Agency Forms Undergoing Paperwork Reduction Act Review, 45257-45258 [2011-19107]
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45257
Federal Register / Vol. 76, No. 145 / Thursday, July 28, 2011 / Notices
Background and Brief Description
Cardiovascular disease is a leading
cause of death and disability for men
and women in the United States, among
the most costly health problems facing
our nation today, and among the most
preventable. Risk factors for
cardiovascular disease include high
blood pressure and high cholesterol.
Because over 50% of diabetics have
high blood pressure, high cholesterol, or
both conditions, the optimal systems to
treat people with hypertension, high
cholesterol, or diabetes are interrelated.
In 2005, CDC’s Division for Heart
Disease and Stroke Prevention (DHDSP)
began developing evaluation indicators
that reflect evidence-based outcomes
from policy, systems, and
environmental changes related to heart
disease and stroke prevention. However,
many of the indicators for short-term
policy and systems changes do not have
readily available data sources. This is
particularly true for outcomes related to
health care systems changes.
conducted two years after completion of
the baseline NSPCP. Approximately 900
physicians will participate in each cycle
of data collection (baseline and followup). On an annualized basis,
approximately 600 physicians will
participate in the NSPCP per year, and
1,333 practices will be screened for
participation.
Information from both cycles of data
collection will be compared to monitor
changes in health systems and
dissemination of health systems
technology. Results will be used by
primary care practices to inform their
systems for managing patients with
chronic conditions and to improve the
quality of care delivered. Results will be
used by CDC to improve technical
assistance to public health partners.
OMB approval is requested for three
years. Participation in the NSPCP is
voluntary, and all responses will be deidentified. There are no costs to
respondents other than their time. The
total estimated annualized burden hours
are 317.
In 2011, CDC proposes to conduct a
new information collection, the
National Survey of Primary Care
Policies for Managing Patients with
High Blood Pressure, High Cholesterol,
or Diabetes (NSPCP). The survey will be
targeted to practice managers of nonfederally run primary care physician
practices that include at least one family
practitioner or at least one physician
specializing in internal medicine.
Respondents will be drawn from a
nationally representative sample of
physician practices. The NSPCP survey
instrument will undergo cognitive
testing before dissemination.
The Web-based NSPCP will collect
information about physician practices’
use of evidence-based systems,
including multidisciplinary team
approaches for chronic disease
treatment, electronic health records
(EHR) with features appropriate for
treating patients with chronic disease
(e.g., clinical decision supports, patient
registries), and patient follow-up
mechanisms. A follow-up survey will be
ESTIMATED ANNUALIZED BURDEN HOURS
Number of respondents
Type of respondents
Form name
Physician .........................................................
Medical Secretary ...........................................
Physician .........................................................
DC 20503 or by fax to (202) 395–5806.
Written comments should be received
within 30 days of this notice.
[FR Doc. 2011–19109 Filed 7–27–11; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Background and Brief Description
[30Day–11–11CD]
Agency Forms Undergoing Paperwork
Reduction Act Review
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) 639–5960 or send an email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
VerDate Mar<15>2010
15:51 Jul 27, 2011
Jkt 223001
Proposed Project
Tourette Syndrome National
Education and Outreach Program—
New—National Center on Birth Defects
and Developmental Disabilities
(NCBDDD), Centers for Disease Control
and Prevention (CDC).
BILLING CODE 4163–18–P
rmajette on DSK89S0YB1PROD with NOTICES
5
1,333
600
1
1
1
Cognitive Testing Interview Guide .................
NSPCP Screener ...........................................
NSPCP ...........................................................
Dated: July 22, 2011.
Daniel Holcomb,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
Number of responses per
respondent
This program will collect program
evaluation data from participants of
educational workshops and recipients of
educational resources on Tourette
Syndrome (TS) conducted by the
Tourette Syndrome Association in a
cooperative agreement with the CDC.
TS is an inherited, neurobiological
movement disorder characterized by
involuntary motor and vocal tics that
typically manifest during childhood.
The exact number of people with TS is
unknown. Data from the National
Survey of Children’s Health 2007
resulted in an estimate that 3 out of
every 1,000 U.S. children (about
148,000) 6 through 17 years of age had
PO 00000
Frm 00037
Fmt 4703
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Avg. burden
per response
(in hr)
75/60
5/60
20/60
been diagnosed with TS. Higher
prevalence estimates obtained from
community studies likely mean that
there are a significant number of
individuals who have TS, but who have
not been diagnosed. TS is three to four
times more common among males than
females.
It is estimated that tens of thousands
or Americans with TS either go
undiagnosed or the clinical care they do
receive is inadequate. There is no
known cure. The disorder may express
itself with mild symptoms for some, and
severe symptoms for others. Depending
on the severity and duration, tic
symptoms may also be diagnosed as
chronic motor or vocal tic disorder,
transient tic disorder, and tic disorder
not otherwise specified. TS is associated
with a high rate of co-morbid
conditions.
There is a lack of accurate treatment
information among the medical
community as well as the general
public, and a limited number of expert
physicians—all resulting in significant
under-diagnosis, misdiagnosis, and
inadequate treatment with scant followup care. Children also meet with stigma
E:\FR\FM\28JYN1.SGM
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45258
Federal Register / Vol. 76, No. 145 / Thursday, July 28, 2011 / Notices
and inadequate responses in
educational settings, limiting their
educational and social success.
To address these issues, the Tourette
Syndrome Association has developed
educational workshops and materials to
improve the recognition and awareness
of TS diagnosis, treatment, co-occurring
conditions, and quality of life for those
impacted by TS. Health education
programs have been developed for 3
groups of audiences: Health
professionals, education professionals,
and people with TS and their families.
The format includes general education
programs for the 3 groups, as well as
two more in-depth medical training
programs for physicians on TS and on
the Comprehensive Behavioral
Intervention for Tics (CBIT) treatment.
In addition, a range of professional
health education materials in various
formats have been developed as
educational resources and will be
disseminated.
CDC requests OMB approval to collect
program evaluation information from
workshop participants and recipients of
educational materials over a three-year
period. Participants of the workshops
and recipients of educational resources
will be completing program evaluation
forms to provide information on
whether the workshop or resource met
the educational goals. The information
will be used to improve future
workshops.
There are no costs to respondents
other than their time. The total
estimated annual burden hours are 277.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondent
Form name
Health professionals ..........................
Health professionals ..........................
Medical Program Evaluation ............
Physician Training Retreat Pre-test
Physician Training Retreat Post-test
Physician Training Retreat 3-Month
Follow-up.
CBIT Program Evaluation ................
CBIT Pre-test ...................................
CBIT Post-test .................................
CBIT Online Program Evaluation ....
CBIT Program 3-Month Follow-up ...
Medical Resource Dissemination ....
Education Program Evaluation ........
Education Program Pre-test ............
Education Program Post-test ...........
Education Resource Dissemination
Family/Public Education Program
Evaluation.
Family/Public
Medical
Program
Evaluation.
Family Resource Dissemination ......
Health professionals ..........................
Health professionals ..........................
Teachers/Educators ..........................
Public .................................................
Dated: July 22, 2011.
Daniel L. Holcomb,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2011–19107 Filed 7–27–11; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: ACF–535 LIHEAP Quarterly
Allocation Estimates.
Number of
responses/
respondent
Average burden/response
(in hours)
Response
burden
(in hours)
1,200
50
50
30
1
1
1
1
2/60
3/60
3/60
2/60
40
3
3
1
500
500
500
50
300
210
1,200
800
800
210
250
1
1
1
1
1
1
1
1
1
1
1
2/60
3/60
3/60
1/60
1/60
2/60
2/60
3/60
3/60
2/60
2/60
17
25
25
1
5
7
40
40
40
7
8
250
1
2/60
8
200
1
2/60
7
OMB No.: 0970–0037.
Description: The LIHEAP Quarterly
Allocation Estimates, ACF Form-535 is
a one-page form that is sent to 50 State
grantees and to the District of Columbia.
It is also sent to Tribal Government
grantees that receive over $1 million
annually for the Low Income Home
Energy Assistance Program (LIHEAP).
Grantees are asked to complete and
submit the form in the 4th quarter of
each year. The data collected on the
form are grantees estimates of
obligations they expect to make each
quarter for the upcoming fiscal year for
the LIHEAP program. This is the only
method used to request anticipated
distributions of the grantees LIHEAP
funds. The information is used to
develop apportionment requests to OMB
and to make grant awards based on
grantees anticipated needs. Information
collected on this form is not available
through any other Federal source.
Submission of the form is voluntary.
Respondents: State Governments.
rmajette on DSK89S0YB1PROD with NOTICES
ANNUAL BURDEN ESTIMATES
Instrument
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
LIHEAP Quarterly Allocation Estimate, ACF–535 ...........................................
55
1
0.25
13.75
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17:52 Jul 27, 2011
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]]>Agencies
[Federal Register Volume 76, Number 145 (Thursday, July 28, 2011)]
[Notices]
[Pages 45257-45258]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-19107]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-11-11CD]
Agency Forms Undergoing Paperwork Reduction Act Review
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) 639-5960 or send an e-mail
to omb@cdc.gov. Send written comments to CDC Desk Officer, Office of
Management and Budget, Washington, DC 20503 or by fax to (202) 395-
5806. Written comments should be received within 30 days of this
notice.
Proposed Project
Tourette Syndrome National Education and Outreach Program--New--
National Center on Birth Defects and Developmental Disabilities
(NCBDDD), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
This program will collect program evaluation data from participants
of educational workshops and recipients of educational resources on
Tourette Syndrome (TS) conducted by the Tourette Syndrome Association
in a cooperative agreement with the CDC.
TS is an inherited, neurobiological movement disorder characterized
by involuntary motor and vocal tics that typically manifest during
childhood. The exact number of people with TS is unknown. Data from the
National Survey of Children's Health 2007 resulted in an estimate that
3 out of every 1,000 U.S. children (about 148,000) 6 through 17 years
of age had been diagnosed with TS. Higher prevalence estimates obtained
from community studies likely mean that there are a significant number
of individuals who have TS, but who have not been diagnosed. TS is
three to four times more common among males than females.
It is estimated that tens of thousands or Americans with TS either
go undiagnosed or the clinical care they do receive is inadequate.
There is no known cure. The disorder may express itself with mild
symptoms for some, and severe symptoms for others. Depending on the
severity and duration, tic symptoms may also be diagnosed as chronic
motor or vocal tic disorder, transient tic disorder, and tic disorder
not otherwise specified. TS is associated with a high rate of co-morbid
conditions.
There is a lack of accurate treatment information among the medical
community as well as the general public, and a limited number of expert
physicians--all resulting in significant under-diagnosis, misdiagnosis,
and inadequate treatment with scant follow-up care. Children also meet
with stigma
[[Page 45258]]
and inadequate responses in educational settings, limiting their
educational and social success.
To address these issues, the Tourette Syndrome Association has
developed educational workshops and materials to improve the
recognition and awareness of TS diagnosis, treatment, co-occurring
conditions, and quality of life for those impacted by TS. Health
education programs have been developed for 3 groups of audiences:
Health professionals, education professionals, and people with TS and
their families. The format includes general education programs for the
3 groups, as well as two more in-depth medical training programs for
physicians on TS and on the Comprehensive Behavioral Intervention for
Tics (CBIT) treatment. In addition, a range of professional health
education materials in various formats have been developed as
educational resources and will be disseminated.
CDC requests OMB approval to collect program evaluation information
from workshop participants and recipients of educational materials over
a three-year period. Participants of the workshops and recipients of
educational resources will be completing program evaluation forms to
provide information on whether the workshop or resource met the
educational goals. The information will be used to improve future
workshops.
There are no costs to respondents other than their time. The total
estimated annual burden hours are 277.
Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of Average burden/ Response
Type of respondent Form name Number of responses/ response (in burden (in
respondents respondent hours) hours)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Health professionals........................... Medical Program Evaluation............. 1,200 1 2/60 40
Health professionals........................... Physician Training Retreat Pre-test.... 50 1 3/60 3
Physician Training Retreat Post-test... 50 1 3/60 3
Physician Training Retreat 3-Month 30 1 2/60 1
Follow-up.
Health professionals........................... CBIT Program Evaluation................ 500 1 2/60 17
CBIT Pre-test.......................... 500 1 3/60 25
CBIT Post-test......................... 500 1 3/60 25
CBIT Online Program Evaluation......... 50 1 1/60 1
CBIT Program 3-Month Follow-up......... 300 1 1/60 5
Health professionals........................... Medical Resource Dissemination......... 210 1 2/60 7
Teachers/Educators............................. Education Program Evaluation........... 1,200 1 2/60 40
Education Program Pre-test............. 800 1 3/60 40
Education Program Post-test............ 800 1 3/60 40
Education Resource Dissemination....... 210 1 2/60 7
Public......................................... Family/Public Education Program 250 1 2/60 8
Evaluation.
Family/Public Medical Program 250 1 2/60 8
Evaluation.
Family Resource Dissemination.......... 200 1 2/60 7
--------------------------------------------------------------------------------------------------------------------------------------------------------
Dated: July 22, 2011.
Daniel L. Holcomb,
Reports Clearance Officer, Centers for Disease Control and Prevention.
[FR Doc. 2011-19107 Filed 7-27-11; 8:45 am]
BILLING CODE 4163-18-P
