Agency Forms Undergoing Paperwork Reduction Act Review, 77836-77838 [2022-27504]
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77836
Federal Register / Vol. 87, No. 243 / Tuesday, December 20, 2022 / Notices
allowed the monitoring of progress
toward these goals. For example,
recipient efforts to establish public
health–health care collaboration has
been integrated into CDC’s 6|18
initiative which connects healthcare
purchasers, payers, and providers with
CDC researchers, economists, and policy
analysts to find ways to improve health
and control costs with the 6|18
interventions;
• Allow the NACP and the state
asthma programs to make more
informed decisions about activities to
achieve objectives. For example, PM
information identified a problem with
enrolling patients most in need of
intervention into recipient programs.
This led to cross-state discussions and
changes in recruitment strategies;
• Motivate use of data and evaluation
findings. For example, the requirement
to report actions taken based on
evaluation findings encourages program
managers and health departments
officials to act on recommendations in
evaluation reports.
CDC requests OMB approval for an
estimated 105 annual burden hours.
There is no cost to respondents other
than their time to participate.
ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden per
response
(in hours)
Total burden
(in hours)
Form name
Funded Asthma Program Recipients
Performance Measures Reporting
Tool.
Emergency Department Visits Reporting Form.
Hospital Discharge Reporting Form
30
1
150/60
75
30
1
30/60
15
30
1
30/60
15
..........................................................
........................
........................
........................
105
Total ...........................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2022–27506 Filed 12–19–22; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–23–1030]
Agency Forms Undergoing Paperwork
Reduction Act Review
lotter on DSK11XQN23PROD with NOTICES1
Number of
responses per
respondent
Number of
respondents
Type of respondents
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘Developmental
Studies to Improve the National Health
Care Surveys’’ to the Office of
Management and Budget (OMB) for
review and approval. CDC previously
published a ‘‘Proposed Data Collection
Submitted for Public Comment and
Recommendations’’ notice on
September 30, 2022 to obtain comments
from the public and affected agencies.
CDC did not receive comments related
to the previous notice. This notice
serves to allow an additional 30 days for
public and affected agency comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
VerDate Sep<11>2014
18:41 Dec 19, 2022
Jkt 259001
(a) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) Minimize the burden of the
collection of information on those who
are to respond, including, through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570.
Comments and recommendations for the
proposed information collection should
be sent within 30 days of publication of
this notice to www.reginfo.gov/public/
do/PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function. Direct written
comments and/or suggestions regarding
the items contained in this notice to the
Attention: CDC Desk Officer, Office of
Management and Budget, 725 17th
PO 00000
Frm 00050
Fmt 4703
Sfmt 4703
Street NW, Washington, DC 20503 or by
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
Proposed Project
Developmental Studies to Improve the
National Health Care Surveys (OMB
Control No. 0920–1030, Exp. 06/30/
2023)—Extension—National Center for
Health Statistics (NCHS), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Section 306 of the Public Health
Service (PHS) Act (42 U.S.C. 242k), as
amended, authorizes the Secretary of
Health and Human Services (DHHS),
acting through the Division of Health
Care Statistics (DHCS) within NCHS,
shall collect statistics on the extent and
nature of illness and disability of the
population of the United States.
The DHCS conducts the National
Health Care Surveys (NHCS), a family of
nationally representative surveys of
encounters and health care providers in
inpatient, ambulatory, and long-term
care settings. This information
collection request (ICR) is for the
extension of a generic clearance to
conduct developmental studies to
improve this family of surveys. This
three-year clearance period will include
studies to evaluate and improve upon
existing survey design and operations,
as well as to examine the feasibility of,
and address challenges that may arise
with, future expansions of the National
Health Care Surveys.
Specifically, this request covers
developmental research with the
E:\FR\FM\20DEN1.SGM
20DEN1
77837
Federal Register / Vol. 87, No. 243 / Tuesday, December 20, 2022 / Notices
following aims: (1) to explore ways to
refine and improve upon existing survey
designs and procedures; and (2) to
explore and evaluate proposed survey
designs and alternative approaches to
data collection. The goal of these
research studies is to further enhance
DHCS existing and future data
collection protocols to increase research
capacity and improve health care data
quality for the purpose of monitoring
public health and well-being at the
national, state and local levels, thereby
informing the health policy decisionmaking process. The information
collected through this Generic ICR will
not be used to make generalizable
statements about the population of
interest or to inform public policy;
however, methodological findings may
be reported.
This Generic ICR would include
studies conducted in person, via the
telephone or internet, and by postal or
electronic mail. Methods covered would
include qualitative (e.g., usability
testing, focus groups, ethnographic
studies, and respondent debriefing
questionnaires) and/or quantitative (e.g.,
pilot tests, pre-tests and split sample
experiments) research methodologies.
Examples of studies to improve existing
survey designs and procedures may
include evaluation of incentive
approaches to improve recruitment and
increase participation rates; testing of
new survey items to obtain additional
data on providers, patients, and their
encounters while minimizing
misinterpretation and human error in
data collection; testing data collection in
panel surveys; triangulating and
validating survey responses from
multiple data sources; assessment of the
feasibility of data retrieval; and
development of protocols that will
locate, identify, and collect accurate
survey data in the least labor-intensive
and burdensome manner at the sampled
practice site.
To explore and evaluate proposed
survey designs and alternative
approaches to collecting data, especially
with the nationwide adoption of
electronic health records, studies may
expand the evaluation of data extraction
of electronic health records and
submission via continuity of care
documentation to small/mid-size/large
medical providers and hospital
networks, managed care health plans,
prison-hospitals, and other inpatient,
outpatient, and long-term care settings
that are currently either in-scope or outof-scope of the National Health Care
Surveys. Research on feasibility, data
quality and respondent burden also may
be carried out in the context of
developing new surveys of health care
providers and establishments that are
currently out-of-scope of the National
Health Care Surveys.
Specific motivations for conducting
developmental studies include: (1)
within the National Ambulatory
Medical Care Survey (NAMCS), new
clinical groups may be expanded to
include dentists, psychologists,
podiatrists, chiropractors, optometrists),
mid-level providers (e.g., physician
assistants, advanced practice nurses,
nurse practitioners, certified nurse
midwives) and allied-health
professionals (e.g., certified nursing
aides, medical assistants, radiology
technicians, laboratory technicians,
pharmacists, dieticians/nutritionists).
Current sampling frames such as those
from the American Medical Association
may be obtained and studied, as well as
frames that are not currently in use by
NAMCS, such as state and
organizational listings of other licensed
providers; (2) within the National Study
of Long-Term Care Providers, additional
new frames may be sought and
evaluated and data items from home
care agencies, long-term care hospitals,
and facilities exclusively serving
individuals with intellectual/
developmental disability may be tested.
Similarly, data may be obtained from
lists compiled by states and other
organizations. Data about the facilities
as well as residents and their visits will
be investigated; and (3) in the inpatient
and outpatient care settings, the
National Hospital Care Survey (NHCS)
and the National Hospital Ambulatory
Medical Care Survey (NHAMCS) may
investigate the addition of facility and
patient information especially as it
relates to insurance and electronic
medical records.
Projects under development or in the
planning stages include two projects
related to opioid use: one that will
investigate adding questions to NAMCS
on physician understanding of
guidelines for opioid use and one that
will test the validation of an algorithm
for identifying opioid-involved hospital
visits. Another study will develop a
Hospital-Based Victim Services Frame.
The NHCSs collect critical, accurate
data that are used to produce reliable
national estimates—and in recent years
(when budget allows), state-level
estimates—of clinical services and of
the providers who delivered those
services in inpatient, outpatient,
ambulatory, and long-term care settings.
The data from these surveys are used by
providers, policy makers and
researchers to address important topics
of interest, including the quality and
disparities of care among populations,
epidemiology of medical conditions,
diffusion of technologies, effects of
policies and practice guidelines, and
changes in health care over time.
Research studies need to be conducted
to improve existing and proposed
survey design and procedures of the
NHCSs, as well as to evaluate
alternative data collection approaches
particularly due to the expansion of
electronic health record use, and to
develop new sample frames of currently
out-of-scope providers and settings of
care.
Average burdens are designed to
cover 15–40 min interviews as well as
90-minute focus groups, as well as
longer on-site visits, and situations
where organizations may be preparing
electronic data files. CDC requests OMB
approval for an estimated 3,000 annual
burden hours. There is no cost to
respondents other than their time to
participate.
lotter on DSK11XQN23PROD with NOTICES1
TABLE 1—ESTIMATED ANNUALIZED BURDEN HOURS
Type of
respondents
Form name
Health Care Providers and .....
Business entities .....................
Health Care Providers,State/
local government agencies,
and business entities.
Interviews, surveys, focus groups, experiments (in person,
phone, internet, postal/electronic mail).
Interviews, surveys, focus groups, experiments (in person,
phone, internet, postal/electronic mail).
VerDate Sep<11>2014
18:41 Dec 19, 2022
Jkt 259001
PO 00000
Frm 00051
Fmt 4703
Number of
respondents
Sfmt 4703
E:\FR\FM\20DEN1.SGM
Number of
responses per
respondent
Average
burden per
response
(in hours)
2,582
1
1
167
1
2.5
20DEN1
77838
Federal Register / Vol. 87, No. 243 / Tuesday, December 20, 2022 / Notices
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2022–27504 Filed 12–19–22; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day-23–1185]
Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘Youth
Outreach Generic Clearance for the
National Center for Health Statistics
(NCGS)’’ to the Office of Management
and Budget (OMB) for review and
approval. CDC previously published a
‘‘Proposed Data Collection Submitted
for Public Comment and
Recommendations’’ notice on
September 23, 2022 to obtain comments
from the public and affected agencies.
CDC did not receive any comments
related to the previous notice. This
notice serves to allow an additional 30
days for public and affected agency
comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) Minimize the burden of the
collection of information on those who
are to respond, including, through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570.
Comments and recommendations for the
proposed information collection should
be sent within 30 days of publication of
this notice to www.reginfo.gov/public/
do/PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function. Direct written
comments and/or suggestions regarding
the items contained in this notice to the
Attention: CDC Desk Officer, Office of
Management and Budget, 725 17th
Street, NW, Washington, DC 20503 or by
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
Proposed Project
Youth Outreach Generic Clearance for
the National Center for Health Statistics
(NCHS) (OMB Control No. 0920–1185,
Exp. 07/31/2023)—Extension—National
Center for Health Statistics (NCHS),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The National Center for Health
Statistics (NCHS) is authorized to
collect data under Section 306 of the
Public Health Service Act (42 U.S.C.
242k). NCHS has a history of reaching
out to young people to encourage their
interest in Science, Technology,
Engineering and Math (STEM).
Examples of past involvement include
adopting local schools, speaking at local
colleges, conducting a Statistics Day for
high school students, and, most
recently, conducting the NCHS Data
Detectives Camp for middle school
students.
The success of these programs has
inspired NCHS leadership and staff to
want to look for new and continuing
opportunities to positively impact the
lives of young people and expand their
interest, understanding of, and
involvement in the sciences. NCHS
requests approval for a New Generic
Clearance mechanism to collect
information for these youth outreach
activities and to inform future NCHS
planning activities.
As stated, these activities include
hosting the Data Detectives Camp
annually; hosting Statistics Day
annually; creating youth poster sessions
for professional conferences (such as the
NCHS National Conference on Health
Statistics or the American Statistical
Association Conference etc.); hosting a
statistical or health sciences fair or other
STEM-related competitions; organizing
a STEM Career Day or similar activity;
developing web-based sites or materials
with youth focus, as well as other
programs developed to meet future
youth outreach needs, particularly
activities that encourage STEM.
Information will be collected using a
combination of methodologies
appropriate to each program. These may
include: registration forms, letters of
recommendation, evaluation forms, mail
surveys, focus groups, automated and
electronic technology (e.g. email, Webbased surveys), and telephone surveys.
OMB approval is requested for three
years to conduct the Youth Outreach
Generic Clearance for the National
Center for Health Statistics (NCHS).
CDC requests OMB approval for an
estimated 1,750 annual burden hours.
Participation is voluntary and there are
no costs to respondents other than their
time.
lotter on DSK11XQN23PROD with NOTICES1
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Average
burden/
response
(in hours)
Number of
responses/
respondent
Type of survey
Respondent
Questionnaires/Applications ............................
Applicants Questionnaire/Application .............
Applications, Recommendations, and Other
applicant-supporting documentation.
Focus Groups .................................................
Student/Youth .................................................
Parents/Guardians of Applicants ...................
School Officials/Community Representatives
800
800
1200
1
1
1
30/60
30/60
30/60
Student/Youth; Parent/Guardian; School Officials; Other.
Student/Youth; Parent/Guardian; School Officials; Other.
50
1
60/60
600
1
30/60
Other Program Surveys ..................................
VerDate Sep<11>2014
18:41 Dec 19, 2022
Jkt 259001
PO 00000
Frm 00052
Fmt 4703
Sfmt 4703
E:\FR\FM\20DEN1.SGM
20DEN1
Agencies
[Federal Register Volume 87, Number 243 (Tuesday, December 20, 2022)]
[Notices]
[Pages 77836-77838]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-27504]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-23-1030]
Agency Forms Undergoing Paperwork Reduction Act Review
In accordance with the Paperwork Reduction Act of 1995, the Centers
for Disease Control and Prevention (CDC) has submitted the information
collection request titled ``Developmental Studies to Improve the
National Health Care Surveys'' to the Office of Management and Budget
(OMB) for review and approval. CDC previously published a ``Proposed
Data Collection Submitted for Public Comment and Recommendations''
notice on September 30, 2022 to obtain comments from the public and
affected agencies. CDC did not receive comments related to the previous
notice. This notice serves to allow an additional 30 days for public
and affected agency comments.
CDC will accept all comments for this proposed information
collection project. The Office of Management and Budget is particularly
interested in comments that:
(a) Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
(b) Evaluate the accuracy of the agencies estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and clarity of the information to
be collected;
(d) Minimize the burden of the collection of information on those
who are to respond, including, through the use of appropriate
automated, electronic, mechanical, or other technological collection
techniques or other forms of information technology, e.g., permitting
electronic submission of responses; and
(e) Assess information collection costs.
To request additional information on the proposed project or to
obtain a copy of the information collection plan and instruments, call
(404) 639-7570. Comments and recommendations for the proposed
information collection should be sent within 30 days of publication of
this notice to www.reginfo.gov/public/do/PRAMain. Find this particular
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function. Direct
written comments and/or suggestions regarding the items contained in
this notice to the Attention: CDC Desk Officer, Office of Management
and Budget, 725 17th Street NW, Washington, DC 20503 or by fax to (202)
395-5806. Provide written comments within 30 days of notice
publication.
Proposed Project
Developmental Studies to Improve the National Health Care Surveys
(OMB Control No. 0920-1030, Exp. 06/30/2023)--Extension--National
Center for Health Statistics (NCHS), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Section 306 of the Public Health Service (PHS) Act (42 U.S.C.
242k), as amended, authorizes the Secretary of Health and Human
Services (DHHS), acting through the Division of Health Care Statistics
(DHCS) within NCHS, shall collect statistics on the extent and nature
of illness and disability of the population of the United States.
The DHCS conducts the National Health Care Surveys (NHCS), a family
of nationally representative surveys of encounters and health care
providers in inpatient, ambulatory, and long-term care settings. This
information collection request (ICR) is for the extension of a generic
clearance to conduct developmental studies to improve this family of
surveys. This three-year clearance period will include studies to
evaluate and improve upon existing survey design and operations, as
well as to examine the feasibility of, and address challenges that may
arise with, future expansions of the National Health Care Surveys.
Specifically, this request covers developmental research with the
[[Page 77837]]
following aims: (1) to explore ways to refine and improve upon existing
survey designs and procedures; and (2) to explore and evaluate proposed
survey designs and alternative approaches to data collection. The goal
of these research studies is to further enhance DHCS existing and
future data collection protocols to increase research capacity and
improve health care data quality for the purpose of monitoring public
health and well-being at the national, state and local levels, thereby
informing the health policy decision-making process. The information
collected through this Generic ICR will not be used to make
generalizable statements about the population of interest or to inform
public policy; however, methodological findings may be reported.
This Generic ICR would include studies conducted in person, via the
telephone or internet, and by postal or electronic mail. Methods
covered would include qualitative (e.g., usability testing, focus
groups, ethnographic studies, and respondent debriefing questionnaires)
and/or quantitative (e.g., pilot tests, pre-tests and split sample
experiments) research methodologies. Examples of studies to improve
existing survey designs and procedures may include evaluation of
incentive approaches to improve recruitment and increase participation
rates; testing of new survey items to obtain additional data on
providers, patients, and their encounters while minimizing
misinterpretation and human error in data collection; testing data
collection in panel surveys; triangulating and validating survey
responses from multiple data sources; assessment of the feasibility of
data retrieval; and development of protocols that will locate,
identify, and collect accurate survey data in the least labor-intensive
and burdensome manner at the sampled practice site.
To explore and evaluate proposed survey designs and alternative
approaches to collecting data, especially with the nationwide adoption
of electronic health records, studies may expand the evaluation of data
extraction of electronic health records and submission via continuity
of care documentation to small/mid-size/large medical providers and
hospital networks, managed care health plans, prison-hospitals, and
other inpatient, outpatient, and long-term care settings that are
currently either in-scope or out-of-scope of the National Health Care
Surveys. Research on feasibility, data quality and respondent burden
also may be carried out in the context of developing new surveys of
health care providers and establishments that are currently out-of-
scope of the National Health Care Surveys.
Specific motivations for conducting developmental studies include:
(1) within the National Ambulatory Medical Care Survey (NAMCS), new
clinical groups may be expanded to include dentists, psychologists,
podiatrists, chiropractors, optometrists), mid-level providers (e.g.,
physician assistants, advanced practice nurses, nurse practitioners,
certified nurse midwives) and allied-health professionals (e.g.,
certified nursing aides, medical assistants, radiology technicians,
laboratory technicians, pharmacists, dieticians/nutritionists). Current
sampling frames such as those from the American Medical Association may
be obtained and studied, as well as frames that are not currently in
use by NAMCS, such as state and organizational listings of other
licensed providers; (2) within the National Study of Long-Term Care
Providers, additional new frames may be sought and evaluated and data
items from home care agencies, long-term care hospitals, and facilities
exclusively serving individuals with intellectual/developmental
disability may be tested. Similarly, data may be obtained from lists
compiled by states and other organizations. Data about the facilities
as well as residents and their visits will be investigated; and (3) in
the inpatient and outpatient care settings, the National Hospital Care
Survey (NHCS) and the National Hospital Ambulatory Medical Care Survey
(NHAMCS) may investigate the addition of facility and patient
information especially as it relates to insurance and electronic
medical records.
Projects under development or in the planning stages include two
projects related to opioid use: one that will investigate adding
questions to NAMCS on physician understanding of guidelines for opioid
use and one that will test the validation of an algorithm for
identifying opioid-involved hospital visits. Another study will develop
a Hospital-Based Victim Services Frame.
The NHCSs collect critical, accurate data that are used to produce
reliable national estimates--and in recent years (when budget allows),
state-level estimates--of clinical services and of the providers who
delivered those services in inpatient, outpatient, ambulatory, and
long-term care settings. The data from these surveys are used by
providers, policy makers and researchers to address important topics of
interest, including the quality and disparities of care among
populations, epidemiology of medical conditions, diffusion of
technologies, effects of policies and practice guidelines, and changes
in health care over time. Research studies need to be conducted to
improve existing and proposed survey design and procedures of the
NHCSs, as well as to evaluate alternative data collection approaches
particularly due to the expansion of electronic health record use, and
to develop new sample frames of currently out-of-scope providers and
settings of care.
Average burdens are designed to cover 15-40 min interviews as well
as 90-minute focus groups, as well as longer on-site visits, and
situations where organizations may be preparing electronic data files.
CDC requests OMB approval for an estimated 3,000 annual burden hours.
There is no cost to respondents other than their time to participate.
Table 1--Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per
Type of respondents Form name respondents responses per response (in
respondent hours)
----------------------------------------------------------------------------------------------------------------
Health Care Providers and.......... Interviews, surveys, focus 2,582 1 1
Business entities.................. groups, experiments (in
person, phone, internet,
postal/electronic mail).
Health Care Providers,State/local Interviews, surveys, focus 167 1 2.5
government agencies, and business groups, experiments (in
entities. person, phone, internet,
postal/electronic mail).
----------------------------------------------------------------------------------------------------------------
[[Page 77838]]
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2022-27504 Filed 12-19-22; 8:45 am]
BILLING CODE 4163-18-P