Proposed Data Collections Submitted for Public Comment and Recommendations, 24029-24030 [2011-10384]
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24029
Federal Register / Vol. 76, No. 83 / Friday, April 29, 2011 / Notices
National Center for Chronic Disease
Prevention and Health Promotion
(NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
CDC has previously examined the role
that schools play in addressing the
health risk behaviors through the School
Health Policies and Programs Study
(SHPPS, OMB No. 0920–0445), a series
of data collections conducted at the
state, district, school, and classroom
levels in 1994 (OMB. No. 0920–0340,
exp. 1/31/1995), in 2000 (OMB No.
0920–0445, exp. 10/31/2002), and in
2006 (OMB No. 0920–0445, exp. 11/30/
2008).
Clearance is being requested for one
year for CDC to conduct SHPPS 2012.
The purpose of the study is to collect
updated information to assess the
characteristics of eight components of
school health programs at the
elementary, middle, and high school
levels. The components are: Health
education, physical education, health
services, mental health and social
services, nutrition services, healthy and
safe school environment, faculty and
staff health promotion, and family and
community involvement. Twenty-two
questionnaires will be used: Six at the
state level, seven at the district level,
seven at the school level, and two at the
classroom level. Data collection at the
state and district levels will be selfadministered via the Internet. Data
collection at the school and classroom
levels will be conducted via computerassisted personal interviews. SHPPS
2012 also will include vending machine
observations in the schools.
SHPPS 2012 data will have significant
implications for policy and program
development for school health programs
nationwide. The data will also be used
to provide the only national source of
data to measure 14 Healthy People 2020
national health objectives, and will
provide the only nationally
representative dataset of snack and
beverage offerings available to students
through school vending machines.
There are no costs to respondents
other than their time. The total
estimated burden hours are 13,262.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondent
Form name
State Officials ..................................................
State Health Education ..................................
State Physical Education and Activity ...........
State Health Services ....................................
State Nutrition Services .................................
State Healthy and Safe School Environment
State Mental Health and Social Services ......
State Recruitment Script ................................
District Health Education ................................
District Physical Education and Activity .........
District Health Services ..................................
District Nutrition Services ...............................
District Healthy and Safe School Environment.
District Mental Health and Social Services ....
District Faculty and Staff Health Promotion ...
District Recruitment Script .............................
School Recruitment Script .............................
School Health Education ................................
School Physical Education and Activity .........
School Health Services ..................................
School Nutrition Services ...............................
Healthy and Safe School Environment ..........
School Mental Health and Social Services ....
School Faculty and Staff Health Promotion ...
Classroom Health Education .........................
Classroom Physical Education and Activity ...
District Officials ...............................................
School Officials ...............................................
Classroom Teachers .......................................
Dated: April 25, 2011.
Carol Walker,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
BILLING CODE 4163–18–P
srobinson on DSKHWCL6B1PROD with NOTICES
[FR Doc. 2011–10391 Filed 4–28–11; 8:45 am]
Centers for Disease Control and
Prevention
[60 Day–11–11EM]
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
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17:39 Apr 28, 2011
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Number
responses per
respondent
Average
burden per
response
(in hours)
51
51
51
51
51
51
51
685
685
685
685
685
1
1
1
1
1
1
1
1
1
1
1
1
30/60
30/60
30/60
30/60
30/60
30/60
1
30/60
40/60
40/60
30/60
1
685
685
1006
1409
1043
1043
1043
1043
1043
1043
1043
2002
2002
1
1
1
1
1
1
1
1
1
1
1
1
1
30/60
20/60
1
1
20/60
40/60
50/60
40/60
75/60
30/60
20/60
50/60
40/60
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 or send
comments to Carol Walker, CDC Acting
Reports Clearance Officer, 1600 Clifton
Road, MS D–74, 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
E:\FR\FM\29APN1.SGM
29APN1
24030
Federal Register / Vol. 76, No. 83 / Friday, April 29, 2011 / Notices
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
National Survey of Primary Care
Policies for Managing Patients with
High Blood Pressure, High Cholesterol,
or Diabetes—New—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Cardiovascular disease is a leading
cause of death for men and women in
the United States, among the most
costly health problems facing our nation
today, and among the most preventable.
Heart disease and stroke also contribute
significantly to disability, with nearly
three million American people reporting
disability from these causes.
Additionally, over 50% of diabetics
have high blood pressure, high
cholesterol, or both conditions. To
reduce the burden of cardiovascular
disease, the federal Centers for Disease
Control and Prevention (CDC) works
with a broad array of public- and
private-sector stakeholders, including
years after completion of the baseline
survey. Information from both cycles of
data collection will be compared to
monitor changes in health systems
uptake and dissemination of health
systems technology. The survey will be
pretested with approximately 16
respondents before dissemination.
The target population for the NSPCP
is practice managers of non-federally
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. OMB approval is
requested for three years.
Approximately 900 physicians will
participate in the first cycle of webbased data collection, and 900
physicians will participate in the twoyear follow-up survey. An average of
600 respondents per year will
participate in the NSPCP.
Results will be used by CDC to
improve services to partners through
development of translation pieces or
technical assistance aids that address
gaps in the use of evidence-based
interventions. Most importantly, the
study will provide primary care
practices with information that can be
used to inform their systems for
managing patients with chronic
conditions and to improve the quality of
care delivered.
Participation is voluntary, and all
responses will be de-identified. There
are no costs to respondents other than
their time.
state and local health departments,
community-based organizations,
professional organizations, and health
care practitioners.
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 for heart disease
and stroke prevention. These indicators
are needed to provide common
measures that CDC, CDC-funded state
Heart Disease and Stroke Prevention
programs, and other partners can use to
show progress toward achieving
outcomes in heart disease and stroke
prevention and control efforts. Many of
the indicators that reflect outcomes of
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.
In 2011, CDC proposes to conduct the
first cycle of data collection for the
National Survey of Primary Care
Policies for Managing Patients with
High Blood Pressure, High Cholesterol,
or Diabetes (NSPCP). The web-based
survey will collect information on
physician practices’ use of evidencebased 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
questionnaire will be distributed two
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Number of
respondents
Avg. burden
per response
(in hr)
Total burden
(in hr)
Type of respondents
Form name
Physician .......................................................
Medical Secretary .........................................
Physician .......................................................
Cognitive Testing Protocol ...
NSPCP Screener ..................
NSPCP .................................
5
1,333
600
1
1
1
75/60
5/60
20/60
6
111
200
Total .......................................................
...............................................
........................
........................
........................
317
Dated: April 25, 2011.
Carol Walker,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention
[FR Doc. 2011–10384 Filed 4–28–11; 8:45 am]
srobinson on DSKHWCL6B1PROD with NOTICES
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel (SEP): Funding
Opportunity Announcement GH11–002,
Initial Review
Correction: This notice was published
in the Federal Register on April 12,
2011, Volume 76, Number 70, Page
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17:39 Apr 28, 2011
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20355. The contact person for the
aforementioned meeting has been
changed to the following:
Contact Person for More Information:
Diana Bartlett, M.P.H., Scientific Review
Officer, CDC, 1600 Clifton Road, NE.,
Mailstop D–72, Atlanta, Georgia 30333,
Telephone: (404) 639–4938.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities, for both the
E:\FR\FM\29APN1.SGM
29APN1
Agencies
[Federal Register Volume 76, Number 83 (Friday, April 29, 2011)]
[Notices]
[Pages 24029-24030]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-10384]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60 Day-11-11EM]
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 or
send comments to Carol Walker, CDC Acting Reports Clearance Officer,
1600 Clifton Road, MS D-74, 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
[[Page 24030]]
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
National Survey of Primary Care Policies for Managing Patients with
High Blood Pressure, High Cholesterol, or Diabetes--New--National
Center for Chronic Disease Prevention and Health Promotion (NCCDPHP),
Centers for Disease Control and Prevention (CDC).
Background and Brief Description
Cardiovascular disease is a leading cause of death for men and
women in the United States, among the most costly health problems
facing our nation today, and among the most preventable. Heart disease
and stroke also contribute significantly to disability, with nearly
three million American people reporting disability from these causes.
Additionally, over 50% of diabetics have high blood pressure, high
cholesterol, or both conditions. To reduce the burden of cardiovascular
disease, the federal Centers for Disease Control and Prevention (CDC)
works with a broad array of public- and private-sector stakeholders,
including state and local health departments, community-based
organizations, professional organizations, and health care
practitioners.
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 for
heart disease and stroke prevention. These indicators are needed to
provide common measures that CDC, CDC-funded state Heart Disease and
Stroke Prevention programs, and other partners can use to show progress
toward achieving outcomes in heart disease and stroke prevention and
control efforts. Many of the indicators that reflect outcomes of 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.
In 2011, CDC proposes to conduct the first cycle of data collection
for the National Survey of Primary Care Policies for Managing Patients
with High Blood Pressure, High Cholesterol, or Diabetes (NSPCP). The
web-based survey will collect information on 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 questionnaire will be distributed two years
after completion of the baseline survey. Information from both cycles
of data collection will be compared to monitor changes in health
systems uptake and dissemination of health systems technology. The
survey will be pretested with approximately 16 respondents before
dissemination.
The target population for the NSPCP is practice managers of non-
federally 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. OMB approval is requested
for three years. Approximately 900 physicians will participate in the
first cycle of web-based data collection, and 900 physicians will
participate in the two-year follow-up survey. An average of 600
respondents per year will participate in the NSPCP.
Results will be used by CDC to improve services to partners through
development of translation pieces or technical assistance aids that
address gaps in the use of evidence-based interventions. Most
importantly, the study will provide primary care practices with
information that can be used to inform their systems for managing
patients with chronic conditions and to improve the quality of care
delivered.
Participation is voluntary, and all responses will be de-
identified. There are no costs to respondents other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Avg. burden
Type of respondents Form name Number of responses per per response Total burden
respondents respondent (in hr) (in hr)
----------------------------------------------------------------------------------------------------------------
Physician..................... Cognitive 5 1 75/60 6
Testing
Protocol.
Medical Secretary............. NSPCP Screener.. 1,333 1 5/60 111
Physician..................... NSPCP........... 600 1 20/60 200
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 317
----------------------------------------------------------------------------------------------------------------
Dated: April 25, 2011.
Carol Walker,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention
[FR Doc. 2011-10384 Filed 4-28-11; 8:45 am]
BILLING CODE 4163-18-P