[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]


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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.

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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
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                                                     Number of                    Average burden
 Type of information collection      Number of     responses per       Total       per response    Total burden
                                    respondents     respondent       responses      (in hours)         hours
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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
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    Total.......................           5,575  ..............           5,575  ..............            3482
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\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]
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