Agency Information Collection Activities: Submission to OMB for Review and Approval; Public Comment Request; Questionnaire and Data Collection Testing, Evaluation, and Research for the Health Resources and Services Administration, OMB No. 0915-0379 Revision, 42083-42085 [2023-13829]
Download as PDF
<![CDATA[
42083
Federal Register / Vol. 88, No. 124 / Thursday, June 29, 2023 / Notices
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form name
Rural Communities Opioid Response Program—Implementation/Neonatal Abstinence Syndrome/MAT Expansion ...................................................................................
Rural Communities Opioid Response Program—
Psychostimulant Support ..................................................
Rural Communities Opioid Response Program—MAT Access—NEW ......................................................................
Rural Communities Opioid Response Program—Behavioral Health Care Support—NEW ....................................
Total ..............................................................................
1.24
719.20
15
1
15
1.30
19.50
11
1
11
1.95
21.45
58
1
58
2.02
117.16
374
........................
664
........................
877.31
To
request a copy of the clearance requests
submitted to OMB for review, email
Samantha Miller, the HRSA Information
Collection Clearance Officer, at (301)
443–3983.
SUPPLEMENTARY INFORMATION:
Information Collection Request Title:
Questionnaire and Data Collection
Testing, Evaluation, and Research for
HRSA—OMB No. 0915–0379—Revision.
Abstract: The purpose of information
collections under this generic umbrella
ICR package is to allow HRSA to
continue collecting feedback from
members of the public for HRSA to use
when developing new questions,
questionnaires, and tools; pilot/pre-test
instruments to be deployed by HRSA;
and to identify problems in instruments
currently in use. This generic clearance
is limited to data collection for the
development or revision of HRSA tools
and data collection instruments, as well
as reports for internal decision-making
and development purposes. Information
collected under this generic clearance
will not be used for data collection,
reports, or policy documents to be
released to the public. It is anticipated
that data collection approved under this
generic clearance will rely heavily on
qualitative techniques and not the
collection of numerical data. In general,
these activities are not designed to yield
results that meet generally accepted
standards of statistical rigor but
designed to obtain information to
develop clearer and more effective and
efficient data collection tools that will
yield more accurate results and decrease
public non-response. The forms
submitted under this generic clearance
will be voluntary, low-burden, and
uncontroversial.
HRSA originally developed this
generic umbrella ICR to support similar
needs across HRSA’s bureaus and
FOR FURTHER INFORMATION CONTACT:
Agency Information Collection
Activities: Submission to OMB for
Review and Approval; Public Comment
Request; Questionnaire and Data
Collection Testing, Evaluation, and
Research for the Health Resources and
Services Administration, OMB No.
0915–0379 Revision
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services.
ACTION: Notice.
AGENCY:
In compliance with the
Paperwork Reduction Act of 1995,
HRSA submitted an Information
Collection Request (ICR) to the Office of
Management and Budget (OMB) for
review and approval. Comments
submitted during the first public review
of this ICR will be provided to OMB.
OMB will accept further comments from
the public during the review and
approval period. OMB may act on
HRSA’s ICR only after the 30-day
comment period for this notice has
closed.
SUMMARY:
Comments on this ICR should be
received no later than July 31, 2023.
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
DATES:
VerDate Sep<11>2014
17:21 Jun 28, 2023
Jkt 259001
PO 00000
Frm 00043
Fmt 4703
Total burden
hours
580
[FR Doc. 2023–13827 Filed 6–28–23; 8:45 am]
Health Resources and Services
Administration
Average
burden per
response
(in hours)
2
Public Comments’’ or by using the
search function.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Total
responses
290
Maria G. Button,
Director, Executive Secretariat.
BILLING CODE 4165–15–P
lotter on DSK11XQN23PROD with NOTICES1
Number of
responses per
respondent
(annually)
Sfmt 4703
offices as reflected in their specific
activities informed by their specific
authorizing statutes. The purpose is to
collect qualitative data from small
groups of people in response to short
questionnaires, using questions posed
on HRSA’s website, through focus
groups and individual interviews of
HRSA staff and members of the public.
The abbreviated clearance process of the
generic clearance helps ensure timely
data gathering on current issues HRSA
is addressing (e.g., allows program
offices to gather a suitable pool of
candidates for piloting future
instruments).
HRSA seeks to extend OMB approval
of this ICR and existing ICRs that fall
under it while including a slight
increase in the burden estimate to
account for HRSA’s implementation of
Executive Order 13985, which calls on
agencies to advance racial equity and
support for underserved communities
through identifying and addressing
barriers to equal opportunity that
underserved communities may face;
HRSA will likely conduct additional
information collection requests so that
HRSA may effectively implement this
Executive Order.
A 60-day notice published in the
Federal Register on April 13, 2023, vol.
88, No. 71; pp. 22459–61. There were no
public comments.
Need and Proposed Use of the
Information: HRSA conducts
interviews, focus groups, usability tests,
and field tests/pilot interviews for data
collection instrument development and
evaluation (including assessment of
response errors in data collection
instruments). HRSA staff use various
techniques to evaluate intervieweradministered, self-administered,
telephone, Computer Assisted Personal
Interviewing, Computer Assisted SelfInterviewing, Audio Computer-Assisted
Self-Interviewing, and web-based
questionnaires.
E:\FR\FM\29JNN1.SGM
29JNN1
42084
Federal Register / Vol. 88, No. 124 / Thursday, June 29, 2023 / Notices
Each information collection under
this generic clearance will specify the
specific testing and evaluation
procedures to be used. Participation will
be fully voluntary, and nonparticipation will not affect eligibility
for, or receipt of, future HRSA health
services research activities or grant
awards, recruitment, or participation.
Appropriate consent procedures will be
customized and used for each
information collection activity and any
collection of personal, privacy-protected
information will be handled in
accordance with all applicable federal
requirements. If HRSA wishes to record
the encounter, the respondent’s
permission to record will be obtained
before beginning the interview. If
consent is not provided, the interview
either will not be recorded or not be
conducted. When screening is used
(e.g., quota sampling), the screening will
be as brief as possible, and the screening
questionnaire will be provided to OMB
for review.
Collection methods—The particular
information collection methods used
will vary, but may include the
following:
• Individual in-depth interviews—Indepth interviews will commonly be
used to ensure that the respondent
understands the meaning of a
questionnaire or strategy. When indepth interviewing is used, the
interview guide will be provided to
OMB for review.
• Focus groups—Focus groups will be
used to obtain insights into beliefs and
understandings of the target audience
early in the development of a
questionnaire or tool. When focus
groups are used, the focus group
discussion guide will be provided to
OMB for review.
• Expert/Gatekeeper review of tools—
In some instances, medical providers or
other gatekeepers may review tools to
provide feedback on the acceptability
and usability of a particular tool. This
will usually be in addition to an
individual user pretesting the tool.
• Record abstractions—On occasion,
the development of a tool or other
information collection requires review
and interaction with records, rather than
individuals.
• ‘‘Dress rehearsal’’ of a specific
protocol—In some instances, the
proposed pre-testing will constitute a
walkthrough of the intended data
collection procedure. In these cases, the
request will mirror what is expected to
occur for the larger scale data collection.
Professionally recognized procedures
are followed in each information
collection activity to ensure collection
of high-quality information. Examples of
these procedures could include the
following:
• Monitoring by supervisory staff of
some telephone interviews;
• Conducting interviews using
methods including ‘‘think-aloud’’
techniques and debriefings;
• Computerizing data-entry from mail
or paper-and-pencil surveys using
scannable forms or double-key entry
(i.e., two people input the data from
mail or paper-and-pencil surveys into
an electronic format, and then
comparing the two sets of entries for
anomalies);
• Monitoring by observers of focus
groups and recording (e.g., video
recording, audio recording) of focus
group proceedings (subject to
participant consent); and
• Employing commonly used
statistical validation techniques to
ensure accuracy (such as disallowing
out-of-range values) of data submitted
through on-line surveys.
HRSA is requesting approval for
generic information collections
previously approved by OMB. These
include:
• Health Center Workforce Well-Being
Survey: Listening Sessions
• Health Center Workforce Well-Being
Survey: Cognitive Sessions
• Health Center Workforce Well-Being
Survey: Pilot Testing
• Health Center Workforce Survey
Evaluation and Technical Assistance:
Pilot Survey
• Fast Track Interviews with National
Hypertension Control Initiative Group
2 Participants
HRSA notes that the previously
approved collections are mostly
unchanged, except that they may have
updates to include any advances in
burden estimation or information
collection protocols. HRSA also
anticipates conducting additional
collections as the agency implements
Executive Order 13985. To identify
areas for improvement, HRSA
anticipates collecting and aggregating
data by race, ethnicity, gender,
disability, income, veteran status, or
other key demographic variables, while
protecting individual privacy, so that
HRSA can use the information to help
increase equity in its programs for
people from a robust range of
demographic groups.
Likely Respondents: Participation in
any collections under this clearance will
be entirely voluntary, and the privacy of
respondents will be preserved to the
extent requested by participants and as
permitted by law.
Respondents will be recruited by
means of advertisements in public
venues or through techniques that
replicate prospective data collection
activities that are the focus of the
project. For instance, a survey on
physician communication, designed to
be administered following an office
visit, might be pretested using the same
procedure. Each ICR will specify the
recruitment procedure to be used.
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
respondents
lotter on DSK11XQN23PROD with NOTICES1
Type of information collection
Mail/email 1 ...........................................................................
Telephone ............................................................................
Web-based ...........................................................................
Focus Groups ......................................................................
In-person ..............................................................................
Automated 2 ..........................................................................
VerDate Sep<11>2014
17:21 Jun 28, 2023
Jkt 259001
PO 00000
Frm 00044
Number of
responses per
respondent
1,000
1,000
1,200
925
250
500
Fmt 4703
Sfmt 4703
Total
responses
1
1
1
1
1
1
E:\FR\FM\29JNN1.SGM
1,000
1,000
1,200
925
250
500
29JNN1
Average
burden per
response
(in hours)
0.26
0.26
0.25
1.00
1.00
1.00
Total burden
hours
260
260
300
925
250
500
42085
Federal Register / Vol. 88, No. 124 / Thursday, June 29, 2023 / Notices
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Number of
respondents
Type of information collection
Total
responses
Average
burden per
response
(in hours)
Total burden
hours
Cognitive Testing .................................................................
700
1
700
1.41
987
Total ..............................................................................
5,575
........................
5,575
........................
3482
1 May
2 May
include telephone non-response follow-up in which case the burden will not change.
include testing of database software, Computer Assisted Personal Interviewing software, or other automated technologies.
Maria G. Button,
Director, Executive Secretariat.
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Submission to OMB for
Review and Approval; Public Comment
Request; Information Collection
Request; Application for Federally
Supported Health Centers Assistance
Act/Federal Tort Claims Act
Particularized Determination of
Coverage, 0906–XXXX, New
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 submitted an
Information Collection Request (ICR),
described below, to the Office of
Management and Budget (OMB) for
review and approval. Comments
submitted during the first public review
of this ICR will be provided to OMB.
OMB will accept further comments from
the public during the review and
approval period. OMB may act on
HRSA’s ICR only after the 30-day
comment period for this notice has
closed.
DATES: Comments on this ICR must be
received no later than July 31, 2023.
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.
SUMMARY:
VerDate Sep<11>2014
17:21 Jun 28, 2023
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 Samantha Miller, the HRSA
Information Collection Clearance
Officer, at paperwork@hrsa.gov or call
(301) 443–3983.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the ICR title
for reference.
Information Collection Request Title:
Application for Federally Supported
Health Centers Assistance Act/Federal
Tort Claims Act Particularized
Determination of Coverage. OMB No.
0906–XXXX–New.
Abstract: Section 224(g)–(n) of the
Public Health Service (PHS) Act (42
U.S.C. 233(g)–(n)), as amended,
authorizes the Secretary to ‘‘deem’’
entities receiving funds under section
330 of the PHS Act (HRSA’s Health
Center Program) as PHS employees for
the purposes of establishing eligibility
for liability protections under the
Federally Supported Health Centers
Assistance Act (FSHCAA) including
Federal Tort Claims Act (FTCA)
coverage, for covered activities and
individuals. Health centers submit
deeming applications annually to
HRSA’s Bureau of Primary Health Care,
which administers the Health Center
Program and the Health Center FTCA
Program, in the prescribed form and
manner to obtain deemed PHS
employee status for this purpose.
FSHCAA and 42 CFR 6.6(d) authorize
FTCA coverage for the provision of
medical services to non-health center
patients in certain situations. Section
224(g)(1)(C) of the PHS Act and 42 CFR
6.6(d) explain the criteria by which the
Secretary will determine whether
FSHCAA’s liability protections,
including FTCA coverage, will extend to
the provision of medical care to
individuals who are not patients of the
health center. 42 CFR 6.6(e) identifies
examples that are approvable for FTCA
coverage under 42 CFR 6.6(d) and
section 224(g)(1)(B)(ii) of the PHS Act if
FOR FURTHER INFORMATION CONTACT:
[FR Doc. 2023–13829 Filed 6–28–23; 8:45 am]
lotter on DSK11XQN23PROD with NOTICES1
Number of
responses per
respondent
Jkt 259001
PO 00000
Frm 00045
Fmt 4703
Sfmt 4703
there is compliance with all other
coverage requirements under FSHCAA.
42 CFR 6.6(e)(4) provides examples of
specific activities that the Department
has determined are eligible for
FSCHAA’s liability protections,
including FTCA coverage, without the
need for a specific application for a
coverage determination. As indicated in
42 CFR 6.6(e)(4), if any element of an
activity or arrangement does not fit
squarely into the examples listed in 42
CFR 6.6(e), the covered entity should
request a particularized determination
of coverage. Acts and omissions related
to services provided to individuals who
are not patients of a covered entity that
do not fit squarely within the examples
in 42 CFR 6.6(e)(4) will be covered only
if the Secretary makes a coverage
determination under 42 CFR 6.6(d). The
FTCA program uses a web-based
application system within HRSA’s
Electronic Handbooks (EHB) system for
deeming applications. These electronic
application forms decrease the time and
effort required to complete the older,
paper-based approved deeming
application forms. HRSA is proposing a
new paper application that will be
transitioned into an electronic
application within the EHB system for
Particularized Determinations (PD). PDs
extend liability protections under
FSCHAA, including FTCA coverage, for
certain medical services provided to
individuals who are not patients of a
covered entity. This application will
help ensure health centers provide all
the necessary information required to
make determinations appropriately and
efficiently in response to their requests.
By including the application within the
EHBs, health centers will have access to
all information from prior applications
and have that information readily
available if making future requests. The
paper form of the application is an
interim solution to support health
centers until the electronic application
becomes available in the FTCA module
of the EHBs. After the electronic
application is available in the EHBs, all
PD requests will be submitted
E:\FR\FM\29JNN1.SGM
29JNN1
]]>Agencies
[Federal Register Volume 88, Number 124 (Thursday, June 29, 2023)]
[Notices]
[Pages 42083-42085]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-13829]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Submission to OMB for
Review and Approval; Public Comment Request; Questionnaire and Data
Collection Testing, Evaluation, and Research for the Health Resources
and Services Administration, OMB No. 0915-0379 Revision
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
submitted an Information Collection Request (ICR) to the Office of
Management and Budget (OMB) for review and approval. Comments submitted
during the first public review of this ICR will be provided to OMB. OMB
will accept further comments from the public during the review and
approval period. OMB may act on HRSA's ICR only after the 30-day
comment period for this notice has closed.
DATES: Comments on this ICR should be received no later than July 31,
2023.
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 a copy of the clearance
requests submitted to OMB for review, email Samantha Miller, the HRSA
Information Collection Clearance Officer, at (301) 443-3983.
SUPPLEMENTARY INFORMATION:
Information Collection Request Title: Questionnaire and Data
Collection Testing, Evaluation, and Research for HRSA--OMB No. 0915-
0379--Revision.
Abstract: The purpose of information collections under this generic
umbrella ICR package is to allow HRSA to continue collecting feedback
from members of the public for HRSA to use when developing new
questions, questionnaires, and tools; pilot/pre-test instruments to be
deployed by HRSA; and to identify problems in instruments currently in
use. This generic clearance is limited to data collection for the
development or revision of HRSA tools and data collection instruments,
as well as reports for internal decision-making and development
purposes. Information collected under this generic clearance will not
be used for data collection, reports, or policy documents to be
released to the public. It is anticipated that data collection approved
under this generic clearance will rely heavily on qualitative
techniques and not the collection of numerical data. In general, these
activities are not designed to yield results that meet generally
accepted standards of statistical rigor but designed to obtain
information to develop clearer and more effective and efficient data
collection tools that will yield more accurate results and decrease
public non-response. The forms submitted under this generic clearance
will be voluntary, low-burden, and uncontroversial.
HRSA originally developed this generic umbrella ICR to support
similar needs across HRSA's bureaus and offices as reflected in their
specific activities informed by their specific authorizing statutes.
The purpose is to collect qualitative data from small groups of people
in response to short questionnaires, using questions posed on HRSA's
website, through focus groups and individual interviews of HRSA staff
and members of the public. The abbreviated clearance process of the
generic clearance helps ensure timely data gathering on current issues
HRSA is addressing (e.g., allows program offices to gather a suitable
pool of candidates for piloting future instruments).
HRSA seeks to extend OMB approval of this ICR and existing ICRs
that fall under it while including a slight increase in the burden
estimate to account for HRSA's implementation of Executive Order 13985,
which calls on agencies to advance racial equity and support for
underserved communities through identifying and addressing barriers to
equal opportunity that underserved communities may face; HRSA will
likely conduct additional information collection requests so that HRSA
may effectively implement this Executive Order.
A 60-day notice published in the Federal Register on April 13,
2023, vol. 88, No. 71; pp. 22459-61. There were no public comments.
Need and Proposed Use of the Information: HRSA conducts interviews,
focus groups, usability tests, and field tests/pilot interviews for
data collection instrument development and evaluation (including
assessment of response errors in data collection instruments). HRSA
staff use various techniques to evaluate interviewer-administered,
self-administered, telephone, Computer Assisted Personal Interviewing,
Computer Assisted Self-Interviewing, Audio Computer-Assisted Self-
Interviewing, and web-based questionnaires.
[[Page 42084]]
Each information collection under this generic clearance will
specify the specific testing and evaluation procedures to be used.
Participation will be fully voluntary, and non-participation will not
affect eligibility for, or receipt of, future HRSA health services
research activities or grant awards, recruitment, or participation.
Appropriate consent procedures will be customized and used for each
information collection activity and any collection of personal,
privacy-protected information will be handled in accordance with all
applicable federal requirements. If HRSA wishes to record the
encounter, the respondent's permission to record will be obtained
before beginning the interview. If consent is not provided, the
interview either will not be recorded or not be conducted. When
screening is used (e.g., quota sampling), the screening will be as
brief as possible, and the screening questionnaire will be provided to
OMB for review.
Collection methods--The particular information collection methods
used will vary, but may include the following:
Individual in-depth interviews--In-depth interviews will
commonly be used to ensure that the respondent understands the meaning
of a questionnaire or strategy. When in-depth interviewing is used, the
interview guide will be provided to OMB for review.
Focus groups--Focus groups will be used to obtain insights
into beliefs and understandings of the target audience early in the
development of a questionnaire or tool. When focus groups are used, the
focus group discussion guide will be provided to OMB for review.
Expert/Gatekeeper review of tools--In some instances,
medical providers or other gatekeepers may review tools to provide
feedback on the acceptability and usability of a particular tool. This
will usually be in addition to an individual user pretesting the tool.
Record abstractions--On occasion, the development of a
tool or other information collection requires review and interaction
with records, rather than individuals.
``Dress rehearsal'' of a specific protocol--In some
instances, the proposed pre-testing will constitute a walkthrough of
the intended data collection procedure. In these cases, the request
will mirror what is expected to occur for the larger scale data
collection.
Professionally recognized procedures are followed in each
information collection activity to ensure collection of high-quality
information. Examples of these procedures could include the following:
Monitoring by supervisory staff of some telephone
interviews;
Conducting interviews using methods including ``think-
aloud'' techniques and debriefings;
Computerizing data-entry from mail or paper-and-pencil
surveys using scannable forms or double-key entry (i.e., two people
input the data from mail or paper-and-pencil surveys into an electronic
format, and then comparing the two sets of entries for anomalies);
Monitoring by observers of focus groups and recording
(e.g., video recording, audio recording) of focus group proceedings
(subject to participant consent); and
Employing commonly used statistical validation techniques
to ensure accuracy (such as disallowing out-of-range values) of data
submitted through on-line surveys.
HRSA is requesting approval for generic information collections
previously approved by OMB. These include:
Health Center Workforce Well-Being Survey: Listening Sessions
Health Center Workforce Well-Being Survey: Cognitive Sessions
Health Center Workforce Well-Being Survey: Pilot Testing
Health Center Workforce Survey Evaluation and Technical
Assistance: Pilot Survey
Fast Track Interviews with National Hypertension Control
Initiative Group 2 Participants
HRSA notes that the previously approved collections are mostly
unchanged, except that they may have updates to include any advances in
burden estimation or information collection protocols. HRSA also
anticipates conducting additional collections as the agency implements
Executive Order 13985. To identify areas for improvement, HRSA
anticipates collecting and aggregating data by race, ethnicity, gender,
disability, income, veteran status, or other key demographic variables,
while protecting individual privacy, so that HRSA can use the
information to help increase equity in its programs for people from a
robust range of demographic groups.
Likely Respondents: Participation in any collections under this
clearance will be entirely voluntary, and the privacy of respondents
will be preserved to the extent requested by participants and as
permitted by law.
Respondents will be recruited by means of advertisements in public
venues or through techniques that replicate prospective data collection
activities that are the focus of the project. For instance, a survey on
physician communication, designed to be administered following an
office visit, might be pretested using the same procedure. Each ICR
will specify the recruitment procedure to be used.
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
Type of information collection Number of responses per Total per response Total burden
respondents respondent responses (in hours) hours
----------------------------------------------------------------------------------------------------------------
Mail/email \1\.................. 1,000 1 1,000 0.26 260
Telephone....................... 1,000 1 1,000 0.26 260
Web-based....................... 1,200 1 1,200 0.25 300
Focus Groups.................... 925 1 925 1.00 925
In-person....................... 250 1 250 1.00 250
Automated \2\................... 500 1 500 1.00 500
[[Page 42085]]
Cognitive Testing............... 700 1 700 1.41 987
-------------------------------------------------------------------------------
Total....................... 5,575 .............. 5,575 .............. 3482
----------------------------------------------------------------------------------------------------------------
\1\ May include telephone non-response follow-up in which case the burden will not change.
\2\ May include testing of database software, Computer Assisted Personal Interviewing software, or other
automated technologies.
Maria G. Button,
Director, Executive Secretariat.
[FR Doc. 2023-13829 Filed 6-28-23; 8:45 am]
BILLING CODE 4165-15-P
