Agency Information Collection Request; 60-Day Public Comment Request, 14400 [2011-6086]
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14400
Federal Register / Vol. 76, No. 51 / Wednesday, March 16, 2011 / Notices
Seleda Perryman,
Office of the Secretary, Paperwork Reduction
Act Reports Clearance Officer.
[FR Doc. 2011–6078 Filed 3–15–11; 8:45 am]
BILLING CODE 4150–30–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Document Identifier: OS–0990–New]
Agency Information Collection
Request; 60-Day Public Comment
Request
Office on Women’s Health,
Office of the Secretary, HHS.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Office of the Secretary (OS), Department
of Health and Human Services, is
publishing the following summary of a
proposed information collection request
for public comment. Interested persons
are invited to send comments regarding
this burden estimate or any other aspect
AGENCY:
of this collection of information,
including any of the following subjects:
(1) The necessity and utility of the
proposed information collection for the
proper performance of the agency’s
functions; (2) the accuracy of the
estimated burden; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4) the
use of automated collection techniques
or other forms of information
technology to minimize the information
collection burden.
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, e-mail your request,
including your address, phone number,
OMB number, and OS document
identifier, to
Sherette.funncoleman@hhs.gov, or call
the Reports Clearance Office on (202)
690–6162. Written comments and
recommendations for the proposed
information collections must be directed
to the OS Paperwork Clearance Officer
Type of
respondent
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
Single Parent Caregivers .....
1,000
1
18/60
300
Forms
Single Parent Caregiver Survey Instrument
Seleda Perryman,
Office of the Secretary, Paperwork Reduction
Act Reports Clearance Officer.
[FR Doc. 2011–6086 Filed 3–15–11; 8:45 am]
BILLING CODE 4150–33–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60-Day–11–11DD]
jlentini on DSKJ8SOYB1PROD 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 Carol E. Walker, CDC
Acting Reports Clearance Officer, 1600
Clifton Road, MS–D74, Atlanta, GA
VerDate Mar<15>2010
16:56 Mar 15, 2011
at the above e-mail address within 60days.
Proposed Project: National Survey of
Single Parent Caregivers—OMB No.
0990-NEW-OWH; HHS, Office on
Women’s Health.
Abstract: The National Survey of
Single Parent Caregivers will measure
the size, characteristics, and unmet
needs of single parents providing care
for an adult family member or friend.
Single parent caregivers provide support
services and financial assistance for two
generations without the aid of a married
partner. Survey results will be used to
develop national estimates of the costs
borne by single parent caregivers, their
psychosocial burden, stress, and
diminished social and leisure
opportunities, and suggest policy
options that mitigate the burden on
single parent caregivers. The survey will
be administered once under a one-year
request, and will contact individuals
using computer-assisted telephone
interviewing (CATI) methods.
Jkt 223001
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: Raising Public
Awareness for Deep Vein Thrombosis/
Pulmonary Embolism—NEW—National
Center on Birth Defects and
Developmental Disabilities (NCBDDD),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The Division of Blood Disorders,
located within the National Center on
Birth Defects and Developmental
Disabilities, implements health
promotion and wellness programs
PO 00000
Frm 00032
Fmt 4703
Sfmt 4703
designed to prevent secondary
conditions in people with bleeding and
clotting disorders.
There are few public health problems
as serious as deep vein thrombosis
(DVT) and pulmonary embolism (PE),
yet these conditions receive little
attention. DVT/PE is an under
diagnosed, serious, preventable medical
condition that occurs when a blood clot
forms in a deep vein. These clots
usually develop in the lower leg, thigh,
or pelvis, but they can also occur in the
arm. In more than one third of people
affected by DVT, clots can travel to the
lungs and cause PE, a potentially fatal
condition.
The precise number of people affected
by DVT/PE is unknown, but estimates
range from 300,000 to 600,000 annually
in the United States. DVT/PE is
associated with substantial morbidity
and mortality: One third of people with
DVT/PE will have a recurrence within
10 years and one third of people die
within 1 month of diagnosis. Among
people who have had a DVT, one third
will have long-term complications (postthrombotic syndrome), such as swelling,
pain, discoloration, and scaling in the
affected limb. In some cases, the
symptoms can be so severe that a person
can become disabled. More troubling,
sudden death is the first symptom in
E:\FR\FM\16MRN1.SGM
16MRN1
]]>Agencies
[Federal Register Volume 76, Number 51 (Wednesday, March 16, 2011)]
[Notices]
[Page 14400]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-6086]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Document Identifier: OS-0990-New]
Agency Information Collection Request; 60-Day Public Comment
Request
AGENCY: Office on Women's Health, Office of the Secretary, HHS.
In compliance with the requirement of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Office of the Secretary (OS),
Department of Health and Human Services, is publishing the following
summary of a proposed information collection request for public
comment. Interested persons are invited to send comments regarding this
burden estimate or any other aspect of this collection of information,
including any of the following subjects: (1) The necessity and utility
of the proposed information collection for the proper performance of
the agency's functions; (2) the accuracy of the estimated burden; (3)
ways to enhance the quality, utility, and clarity of the information to
be collected; and (4) the use of automated collection techniques or
other forms of information technology to minimize the information
collection burden.
To obtain copies of the supporting statement and any related forms
for the proposed paperwork collections referenced above, e-mail your
request, including your address, phone number, OMB number, and OS
document identifier, to Sherette.funncoleman@hhs.gov, or call the
Reports Clearance Office on (202) 690-6162. Written comments and
recommendations for the proposed information collections must be
directed to the OS Paperwork Clearance Officer at the above e-mail
address within 60-days.
Proposed Project: National Survey of Single Parent Caregivers--OMB
No. 0990-NEW-OWH; HHS, Office on Women's Health.
Abstract: The National Survey of Single Parent Caregivers will
measure the size, characteristics, and unmet needs of single parents
providing care for an adult family member or friend. Single parent
caregivers provide support services and financial assistance for two
generations without the aid of a married partner. Survey results will
be used to develop national estimates of the costs borne by single
parent caregivers, their psychosocial burden, stress, and diminished
social and leisure opportunities, and suggest policy options that
mitigate the burden on single parent caregivers. The survey will be
administered once under a one-year request, and will contact
individuals using computer-assisted telephone interviewing (CATI)
methods.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of Average burden
Forms Type of respondent Number of responses per hours per Total burden
respondents respondent response hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Single Parent Caregiver Survey Instrument..... Single Parent Caregivers............ 1,000 1 18/60 300
--------------------------------------------------------------------------------------------------------------------------------------------------------
Seleda Perryman,
Office of the Secretary, Paperwork Reduction Act Reports Clearance
Officer.
[FR Doc. 2011-6086 Filed 3-15-11; 8:45 am]
BILLING CODE 4150-33-P
