs for efficacy and efficiency in identifying adult and adolescent
subjects with CFS who are
[[Page 41759]]
receiving medical and ancillary medical care. Specifically, the CFS
Registry Pilot Test will evaluate surveillance of patients with CFS
identified through physician practices and a surveillance of CFS
patients identified by physicians and other health care providers.
The proposed study will begin when a provider refers a patient to
the registry. Patients who consent to be contacted for the registry
will be asked to complete a detailed telephone interview that screens
for medical and psychiatric eligibility. Eligible subjects will be
invited to have a clinical evaluation that comprises a physical
examination; collection of blood, urine, and saliva specimens; a mental
health interview; and self-administered questionnaires.
There is no cost to respondents other than their time. Patients who
are clinically evaluated will be reimbursed for their time and effort.
The total annualized burden hours are 2,557.
Estimate of Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Respondent respondents responses per response (hours)
respondent (hours)
----------------------------------------------------------------------------------------------------------------
Referring Providers............................. 400 2 5/60 67
Patient Consent to be Contacted................. 677 1 10/60 113
Patient Telephone Interview..................... 541 1 30/60 271
Patient Clinical Evaluation..................... 234 1 540/60 2,106
---------------------------------------------------------------
Total Burden................................ .............. .............. .............. 2,557
----------------------------------------------------------------------------------------------------------------
Dated: July 24, 2007.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E7-14704 Filed 7-30-07; 8:45 am]
BILLING CODE 4163-18-P
