Proposed Data Collection Submitted for Public Comment and Recommendations, 70828-70830 [2022-25245]
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70828
Federal Register / Vol. 87, No. 223 / Monday, November 21, 2022 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
Applicants or fellows .......................................
Mentors, supervisors, or employers ...............
Alumni .............................................................
Fellowship Data Collection Instrument ..........
Fellowship Data Collection Instrument ..........
Fellowship Data Collection Instrument ..........
Jeffery M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2022–25244 Filed 11–18–22; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–23–0950; Docket No. CDC–2022–
0133]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other federal
agencies the opportunity to comment on
a continuing information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed revision of the
information collection project titled
National Health and Nutrition
Examination Survey (NHANES).
NHANES produces descriptive
statistics, which measure the health and
nutrition status of the general
population.
SUMMARY:
CDC must receive written
comments on or before January 20,
2023.
DATES:
You may submit comments,
identified by Docket No. CDC–2022–
0133 by either of the following methods:
• Federal eRulemaking Portal:
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS H21–8, Atlanta,
Georgia 30329.
ADDRESSES:
lotter on DSK11XQN23PROD with NOTICES1
Number
respondents
Type of respondents
VerDate Sep<11>2014
21:25 Nov 18, 2022
Jkt 259001
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
www.regulations.gov.
Please note: Submit all Federal
comments through the Federal
eRulemaking portal
(www.regulations.gov) or by U.S. mail to
the address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS
H21–8, Atlanta, Georgia 30329;
Telephone: 404–639–7570; Email: omb@
cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. 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;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected;
PO 00000
Frm 00059
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
966
193
1932
1
1
1
Average
burden per
response
(in hours)
30/60
30/60
30/60
4. 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 submissions
of responses; and
5. Assess information collection costs.
Proposed Project
The National Health and Nutrition
Examination Survey (NHANES), (OMB
Control No. 0920–0950, Exp. 04/30/
2023)—Revision—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 that the Secretary
of Health and Human Services (DHHS),
acting through NCHS, shall collect
statistics on the extent and nature of
illness and disability; environmental,
social and other health hazards; and
determinants of health of the population
of the United States.
The National Health and Nutrition
Examination Survey (NHANES) has
been conducted periodically between
1970 and 1994, and continuously since
1999 by the National Center for Health
Statistics (NCHS), CDC.
NHANES produces descriptive
statistics, which measure the health and
nutrition status of the general
population. With physical
examinations, laboratory tests, and
interviews, NHANES studies the
relationship between diet, nutrition and
health in a representative sample of the
United States. NHANES monitors the
prevalence of chronic conditions and
risk factors and is used to produce
national reference data on height,
weight, and nutrient levels in the blood.
Results from more recent NHANES can
be compared to findings reported from
previous surveys to monitor changes in
the health of the U.S. population over
time.
In this Revision, the program is not
considering any substantial changes to
NHANES content or procedures. The
proposed changes being requested
E:\FR\FM\21NON1.SGM
21NON1
70829
Federal Register / Vol. 87, No. 223 / Monday, November 21, 2022 / Notices
include modifications previously
approved via non-substantive change
requests in addition to a request for
three years of approval. As in previous
years, the base sample will remain at
approximately 5,000 interviewed and
examined individuals annually. It is
possible that the survey may have to
adapt its plans in response to the novel
Coronavirus Disease (COVID–19) or
related concerns.
NCHS collects personally identifiable
information (PII). Participant level data
items will include basic demographic
information, name, address, Social
Security number, Medicare number and
participant health information to allow
for linkages to other data sources such
as the National Death Index and data
from the Centers for Medicare and
Medicaid Services (CMS).
A variety of agencies sponsors data
collection components on NHANES. To
keep burden down and respond to
changing public health research needs,
NCHS cycles in and out various
components. The 2021–22 NHANES
physical examination includes the
following components: anthropometry
(all ages), liver elastography (ages 12
and older), standing balance (ages 20–
69), 24-hour dietary recall via phone (all
ages), blood pressure measurement (ages
eight and older), and dual X-ray
absorptiometry (DXA) (ages 8–69, total
body scan). While at the examination
center, additional interview questions
are asked of participants and a second
24-hour dietary recall (all ages) is
scheduled to be conducted by phone 3–
10 days later.
The 2021–22 survey is similar to what
was fielded in 2019–20. NHANES may
conduct developmental projects, with a
focus on planning for NHANES 2024
and beyond. These may include
activities such as tests of new
equipment, crossover studies between
current and proposed methods, test of
different study modes, settings or
technology, outreach materials,
incentive strategies, sample storage and
processing or sample designs. The
biospecimens collected for laboratory
tests include urine and blood. Serum,
plasma and urine specimens are stored
for future testing, including genetic
research, if the participant consents.
Consent to store DNA is continuing in
NHANES.
Beginning in 2021, NHANES added
the following laboratory tests:
Acetylcholinesterase Enzyme Activity
in whole blood; an Environmental
Toxicant in Washed Red Blood Cells
(Hemoglobin Adducts); Environmental
Toxicants in serum (seven terpenes);
Environmental Toxicants in urine
(seven volatile organic compound (VOC)
metabolites); Infectious Disease Markers
in serum (Enterovirus 68 (EV–D68) and
Human Papilloma Virus (HPV) in
serum); Nutritional Biomarkers in
plasma (Four trans-fatty acids (TFA));
and two Nutritional Biomarkers in
serum.
Additionally, at the start of the 2021
survey year, the following Laboratory
Tests were modified: Steroid hormones
in serum (eleven steroid hormones).
Cycling out of NHANES is the Blood
Pressure Methodology Study and
laboratory tests of Adducts of
Hemoglobin (Acrylamide, Glycidamide)
and Urine flow rate.
Most sections of the NHANES
interviews provide self-reported
information to be used in combination
with specific examination or laboratory
content, as independent prevalence
estimates, or as covariates in statistical
analysis (e.g., socio-demographic
characteristics). Some examples include
alcohol, drug, and tobacco use, sexual
behavior, prescription and aspirin use,
and indicators of oral, bone,
reproductive, and mental health.
Several interview components support
the nutrition-monitoring objective of
NHANES, including questions about
food security and nutrition program
participation, dietary supplement use,
and weight history/self-image related
behavior.
NHANES will continue multi-mode
screening and electronic consent
procedures. Our yearly goal for
interview, exam and post exam
components is 5,600 participants. To
achieve this goal, we may need to screen
up to 8,300 individuals annually.
Burden for individuals will vary based
on their level of participation. For
example, infants and children tend to
have shorter interviews and exams than
adults. This is because young people
may have fewer health conditions or
medications to report so their interviews
take less time or because certain exams
are only conducted on individuals 18
and older. In addition, adults often
serve as proxy respondents for young
people in their families.
Participation in NHANES is voluntary
and confidential. CDC requests OMB
approval for a three-year extension, with
65,630 annualized burden hours. There
is no cost to respondents other than
their time to participate.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total
burden
(in hours)
Form name
Individuals ..........................................................
in households ....................................................
Individuals in households ..................................
Individuals in households ..................................
Individuals in households ..................................
Screener ...........................................................
8,300
1
10/60
1,383
5,600
5,600
5,600
1
1
1
1
2.5
1.3
5,600
14,000
7,280
5,600
1
20/60
1,867
Individuals in households ..................................
Individuals in households ..................................
Household Interview .........................................
MEC Interview & Examination ..........................
Telephone Dietary Recall & Dietary Supplements.
Flexible Consumer Behavior Survey Phone
Follow-Up.
Developmental Projects & Special Studies ......
24-hour wearable device projects .....................
3,500
1,000
1
1
3
25
10,500
25,000
Total ............................................................
...........................................................................
........................
........................
........................
65,630
Individuals in households ..................................
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E:\FR\FM\21NON1.SGM
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70830
Federal Register / Vol. 87, No. 223 / Monday, November 21, 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. 2022–25245 Filed 11–18–22; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30 Day–23–0010]
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 ‘‘Birth Defects
Study To Evaluate Pregnancy exposureS
(BD–STEPS)’’ 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 March 1,
2022 to obtain comments from the
public and affected agencies. CDC
received two 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
Birth Defects Study To Evaluate
Pregnancy exposureS (BD–STEPS)
(OMB Control No. 0920–0010, Exp. 2/
28/2023)—Revision—National Center
on Birth Defects and Developmental
Disabilities (NCBDDD), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Birth defects are associated with
substantial morbidity and mortality in
the United States. About one in every 33
babies is born with a birth defect. Birth
defects contributed to more than one
million hospital stays in the U.S. in
2013, resulting in $22.9 billion in
hospital costs. Birth defects are the
leading cause of infant mortality and the
fifth leading cause of loss of potential
years of life before age 65. One in five
infant deaths is due to birth defects.
For most birth defects, the causes are
not known, making prevention efforts
challenging to develop. To date, primary
preventive measures are available for
only a few birth defects. For example,
vaccination programs have reduced the
incidence of congenital rubella
syndrome, Rh hemolytic disease of the
newborn can be prevented by
appropriate medical practice, and
genetic counseling can provide parents
with information about the increased
risk of Down syndrome associated with
advanced maternal age. Perhaps most
importantly, folic acid intake before and
during pregnancy can prevent many
cases of fatal or permanently disabling
neural tube defects such as anencephaly
and spina bifida.
This continued burden justifies
reasonable attempts to reduce the
prevalence of birth defects. To help
reduce birth defects among U.S. babies,
in 1996 Congress directed the CDC to
establish Centers of Excellence for Birth
Defects Research and Prevention. The
mandate was formalized with passage of
the Birth Defects Prevention Act of
1998. This Act amended Section 317C
of the Public Health Service Act (42
U.S.C. 247b–4) and authorized CDC to:
(1) collect, analyze, and make available
data on birth defects; (2) operate
regional centers that will conduct
applied epidemiological research for the
prevention of birth defects; and (3)
provide the public with information on
preventing birth defects.
In response to this mandate, the
Division of Birth Defects and Infant
Disorders (DBDID) obtained OMB
clearance for data collection that is
carried out by the Centers for Birth
Defects Research and Prevention
(CBDRP). The CBDRP’s first research
effort was the National Birth Defects
Prevention Study (NBDPS), which
began data collection in 1997 and ended
in 2013. The CBDRPs transitioned from
NBDPS to the Birth Defects Study To
Evaluate Pregnancy exposureS (BD–
STEPS), which began data collection in
2014. One of the main activities for each
Center is to conduct BD–STEPS in their
state, and the purpose of BD–STEPS is
to evaluate factors associated with the
occurrence of birth defects and
stillbirths, and ultimately to work to
prevent major birth defects and
stillbirths associated with maternal risk
factors.
CDC requests OMB approval for an
estimated 4,473 annual burden hours.
There is no cost to respondents other
than their time to participate.
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ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Mothers (Interview) ................
VerDate Sep<11>2014
21:25 Nov 18, 2022
Number of
respondents
Form name
Core Computer Assisted
Telephone Interview.
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Average
burden per
response
(in hours)
Number of
responses per
respondent
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]]>Agencies
[Federal Register Volume 87, Number 223 (Monday, November 21, 2022)]
[Notices]
[Pages 70828-70830]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-25245]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-23-0950; Docket No. CDC-2022-0133]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing efforts to reduce public burden and maximize the
utility of government information, invites the general public and other
federal agencies the opportunity to comment on a continuing information
collection, as required by the Paperwork Reduction Act of 1995. This
notice invites comment on a proposed revision of the information
collection project titled National Health and Nutrition Examination
Survey (NHANES). NHANES produces descriptive statistics, which measure
the health and nutrition status of the general population.
DATES: CDC must receive written comments on or before January 20, 2023.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2022-
0133 by either of the following methods:
Federal eRulemaking Portal: www.regulations.gov. Follow
the instructions for submitting comments.
Mail: Jeffrey M. Zirger, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road
NE, MS H21-8, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. CDC will post, without change, all relevant comments
to www.regulations.gov.
Please note: Submit all Federal comments through the Federal
eRulemaking portal (www.regulations.gov) or by U.S. mail to the address
listed above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact Jeffrey M. Zirger, Information Collection
Review Office, Centers for Disease Control and Prevention, 1600 Clifton
Road NE, MS H21-8, Atlanta, Georgia 30329; Telephone: 404-639-7570;
Email: [email protected].
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3520), federal agencies must obtain approval from
the Office of Management and Budget (OMB) for each collection of
information they conduct or sponsor. In addition, the PRA also requires
federal agencies to provide a 60-day notice in the Federal Register
concerning each proposed collection of information, including each new
proposed collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to the OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. 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;
2. Evaluate the accuracy of the agency's estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and clarity of the information to
be collected;
4. 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
submissions of responses; and
5. Assess information collection costs.
Proposed Project
The National Health and Nutrition Examination Survey (NHANES), (OMB
Control No. 0920-0950, Exp. 04/30/2023)--Revision--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 that the Secretary of Health and Human
Services (DHHS), acting through NCHS, shall collect statistics on the
extent and nature of illness and disability; environmental, social and
other health hazards; and determinants of health of the population of
the United States.
The National Health and Nutrition Examination Survey (NHANES) has
been conducted periodically between 1970 and 1994, and continuously
since 1999 by the National Center for Health Statistics (NCHS), CDC.
NHANES produces descriptive statistics, which measure the health
and nutrition status of the general population. With physical
examinations, laboratory tests, and interviews, NHANES studies the
relationship between diet, nutrition and health in a representative
sample of the United States. NHANES monitors the prevalence of chronic
conditions and risk factors and is used to produce national reference
data on height, weight, and nutrient levels in the blood. Results from
more recent NHANES can be compared to findings reported from previous
surveys to monitor changes in the health of the U.S. population over
time.
In this Revision, the program is not considering any substantial
changes to NHANES content or procedures. The proposed changes being
requested
[[Page 70829]]
include modifications previously approved via non-substantive change
requests in addition to a request for three years of approval. As in
previous years, the base sample will remain at approximately 5,000
interviewed and examined individuals annually. It is possible that the
survey may have to adapt its plans in response to the novel Coronavirus
Disease (COVID-19) or related concerns.
NCHS collects personally identifiable information (PII).
Participant level data items will include basic demographic
information, name, address, Social Security number, Medicare number and
participant health information to allow for linkages to other data
sources such as the National Death Index and data from the Centers for
Medicare and Medicaid Services (CMS).
A variety of agencies sponsors data collection components on
NHANES. To keep burden down and respond to changing public health
research needs, NCHS cycles in and out various components. The 2021-22
NHANES physical examination includes the following components:
anthropometry (all ages), liver elastography (ages 12 and older),
standing balance (ages 20-69), 24-hour dietary recall via phone (all
ages), blood pressure measurement (ages eight and older), and dual X-
ray absorptiometry (DXA) (ages 8-69, total body scan). While at the
examination center, additional interview questions are asked of
participants and a second 24-hour dietary recall (all ages) is
scheduled to be conducted by phone 3-10 days later.
The 2021-22 survey is similar to what was fielded in 2019-20.
NHANES may conduct developmental projects, with a focus on planning for
NHANES 2024 and beyond. These may include activities such as tests of
new equipment, crossover studies between current and proposed methods,
test of different study modes, settings or technology, outreach
materials, incentive strategies, sample storage and processing or
sample designs. The biospecimens collected for laboratory tests include
urine and blood. Serum, plasma and urine specimens are stored for
future testing, including genetic research, if the participant
consents. Consent to store DNA is continuing in NHANES.
Beginning in 2021, NHANES added the following laboratory tests:
Acetylcholinesterase Enzyme Activity in whole blood; an Environmental
Toxicant in Washed Red Blood Cells (Hemoglobin Adducts); Environmental
Toxicants in serum (seven terpenes); Environmental Toxicants in urine
(seven volatile organic compound (VOC) metabolites); Infectious Disease
Markers in serum (Enterovirus 68 (EV-D68) and Human Papilloma Virus
(HPV) in serum); Nutritional Biomarkers in plasma (Four trans-fatty
acids (TFA)); and two Nutritional Biomarkers in serum.
Additionally, at the start of the 2021 survey year, the following
Laboratory Tests were modified: Steroid hormones in serum (eleven
steroid hormones). Cycling out of NHANES is the Blood Pressure
Methodology Study and laboratory tests of Adducts of Hemoglobin
(Acrylamide, Glycidamide) and Urine flow rate.
Most sections of the NHANES interviews provide self-reported
information to be used in combination with specific examination or
laboratory content, as independent prevalence estimates, or as
covariates in statistical analysis (e.g., socio-demographic
characteristics). Some examples include alcohol, drug, and tobacco use,
sexual behavior, prescription and aspirin use, and indicators of oral,
bone, reproductive, and mental health. Several interview components
support the nutrition-monitoring objective of NHANES, including
questions about food security and nutrition program participation,
dietary supplement use, and weight history/self-image related behavior.
NHANES will continue multi-mode screening and electronic consent
procedures. Our yearly goal for interview, exam and post exam
components is 5,600 participants. To achieve this goal, we may need to
screen up to 8,300 individuals annually. Burden for individuals will
vary based on their level of participation. For example, infants and
children tend to have shorter interviews and exams than adults. This is
because young people may have fewer health conditions or medications to
report so their interviews take less time or because certain exams are
only conducted on individuals 18 and older. In addition, adults often
serve as proxy respondents for young people in their families.
Participation in NHANES is voluntary and confidential. CDC requests
OMB approval for a three-year extension, with 65,630 annualized burden
hours. There is no cost to respondents other than their time to
participate.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form name Number of responses per per response Total burden
respondents respondent (in hours) (in hours)
----------------------------------------------------------------------------------------------------------------
Individuals................... Screener........ 8,300 1 10/60 1,383
in households.................
Individuals in households..... Household 5,600 1 1 5,600
Interview.
Individuals in households..... MEC Interview & 5,600 1 2.5 14,000
Examination.
Individuals in households..... Telephone 5,600 1 1.3 7,280
Dietary Recall
& Dietary
Supplements.
Individuals in households..... Flexible 5,600 1 20/60 1,867
Consumer
Behavior Survey
Phone Follow-Up.
Individuals in households..... Developmental 3,500 1 3 10,500
Projects &
Special Studies.
Individuals in households..... 24-hour wearable 1,000 1 25 25,000
device projects.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 65,630
----------------------------------------------------------------------------------------------------------------
[[Page 70830]]
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2022-25245 Filed 11-18-22; 8:45 am]
BILLING CODE 4163-18-P
