Submission for OMB Review; Comment Request; the Jackson Heart Study (JHS), 17744-17745 [2010-7895]
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Federal Register / Vol. 75, No. 66 / Wednesday, April 7, 2010 / Notices
Sandra L. Kusumoto,
Director, Bureau of Certification and
Licensing.
[FR Doc. 2010–7890 Filed 4–6–10; 8:45 am]
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Sandra L. Kusumoto,
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
WReier-Aviles on DSKGBLS3C1PROD with NOTICES
Office of the National Coordinator for
Health Information Technology HIT
Policy Committee Advisory Meeting;
Notice of Meeting
AGENCY: Office of the National
Coordinator for Health Information
Technology, HHS.
ACTION: Notice of change of location for
meetings.
This notice references forthcoming
meetings of public advisory committees
of the Office of the National Coordinator
for Health Information Technology
(ONC). The meeting will be open to the
public.
Name of Committee: HIT Policy
Committee; Meaningful Use Workgroup.
VerDate Nov<24>2008
15:18 Apr 06, 2010
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General Function of the Committee: to
provide recommendations to the
National Coordinator on a policy
framework for the development and
adoption of a nationwide health
information technology infrastructure
that permits the electronic exchange and
use of health information as is
consistent with the Federal Health IT
Strategic Plan and that includes
recommendations on the areas in which
standards, implementation
specifications, and certification criteria
are needed.
Date and Time: The meetings will be
held on April 20, 2010, from 9 a.m. to
5 p.m./Eastern Time (the Meaningful
Use Workgroup); and April 21, 2010,
from 10 a.m. to 4 p.m./Eastern Time
(HIT Policy Committee).
Location: The location for both
meetings has changed to the
Renaissance Dupont Circle Hotel, 1143
New Hampshire Avenue, NW.,
Washington, DC. The hotel telephone
number is 202–775–0800.
Contact Person: Judy Sparrow, Office
of the National Coordinator, HHS, 330 C
Street, SW., Washington, DC 20201,
202–205–4528, Fax: 202–690–6079, email: judy.sparrow@hhs.gov Please call
the contact person for up-to-date
information on these meetings. A notice
in the Federal Register about last
minute modifications that impact a
previously announced advisory
committee meeting cannot always be
published quickly enough to provide
timely notice.
Agenda: The Meaningful Use
Workgroup meeting will concern
Patient/Consumer Engagement, and hear
testimony from experts; the HIT Policy
Committee will hear reports from its
workgroups, including the Meaningful
Use Workgroup, the Certification/
Adoption Workgroup, the NHIN
Workgroup, the Privacy & Security
Policy Workgroup, and the Strategic
Plan Workgroup. ONC intends to make
background material available to the
public no later than two (2) business
days prior to the meeting. If ONC is
unable to post the background material
on its Web site prior to the meeting, it
will be made publicly available at the
location of the advisory committee
meeting, and the background material
will be posed on ONC’s Web site after
the meeting, at https://healthit.hhs.gov.
Procedure: Interested persons may
present data, information, or views,
orally or in writing, on issues pending
before the committee. Written
submissions may be made to the contact
person on or before April 13, 2010. Oral
comments from the public will be
scheduled between approximately 3:30
p.m. to 4 p.m. Time allotted for each
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presentation is limited to three minutes.
If the number of speakers requesting to
comment is greater than can be
reasonably accommodated during the
scheduled open public hearing session,
ONC will take written comments after
the meeting until close of business.
Persons attending ONC’s advisory
committee meetings are advised that the
agency is not responsible for providing
access to electrical outlets.
ONC welcomes the attendance of the
public at its advisory committee
meetings. Seating is limited at the
location, and ONC will make every
effort to accommodate persons with
physical disabilities or special needs. If
you require special accommodations
due to a disability, please contact Judy
Sparrow at least seven (7) days in
advance of the meeting.
ONC is committed to the orderly
conduct of its advisory committee
meetings. Please visit our Web site at
https://healthit.hhs.gov for procedures
on public conduct during advisory
committee meetings.
Notice of this meeting is given under
the Federal Advisory Committee Act
(Pub. L. 92–463, 5 U.S.C., App. 2).
Dated: April 1, 2010.
Judith Sparrow,
Office of Programs and Coordination, Office
of the National Coordinator for Health
Information Technology.
[FR Doc. 2010–7902 Filed 4–6–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Submission for OMB Review;
Comment Request; the Jackson Heart
Study (JHS)
Summary: Under the provisions of
Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National
Heart, Lung, and Blood Institute
(NHLBI), the National Institutes of
Health (NIH) has submitted to the Office
of Management and Budget (OMB) a
request for review and approval the
information collection listed below.
This proposed information collection
was previously published in the Federal
Register on January 13, 2010, page 1789,
and allowed 60 days for public
comment. No comments were received.
The purpose of this notice is to allow an
additional 30 days for public comment.
The National Institutes of Health may
not conduct or sponsor, and the
respondent is not required to respond
to, an information collection that has
been extended, revised, or implemented
E:\FR\FM\07APN1.SGM
07APN1
17745
Federal Register / Vol. 75, No. 66 / Wednesday, April 7, 2010 / Notices
on or after October 1, 1995, unless it
displays a currently valid OMB control
number.
Proposed Collection: Title: The
Jackson Heart Study: Annual Follow-up
with Third Party Respondents. Type of
Information Collection Request:
Revision of a currently approved
collection (OMB No. 0925–0491). Need
and Use of Information Collection: This
project involves contacting next-of-kin
and family physicians of deceased
participants who were part of the
Jackson Heart Study exam. Interviewers
will contact doctors and hospitals to
ascertain participants’ cardiovascular
events. Information gathered will be
used to further describe the risk factors,
occurrence rates, and consequences of
cardiovascular disease in African
American men and women. Recruitment
of 5,500 JHS participants began in
September 2000 and was completed in
March 2004. 5,302 participants
completed a baseline Exam 1 that
included demographics, psychosocial
inventories, medical history,
anthropometry, resting and ambulatory
blood pressure, phlebotomy and 24hour urine collection, ECG,
echocardiography, and pulmonary
function. JHS Exam 2 began September
26, 2005, followed by a more
comprehensive Exam 3 that began in
February 2009. The two new exams
include some repeated measures from
Exam 1 and several new components,
including distribution of self-monitoring
blood pressure devices. The
continuation of the study allows
continued assessment of subclinical
coronary disease, left ventricular
dysfunction, progression of carotid
atherosclerosis and left ventricular
hypertrophy, and responses to stress,
racism, and discrimination as well as
new components such as renal disease,
body fat distribution and body
composition, and metabolic
consequences of obesity.
Frequency of Response: One-time.
Affected Public: Individuals or
households; businesses or other for
profit; not-for-profit institutions. Type of
Respondents: Adults; doctors and staff
of hospitals and nursing homes. The
annual reporting burden is as follows:
Estimated Number of Respondents: 400;
Estimated Number of Responses per
Respondent: 1.0; Average Burden Hours
per Response: (84 hours/400
respondents) 0.20; and Estimated Total
Annual Burden Hours Requested: 84.
The annualized cost to respondents is
estimated at $3,760, assuming $15 per
burden hour for informants and $65 per
burden hour for physicians. There are
no Capital Costs to report. There are no
Operating or Maintenance Costs to
report.
ESTIMATE OF ANNUAL HOUR BURDEN
Number of
respondents
Type of response
Frequency of
response
Average time
per response
Annual hour
burden
200
200
1
1
0.17
0.25
34
50
Total ..........................................................................................................
WReier-Aviles on DSKGBLS3C1PROD with NOTICES
Morbidity & Mortality AFU 3rd Party/Next-of-kin decedents ............................
Morbidity & Mortality AFU 3rd Party Physicians .............................................
400
........................
........................
84
Request for Comments: Written
comments and/or suggestions from the
public and affected agencies should
address one or more of the following
points: (1) Evaluate whether the
proposed collection of information is
necessary for the proper performance of
the function of the agency, including
whether the information will have
practical utility; (2) Evaluate the
accuracy of the agency’s estimate of the
burden of the proposed collection of
information, including the validity of
the methodology and assumptions used;
(3) Enhance the quality, utility, and
clarity of the information to be
collected; and (4) Minimize the burden
of the collection of information on those
who are to respond, including the use
of appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
Direct Comments to OMB: Written
comments and/or suggestions regarding
the item(s) contained in this notice,
especially regarding the estimated
public burden and associated response
time, should be directed to the: Office
of Management and Budget, Office of
Regulatory Affairs,
OIRA_submission@omb.eop.gov or by
fax to 202–395–6974, Attention: Desk
VerDate Nov<24>2008
15:18 Apr 06, 2010
Jkt 220001
Officer for NIH. To request more
information on the proposed project or
to obtain a copy of the data collection
plans and instruments, contact: Ms.
Cheryl Nelson, Project Officer, NIH,
NHLBI, 6701 Rockledge Drive, MSC
7934, Bethesda, MD 20892–7934, or call
non-toll-free number 301–435–0451 or
e-mail your request, including your
address to: NelsonC@nhlbi.nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 30 days of the date of
this publication.
Suzanne Freeman,
NHLBI Project Clearance Liaison, National
Institutes of Health.
Michael Lauer,
Director, DCVS, National Institutes of Health.
[FR Doc. 2010–7895 Filed 4–6–10; 8:45 am]
BILLING CODE 4140–01–P
PO 00000
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Indian Health Service
[Funding Announcement Number: HHS–
2011–IHS–TMD–0001]
Tribal Management Grant Program;
Announcement Type: New and
Competing Continuation Discretionary
Funding Cycle for Fiscal Year 2011
Catalog of Federal Domestic
Assistance Number(s): 93.228.
Key Dates: Program Requirements
Session: April 21–22 and May 5–6,
2010.
Grant Writing Session: May 17–21,
2010.
TMG WebEx Session: June 3, 2010.
Application Deadline Date: August 6,
2010.
Receipt Date for Final Tribal
Resolution: October 1, 2010.
Review Date: October 4–8, 2010.
Application Notification Date:
November 12, 2010.
Earliest Anticipated Start Date:
January 1, 2011.
I. Funding Opportunity Description
The Indian Health Service (IHS)
announces competitive grant
applications for the Tribal Management
Frm 00065
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Agencies
[Federal Register Volume 75, Number 66 (Wednesday, April 7, 2010)]
[Notices]
[Pages 17744-17745]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-7895]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Submission for OMB Review; Comment Request; the Jackson Heart
Study (JHS)
Summary: Under the provisions of Section 3507(a)(1)(D) of the
Paperwork Reduction Act of 1995, the National Heart, Lung, and Blood
Institute (NHLBI), the National Institutes of Health (NIH) has
submitted to the Office of Management and Budget (OMB) a request for
review and approval the information collection listed below. This
proposed information collection was previously published in the Federal
Register on January 13, 2010, page 1789, and allowed 60 days for public
comment. No comments were received. The purpose of this notice is to
allow an additional 30 days for public comment. The National Institutes
of Health may not conduct or sponsor, and the respondent is not
required to respond to, an information collection that has been
extended, revised, or implemented
[[Page 17745]]
on or after October 1, 1995, unless it displays a currently valid OMB
control number.
Proposed Collection: Title: The Jackson Heart Study: Annual Follow-
up with Third Party Respondents. Type of Information Collection
Request: Revision of a currently approved collection (OMB No. 0925-
0491). Need and Use of Information Collection: This project involves
contacting next-of-kin and family physicians of deceased participants
who were part of the Jackson Heart Study exam. Interviewers will
contact doctors and hospitals to ascertain participants' cardiovascular
events. Information gathered will be used to further describe the risk
factors, occurrence rates, and consequences of cardiovascular disease
in African American men and women. Recruitment of 5,500 JHS
participants began in September 2000 and was completed in March 2004.
5,302 participants completed a baseline Exam 1 that included
demographics, psychosocial inventories, medical history, anthropometry,
resting and ambulatory blood pressure, phlebotomy and 24-hour urine
collection, ECG, echocardiography, and pulmonary function. JHS Exam 2
began September 26, 2005, followed by a more comprehensive Exam 3 that
began in February 2009. The two new exams include some repeated
measures from Exam 1 and several new components, including distribution
of self-monitoring blood pressure devices. The continuation of the
study allows continued assessment of subclinical coronary disease, left
ventricular dysfunction, progression of carotid atherosclerosis and
left ventricular hypertrophy, and responses to stress, racism, and
discrimination as well as new components such as renal disease, body
fat distribution and body composition, and metabolic consequences of
obesity.
Frequency of Response: One-time. Affected Public: Individuals or
households; businesses or other for profit; not-for-profit
institutions. Type of Respondents: Adults; doctors and staff of
hospitals and nursing homes. The annual reporting burden is as follows:
Estimated Number of Respondents: 400; Estimated Number of Responses per
Respondent: 1.0; Average Burden Hours per Response: (84 hours/400
respondents) 0.20; and Estimated Total Annual Burden Hours Requested:
84. The annualized cost to respondents is estimated at $3,760, assuming
$15 per burden hour for informants and $65 per burden hour for
physicians. There are no Capital Costs to report. There are no
Operating or Maintenance Costs to report.
Estimate of Annual Hour Burden
----------------------------------------------------------------------------------------------------------------
Number of Frequency of Average time Annual hour
Type of response respondents response per response burden
----------------------------------------------------------------------------------------------------------------
Morbidity & Mortality AFU 3rd Party/Next-of-kin 200 1 0.17 34
decedents......................................
Morbidity & Mortality AFU 3rd Party Physicians.. 200 1 0.25 50
---------------------------------------------------------------
Total....................................... 400 .............. .............. 84
----------------------------------------------------------------------------------------------------------------
Request for Comments: Written comments and/or suggestions from the
public and affected agencies should address one or more of the
following points: (1) Evaluate whether the proposed collection of
information is necessary for the proper performance of the function of
the agency, including whether the information will have practical
utility; (2) Evaluate the accuracy of the agency's estimate of the
burden of the proposed collection of information, including the
validity of the methodology and assumptions used; (3) Enhance the
quality, utility, and clarity of the information to be collected; and
(4) Minimize the burden of the collection of information on those who
are to respond, including the use of appropriate automated, electronic,
mechanical, or other technological collection techniques or other forms
of information technology.
Direct Comments to OMB: Written comments and/or suggestions
regarding the item(s) contained in this notice, especially regarding
the estimated public burden and associated response time, should be
directed to the: Office of Management and Budget, Office of Regulatory
Affairs, OIRA_submission@omb.eop.gov or by fax to 202-395-6974,
Attention: Desk Officer for NIH. To request more information on the
proposed project or to obtain a copy of the data collection plans and
instruments, contact: Ms. Cheryl Nelson, Project Officer, NIH, NHLBI,
6701 Rockledge Drive, MSC 7934, Bethesda, MD 20892-7934, or call non-
toll-free number 301-435-0451 or e-mail your request, including your
address to: NelsonC@nhlbi.nih.gov.
Comments Due Date: Comments regarding this information collection
are best assured of having their full effect if received within 30 days
of the date of this publication.
Suzanne Freeman,
NHLBI Project Clearance Liaison, National Institutes of Health.
Michael Lauer,
Director, DCVS, National Institutes of Health.
[FR Doc. 2010-7895 Filed 4-6-10; 8:45 am]
BILLING CODE 4140-01-P