Agency Information Collection Activities: Proposed Collection: Public Comment Request; Information Collection Request Title: National Survey of Organ Donation Attitudes and Practices, OMB No. 0915-0290-Revision, 3409-3410 [2024-00819]
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Federal Register / Vol. 89, No. 12 / Thursday, January 18, 2024 / Notices
Review Board Waiver or Alteration of
Informed Consent for Minimal Risk
Clinical Investigations’’ has been
approved by the Office of Management
and Budget (OMB) under the Paperwork
Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT:
Domini Bean, Office of Operations,
Food and Drug Administration, Three
White Flint North, 10A–12M, 11601
Landsdown St., North Bethesda, MD
20852, 301–796–5733, PRAStaff@
fda.hhs.gov.
On
November 27, 2023, the Agency
submitted a proposed collection of
information entitled ‘‘Institutional
Review Board Waiver or Alteration of
Informed Consent for Minimal Risk
Clinical Investigations’’ to OMB for
review and clearance under 44 U.S.C.
3507. An Agency may not conduct or
sponsor, and a person is not required to
respond to, a collection of information
unless it displays a currently valid OMB
control number. OMB has now
approved the information collection and
has assigned OMB control number
0910–0130. The approval expires on
December 31, 2026. A copy of the
supporting statement for this
information collection is available on
the internet at https://www.reginfo.gov/
public/do/PRAMain.
SUPPLEMENTARY INFORMATION:
Dated: January 12, 2024.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2024–00886 Filed 1–17–24; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection: Public
Comment Request; Information
Collection Request Title: National
Survey of Organ Donation Attitudes
and Practices, OMB No. 0915–0290—
Revision
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services.
ACTION: Notice.
khammond on DSKJM1Z7X2PROD with NOTICES
AGENCY:
In compliance with the requirement
for opportunity for public comment on
proposed data collection projects of the
Paperwork Reduction Act of 1995,
HRSA announces plans to submit an
Information Collection Request (ICR),
described below, to the Office of
Management and Budget (OMB). Prior
VerDate Sep<11>2014
17:32 Jan 17, 2024
Jkt 262001
to submitting the ICR to OMB, HRSA
seeks comments from the public
regarding the burden estimate, below, or
any other aspect of the ICR.
DATES: Comments on this ICR should be
received no later than March 18, 2024.
ADDRESSES: Submit your comments to
paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance
Officer, Room 14N39, 5600 Fishers
Lane, Rockville, Maryland, 20857.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and draft
instruments, email paperwork@hrsa.gov
or call Joella Roland, the HRSA
Information Collection Clearance
Officer, at (301) 443–3983.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the ICR title
for reference.
Information Collection Request Title:
National Survey of Organ Donation
Attitudes and Practices (NSODAP) OMB
No. 0915–0290—Revision with changes.
Abstract: The overall purpose of this
study is to conduct an independent
multi-mode (web and telephone) survey
of public opinion regarding various
issues related to organ donation. The
survey will measure public opinion on
issues such as willingness to become an
organ donor, financial incentives for
donation, living donation, impediments
to donation, and level of public
knowledge about donation. Previous
NSODAPs were conducted during 1993,
2005, 2012, and 2019. Similar to the
2019 survey, the goal is to complete
10,000 interviews with adults (18 years
of age or older) nationwide. Specifically,
this will include 1,000 equal-probability
of selection method computer-assisted
telephone interviewing (CATI)
interviews, 1,000 ethnic oversamples
CATI interviews, and a supplemental
web panel of 8,000 respondents. The
final sample will include 1,000
interviews each with Black/African
Americans, Asians, Hispanics, and
Native Americans, and a statistically
sufficient sample for meaningful
comparisons across demographic levels
of age group, education, and income
groups. A total sample of 10,000 is
necessary to achieve sufficiently large
subgroups for statistical analysis across
demographic groups.
Need and Proposed Use of the
Information: The Division of
Transplantation, within the Health
Systems Bureau of HRSA at the
Department of Health and Human
Services, is the primary federal entity
responsible for oversight of the solid
organ and blood stem cell transplant
PO 00000
Frm 00040
Fmt 4703
Sfmt 4703
3409
systems in the United States and for
initiatives to increase organ donor
registration and donation. Sponsorship
of a national survey on the American
public’s donation attitudes and
practices is one of the services that the
Division of Transplantation provides for
the larger donation community,
consistent with its legal authority to
establish a public education and
awareness program (section 377A of the
Public Health Service Act, 42 U.S.C.
274f–1).
Patients in need of organ
transplantation in the United States face
a longstanding critical shortage of
organs. Approximately 103,000
Americans were on the waiting list for
transplantation by the end of 2022, but
only 42,000 transplants were performed,
only meeting two-fifths of the national
need. While this represents an increase
in the number of transplants performed
in 2021, the organ shortage remains in
the United States. Understanding public
attitudes about organ donation and how
the attitudes change over time is critical
to addressing organ shortage through
public awareness and education efforts.
The information from this survey will
facilitate appropriate tailoring and
targeting of donation outreach messages
and strategies and provide an overall
assessment of the impact of previous
outreach messages and strategies. The
data will also inform the development
of policies related to organ donation and
transplantation.
Likely Respondents: A nationally
representative sample of adults over the
age of 18 with a higher number of
responses from populations of interest
such as racial-ethnic minorities,
including African American, Asian,
Native American, and Hispanic
respondents, as well as respondents of
all age groups and education levels.
Burden Statement: The modes of data
collection are web surveys and CATI
interviews and include both landline
and cell phones. Respondent burden is
minimized by having automatic data
entry either electronically by the
respondent answering the online survey
or by a trained CATI interviewer for a
telephone survey that includes no
additional requirements for
respondents. The survey will capture
only the minimum necessary
information for analysis and will take
only about 22 minutes of the
respondent’s time for the CATI survey
and 16 minutes for the web survey. The
questions are the same in both the CATI
and web surveys, but prior research
experience by the contractor has found
web surveys take 25 percent less time to
complete than the same survey
conducted via phone, because
E:\FR\FM\18JAN1.SGM
18JAN1
3410
Federal Register / Vol. 89, No. 12 / Thursday, January 18, 2024 / Notices
respondents can read and click faster
than a phone interviewer can read
survey questions.
Burden in this context means the time
expended by persons to generate,
maintain, retain, disclose, or provide the
information requested. This includes
the time needed to review instructions;
to develop, acquire, install, and utilize
technology and systems for the purpose
of collecting, validating, and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information; to search
data sources; to complete and review
the collection of information; and to
transmit or otherwise disclose the
information. The total annual burden
hours estimated for this ICR are
summarized in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS
Form name
The National Survey of Organ Donation Attitudes and Practices
(NSODAP)—Telephone (English and Spanish versions) ..................
The National Survey of Organ Donation Attitudes and Practices
(NSODAP)—Web (English and Spanish versions) ............................
Total ................................................................................................
HRSA specifically requests comments
on: (1) the necessity and utility of the
proposed information collection for the
proper performance of the agency’s
functions; (2) the accuracy of the
estimated burden; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4) the
use of automated collection techniques
or other forms of information
technology to minimize the information
collection burden.
Maria G. Button,
Director, Executive Secretariat.
[FR Doc. 2024–00819 Filed 1–17–24; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
khammond on DSKJM1Z7X2PROD with NOTICES
National Institute of Neurological
Disorders and Stroke; Notice of Closed
Meetings
Pursuant to section 1009 of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meetings.
The meetings 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. 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: National Institute of
Neurological Disorders and Stroke Special
VerDate Sep<11>2014
17:32 Jan 17, 2024
Jkt 262001
Number of
responses per
respondent
2,000
1
2,000
0.37
740
8,000
1
8,000
0.27
2,160
10,000
........................
10,000
....................
2,900
Emphasis Panel; T90/R90 Interdisciplinary
Training Awards in Clinical Pain Research
(RFA–NS–24–015).
Date: February 12, 2024.
Time: 9:30 a.m. to 3:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Neuroscience Center, 6001 Executive
Boulevard, Rockville, MD 20852 (Virtual
Meeting).
Contact Person: Steven G. Britt, Scientific
Review Officer, Scientific Review Branch,
Division of Extramural Activities, NINDS/
NIH, NSC, 6001 Executive Blvd., Rockville,
MD 20852, 301–480–1953, steve.britt@
nih.gov.
Name of Committee: National Institute of
Neurological Disorders and Stroke Special
Emphasis Panel; Initial Translation Efforts for
Non-addictive Analgesic Therapeutics
Development (HEAL U19).
Date: February 13–14, 2024.
Time: 10:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate
cooperative agreement applications.
Place: National Institutes of Health,
Neuroscience Center, 6001 Executive
Boulevard, Rockville, MD 20852 (Virtual
Meeting).
Contact Person: Abhignya Subedi, Ph.D.,
Scientific Review Officer, Scientific Review
Branch, Division of Extramural Activities,
NINDS/NIH, NSC, 6001 Executive Blvd.,
Rockville, MD 20852, 301–496–9223,
abhi.subedi@nih.gov.
Name of Committee: National Institute of
Neurological Disorders and Stroke Special
Emphasis Panel; HEAL Initiative: Planning
Studies for Initial Analgesic Development
[Small Molecules and Biologics] (R61
Clinical Trial Not Allowed).
Date: February 16, 2024.
Time: 11:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Neuroscience Center, 6001 Executive
Boulevard, Rockville, MD 20852 (Virtual
Meeting).
PO 00000
Frm 00041
Fmt 4703
Average
burden per
response
(in hours)
Number of
respondents
Sfmt 4703
Total
responses
Total
burden
hours
Contact Person: Bo-Shiun Chen, Ph.D.,
Scientific Review Officer, Scientific Review
Branch, Division of Extramural Activities,
NINDS/NIH, NSC, 6001 Executive Blvd.,
Rockville, MD 20852, 301–496–9223, boshiun.chen@nih.gov.
Name of Committee: National Institute of
Neurological Disorders and Stroke Special
Emphasis Panel; R25 Review.
Date: February 22, 2024.
Time: 10:00 a.m. to 4:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Neuroscience Center, 6001 Executive
Boulevard, Rockville, MD 20852 (Virtual
Meeting).
Contact Person: Lataisia Cherie Jones,
Ph.D., Scientific Review Officer, Scientific
Review Branch, Division of Extramural
Activities, NINDS/NIH, 6001 Executive
Blvd., Rockville, MD 20852, 301–496–9223,
lataisia.jones@nih.gov.
Name of Committee: National Institute of
Neurological Disorders and Stroke Special
Emphasis Panel; Research Opportunities in
the Human Brain (ROH) U01/R61.
Date: February 26–27, 2024.
Time: 9:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Canopy by Hilton, 940 Rose Avenue,
North Bethesda, MD 20852.
Contact Person: Tatiana Pasternak, Ph.D.,
Scientific Review Officer, Scientific Review
Branch, Division of Extramural Activities,
NSC, 6001 Executive Blvd., NINDS/NIH,
Rockville, MD 20852, 301–496–9223,
tatiana.pasternak@nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.853, Clinical Research
Related to Neurological Disorders; 93.854,
Biological Basis Research in the
Neurosciences, National Institutes of Health,
HHS.)
E:\FR\FM\18JAN1.SGM
18JAN1
]]>Agencies
[Federal Register Volume 89, Number 12 (Thursday, January 18, 2024)]
[Notices]
[Pages 3409-3410]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-00819]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Proposed Collection:
Public Comment Request; Information Collection Request Title: National
Survey of Organ Donation Attitudes and Practices, OMB No. 0915-0290--
Revision
AGENCY: Health Resources and Services Administration (HRSA), Department
of Health and Human Services.
ACTION: Notice.
-----------------------------------------------------------------------
In compliance with the requirement for opportunity for public
comment on proposed data collection projects of the Paperwork Reduction
Act of 1995, HRSA announces plans to submit an Information Collection
Request (ICR), described below, to the Office of Management and Budget
(OMB). Prior to submitting the ICR to OMB, HRSA seeks comments from the
public regarding the burden estimate, below, or any other aspect of the
ICR.
DATES: Comments on this ICR should be received no later than March 18,
2024.
ADDRESSES: Submit your comments to [email protected] or mail the HRSA
Information Collection Clearance Officer, Room 14N39, 5600 Fishers
Lane, Rockville, Maryland, 20857.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the data collection plans and
draft instruments, email [email protected] or call Joella Roland, the
HRSA Information Collection Clearance Officer, at (301) 443-3983.
SUPPLEMENTARY INFORMATION: When submitting comments or requesting
information, please include the ICR title for reference.
Information Collection Request Title: National Survey of Organ
Donation Attitudes and Practices (NSODAP) OMB No. 0915-0290--Revision
with changes.
Abstract: The overall purpose of this study is to conduct an
independent multi-mode (web and telephone) survey of public opinion
regarding various issues related to organ donation. The survey will
measure public opinion on issues such as willingness to become an organ
donor, financial incentives for donation, living donation, impediments
to donation, and level of public knowledge about donation. Previous
NSODAPs were conducted during 1993, 2005, 2012, and 2019. Similar to
the 2019 survey, the goal is to complete 10,000 interviews with adults
(18 years of age or older) nationwide. Specifically, this will include
1,000 equal-probability of selection method computer-assisted telephone
interviewing (CATI) interviews, 1,000 ethnic oversamples CATI
interviews, and a supplemental web panel of 8,000 respondents. The
final sample will include 1,000 interviews each with Black/African
Americans, Asians, Hispanics, and Native Americans, and a statistically
sufficient sample for meaningful comparisons across demographic levels
of age group, education, and income groups. A total sample of 10,000 is
necessary to achieve sufficiently large subgroups for statistical
analysis across demographic groups.
Need and Proposed Use of the Information: The Division of
Transplantation, within the Health Systems Bureau of HRSA at the
Department of Health and Human Services, is the primary federal entity
responsible for oversight of the solid organ and blood stem cell
transplant systems in the United States and for initiatives to increase
organ donor registration and donation. Sponsorship of a national survey
on the American public's donation attitudes and practices is one of the
services that the Division of Transplantation provides for the larger
donation community, consistent with its legal authority to establish a
public education and awareness program (section 377A of the Public
Health Service Act, 42 U.S.C. 274f-1).
Patients in need of organ transplantation in the United States face
a longstanding critical shortage of organs. Approximately 103,000
Americans were on the waiting list for transplantation by the end of
2022, but only 42,000 transplants were performed, only meeting two-
fifths of the national need. While this represents an increase in the
number of transplants performed in 2021, the organ shortage remains in
the United States. Understanding public attitudes about organ donation
and how the attitudes change over time is critical to addressing organ
shortage through public awareness and education efforts.
The information from this survey will facilitate appropriate
tailoring and targeting of donation outreach messages and strategies
and provide an overall assessment of the impact of previous outreach
messages and strategies. The data will also inform the development of
policies related to organ donation and transplantation.
Likely Respondents: A nationally representative sample of adults
over the age of 18 with a higher number of responses from populations
of interest such as racial-ethnic minorities, including African
American, Asian, Native American, and Hispanic respondents, as well as
respondents of all age groups and education levels.
Burden Statement: The modes of data collection are web surveys and
CATI interviews and include both landline and cell phones. Respondent
burden is minimized by having automatic data entry either
electronically by the respondent answering the online survey or by a
trained CATI interviewer for a telephone survey that includes no
additional requirements for respondents. The survey will capture only
the minimum necessary information for analysis and will take only about
22 minutes of the respondent's time for the CATI survey and 16 minutes
for the web survey. The questions are the same in both the CATI and web
surveys, but prior research experience by the contractor has found web
surveys take 25 percent less time to complete than the same survey
conducted via phone, because
[[Page 3410]]
respondents can read and click faster than a phone interviewer can read
survey questions.
Burden in this context means the time expended by persons to
generate, maintain, retain, disclose, or provide the information
requested. This includes the time needed to review instructions; to
develop, acquire, install, and utilize technology and systems for the
purpose of collecting, validating, and verifying information,
processing and maintaining information, and disclosing and providing
information; to train personnel and to be able to respond to a
collection of information; to search data sources; to complete and
review the collection of information; and to transmit or otherwise
disclose the information. The total annual burden hours estimated for
this ICR are summarized in the table below.
Total Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of Total burden per Total
Form name respondents responses per responses response burden
respondent (in hours) hours
----------------------------------------------------------------------------------------------------------------
The National Survey of Organ Donation 2,000 1 2,000 0.37 740
Attitudes and Practices (NSODAP)--Telephone
(English and Spanish versions)..............
The National Survey of Organ Donation 8,000 1 8,000 0.27 2,160
Attitudes and Practices (NSODAP)--Web
(English and Spanish versions)..............
------------------------------------------------------------------
Total.................................... 10,000 .............. 10,000 ........... 2,900
----------------------------------------------------------------------------------------------------------------
HRSA specifically requests comments on: (1) the necessity and
utility of the proposed information collection for the proper
performance of the agency's functions; (2) the accuracy of the
estimated burden; (3) ways to enhance the quality, utility, and clarity
of the information to be collected; and (4) the use of automated
collection techniques or other forms of information technology to
minimize the information collection burden.
Maria G. Button,
Director, Executive Secretariat.
[FR Doc. 2024-00819 Filed 1-17-24; 8:45 am]
BILLING CODE 4165-15-P
