Agency Information Collection Activities: Proposed Collection: Comment Request; Information Collection Request Title: Survey of Eligible Users of the National Practitioner Data Bank, OMB No. 0915-0366-Reinstatement With Change, 8917 [2021-02757]
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Federal Register / Vol. 86, No. 26 / Wednesday, February 10, 2021 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection:
Comment Request; Information
Collection Request Title: Survey of
Eligible Users of the National
Practitioner Data Bank, OMB No. 0915–
0366—Reinstatement With Change
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services.
ACTION: Notice.
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 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 12, 2021.
ADDRESSES: Written 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 Review—Open for
Public Comments’’ or by using the
search function.
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
SUMMARY:
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:
Survey of Eligible Users of the National
Practitioner Data Bank, OMB No. 0915–
0366—Reinstatement with Change.
Abstract: HRSA plans to survey
National Practitioner Data Bank (NPDB)
users. The purpose of this survey is to
assess the overall satisfaction of the
eligible users of the NPDB. This survey
will evaluate the effectiveness of the
NPDB as a flagging system, source of
information, and its use in decision
making. Furthermore, this survey will
collect information from organizations
and individuals who query the NPDB to
understand and improve their user
experience. This survey is a
reinstatement of the 2012 NPDB survey
with some changes.
A 60-day Notice published in the
Federal Register on October 16, 2020,
vol. 85, No. 201; pp. 65833–34. There
were no comments.
Need and Proposed Use of the
Information: The survey will collect
information regarding the participants’
experiences of querying and reporting to
the NPDB, perceptions of health care
practitioners with reports, impact of
NPDB reports on organizations’
decision-making, and satisfaction with
various NPDB products and services.
The survey will also be administered
to health care practitioners that use the
self-query service provided by the
NPDB. The self-queriers will be asked
about their experiences of querying, the
impact of having reports in the NPDB on
their careers and health care
organizations’ perceptions, and their
satisfaction with various NPDB products
and services. Understanding selfNumber of
respondents
Form name
Number of
responses per
respondent
queriers’ satisfaction and their use of the
information is an important component
of the survey.
Proposed changes to this ICR include
the following:
1. In the proposed entity survey, there
are 37 modules and 258 questions. From
the previous 2012 survey, there are 15
deleted questions and 13 new questions
in addition to proposed changes to 12
survey questions.
2. In the proposed self-query survey,
there are 22 modules and 88 questions.
From the previous 2012 survey, there
are five deleted questions and five new
questions in addition to proposed
changes to two survey questions.
Likely Respondents: Health care
entities and health care practitioners
who are eligible users of the NPDB will
be asked to complete a web-based
survey. Data gathered from the survey
will be compared with previous survey
results. This survey will provide HRSA
with the information necessary for
research purposes and for improving the
usability and effectiveness of the NPDB.
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 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:
Total
responses
Average
burden per
response
(in hours)
Total
burden hours
NPDB Users Entities Respondents .....................................
NPDB Self-Query Respondents ..........................................
15,000
2,000
1
1
15,000
2,000
0.25
0.10
3,750
200
Total ..............................................................................
17,000
........................
17,000
........................
3,950
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
VerDate Sep<11>2014
18:53 Feb 09, 2021
Jkt 253001
use of automated collection techniques
or other forms of information
PO 00000
technology to minimize the information
collection burden.
Maria G. Button,
Director, Executive Secretariat.
[FR Doc. 2021–02757 Filed 2–9–21; 8:45 am]
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Agencies
[Federal Register Volume 86, Number 26 (Wednesday, February 10, 2021)]
[Notices]
[Page 8917]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-02757]
[[Page 8917]]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Proposed Collection:
Comment Request; Information Collection Request Title: Survey of
Eligible Users of the National Practitioner Data Bank, OMB No. 0915-
0366--Reinstatement With Change
AGENCY: Health Resources and Services Administration (HRSA), Department
of Health and Human Services.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: 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 12,
2021.
ADDRESSES: Written 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 Review--Open for
Public Comments'' or by using the search function.
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: Survey of Eligible Users of
the National Practitioner Data Bank, OMB No. 0915-0366--Reinstatement
with Change.
Abstract: HRSA plans to survey National Practitioner Data Bank
(NPDB) users. The purpose of this survey is to assess the overall
satisfaction of the eligible users of the NPDB. This survey will
evaluate the effectiveness of the NPDB as a flagging system, source of
information, and its use in decision making. Furthermore, this survey
will collect information from organizations and individuals who query
the NPDB to understand and improve their user experience. This survey
is a reinstatement of the 2012 NPDB survey with some changes.
A 60-day Notice published in the Federal Register on October 16,
2020, vol. 85, No. 201; pp. 65833-34. There were no comments.
Need and Proposed Use of the Information: The survey will collect
information regarding the participants' experiences of querying and
reporting to the NPDB, perceptions of health care practitioners with
reports, impact of NPDB reports on organizations' decision-making, and
satisfaction with various NPDB products and services.
The survey will also be administered to health care practitioners
that use the self-query service provided by the NPDB. The self-queriers
will be asked about their experiences of querying, the impact of having
reports in the NPDB on their careers and health care organizations'
perceptions, and their satisfaction with various NPDB products and
services. Understanding self-queriers' satisfaction and their use of
the information is an important component of the survey.
Proposed changes to this ICR include the following:
1. In the proposed entity survey, there are 37 modules and 258
questions. From the previous 2012 survey, there are 15 deleted
questions and 13 new questions in addition to proposed changes to 12
survey questions.
2. In the proposed self-query survey, there are 22 modules and 88
questions. From the previous 2012 survey, there are five deleted
questions and five new questions in addition to proposed changes to two
survey questions.
Likely Respondents: Health care entities and health care
practitioners who are eligible users of the NPDB will be asked to
complete a web-based survey. Data gathered from the survey will be
compared with previous survey results. This survey will provide HRSA
with the information necessary for research purposes and for improving
the usability and effectiveness of the NPDB.
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 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:
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Form name Number of responses per Total per response Total burden
respondents respondent responses (in hours) hours
----------------------------------------------------------------------------------------------------------------
NPDB Users Entities Respondents. 15,000 1 15,000 0.25 3,750
NPDB Self-Query Respondents..... 2,000 1 2,000 0.10 200
-------------------------------------------------------------------------------
Total....................... 17,000 .............. 17,000 .............. 3,950
----------------------------------------------------------------------------------------------------------------
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. 2021-02757 Filed 2-9-21; 8:45 am]
BILLING CODE 4165-15-P