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Federal Register / Vol. 86, No. 159 / Friday, August 20, 2021 / Notices
time points: Pre before the training, post after the training, and follow-up 46 weeks after the training. The survey will assess; 1 foundational OSH
knowledge; 2 OSH attitudes; 3 selfefficacy for OSH; 4 behavioral intention to use newly learned OSH
skills; 5 OSH training perceptions; and 6 job safety perceptions. Basic demographics and work experience information will also be collected from field pilot participants, but no sensitive or personally identifiable information PII will be collected by NIOSH.
Participants in the training group will be asked to provide reactions to the training during brief post-training feedback sessions, and this data will be
workforce development program participants, and the two trained PacMtn WDC will conduct post-training feedback sessions with the 36 training group participants after each training session. Each survey will take approximately 30 minutes to complete, for a total of 90 minutes per participant to complete all three surveys. The training will take three hours and 20
minutes to administer, and the post training feedback session will take 10
minutes to complete.
CDC requests approval for an estimated 43 annual burden hours.
There are no costs to respondents other than their time to participate.

audio recorded. This field pilot will follow the CDC COVID19 interim guidance for research activities, including in-person activities, in place at the time of the activity. This data collection will serve as a first step in addressing the need for evidence-based, foundational OSH training programs for the workforce development sector, and is aligned with the National Occupational Research Agenda NORA
Healthy Work Design and Well-Being, Services, and Manufacturing goals related to promoting OSH among contingent workers.
As part of the proposed field pilot, NIOSH will administer three online surveys pre, post, and follow-up to 72

ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Workforce Workforce Workforce Workforce
development development development development
program program program program
participant participant participant participant
Number of responses per respondent
Average burden per response in hours
Total burden in hours

Pre-survey
Post-survey
Follow-up Survey
Post training feedback session.

34
29
15
18

1
1 1
1

30/60
30/60
30/60
10/60

17
15
8 3

Total

43

Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Scientific Integrity, Office of Science, Centers for Disease Control and Prevention.
FR Doc. 202117864 Filed 81921; 8:45 am BILLING CODE 416318P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

60Day2121HI; Docket No. CDC2021
0086

Proposed Data Collection Submitted for Public Comment and Recommendations Centers for Disease Control and Prevention CDC, Department of Health and Human Services HHS.
ACTION: Notice with comment period.
AGENCY:

The Centers for Disease Control and Prevention CDC, as part of its continuing effort to reduce public burden and maximize the utility of government information, invites the general public and other Federal agencies the opportunity to comment on a proposed and/or continuing information collection, as required by the Paperwork Reduction Act of 1995.
This notice invites comment on a
SUMMARY:

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proposed information collection project titled Red Carpet Entry RCE Program Implementation Project. This study will prepare for, implement, and evaluate an implementation model of linkage and reengagement to HIV care via a toolkit.
DATES: CDC must receive written comments on or before October 19, 2021.
You may submit comments, identified by Docket No. CDC2021
0086 by any of the following methods:
Federal eRulemaking Portal:
Regulations.gov. Follow the instructions for submitting comments.
Mail: Jeffrey M. Zirger, Information Collection Review Office, Centers for Disease Control and Prevention, 1600
Clifton Road NE, MSD74, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name and Docket Number. CDC will post, without change, all relevant comments to Regulations.gov.

ADDRESSES:

Centers for Disease Control and Prevention
khammond on DSKJM1Z7X2PROD with NOTICES

Number of respondents
Form name
Please note: Submit all comments through the Federal eRulemaking portal regulations.gov or by U.S. mail to the address listed above.

To request more information on the proposed project or to obtain a copy of the information collection plan and instruments, contact Jeffrey M. Zirger,
FOR FURTHER INFORMATION CONTACT:

PO 00000

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Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road, NE, MS
D74, Atlanta, Georgia 30329; phone:
4046397118; Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995 PRA
44 U.S.C. 35013520, Federal agencies must obtain approval from the Office of Management and Budget OMB for each collection of information they conduct or sponsor. In addition, the PRA also requires Federal agencies to provide a 60-day notice in the Federal Register concerning each proposed collection of information, including each new proposed collection, each proposed extension of existing collection of information, and each reinstatement of previously approved information collection before submitting the collection to the OMB for approval. To comply with this requirement, we are publishing this notice of a proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility;
2. Evaluate the accuracy of the agencys estimate of the burden of the
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