Proposed Data Collections Submitted for Public Comment and Recommendations, 24435-24437 [2014-09767]
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24435
Federal Register / Vol. 79, No. 83 / Wednesday, April 30, 2014 / Notices
the doctor responded to the parent’s
concerns and whether the child
accessed screening, diagnostic and
treatment services. We estimate each
parent will return to the clinic twice
during the study for activities such as
WIC eligibility re-certification. This
offers the opportunity to track referral
outcomes over time. The Referral
Outcome Tracking Form will be
completed twice by the same 100
parent/guardian respondents.
In Phase 3, two measures will
evaluate the WIC staff’s response to the
study to help determine program and
message improvements, feasibility and
programming and establish the
estimated time required to complete this
data collection process.
The estimate for burden hours is
based on the number of questions
included in the questionnaires, as well
as survey pre-testing to determine the
typical length of time for completion. To
obtain maximum potential burden
estimates, we did not factor in attrition
during the course of the study but rather
assumed that all participants would
complete all measures.
The total estimated burden is 255
hours. There is no cost to respondents
other than their time.
sustainability. An online survey will
assess staff perceptions of factors such
as key elements, such as ease of use,
time requirements and perceived impact
on children and families. The WIC
Developmental Milestones Staff Survey
will be completed by 47 WIC staff
members who work in the WIC clinics
in the 9 sites where the project will be
implemented. Each staff member also
will be sent an email invitation to attend
one 60-minute focus group meeting.
This will allow for further clarification
of the group’s response. WIC staff
members have provided feedback to
refine questions, ensure accurate
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Number of
respondents
Average
burden per
response
(in hours)
Total burden
hours
Type of respondent
Form name
Parents/guardians of children receiving WIC enrolled in Phase 1.
Pre-Intervention Survey ...................
450
1
10/60
75
Post-Intervention Survey ..................
Referral Outcome Tracking Form ....
450
100
1
2
10/60
15/60
75
50
47
1
10/60
8
WIC staff enrolled in Phase 3 ...........
WIC
Developmental
Milestones
Staff Survey.
Focus Group Questions ...................
47
1
1
47
Total ...........................................
...........................................................
........................
........................
........................
255
Parents/guardians of children enrolled in Phase 2.
WIC staff enrolled in Phase 3 ...........
LeRoy Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2014–09768 Filed 4–29–14; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–14–14VS]
mstockstill on DSK4VPTVN1PROD 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 404–639–7570 or send
comments to Leroy Richardson, at 1600
VerDate Mar<15>2010
17:41 Apr 29, 2014
Jkt 232001
Clifton Road, MS D74, Atlanta, GA
30333 or send an email 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
Developmental Studies to improve the
National Health Care Surveys—New—
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
PO 00000
Frm 00065
Fmt 4703
Sfmt 4703
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, a family of
nationally representative surveys of
encounters and health care providers in
inpatient, outpatient, and long-term care
settings. This information collection
request (ICR) is for a new generic 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
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
E:\FR\FM\30APN1.SGM
30APN1
24436
Federal Register / Vol. 79, No. 83 / Wednesday, April 30, 2014 / Notices
national, state and local levels, thereby
informing 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. (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.
The National Health Care Surveys
collect critical, accurate data that are
used to produce reliable national
estimates—and in recent years, statelevel 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
National Health Care Surveys, 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. There is no cost to
respondents other than their time to
participate. Average burdens are
designed to cover 15–40 minute
interviews as well as 90-minute focus
groups, longer on-site visits, and
situations where organizations may be
preparing electronic data files.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
Health Care Providers and Business
entities.
Health Care Providers, State/local
government agencies, and business entities.
Average
burden
per response
(in hours)
18,000
1
1
500
1
2.5
1,250
........................
........................
..........................
19,250
Interviews, surveys, focus groups,
experiments (in person, phone,
internet, postal/electronic mail).
Interviews, surveys, focus groups,
experiments (in person, phone,
internet, postal/electronic mail).
Total ..........................................
mstockstill on DSK4VPTVN1PROD with NOTICES
Number of
responses per
respondent
Number of
respondents
Type of respondents
..........................................................
VerDate Mar<15>2010
17:41 Apr 29, 2014
Jkt 232001
PO 00000
Frm 00066
Fmt 4703
Sfmt 4703
E:\FR\FM\30APN1.SGM
30APN1
Total
burden
(in hours)
18,000
Federal Register / Vol. 79, No. 83 / Wednesday, April 30, 2014 / Notices
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2014–09767 Filed 4–29–14; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–14–14VU]
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 404–639–7570 and
send comments to Leroy Richardson,
1600 Clifton Road, MS–D74, Atlanta,
GA 30333 or send an email 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.
mstockstill on DSK4VPTVN1PROD with NOTICES
Proposed Project
Promoting Adolescent Health
Through School-Based HIV/STD
Prevention—New—National Center for
HIV/AIDS, Viral Hepatitis, STD, and TB
Prevention (NHHSTP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Many young people engage in sexual
behaviors that place them at risk for HIV
infection, other sexually transmitted
diseases (STD), and pregnancy.
VerDate Mar<15>2010
17:41 Apr 29, 2014
Jkt 232001
According to the 2011 National Youth
Risk Behavior Survey (YRBS) results,
47% of U.S. high school students never
had sexual intercourse; 34% had sexual
intercourse with at least one person
during the 3 months before the survey;
and 15% had had sexual intercourse
with four or more persons during their
lifetime. Of those sexually active high
school students, 40% reported that
either they or their partner had not used
a condom during last sexual intercourse,
and 77% reported that either they or
their partner had not used birth control
pills or Depo-Provera (or any injectable
birth control), Nuva Ring (or any birth
control ring), Implanon (or any
implant), or any intrauterine device
(IUD) before last sexual intercourse.
Establishing healthy behaviors during
childhood and adolescence is easier and
more effective than trying to change
unhealthy behaviors during adulthood.
Since 1987, the Division of Adolescent
and School Health (DASH), which is
now a part of the National Center for
HIV/AIDS, Viral Hepatitis, STD, and TB
Prevention, Centers for Disease Control
and Prevention (CDC), has been a
unique source of support for HIV
prevention efforts in the Nation’s
schools.
CDC requests Office of Management
and Budget (OMB) approval to collect
data over a three-year period from
funded agencies under award PS13–
1308: Promoting Adolescent Health
through School-Based HIV/STD
Prevention and School-Based
Surveillance. Funded agencies include
non-governmental organizations, state
education agencies, and local education
agencies. The primary purpose of PS–
13–1308 is to build the capacity of
priority districts and priority schools to
effectively contribute to the reduction of
HIV infection and other STD among
adolescents; the reduction of disparities
in HIV infection and other STD
experienced by specific adolescent subpopulations; and the conducting of
school-based surveillance, a component
not included in this data collection for
evaluation.
CDC will be using a web-based system
to collect data on the approaches that
funded agencies are using to meet their
goals. Approaches include helping
districts and schools deliver exemplary
sexual health education emphasizing
HIV and other STD prevention;
increasing adolescent access to key
sexual health services; and establishing
safe and supportive environments for
students and staff.
To track funded agency progress and
evaluate the effectiveness of program
activities, CDC will be collecting data
using a mix of process and performance
PO 00000
Frm 00067
Fmt 4703
Sfmt 4703
24437
measures. Process measures, which will
be completed by all funded agencies, are
important to assess the extent to which
planned program activities have been
implemented and lead to feasible and
sustainable programmatic outcomes.
Process measures include items on
school health policy assessment and
monitoring, and on providing training
and technical assistance to partner
education agencies and schools.
Performance measures, which will be
completed by only state and local
education agencies, assess whether
funded activities at each site are leading
to intended outcomes including public
health impact of systemic change in
schools. These measures drove the
development of questionnaires that have
been tailored to each funded agencies’
approach (i.e., exemplary sexual health
education, sexual health services, and
safe and supportive environments).
Respondents include 19 state
education agencies, 17 local education
agencies, and 6 non-governmental
organizations that have all been funded
under PS13–1308. The questionnaires
will be submitted to CDC semi-annually
using the Program Evaluation and
Reporting System, an electronic webbased interface specifically designed for
this data collection.
Each funded agency will receive a
unique log-in to the system and
technical assistance to ensure they can
use the system easily. The dates when
data are requested reflect Procurement
and Grants Office deadlines to provide
timely feedback to funded agencies and
CDC staff for accountability and optimal
use of funds. CDC anticipates that semiannual information collection will begin
in October 2014 and will describe
activities conducted during the period
August 2014–July 2017.
The estimated burden per response
ranges from 0.5 hours to 6 hours. This
variation in burden is due to the
variability in the questions on the forms
based on the approach and type of
funded agency. For instance, nongovernmental organizations have fewer
questions to respond to because they
only have questions for process
evaluation. Local education agencies
have the highest burden because it takes
more time to gather information as they
gather data at the school- and studentlevel as compared with state education
agencies that report only state- and
district-level data. Annualizing this
collection over three years results in an
estimated annualized burden of 820
hours for all funded agencies.
There are no costs to respondents
other than their time.
E:\FR\FM\30APN1.SGM
30APN1
Agencies
[Federal Register Volume 79, Number 83 (Wednesday, April 30, 2014)]
[Notices]
[Pages 24435-24437]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-09767]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-14-14VS]
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 404-639-7570 or
send comments to Leroy Richardson, at 1600 Clifton Road, MS D74,
Atlanta, GA 30333 or send an email 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
Developmental Studies to improve the National Health Care Surveys--
New--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, a family of
nationally representative surveys of encounters and health care
providers in inpatient, outpatient, and long-term care settings. This
information collection request (ICR) is for a new generic 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
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
[[Page 24436]]
national, state and local levels, thereby informing 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. (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.
The National Health Care Surveys collect critical, accurate data
that are used to produce reliable national estimates--and in recent
years, 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
National Health Care Surveys, 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. There is no cost to
respondents other than their time to participate. Average burdens are
designed to cover 15-40 minute interviews as well as 90-minute focus
groups, longer on-site visits, and situations where organizations may
be preparing electronic data files.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response Total burden
respondents respondent (in hours) (in hours)
----------------------------------------------------------------------------------------------------------------
Health Care Providers and Interviews, 18,000 1 1 18,000
Business entities. surveys, focus
groups,
experiments (in
person, phone,
internet,
postal/
electronic
mail).
Health Care Providers, State/ Interviews, 500 1 2.5 1,250
local government agencies, surveys, focus
and business entities. groups,
experiments (in
person, phone,
internet,
postal/
electronic
mail).
----------------------------------------------------------------
Total.................... ................ .............. .............. ............... 19,250
----------------------------------------------------------------------------------------------------------------
[[Page 24437]]
Leroy A. Richardson,
Chief, Information Collection Review Office, Office of Scientific
Integrity, Office of the Associate Director for Science, Office of the
Director, Centers for Disease Control and Prevention.
[FR Doc. 2014-09767 Filed 4-29-14; 8:45 am]
BILLING CODE 4163-18-P