Agency Information Collection Activities: Proposed Collection: Public Comment Request; Questionnaire and Data Collection Testing, Evaluation, and Research for the Health Resources and Services Administration, 11230-11231 [2017-03342]
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11230
Federal Register / Vol. 82, No. 33 / Tuesday, February 21, 2017 / Notices
This data collection enables an
efficient award determination process,
and facilitates reporting on the use of
funds and analysis of program
outcomes.
Likely Respondents: NFLP eligible
applicants. This includes accredited
schools of nursing offering eligible
advanced masters and/or doctoral
degree nursing education programs that
will prepare students to serve as
qualified nursing faculty.
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
Form name
Number of
responses per
respondent
Total
responses
Average
burden per
response
(in hours)
Total burden
hours
NFLP—Program Specific Data Form ..................................
90
1
90
8
720
Total ..............................................................................
90
........................
90
........................
720
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.
Jason E. Bennett,
Director, Division of the Executive Secretariat.
[FR Doc. 2017–03339 Filed 2–17–17; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection: Public
Comment Request; Questionnaire and
Data Collection Testing, Evaluation,
and Research for the Health Resources
and Services Administration
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
sradovich on DSK3GMQ082PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:15 Feb 17, 2017
Jkt 241001
public regarding the burden estimate,
below, or any other aspect of the ICR.
DATES: Comments on this ICR must be
received no later than April 24, 2017.
ADDRESSES: Submit your comments to
paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance
Officer, Room 14N–39, 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 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, in compliance with Section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995.
Information Collection Request Title:
Questionnaire and Data Collection
Testing, Evaluation, and Research for
the Health Resources and Services
Administration, OMB No. 0915–0379—
Extension.
Abstract: The purpose of collections
under this generic clearance is to obtain
formative information from respondents
to develop new questions,
questionnaires, and tools and to identify
problems in instruments currently in
use. This clearance request is limited to
formative research activities
emphasizing data collection, toolkit
development, and estimation
procedures and reports for internal
decision-making and development
purposes and does not extend to the
collection of data for public release or
policy formation. It is anticipated that
these studies will rely heavily on
PO 00000
Frm 00060
Fmt 4703
Sfmt 4703
qualitative techniques to meet their
objective. In general, these activities are
not designed to yield results that meet
generally accepted standards of
statistical rigor but are designed to
obtain valuable formative information to
develop more effective and efficient
data collection tools that will yield more
accurate results and decrease nonresponse.
Need and Proposed Use of the
Information: HRSA conducts cognitive
interviews, focus groups, usability tests,
field tests/pilot interviews, and
experimental research in laboratory and
field settings, both for applied
questionnaire development and for
evaluation as well as more basic
research on response errors in surveys.
HRSA staff use various techniques to
evaluate interviewer administered, selfadministered, telephone, Computer
Assisted Personal Interviewing (CAPI),
Computer Assisted Self-Interviewing
(CASI), Audio Computer-Assisted SelfInterviewing (ACASI), and web-based
questionnaires.
Professionally recognized procedures
are followed in each information
collection activity to ensure high quality
data. Examples of these procedures
could include the following:
• Monitoring by supervisory staff of a
certain percent of telephone interviews;
• Conducting cognitive interviewing
techniques, including think-aloud
techniques and debriefings;
• Data-entry from mail or paper-andpencil surveys will be computerized
through scannable forms or checked
through double-key entry;
• Observers will monitor focus
groups, and focus group proceedings
will be recorded; and
• Data submitted through on-line
surveys will be subjected to statistical
E:\FR\FM\21FEN1.SGM
21FEN1
11231
Federal Register / Vol. 82, No. 33 / Tuesday, February 21, 2017 / Notices
validation techniques to ensure
accuracy, such as disallowing out-ofrange values.
Each request under this generic
clearance will specify the procedures to
be used. Participation will be voluntary,
and non-participation will not affect
eligibility for, or receipt of, future HRSA
health services research activities or
grant awards, recruitment, or
participation. Specific testing and
evaluation procedures will be described
when we notify OMB about each new
request. Consent procedures will be
customized for each information
collection activity, but will include
assurances of confidentiality and the
legislative authority for the activity. If
the encounter is to be recorded, the
respondent’s permission to record will
be obtained before beginning the
interview.
Screening: When screening is
required (e.g., quota sampling), the
screening will be as brief as possible
and the screening questionnaire will be
provided as part of the submission to
OMB.
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 meaning of a
questionnaire or strategy is understood
by the respondent. 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, tools designed for
patients may be reviewed in-depth by
medical providers or other gatekeepers
to provide feedback on the acceptability
and usability of a particular tool. This
would usually be in addition to
pretesting of the tool by the actual
patient or other user.
• 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 pretesting will constitute a
walkthrough of the intended data
collection procedure. In these instances,
the request will mirror what is expected
to occur for the larger scale data
collection.
Likely Respondents: 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 submission to OMB
will specify the specific 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 Information
Collection Request are summarized in
the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of information collection
Number of
responses per
respondent
Total
responses
Average
burden per
response
(in hours)
Total burden
hours
Mail/email 1 ...........................................................................
Telephone ............................................................................
Web-based ...........................................................................
Focus Groups ......................................................................
In-person ..............................................................................
Automated 2 ..........................................................................
Cognitive Testing .................................................................
1,666
1,666
1,666
1,666
1,666
1,666
5,000
1
1
1
1
1
1
1
1,666
1,666
1,666
1,666
1,666
1,666
5,000
0.25
0.25
0.25
1.0
1.0
1.0
1.41
416.5
416.5
416.5
1,666
1,666
1,666
7,050
Total ..............................................................................
14,996
........................
14,996
........................
13,298
1 May
sradovich on DSK3GMQ082PROD with NOTICES
2 May
include telephone non-response follow-up in which case the burden will not change.
include testing of database software, CAPI software, or other automated technologies.
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.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Jason E. Bennett,
Director, Division of the Executive Secretariat.
Health Resources and Services
Administration
[FR Doc. 2017–03342 Filed 2–17–17; 8:45 am]
Agency Information Collection
Activities: Proposed Collection: Public
Comment Request; The National
Health Service Corps and NURSE
Corps Interest Capture Form
BILLING CODE 4165–15–P
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services.
AGENCY:
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17:15 Feb 17, 2017
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PO 00000
Frm 00061
Fmt 4703
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E:\FR\FM\21FEN1.SGM
21FEN1
Agencies
[Federal Register Volume 82, Number 33 (Tuesday, February 21, 2017)]
[Notices]
[Pages 11230-11231]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-03342]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Proposed Collection:
Public Comment Request; Questionnaire and Data Collection Testing,
Evaluation, and Research for the Health Resources and Services
Administration
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 must be received no later than April 24,
2017.
ADDRESSES: Submit your comments to paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance Officer, Room 14N-39, 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 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, in compliance with Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995.
Information Collection Request Title: Questionnaire and Data
Collection Testing, Evaluation, and Research for the Health Resources
and Services Administration, OMB No. 0915-0379--Extension.
Abstract: The purpose of collections under this generic clearance
is to obtain formative information from respondents to develop new
questions, questionnaires, and tools and to identify problems in
instruments currently in use. This clearance request is limited to
formative research activities emphasizing data collection, toolkit
development, and estimation procedures and reports for internal
decision-making and development purposes and does not extend to the
collection of data for public release or policy formation. It is
anticipated that these studies will rely heavily on qualitative
techniques to meet their objective. In general, these activities are
not designed to yield results that meet generally accepted standards of
statistical rigor but are designed to obtain valuable formative
information to develop more effective and efficient data collection
tools that will yield more accurate results and decrease non-response.
Need and Proposed Use of the Information: HRSA conducts cognitive
interviews, focus groups, usability tests, field tests/pilot
interviews, and experimental research in laboratory and field settings,
both for applied questionnaire development and for evaluation as well
as more basic research on response errors in surveys.
HRSA staff use various techniques to evaluate interviewer
administered, self-administered, telephone, Computer Assisted Personal
Interviewing (CAPI), Computer Assisted Self-Interviewing (CASI), Audio
Computer-Assisted Self-Interviewing (ACASI), and web-based
questionnaires.
Professionally recognized procedures are followed in each
information collection activity to ensure high quality data. Examples
of these procedures could include the following:
Monitoring by supervisory staff of a certain percent of
telephone interviews;
Conducting cognitive interviewing techniques, including
think-aloud techniques and debriefings;
Data-entry from mail or paper-and-pencil surveys will be
computerized through scannable forms or checked through double-key
entry;
Observers will monitor focus groups, and focus group
proceedings will be recorded; and
Data submitted through on-line surveys will be subjected
to statistical
[[Page 11231]]
validation techniques to ensure accuracy, such as disallowing out-of-
range values.
Each request under this generic clearance will specify the
procedures to be used. Participation will be voluntary, and non-
participation will not affect eligibility for, or receipt of, future
HRSA health services research activities or grant awards, recruitment,
or participation. Specific testing and evaluation procedures will be
described when we notify OMB about each new request. Consent procedures
will be customized for each information collection activity, but will
include assurances of confidentiality and the legislative authority for
the activity. If the encounter is to be recorded, the respondent's
permission to record will be obtained before beginning the interview.
Screening: When screening is required (e.g., quota sampling), the
screening will be as brief as possible and the screening questionnaire
will be provided as part of the submission to OMB.
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 meaning of a questionnaire or
strategy is understood by the respondent. 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,
tools designed for patients may be reviewed in-depth by medical
providers or other gatekeepers to provide feedback on the acceptability
and usability of a particular tool. This would usually be in addition
to pretesting of the tool by the actual patient or other user.
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 pretesting will constitute a walkthrough of the
intended data collection procedure. In these instances, the request
will mirror what is expected to occur for the larger scale data
collection.
Likely Respondents: 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 submission to OMB will specify the specific
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 Information Collection Request 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\.................. 1,666 1 1,666 0.25 416.5
Telephone....................... 1,666 1 1,666 0.25 416.5
Web-based....................... 1,666 1 1,666 0.25 416.5
Focus Groups.................... 1,666 1 1,666 1.0 1,666
In-person....................... 1,666 1 1,666 1.0 1,666
Automated \2\................... 1,666 1 1,666 1.0 1,666
Cognitive Testing............... 5,000 1 5,000 1.41 7,050
-------------------------------------------------------------------------------
Total....................... 14,996 .............. 14,996 .............. 13,298
----------------------------------------------------------------------------------------------------------------
\1\ May include telephone non-response follow-up in which case the burden will not change.
\2\ May include testing of database software, CAPI software, or other automated technologies.
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.
Jason E. Bennett,
Director, Division of the Executive Secretariat.
[FR Doc. 2017-03342 Filed 2-17-17; 8:45 am]
BILLING CODE 4165-15-P