Proposed Data Collection Submitted for Public Comment and Recommendations, 11442-11444 [2022-04191]
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Federal Register / Vol. 87, No. 40 / Tuesday, March 1, 2022 / Notices
other than their time. Based on a
maximum of 12 EIs per year and 100
participants each, the total estimated
annualized burden hours are 600.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
Exposure Investigation Participants ................
Chemical Exposure Questions .......................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2022–04189 Filed 2–28–22; 8:45 am]
BILLING CODE 4163–70–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
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 effort 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 proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled Birth Defects Study To Evaluate
Pregnancy exposureS (BD–STEPS). Data
from BD–STEPS will play an important
part in the decision-making process that
determines federal research agendas,
birth defect prevention activities, and
the direction of funding programs such
as cooperative agreements.
DATES: CDC must receive written
comments on or before May 2, 2022.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2022–
0030 by either of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
SUMMARY:
VerDate Sep<11>2014
19:01 Feb 28, 2022
Jkt 256001
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
regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
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; phone:
404–639–7570; Email: omb@cdc.gov.
FOR FURTHER INFORMATION CONTACT:
[60Day–22–0010; Docket No. CDC–2022–
0030]
jspears on DSK121TN23PROD with NOTICES1
Number of
respondents
Type of respondents
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;
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00048
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
1,200
1
Average
burden
per response
(in hours)
30/60
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
Birth Defects Study to Evaluate
Pregnancy exposureS (BD–STEPS)
(OMB Control No. 0920–0010, Exp. 2/
28/2023)—Extension—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. However, 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 practices, 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
E:\FR\FM\01MRN1.SGM
01MRN1
11443
Federal Register / Vol. 87, No. 40 / Tuesday, March 1, 2022 / Notices
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. The 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.
BD–STEPS is made up of a number of
information collection activities. The
interview is estimated to take
approximately 55 minutes and is titled
‘‘Birth Defects Prevention Study:
Computer Assisted Telephone
Interview.’’ For the five Centers not
participating in the stillbirth component
of the study, a maximum of 370
questionnaire), a maximum of 830
women would receive the online
questionnaire. Completion of the online
questionnaire is estimated to take 20
minutes including reading introductory
communication. The anticipated
maximum burden for the online
questionnaire is 277 hours annually.
CDC requests the release of reportable
infectious diseases information from all
women who complete the CATI except
for women who experienced a stillbirth
without a birth defect. A maximum of
2,590 women would receive the
infectious disease information request.
Based on experience with consent
forms, we expect the review, signing
and mailing of the release of reportable
infectious diseases information to take a
maximum of 15 minutes for
participants. The anticipated maximum
burden for the reportable infectious
diseases information is 648 hours
annually.
In the two Centers participating in the
supplemental interview, mothers of
infants with or without birth defects
that are stillborn and controls are asked
to participate in a supplemental
telephone interview. The 25-minute
supplemental interview includes the
time for informed consent. Based on a
maximum of 640 women to be
interviewed with the supplemental
questionnaire, the maximum burden
time would be 267 hours annually.
Although participation rates may
vary, the total estimates of annual
burden hours for all activities, all
individuals, and all Centers is 4,433
hours. There is no cost to respondents
other than their time to participate.
interviews are planned per year per
center, 270 cases and 100 controls; for
the two Centers participating in
additional stillbirth interviews, 590
interviews are planned per Center, 270
cases with birth defects, 100 controls,
and 220 stillbirths without birth defects.
With seven Centers and a maximum of
3,030 interviews, the maximum
interview burden for all Centers
combined would be 2,778 hours per
year. The 55-minute burden includes
the time for the telephone consent script
which is reviewed with the mother at
the beginning of the call to collect the
information via the computer assisted
telephone interview (CATI).
Five of the seven BD–STEPS Centers
request consent for retrieval of leftover
newborn bloodspots. If a maximum of
2,590 interviews would be expected for
seven Centers (not including interviews
of stillbirths without birth defects), a
maximum of 1,850 would be expected
for five Centers requesting consent for
retrieval of leftover newborn bloodspots
(excluding stillbirths, for which
newborn bloodspots are not available).
A maximum of 15 minutes would be
expected for the participant to read the
bloodspot retrieval consent request and
sign the consent form. The anticipated
maximum burden for bloodspot consent
would be 463 hours annually.
With a maximum of 2,590 interviews
planned annually (not including
interviews of stillbirths without birth
defects since they are not eligible for the
online questionnaire), and
approximately one-third of the
respondents eligible for the online
questionnaire (selected based on
reporting occupations queried in the
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
Mother’s Interview .............................
Telephone
Consent
Script/BD–
STEPS Computer Assisted Telephone Interview.
Consent for bloodspot retrieval ........
Mother’s Consent for Bloodspot Retrieval.
Mother’s Online Occupational Questionnaire.
Mothers Infectious Disease Release
Review.
Mothers of AR/MA Stillbirths and
Controls (Supplemental Telephone
Interview).
jspears on DSK121TN23PROD with NOTICES1
Number of
respondents
Type of respondents
Total .......................................
VerDate Sep<11>2014
19:01 Feb 28, 2022
Average
burden per
response
(in hours)
Number of
responses per
respondent
Total burden
(in hours)
3,030
1
55/60
2,778
1,850
1
15/60
463
830
1
20/60
277
Infectious Disease Request Form ....
2,590
1
15/60
648
Telephone Consent and Supplemental Interview.
640
1
25/60
267
...........................................................
........................
........................
........................
4,433
Online Occupational Questionnaire
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Federal Register / Vol. 87, No. 40 / Tuesday, March 1, 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. 2022–04191 Filed 2–28–22; 8:45 am]
BILLING CODE 4163–18–P
Prevention and the Agency for Toxic
Substances and Disease Registry.
Kalwant Smagh,
Director, Strategic Business Initiatives Unit,
Office of the Chief Operating Officer, Centers
for Disease Control and Prevention.
[FR Doc. 2022–04262 Filed 2–28–22; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
BILLING CODE 4163–18–P
Centers for Disease Control and
Prevention
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Notice of Closed Meeting
Centers for Disease Control and
Prevention
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended, and the Determination of
the Director, Strategic Business
Initiatives Unit, Office of the Chief
Operating Officer, CDC, pursuant to
Public Law 92–463. The grant
applications and the discussions could
disclose confidential trade secrets or
commercial property such as patentable
material, and personal information
concerning individuals associated with
the grant applications, the disclosure of
which would constitute a clearly
unwarranted invasion of personal
privacy.
Name of Committee: Disease,
Disability, and Injury Prevention and
Control Special Emphasis Panel (SEP)—
SIP22–005, Building Resilience Against
Climate Effects (BRACE): Enhancing
Practical Guidance to Support Climate
and Health Adaptation Planning.
Date: May 4, 2022.
Time: 11:00 a.m.–6:00 p.m., EDT.
Place: Teleconference.
Agenda: To review and evaluate grant
applications.
Jaya
Raman, Ph.D., Scientific Review Officer,
National Center for Chronic Disease
Prevention and Health Promotion, CDC,
4770 Buford Highway, Mailstop S107–
B, Atlanta, Georgia 30341, Telephone:
(770) 488–6511, email: JRaman@
cdc.gov.
The Director, Strategic Business
Initiatives Unit, Office of the Chief
Operating Officer, Centers for Disease
Control and Prevention, has been
delegated the authority to sign Federal
Register notices pertaining to
announcements of meetings and other
committee management activities, for
both the Centers for Disease Control and
jspears on DSK121TN23PROD with NOTICES1
FOR FURTHER INFORMATION CONTACT:
VerDate Sep<11>2014
19:01 Feb 28, 2022
Jkt 256001
Notice of Closed Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended, and the Determination of
the Director, Strategic Business
Initiatives Unit, Office of the Chief
Operating Officer, CDC, pursuant to
Public Law 92–463. The grant
applications and the discussions could
disclose confidential trade secrets or
commercial property such as patentable
material, and personal information
concerning individuals associated with
the grant applications, the disclosure of
which would constitute a clearly
unwarranted invasion of personal
privacy.
Name of Committee: Disease,
Disability, and Injury Prevention and
Control Special Emphasis Panel (SEP)RFA–CK-22–001, Investigation of
Monkeypox and Other Zoonotic
Diseases in the Democratic Republic of
the Congo (DRC); RFA–CK–22–002,
Technological Advancement of Global
Rabies Surveillance and Control; and
RFA–CK–22–004, Optimization and
Standardization of Methods to Suppress
Ixodes scapularis and Disrupt Enzootic
Pathogen Transmission in Settings
Posing an Elevated Risk to Humans.
Date: April 28, 2022.
Time: 10:00 a.m.–5:00 p.m. (EDT).
Place: Teleconference, Centers for
Disease Control and Prevention, Room
1080, 8 Corporate Square Blvd., Atlanta,
GA 30329.
Agenda: To review and evaluate grant
applications.
For Further Information Contact:
Gregory Anderson, M.S., M.P.H.,
Scientific Review Officer, National
Center for HIV, Viral Hepatitis, STD,
and TB Prevention, CDC, 1600 Clifton
Road NE, Mailstop US8–1, Atlanta,
PO 00000
Frm 00050
Fmt 4703
Sfmt 4703
Georgia 30329, (404) 718–8833,
ganderson@cdc.gov.
The Director, Strategic Business
Initiatives Unit, Office of the Chief
Operating Officer, Centers for Disease
Control and Prevention, has been
delegated the authority to sign Federal
Register notices pertaining to
announcements of meetings and other
committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Kalwant Smagh,
Director, Strategic Business Initiatives Unit,
Office of the Chief Operating Officer, Centers
for Disease Control and Prevention.
[FR Doc. 2022–04261 Filed 2–28–22; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Notice of Closed Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended, and the Determination of
the Director, Strategic Business
Initiatives Unit, Office of the Chief
Operating Officer, CDC, pursuant to
Public Law 92–463. The grant
applications and the discussions could
disclose confidential trade secrets or
commercial property such as patentable
material, and personal information
concerning individuals associated with
the grant applications, the disclosure of
which would constitute a clearly
unwarranted invasion of personal
privacy.
Name of Committee: Disease,
Disability, and Injury Prevention and
Control Special Emphasis Panel (SEP)—
PAR 20–297, NIOSH Centers of
Excellence for Total Worker Health
(TWH).
Date: April 21, 2022.
Time: 1:00 p.m.–4:00 p.m., EDT.
Place: Video-Assisted Meeting.
Agenda: To review and evaluate grant
applications.
For Further Information Contact: Dan
Hartley, Ed.D., Scientific Review
Officer, Office of Extramural Programs,
National Institute for Occupational
Safety and Health, CDC, 1095
Willowdale Road, Morgantown, West
E:\FR\FM\01MRN1.SGM
01MRN1
]]>Agencies
[Federal Register Volume 87, Number 40 (Tuesday, March 1, 2022)]
[Notices]
[Pages 11442-11444]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-04191]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-22-0010; Docket No. CDC-2022-0030]
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 effort 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 proposed and/or
continuing information collection, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on a proposed
information collection project titled Birth Defects Study To Evaluate
Pregnancy exposureS (BD-STEPS). Data from BD-STEPS will play an
important part in the decision-making process that determines federal
research agendas, birth defect prevention activities, and the direction
of funding programs such as cooperative agreements.
DATES: CDC must receive written comments on or before May 2, 2022.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2022-
0030 by either of the following methods:
Federal eRulemaking Portal: 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 regulations.gov.
Please note: Submit all comments through the Federal eRulemaking
portal (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; phone: 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
Birth Defects Study to Evaluate Pregnancy exposureS (BD-STEPS) (OMB
Control No. 0920-0010, Exp. 2/28/2023)--Extension--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. However, 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 practices, 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
[[Page 11443]]
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.
The 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.
BD-STEPS is made up of a number of information collection
activities. The interview is estimated to take approximately 55 minutes
and is titled ``Birth Defects Prevention Study: Computer Assisted
Telephone Interview.'' For the five Centers not participating in the
stillbirth component of the study, a maximum of 370 interviews are
planned per year per center, 270 cases and 100 controls; for the two
Centers participating in additional stillbirth interviews, 590
interviews are planned per Center, 270 cases with birth defects, 100
controls, and 220 stillbirths without birth defects. With seven Centers
and a maximum of 3,030 interviews, the maximum interview burden for all
Centers combined would be 2,778 hours per year. The 55-minute burden
includes the time for the telephone consent script which is reviewed
with the mother at the beginning of the call to collect the information
via the computer assisted telephone interview (CATI).
Five of the seven BD-STEPS Centers request consent for retrieval of
leftover newborn bloodspots. If a maximum of 2,590 interviews would be
expected for seven Centers (not including interviews of stillbirths
without birth defects), a maximum of 1,850 would be expected for five
Centers requesting consent for retrieval of leftover newborn bloodspots
(excluding stillbirths, for which newborn bloodspots are not
available). A maximum of 15 minutes would be expected for the
participant to read the bloodspot retrieval consent request and sign
the consent form. The anticipated maximum burden for bloodspot consent
would be 463 hours annually.
With a maximum of 2,590 interviews planned annually (not including
interviews of stillbirths without birth defects since they are not
eligible for the online questionnaire), and approximately one-third of
the respondents eligible for the online questionnaire (selected based
on reporting occupations queried in the questionnaire), a maximum of
830 women would receive the online questionnaire. Completion of the
online questionnaire is estimated to take 20 minutes including reading
introductory communication. The anticipated maximum burden for the
online questionnaire is 277 hours annually.
CDC requests the release of reportable infectious diseases
information from all women who complete the CATI except for women who
experienced a stillbirth without a birth defect. A maximum of 2,590
women would receive the infectious disease information request. Based
on experience with consent forms, we expect the review, signing and
mailing of the release of reportable infectious diseases information to
take a maximum of 15 minutes for participants. The anticipated maximum
burden for the reportable infectious diseases information is 648 hours
annually.
In the two Centers participating in the supplemental interview,
mothers of infants with or without birth defects that are stillborn and
controls are asked to participate in a supplemental telephone
interview. The 25-minute supplemental interview includes the time for
informed consent. Based on a maximum of 640 women to be interviewed
with the supplemental questionnaire, the maximum burden time would be
267 hours annually.
Although participation rates may vary, the total estimates of
annual burden hours for all activities, all individuals, and all
Centers is 4,433 hours. There is no cost to respondents other than
their time to participate.
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)
----------------------------------------------------------------------------------------------------------------
Mother's Interview............ Telephone 3,030 1 55/60 2,778
Consent Script/
BD-STEPS
Computer
Assisted
Telephone
Interview.
Mother's Consent for Bloodspot Consent for 1,850 1 15/60 463
Retrieval. bloodspot
retrieval.
Mother's Online Occupational Online 830 1 20/60 277
Questionnaire. Occupational
Questionnaire.
Mothers Infectious Disease Infectious 2,590 1 15/60 648
Release Review. Disease Request
Form.
Mothers of AR/MA Stillbirths Telephone 640 1 25/60 267
and Controls (Supplemental Consent and
Telephone Interview). Supplemental
Interview.
---------------------------------------------------------------
Total................... ................ .............. .............. .............. 4,433
----------------------------------------------------------------------------------------------------------------
[[Page 11444]]
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2022-04191 Filed 2-28-22; 8:45 am]
BILLING CODE 4163-18-P
