Notice2021-19383
Proposed Collection; 60-Day Comment Request: Federal COVID Response-Audience Feedback To Inform Ongoing Messaging and Strategies for “Combat COVID”
Primary source
Metadata and text below are from the Federal Register, a public-domain U.S. government work. Always verify the official published version before relying on it for any legal matter.
Published
September 7, 2021
Issuing agencies
Health and Human Services DepartmentNational Institutes of Health
Abstract
In compliance with the requirement of the Paperwork Reduction Act of 1995 to provide opportunity for public comment on proposed data collection projects, the National Institutes of Health (NIH), Clinical Center (CC) will publish periodic summaries of proposed projects to be submitted to the Office of Management and Budget (OMB) for review and approval.
Full Text
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[Federal Register Volume 86, Number 170 (Tuesday, September 7, 2021)]
[Notices]
[Pages 50143-50144]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2021-19383]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Proposed Collection; 60-Day Comment Request: Federal COVID
Response--Audience Feedback To Inform Ongoing Messaging and Strategies
for ``Combat COVID''
AGENCY: National Institutes of Health, HHS.
ACTION: Notice.
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SUMMARY: In compliance with the requirement of the Paperwork Reduction
Act of 1995 to provide opportunity for public comment on proposed data
collection projects, the National Institutes of Health (NIH), Clinical
Center (CC) will publish periodic summaries of proposed projects to be
submitted to the Office of Management and Budget (OMB) for review and
approval.
DATES: Comments regarding this information collection are best assured
of having their full effect if received within 60 days of the date of
this publication.
FOR FURTHER INFORMATION CONTACT: To obtain a copy of the data
collection plans and instruments, submit comments in writing, or
request more information on the proposed project, contact: Ms. Mikia P.
Currie, Office of Policy for Extramural Research Administration, 6705
Rockledge Drive, Suite 350, Bethesda, Maryland 20892, or call a non-
toll free number (301) 435-0941 or Email your request, including your
address to: <a href="/cdn-cgi/l/email-protection#4313312c29262037002f262231222d20260131222d202b032e222a2f6d2d2a2b6d242c35"><span class="__cf_email__" data-cfemail="3262405d58575146715e575340535c51577040535c515a725f535b5e1c5c5b5a1c555d44">[email protected]</span></a>. Formal requests for
additional plans and instruments must be requested in writing.
SUPPLEMENTARY INFORMATION: Section 3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 requires: written comments and/or suggestions
from the public and affected agencies are invited to address one or
more of the following points: (1) Whether the proposed collection of
information is necessary for the proper performance of the function of
the agency, including whether the information will have practical
utility; (2) The accuracy of the agency's estimate of the burden of the
proposed collection of information, including the validity of the
methodology and assumptions used; (3) Ways to enhance the quality,
utility, and clarity of the information to be collected; and (4) Ways
to minimize the burden of the collection of information on those who
are to respond, including the use of appropriate automated, electronic,
mechanical, or other technological collection techniques or other forms
of information technology.
Proposed Collection Title: Federal COVID Response--Audience
Feedback to Inform Ongoing Messaging and Strategies for ``Combat
COVID,'' OMB #0925-0769, exp.12/31/2021, EXTENSION, National Institutes
of Health (NIH).
Need and Use of Information Collection: The purpose of the
information collection is to collect routine feedback from the Combat
COVID Initiative's two target audiences (the general public and
healthcare providers) to identify evolving needs and better disseminate
relevant information as it relates to COVID-19 treatment and ACTIV
clinical trial resources, specifically. Data collected will be used to
inform the development and broad dissemination of Combat COVID
resources, including new or enhanced message and material concepts
(e.g., social media ads, digital display ads, out-of-home ads), and/or
web pages (<a href="http://combatcovid.hhs.gov">combatcovid.hhs.gov</a>). Because the COVID-19 treatment
landscape continues to evolve, new evidence-based information continues
to come to the forefront, and audience needs continue to change, it is
critical for the Federal COVID Response (FCR) Team to collect quick
audience feedback from the general public (especially from groups who
have not historically been well-represented in clinical trials) and
healthcare providers to identify these evolving needs. By understanding
target audience needs, the FCR team will be able to properly develop
and broadly disseminate relevant COVID-19 treatment and ACTIV clinical
trial resources.
OMB approval is requested for 1 year. There are no costs to
respondents other than their time. The total estimated annualized
burden hours are 3,528.
Estimated Annualized Burden Hours
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Number of Average time
Type of respondent Number of responses per per response Total annual
respondents respondent (in hours) burden hours
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Consumer Audience Feedback Team Screener........ 120 1 5/60 10
HCP Audience Feedback Team Screener............. 40 1 5/60 3
[[Page 50144]]
Consumer Audience Feedback Activity............. 60 8 1 480
HCP Audience Feedback Activity.................. 20 8 1 160
Benchmark & Follow-Up Web Surveys--Consumer 2,000 5 15/60 2,500
Audience.......................................
Benchmark & Follow-Up Web Survey--HCP Audience.. 300 5 15/60 375
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Total....................................... 2,540 12,300 .............. 3,528
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Dated: September 1, 2021.
Lawrence A. Tabak,
Principal Deputy Director, National Institutes of Health.
[FR Doc. 2021-19383 Filed 9-3-21; 8:45 am]
BILLING CODE 4140-01-P
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