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-Extension, 20374 [2021-07996]
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Federal Register / Vol. 86, No. 73 / Monday, April 19, 2021 / Notices
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. 2021–07971 Filed 4–16–21; 8:45 am]
BILLING CODE 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—
Extension
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services.
AGENCY:
ACTION:
Notice.
In compliance with 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
SUMMARY:
regarding the burden estimate below or
any other aspect of the ICR.
DATES: Comments on this ICR should be
received no later than June 18, 2021.
ADDRESSES: Submit your comments to
paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance
Officer, 14N136B, 5600 Fishers Lane,
Rockville, MD 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 Lisa Wright-Solomon, the HRSA
Information Collection Clearance Officer
at (301) 443–1984.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the
information request collection title for
reference.
Information Collection Request Title:
National Survey of Organ Donation
Attitudes and Practices, OMB No. 0915–
0290—Extension.
Abstract: HRSA is requesting
approval by OMB for a revision of a
previously approved collection of
information (OMB control number
0915–0290). The National Survey of
Organ Donation Attitudes and Practices
(NSODAP) is conducted approximately
every 6–7 years and serves a critical role
in providing HRSA and the donation
community with data regarding why
Americans choose to donate organs,
current barriers to donation, and
possible paths to increasing donations.
Survey data and derived analytic
insights help HRSA develop and target
appropriate messages for public
outreach and educational initiatives.
Need and Proposed Use of the
Information: HRSA is the primary
federal entity responsible for oversight
of the solid organ and blood stem cell
transplant systems and initiatives to
increase organ donor registration and
donation in the United States. This
survey is the primary method by which
HRSA can obtain information from
Americans about organ donation
attitudes and beliefs. OMB previously
approved this survey and HRSA fielded
it during 2005, 2012, and 2019. Results
of the data collected from this survey
will help develop appropriate messages
for future public outreach and
educational initiatives to increase
awareness about organ donation and
ultimately the number of registered
donors.
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: 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 collecting,
validating, verifying, processing and
maintaining information, and disclosing
and providing information; to train
personnel and 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. A summary of the total
annual burden hours estimated for this
ICR is in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS
jbell on DSKJLSW7X2PROD with NOTICES
Number of
responses per
respondent
Number of
respondents
Form name
Total
responses
Average
burden per
response
(in hours)
Total burden
hours
NSODAP Revised Survey—Telephone .............................
NSODAP Revised Survey—Online Panel .........................
2,000
8,000
1
1
2,000
8,000
0.37
0.27
740
2,160
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
VerDate Sep<11>2014
17:11 Apr 16, 2021
Jkt 253001
or other forms of information
technology to minimize the information
collection burden.
Maria G. Button,
Director, Executive Secretariat.
[FR Doc. 2021–07996 Filed 4–16–21; 8:45 am]
BILLING CODE 4165–15–P
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Meeting of the COVID–19 Health Equity
Task Force
Office of the Assistant
Secretary for Health, Office of the
Secretary, Department of Health and
Human Services.
AGENCY:
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[Federal Register Volume 86, Number 73 (Monday, April 19, 2021)]
[Notices]
[Page 20374]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-07996]
-----------------------------------------------------------------------
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--
Extension
AGENCY: Health Resources and Services Administration (HRSA), Department
of Health and Human Services.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with 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 June 18,
2021.
ADDRESSES: Submit your comments to [email protected] or mail the HRSA
Information Collection Clearance Officer, 14N136B, 5600 Fishers Lane,
Rockville, MD 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 Lisa Wright-
Solomon, the HRSA Information Collection Clearance Officer at (301)
443-1984.
SUPPLEMENTARY INFORMATION: When submitting comments or requesting
information, please include the information request collection title
for reference.
Information Collection Request Title: National Survey of Organ
Donation Attitudes and Practices, OMB No. 0915-0290--Extension.
Abstract: HRSA is requesting approval by OMB for a revision of a
previously approved collection of information (OMB control number 0915-
0290). The National Survey of Organ Donation Attitudes and Practices
(NSODAP) is conducted approximately every 6-7 years and serves a
critical role in providing HRSA and the donation community with data
regarding why Americans choose to donate organs, current barriers to
donation, and possible paths to increasing donations. Survey data and
derived analytic insights help HRSA develop and target appropriate
messages for public outreach and educational initiatives.
Need and Proposed Use of the Information: HRSA is the primary
federal entity responsible for oversight of the solid organ and blood
stem cell transplant systems and initiatives to increase organ donor
registration and donation in the United States. This survey is the
primary method by which HRSA can obtain information from Americans
about organ donation attitudes and beliefs. OMB previously approved
this survey and HRSA fielded it during 2005, 2012, and 2019. Results of
the data collected from this survey will help develop appropriate
messages for future public outreach and educational initiatives to
increase awareness about organ donation and ultimately the number of
registered donors.
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: 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 collecting, validating, verifying, processing and
maintaining information, and disclosing and providing information; to
train personnel and 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. A
summary of the total annual burden hours estimated for this ICR is in
the table below.
Total Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of Total burden per Total burden
Form name respondents responses per responses response (in hours
respondent hours)
----------------------------------------------------------------------------------------------------------------
NSODAP Revised Survey-- 2,000 1 2,000 0.37 740
Telephone.....................
NSODAP Revised Survey--Online 8,000 1 8,000 0.27 2,160
Panel.........................
--------------------------------------------------------------------------------
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. 2021-07996 Filed 4-16-21; 8:45 am]
BILLING CODE 4165-15-P
