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Federal Register / Vol. 86, No. 17 / Thursday, January 28, 2021 / Notices ESTIMATED ANNUALIZED BURDEN HOURSContinued Type of respondents
Number of respondents
Form name
Actual Experiment 1Mobile Robot
Actual Experiment 2Collaborative Robot
NASA Task Load Index
Perceived Safety Questionnaire
Robot Trust Questionnaire

Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Scientific Integrity, Office of Science, Centers for Disease Control and Prevention.
FR Doc. 202101692 Filed 12721; 8:45 am BILLING CODE 416318P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and Prevention 30Day2120QS

Agency Forms Undergoing Paperwork Reduction Act Review In accordance with the Paperwork Reduction Act of 1995, the Centers for Disease Control and Prevention CDC
has submitted the information collection request titled Proposed Data Collection Multi-Site Clinical Assessment of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome MCAM to the Office of Management and Budget OMB for review and approval. CDC previously published a 60-day notice titled Proposed Data Collection Submitted for Public Comment and Recommendations on August 3, 2020
to obtain comments from the public and affected agencies. CDC received three comments related to the previous notice. This notice serves to allow an additional 30 days for public and affected agency comments.
CDC will accept all comments for this proposed information collection project.
The Office of Management and Budget is particularly interested in comments that:

a 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;
b Evaluate the accuracy of the agencies estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used;
c Enhance the quality, utility, and clarity of the information to be collected;
d Minimize the burden of the collection of information on those who are to respond, including, through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submission of responses; and e Assess information collection costs.
To request additional information on the proposed project or to obtain a copy of the information collection plan and instruments, call 404 6397570.
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 30-day ReviewOpen for Public Comments or by using the search function. Direct written comments and/or suggestions regarding the items contained in this notice to the Attention: CDC Desk Officer, Office of Management and Budget, 725 17th Street NW, Washington, DC 20503 or by
Number of responses per respondent
37
37
37
37
37

Average burden per response in hours
1 1
63
63
63

70/60
70/60
1/60
1/60
1/60

fax to 202 3955806. Provide written comments within 30 days of notice publication.
Proposed Project Multi-Site Clinical Assessment of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome MCAMExisting collection in use without an OMB
Control NumberNational Center for Emerging and Zoonotic Infectious Diseases NCEZID, Centers for Disease Control and Prevention CDC.
Background and Brief Description This Multi-site Clinical Assessment of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome MCAM study uses a standardized approach for data collection to examine the heterogeneity of patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome ME/CFS using a clinical epidemiologic longitudinal study with a retrospective and prospective rolling cohort design. The study also aims to address the issue of ME/CFS case definition and improve measures of illness domains by using evidencebased data from multiple clinical practices in the United States. Healthy adults and those with illnesses that share some features with ME/CFS were enrolled in comparison groups.
Children and adolescents with ME/CFS
and healthy participants were also enrolled.
The MCAM study has been conducted in multiple stages following multiple study protocols. The time burden estimates are based on the 20122019
data collection, which is the most recent stage of data collection completed.

ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents Adult Adult Adult Adult Adult

VerDate Sep<11>2014

17:16 Jan 27, 2021

Number of participants
Form name
CDC Symptom Inventory CDCSI/Form A
CDC Symptom Inventory CDCSI/Form B
CDC Symptom Inventory CDCSI
Short Form CDCSI/Checklist
Medical Outcomes Study Short Form 36

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45
20
20
85
85

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Number of responses per participant 1
1 1
1 1

Average burden per response in hrs.
12/60
10/60
8/60
10/60
7/60