Proposed Data Collections Submitted for Public Comment and Recommendations, 5596-5598 [2010-2275]
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5596
jlentini on DSKJ8SOYB1PROD with NOTICES
ACTION:
Federal Register / Vol. 75, No. 22 / Wednesday, February 3, 2010 / Notices
Notice of meeting.
This notice announces a forthcoming
meeting of a public advisory committee
of the Office of the National Coordinator
for Health Information Technology
(ONC). The meeting will be open to the
public.
Name of Committee: HIT Standards
Committee.
General Function of the Committee:
To provide recommendations to the
National Coordinator on standards,
implementation specifications, and
certification criteria for the electronic
exchange and use of health information
for purposes of adoption, consistent
with the implementation of the Federal
Health IT Strategic Plan, and in
accordance with policies developed by
the HIT Policy Committee.
Date and Time: The meeting will be
held on February 24, 2010, from 9 a.m.
to 4 p.m./Eastern Time.
Location: The Omni Shoreham Hotel,
2500 Calvert Street, NW., Washington,
DC. The hotel telephone number is 202–
234–0700.
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 this meeting. 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 committee will hear
comments from its workgroups,
including the Clinical Operations,
Clinical Quality, Privacy & Security, and
Implementation Workgroups, on the
Interim Final Rule (IFR) on Standards,
Implementation Specifications, and
Certification Criteria for EHRs, and on
the Notice of Proposed Rulemaking
(NPRM) on EHR Incentive Program for
Medicare and Medicaid. 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 February 16, 2010.
Oral comments from the public will be
scheduled between approximately 3
VerDate Nov<24>2008
16:34 Feb 02, 2010
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p.m. and 3:30 p.m./Eastern Time. Time
allotted for each presentation will be
limited to three minutes each. 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. No. 92–463, 5 U.S.C., App. 2).
Dated: January 27, 2010.
Judith Sparrow,
Office of Programs and Coordination, Office
of the National Coordinator for Health
Information Technology.
[FR Doc. 2010–2214 Filed 2–2–10; 8:45 am]
BILLING CODE 4150–45–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day-10–09AL]
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 Maryam I. Daneshvar,
CDC Acting Reports Clearance Officer,
1600 Clifton Road, MS–D74, Atlanta,
GA 30333 or send an e-mail to
omb@cdc.gov.
PO 00000
Frm 00036
Fmt 4703
Sfmt 4703
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
Environmental Health Impacts on
Women and Children in Low-income
Multifamily Housing—NEW—National
Center for Environmental Health
(NCEH) and Agency for Toxic
Substances and Disease Registry
(ATSDR), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
Green building principles and
practices have been shown to reduce
energy consumption, but their efficacy
in reducing environmental agents such
as pesticides, volatile organic
compounds (VOCs), fungi, and indoor
allergens is not clear. Furthermore, little
research has been conducted on health
impacts that might be related to green
buildings, especially on a nationwide
scale. Three main goals of this study are:
(1) To compare levels of certain
environmental chemical and biological
agents in green vs. traditional, multifamily, low-income housing; (2) to
ascertain differences in the health of the
residents in these homes; and (3) to
assess the economic impacts of the
‘‘greening’’ of housing—particularly
those related to health. These goals will
be accomplished in ongoing low-income
multi-family building renovation
programs sponsored by the Department
of Housing and Urban Development
(HUD). In partnership with HUD, the
CDC will leverage this opportunity to
collect survey and biomarker data from
residents and to collect environmental
measurements in their homes in order to
evaluate associations between green
housing and health (notably childhood
asthma morbidity and premature/low
birth weight outcomes).
This study directly supports the
Healthy Homes’ health protection goal
of the Centers for Disease Control and
Prevention (CDC). This investigation is
also consistent with CDC’s Health
Protection Research Agenda, which
E:\FR\FM\03FEN1.SGM
03FEN1
5597
Federal Register / Vol. 75, No. 22 / Wednesday, February 3, 2010 / Notices
calls for research to identify the major
environmental causes of disease and
disability and related risk factors.
Indoor allergens such as those from
cockroaches, dust mites, mice, and fungi
have been associated with childhood
asthma. Also, VOCs and pesticides have
been associated with adverse birth
outcomes (e.g., low birth weight and
prematurity). Given that green
principles such as improvement of
ventilation systems and elimination of
spray pesticides can directly affect the
concentrations of chemical and
biological agents in air, residents in
green housing should theoretically have
better health outcomes (e.g., asthma and
birth outcomes). Better health outcomes
characteristics and respiratory
symptoms will be administered at 3month intervals over a 1-year period.
Environmental sampling of the air and
dust in the participants’ homes will be
conducted over a 1-year period (once in
the home before rehabilitation (baseline
1), and then at three time points after
rehabilitation has been completed:
baseline 2, 6 months, and 12 months).
Environmental sampling includes
measurements of air exchange rate,
pesticides, VOCs, indoor allergens,
fungi, temperature, humidity, and
particulate matter.
There is no cost to respondents other
than their time.
will, in turn, lead to lower healthcare
utilization resulting in overall costs to
society.
Participants will include pregnant
women and children living in HUDsubsidized housing that has either been
rehabilitated in a green (e.g., case) or a
traditional manner (e.g., control) from
study sites across the United States.
Pregnant women and children with
asthma (ages 7–12 years) will donate
blood samples (for assessment of
allergy) and urine samples (for
assessment of pesticide and VOC
exposures). The children with asthma
(ages 7–12 years) will be also tested for
lung function and lung inflammatory
markers. Questionnaires regarding home
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
(in hours)
Respondents
Forms
Mothers of enrolled children.
Screening questionnaire ......................................
800
1
10/60
133
Baseline Questionnaire (Home Characteristics)
Baseline Questionnaire (for Mother) ...................
Baseline Questionnaire (for Children with asthma 7–12 years).
Baseline Questionnaire (for Children 0–6 years)
3- and 9-month Phone contact ............................
6- and 12-month Follow-up Questionnaire (for
environment).
6- and 12-month Follow-up Questionnaire (for
women).
6- and 12-month Follow-up Questionnaire (for
Children with asthma 7–12 years).
6- and 12-month Follow-up Questionnaire (for
children 0–6).
Time/Activity form (for Children with asthma 7–
12 years).
Time/Activity form (for Children 0–6 years) ........
Time/Activity form (for Pregnant women or
mothers).
Screening questionnaire ......................................
Baseline Questionnaire (Home Characteristics)
Baseline Questionnaire (for Pregnant woman) ...
3- and 9-month Phone contact ............................
6- and 12-month Follow-up Questionnaire (for
environment).
6- and 12-month Follow-up Questionnaire (for
women).
Post-delivery questionnaire .................................
Time/Activity form (for Pregnant women or
mothers).
688
688
688
1
1
1
15/60
15/60
15/60
172
172
172
688
688
688
1
2
2
15/60
5/60
10/60
172
115
229
688
2
10/60
229
688
2
10/60
229
688
2
10/60
229
688
4
5/60
229
688
688
4
4
5/60
5/60
229
229
800
688
688
688
688
1
1
1
2
2
10/60
15/60
15/60
5/60
10/60
133
172
172
115
229
688
2
10/60
229
688
688
1
4
5/60
5/60
57
229
........................
........................
........................
3,875
Pregnant women ...........
jlentini on DSKJ8SOYB1PROD with NOTICES
Total ........................
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Sfmt 9990
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03FEN1
5598
Federal Register / Vol. 75, No. 22 / Wednesday, February 3, 2010 / Notices
Dated: January 27, 2010.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. 2010–2275 Filed 2–2–10; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Substance Abuse and Mental Health
Services Administration
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Periodically, the Substance Abuse and
Mental Health Services Administration
(SAMHSA) will publish a summary of
information collection requests under
OMB review, in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
documents, call the SAMHSA Reports
Clearance Officer on (240) 276–1243.
Project: Protection and Advocacy for
Individuals With Mental Illness
(PAIMI) Final Rule, 42 CFR Part 51
(OMB No. 0930–0172)—Extension
These regulations meet the directive
under 42 U.S.C. 10826(b) requiring the
Secretary to promulgate final
regulations to carry out the PAIMI Act.
The regulations contain information
collection requirements. The Act
authorizes funds to support activities on
behalf of individuals with significant
(severe) mental illness (adults) or
emotional impairment (children/youth)
[42 U.S.C. 10802(4)]. Only entities that
are designated by the governors of each
State, the District of Columbia (Mayor),
five (5) jurisdictions (American Samoa,
Guam, the Commonwealth of the
Northern Mariana Islands, The
Commonwealth of Puerto Rico, and the
U.S. Virgin Islands), and the American
Indian Consortium (the Tribal Councils
of the Hopi and Navajo Nations in the
Southwest) to protect and advocate the
rights of persons with developmental
disabilities under Title I, Subtitle C—
Protection and Advocacy of Individual
Rights of the Developmental Disabilities
Assistance and Bill of Rights Act of
2000 [42 U.S.C. 150041 et seq.], are
eligible to receive PAIMI Program grants
[42 U.S.C. 10802 (2)]. These grants are
based on a formula prescribed by the
Secretary [42 U.S.C. at 10822(a)(1)(A)].
On January 1, each eligible State
protection and advocacy (P&A) system
is required to prepare a report that
describes its activities,
accomplishments, and expenditures to
protect the rights of individuals with
mental illness supported with payments
from PAIMI Program allotments during
the most recently completed fiscal year.
The PAIMI Act at 42 U.S.C. 10824(a)
requires that each P&A system transmit
a copy of its annual report to the
Secretary (via SAMHSA/CMHS) and to
the State Mental Health Agency where
the system is located. These annual
PAIMI Program Performance Reports
(PPR) to the Secretary must include the
following information:
• The number of (PAIMI-eligible)
individuals with mental illness served;
• A description of the types of
activities undertaken;
• A description of the types of
facilities providing care or treatment to
which such activities are undertaken;
• A description of the manner in
which the activities are initiated;
• A description of the
accomplishments resulting from such
activities;
Number of
respondents
42 CFR citation
• A description of systems to protect
and advocate the rights of individuals
with mental illness supported with
payments from PAIMI Program
allotments;
• A description of activities
conducted by States to protect and
advocate such rights;
• A description of mechanisms
established by residential facilities for
individuals with mental illness to
protect such rights;
• A description of the coordination
among such systems, activities and
mechanisms;
• Specification of the number systems
that are public and nonprofit systems
established with PAIMI Program
allotments;
• Recommendations for activities and
services to improve the protection and
advocacy of the rights of individuals
with mental illness and a description of
the need for such activities and services
that were not met by the State P&A
systems established under the PAIMI
Act due to resource or annual program
priority limitations.
** [The PAIMI Rules [42 CFR
51.32(b)] state that P&A systems may
place restrictions on case or client
acceptance criteria developed as part of
its annual PAIMI priorities. Each P&A
system is required to inform prospective
clients of any such restrictions when he/
she requests a service].
This PAIMI PPR summary must
include a separate section, prepared by
the PAIMI Advisory Council (PAC) that
describes the council’s activities and its
assessment of the operations of the State
P&A system [42 U.S.C. 10805(7)].
The estimated annual burden under
the PAIMI Final Rule is summarized
below:
Responses
per
respondent
Burden/
response
(hrs.)
Total hour
burden
* 51.8(a)(2) Program Performance Report .......................................................
* 51.8(8)(a)(8) Advisory Council Report ...........................................................
51.10 Remedial Actions:.
Corrective Action Plan ..............................................................................
Implementation Status Reports ................................................................
51.23(c) Reports, materials and fiscal data provided to the PAC ...................
51.25(b)(3) Grievance Procedure ....................................................................
† 51.43 Written denial of access by P&A system ............................................
57
57
1
1
26
10
(1482)
(570)
7
7
57
57
........................
1
3
1
1
........................
8
2
1
0.5
........................
56
42
57
29
........................
Total ..........................................................................................................
57
........................
........................
184
jlentini on DSKJ8SOYB1PROD with NOTICES
* Responses and burden hours associated with these reports were approved under OMB Control No. 0930–0169.
Written comments and
recommendations concerning the
proposed information collection should
be sent by March 5, 2010 to: SAMHSA
Desk Officer, Human Resources and
Housing Branch, Office of Management
VerDate Nov<24>2008
16:34 Feb 02, 2010
Jkt 220001
and Budget, New Executive Office
Building, Room 10235, Washington, DC
20503; due to potential delays in OMB’s
receipt and processing of mail sent
through the U.S. Postal Service,
PO 00000
Frm 00038
Fmt 4703
Sfmt 4703
respondents are encouraged to submit
comments by fax to: 202–395–5806.
E:\FR\FM\03FEN1.SGM
03FEN1
Agencies
[Federal Register Volume 75, Number 22 (Wednesday, February 3, 2010)]
[Notices]
[Pages 5596-5598]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-2275]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-10-09AL]
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 Maryam I. Daneshvar, CDC Acting 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
Environmental Health Impacts on Women and Children in Low-income
Multifamily Housing--NEW--National Center for Environmental Health
(NCEH) and Agency for Toxic Substances and Disease Registry (ATSDR),
Centers for Disease Control and Prevention (CDC).
Background and Brief Description
Green building principles and practices have been shown to reduce
energy consumption, but their efficacy in reducing environmental agents
such as pesticides, volatile organic compounds (VOCs), fungi, and
indoor allergens is not clear. Furthermore, little research has been
conducted on health impacts that might be related to green buildings,
especially on a nationwide scale. Three main goals of this study are:
(1) To compare levels of certain environmental chemical and biological
agents in green vs. traditional, multi-family, low-income housing; (2)
to ascertain differences in the health of the residents in these homes;
and (3) to assess the economic impacts of the ``greening'' of housing--
particularly those related to health. These goals will be accomplished
in ongoing low-income multi-family building renovation programs
sponsored by the Department of Housing and Urban Development (HUD). In
partnership with HUD, the CDC will leverage this opportunity to collect
survey and biomarker data from residents and to collect environmental
measurements in their homes in order to evaluate associations between
green housing and health (notably childhood asthma morbidity and
premature/low birth weight outcomes).
This study directly supports the Healthy Homes' health protection
goal of the Centers for Disease Control and Prevention (CDC). This
investigation is also consistent with CDC's Health Protection Research
Agenda, which
[[Page 5597]]
calls for research to identify the major environmental causes of
disease and disability and related risk factors.
Indoor allergens such as those from cockroaches, dust mites, mice,
and fungi have been associated with childhood asthma. Also, VOCs and
pesticides have been associated with adverse birth outcomes (e.g., low
birth weight and prematurity). Given that green principles such as
improvement of ventilation systems and elimination of spray pesticides
can directly affect the concentrations of chemical and biological
agents in air, residents in green housing should theoretically have
better health outcomes (e.g., asthma and birth outcomes). Better health
outcomes will, in turn, lead to lower healthcare utilization resulting
in overall costs to society.
Participants will include pregnant women and children living in
HUD-subsidized housing that has either been rehabilitated in a green
(e.g., case) or a traditional manner (e.g., control) from study sites
across the United States. Pregnant women and children with asthma (ages
7-12 years) will donate blood samples (for assessment of allergy) and
urine samples (for assessment of pesticide and VOC exposures). The
children with asthma (ages 7-12 years) will be also tested for lung
function and lung inflammatory markers. Questionnaires regarding home
characteristics and respiratory symptoms will be administered at 3-
month intervals over a 1-year period. Environmental sampling of the air
and dust in the participants' homes will be conducted over a 1-year
period (once in the home before rehabilitation (baseline 1), and then
at three time points after rehabilitation has been completed: baseline
2, 6 months, and 12 months). Environmental sampling includes
measurements of air exchange rate, pesticides, VOCs, indoor allergens,
fungi, temperature, humidity, and particulate matter.
There is no cost to respondents other than their time.
Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of Average burden
Respondents Forms Number of responses per per response Total burden
respondents respondent (in hours) (in hours)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Mothers of enrolled children................... Screening questionnaire................ 800 1 10/60 133
Baseline Questionnaire (Home 688 1 15/60 172
Characteristics).
Baseline Questionnaire (for Mother).... 688 1 15/60 172
Baseline Questionnaire (for Children 688 1 15/60 172
with asthma 7-12 years).
Baseline Questionnaire (for Children 0- 688 1 15/60 172
6 years).
3- and 9-month Phone contact........... 688 2 5/60 115
6- and 12-month Follow-up Questionnaire 688 2 10/60 229
(for environment).
6- and 12-month Follow-up Questionnaire 688 2 10/60 229
(for women).
6- and 12-month Follow-up Questionnaire 688 2 10/60 229
(for Children with asthma 7-12 years).
6- and 12-month Follow-up Questionnaire 688 2 10/60 229
(for children 0-6).
Time/Activity form (for Children with 688 4 5/60 229
asthma 7-12 years).
Time/Activity form (for Children 0-6 688 4 5/60 229
years).
Time/Activity form (for Pregnant women 688 4 5/60 229
or mothers).
Pregnant women................................. Screening questionnaire................ 800 1 10/60 133
Baseline Questionnaire (Home 688 1 15/60 172
Characteristics).
Baseline Questionnaire (for Pregnant 688 1 15/60 172
woman).
3- and 9-month Phone contact........... 688 2 5/60 115
6- and 12-month Follow-up Questionnaire 688 2 10/60 229
(for environment).
6- and 12-month Follow-up Questionnaire 688 2 10/60 229
(for women).
Post-delivery questionnaire............ 688 1 5/60 57
Time/Activity form (for Pregnant women 688 4 5/60 229
or mothers).
--------------------------------------------------------------------------------------------------------
Total...................................... ....................................... .............. .............. .............. 3,875
--------------------------------------------------------------------------------------------------------------------------------------------------------
[[Page 5598]]
Dated: January 27, 2010.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. 2010-2275 Filed 2-2-10; 8:45 am]
BILLING CODE 4163-18-P