Agency Forms Undergoing Paperwork Reduction Act Review, 7394-7396 [2021-01914]
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7394
Federal Register / Vol. 86, No. 17 / Thursday, January 28, 2021 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Type of respondents
Number of
respondents
Form name
Actual Experiment 1—Mobile Robot .............................
Actual Experiment 2—Collaborative 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. 2021–01692 Filed 1–27–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–21–20QS]
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) 639–7570.
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 Review—Open
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) 395–5806. Provide written
comments within 30 days of notice
publication.
Proposed Project
Multi-Site Clinical Assessment of
Myalgic Encephalomyelitis/Chronic
Fatigue Syndrome (MCAM)—Existing
collection in use without an OMB
Control Number—National 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 2012–2019
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 (CDC–SI)/Form A ..........................
CDC Symptom Inventory (CDC–SI)/Form B ..........................
CDC Symptom Inventory (CDC–SI) .......................................
Short Form CDC–SI/Checklist ...............................................
Medical Outcomes Study Short Form 36 ...............................
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Fmt 4703
Sfmt 4703
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45
20
20
85
85
28JAN1
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
7395
Federal Register / Vol. 86, No. 17 / Thursday, January 28, 2021 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Type of
respondents
Adult
Adult
Adult
Adult
Adult
........................................
........................................
........................................
........................................
........................................
Adult ........................................
Adult ........................................
Adult ........................................
Adult
Adult
Adult
Adult
Adult
Adult
Adult
Adult
Adult
Adult
Adult
Adult
Adult
Adult
Adult
Adult
Adult
........................................
........................................
........................................
........................................
........................................
........................................
........................................
........................................
........................................
........................................
........................................
........................................
........................................
........................................
........................................
........................................
........................................
Adult ........................................
Adult ........................................
Adult ........................................
Adult ........................................
Adult ........................................
Adult ........................................
Adult ........................................
Adult ........................................
Adult ........................................
Adult ........................................
Pediatric ..................................
Pediatric ..................................
Pediatric ..................................
Pediatric ..................................
Pediatric ..................................
Pediatric
Pediatric
Pediatric
Pediatric
Pediatric
Pediatric
Pediatric
Pediatric
Pediatric
Pediatric
..................................
..................................
..................................
..................................
..................................
..................................
..................................
..................................
..................................
..................................
Pediatric ..................................
Pediatric ..................................
Pediatric ..................................
Pediatric
Pediatric
Pediatric
Pediatric
Pediatric
Pediatric
..................................
..................................
..................................
..................................
..................................
..................................
VerDate Sep<11>2014
17:16 Jan 27, 2021
Multidimensional Fatigue Inventory (MFI–20) ........................
DePaul Symptom Questionnaire (DSQ) ................................
DSQ, 26 selected questions ..................................................
DSQ, 18 selected questions ..................................................
PROMIS Short Form (PROMIS SF—Fatigue, SD, SRI, PB,
PI) & Sleep Data Collection Form.
PROMIS SF—Fatigue, SD, SRI, PB, PI ................................
Brief Pain Inventory (BPI) ......................................................
Patient Health Questionnaire (PHQ–8), Generalized Anxiety
Disorder (GAD–7), CDC Health-Related Quality of Life
(HRQoL–4).
CDC HRQoL–4 .......................................................................
CDC HRQoL–4 with activity limitation questions ...................
Self-Rating Depression Scale (SDS) .....................................
Illness Impact Questionnaire ..................................................
Saliva Data Collection Sheet .................................................
Orthostatic Grading Scale (OGS) ..........................................
COMPosite Autonomic Symptom Score 31 (COMPASS–31)
CDC Symptom Inventory (CDC–SI)/Form A ..........................
CDC Symptom Inventory (CDC–SI)/Form B ..........................
CDC Symptom Inventory (CDC–SI) .......................................
Short Form CDC–SI/Checklist ...............................................
Medical Outcomes Study Short Form 36 ...............................
Multidimensional Fatigue Inventory (MFI–20) ........................
DePaul Symptom Questionnaire (DSQ) ................................
DSQ, 26 selected questions ..................................................
DSQ, 18 selected questions ..................................................
PROMIS Short Form (PROMIS SF—Fatigue, SD, SRI, PB,
PI) & Sleep Data Collection Form.
PROMIS SF—Fatigue, SD, SRI, PB, PI ................................
Brief Pain Inventory (BPI) ......................................................
Patient Health Questionnaire (PHQ–8), Generalized Anxiety
Disorder (GAD–7), CDC Health-Related Quality of Life
(HRQoL–4).
CDC HRQoL–4 .......................................................................
CDC HRQoL–4 with activity limitation questions ...................
Self-Rating Depression Scale (SDS) .....................................
Illness Impact Questionnaire ..................................................
Saliva Data Collection Sheet .................................................
Orthostatic Grading Scale (OGS) ..........................................
COMPosite Autonomic Symptom Score 31 (COMPASS–31)
CDC Symptom Inventory: For Baseline Subjects Pediatrics
CDC Symptom Inventory: For the Follow-Up Subjects Pediatrics.
SF–36 Health Survey .............................................................
Multidimensional Fatigue Inventory (MFI–20) ........................
Selected Questions from DePaul Pediatric Health Questionnaire (DPHQ), 19 Questions.
PROMIS Pediatric Instruments (Fatigue & Pain) ...................
Pediatric Pain Questionnaire (PPQ) ......................................
Visual Analogue Scale ...........................................................
Hospital Anxiety and Depression Scale .................................
Pediatric Daytime Sleepiness Scale ......................................
Social Participation Form Pediatric ........................................
Sociability Form ......................................................................
Saliva Collection Form ...........................................................
CDC Symptom Inventory: For Baseline Subjects Pediatrics
CDC Symptom Inventory: For the Follow-Up Subjects Pediatrics.
SF–36 Health Survey .............................................................
Multidimensional Fatigue Inventory (MFI–20) ........................
Selected Questions from DePaul Pediatric Health Questionnaire (DPHQ), 19 Questions.
PROMIS Pediatric Instruments (Fatigue & Pain) ...................
Pediatric Pain Questionnaire (PPQ) ......................................
Visual Analogue Scale ...........................................................
Hospital Anxiety and Depression Scale .................................
Pediatric Daytime Sleepiness Scale ......................................
Social Participation Form Pediatric ........................................
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PO 00000
Frm 00043
Fmt 4703
Number of
responses per
participant
Number of
participants
Form name
Sfmt 4703
E:\FR\FM\28JAN1.SGM
Average
burden per
response
(in hrs.)
85
45
65
85
85
1
1
1
1
1
5/60
24/60
12/60
6/60
5/60
85
85
85
1
1
1
4/60
13/60
10/60
85
85
45
85
85
85
85
24
30
15
69
69
69
24
45
69
24
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
3/60
4/60
7/60
3/60
5/60
3/60
5/60
42/60
20/60
10/60
20/60
17/60
10/60
36/60
18/60
20/60
6/60
69
24
24
1
1
1
5/60
13/60
10/60
69
69
24
69
69
69
69
36
29
1
1
1
1
1
1
1
1
1
4/60
7/60
7/60
3/60
5/60
5/60
7/60
8/60
6/60
64
64
64
1
1
1
5/60
2/60
5/60
64
64
64
64
64
64
64
64
3
3
1
1
1
1
1
1
1
1
1
1
2/60
7/60
6/60
5/60
2/60
7/60
3/60
5/60
20/60
9/60
3
3
3
1
1
1
9/60
7/60
10/60
3
3
3
3
3
3
1
1
1
1
1
1
3/60
15/60
8/60
7/60
3/60
10/60
28JAN1
7396
Federal Register / Vol. 86, No. 17 / Thursday, January 28, 2021 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Type of
respondents
Form name
Pediatric ..................................
Pediatric ..................................
Adult ........................................
Adult ........................................
Adult ........................................
Adult ........................................
Adult ........................................
Adult ........................................
Adult ........................................
Adult ........................................
Adult ........................................
Adult ........................................
Adult ........................................
Adult ........................................
Adult ........................................
Sociability Form ......................................................................
Saliva Collection Form ...........................................................
CogState Practice Section .....................................................
CogState Baseline Section ....................................................
WAIS IV DS F+B, TOPF ........................................................
Exercise (Bike) Testing ..........................................................
CogState Time 1 Section .......................................................
CogState Time 2 Section .......................................................
CogState Time 3 Section .......................................................
CogState Time 4 Section .......................................................
Visual Analogue Scale for CFS Symptoms ...........................
EQ–5D–Y Health Questionnaire ............................................
PROMIS SF v1—Physical Function .......................................
Physical Fitness and Exercise Activity Levels of Scale .........
International Physical Activity Questionnaire (Self-Administered Long Form).
Physical Activity Readiness Questionnaire ............................
Visual Analogue Scale for CFS Symptoms ...........................
EQ–5D–Y Health Questionnaire ............................................
PROMIS SF v1—Physical Function .......................................
Physical Fitness and Exercise Activity Levels of Scale .........
International Physical Activity Questionnaire (Self-Administered Long Form).
Physical Activity Readiness Questionnaire ............................
Adult
Adult
Adult
Adult
Adult
Adult
........................................
........................................
........................................
........................................
........................................
........................................
Adult ........................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–01914 Filed 1–27–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–21–1129]
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 Improving Fetal
Alcohol Spectrum Disorders Prevention
and Practice through National
Partnerships to the Office of
Management and Budget (OMB) for
review and approval. CDC previously
published a ‘‘Proposed Data Collection
Submitted for Public Comment and
Recommendations’’ notice on October
13, 2020 to obtain comments from the
public and affected agencies. CDC did
not receive 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.
VerDate Sep<11>2014
17:16 Jan 27, 2021
Jkt 253001
Number of
participants
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) 639–7570.
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
PO 00000
Frm 00044
Fmt 4703
Sfmt 4703
Number of
responses per
participant
Average
burden per
response
(in hrs.)
3
3
109
109
109
64
109
109
109
109
60
60
60
60
60
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
5/60
5/60
17/60
27/60
10/60
30/60
22/60
12/60
12/60
12/60
8/60
6/60
5/60
2/60
5/60
60
49
49
49
49
49
1
1
1
1
1
1
5/60
8/60
6/60
5/60
2/60
5/60
49
1
5/60
‘‘Currently under 30-day Review—Open
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
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
Proposed Project
Improving Fetal Alcohol Spectrum
Disorders Prevention and Practice
through National Partnerships (OMB
Control No. 0920–1129, Exp. 8/31/
2019)—Reinstatement with Change—
National Centrer for Birth Defects and
Developmental Disabilities (NCBDDD),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The National Center on Birth Defects
and Developmental Disabilities
(NCBDDD) seeks to collect training
evaluation data from healthcare
practitioners and staff in health systems
where FASD-related practice and
systems changes are implemented, and
from grantees of national partner
organizations related to prevention,
identification, and treatment of fetal
alcohol spectrum disorders (FASDs).
Prenatal exposure to alcohol is a
leading preventable cause of birth
defects and developmental disabilities.
E:\FR\FM\28JAN1.SGM
28JAN1
Agencies
[Federal Register Volume 86, Number 17 (Thursday, January 28, 2021)]
[Notices]
[Pages 7394-7396]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-01914]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-21-20QS]
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) 639-7570. 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 Review--
Open 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 fax to (202)
395-5806. Provide written comments within 30 days of notice
publication.
Proposed Project
Multi-Site Clinical Assessment of Myalgic Encephalomyelitis/Chronic
Fatigue Syndrome (MCAM)--Existing collection in use without an OMB
Control Number--National 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
evidence-based 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
2012-2019 data collection, which is the most recent stage of data
collection completed.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response
participants participant (in hrs.)
----------------------------------------------------------------------------------------------------------------
Adult.............................. CDC Symptom Inventory (CDC- 45 1 12/60
SI)/Form A.
Adult.............................. CDC Symptom Inventory (CDC- 20 1 10/60
SI)/Form B.
Adult.............................. CDC Symptom Inventory (CDC- 20 1 8/60
SI).
Adult.............................. Short Form CDC-SI/Checklist 85 1 10/60
Adult.............................. Medical Outcomes Study 85 1 7/60
Short Form 36.
[[Page 7395]]
Adult.............................. Multidimensional Fatigue 85 1 5/60
Inventory (MFI-20).
Adult.............................. DePaul Symptom 45 1 24/60
Questionnaire (DSQ).
Adult.............................. DSQ, 26 selected questions. 65 1 12/60
Adult.............................. DSQ, 18 selected questions. 85 1 6/60
Adult.............................. PROMIS Short Form (PROMIS 85 1 5/60
SF--Fatigue, SD, SRI, PB,
PI) & Sleep Data
Collection Form.
Adult.............................. PROMIS SF--Fatigue, SD, 85 1 4/60
SRI, PB, PI.
Adult.............................. Brief Pain Inventory (BPI). 85 1 13/60
Adult.............................. Patient Health 85 1 10/60
Questionnaire (PHQ-8),
Generalized Anxiety
Disorder (GAD-7), CDC
Health-Related Quality of
Life (HRQoL-4).
Adult.............................. CDC HRQoL-4................ 85 1 3/60
Adult.............................. CDC HRQoL-4 with activity 85 1 4/60
limitation questions.
Adult.............................. Self-Rating Depression 45 1 7/60
Scale (SDS).
Adult.............................. Illness Impact 85 1 3/60
Questionnaire.
Adult.............................. Saliva Data Collection 85 1 5/60
Sheet.
Adult.............................. Orthostatic Grading Scale 85 1 3/60
(OGS).
Adult.............................. COMPosite Autonomic Symptom 85 1 5/60
Score 31 (COMPASS-31).
Adult.............................. CDC Symptom Inventory (CDC- 24 1 42/60
SI)/Form A.
Adult.............................. CDC Symptom Inventory (CDC- 30 1 20/60
SI)/Form B.
Adult.............................. CDC Symptom Inventory (CDC- 15 1 10/60
SI).
Adult.............................. Short Form CDC-SI/Checklist 69 1 20/60
Adult.............................. Medical Outcomes Study 69 1 17/60
Short Form 36.
Adult.............................. Multidimensional Fatigue 69 1 10/60
Inventory (MFI-20).
Adult.............................. DePaul Symptom 24 1 36/60
Questionnaire (DSQ).
Adult.............................. DSQ, 26 selected questions. 45 1 18/60
Adult.............................. DSQ, 18 selected questions. 69 1 20/60
Adult.............................. PROMIS Short Form (PROMIS 24 1 6/60
SF--Fatigue, SD, SRI, PB,
PI) & Sleep Data
Collection Form.
Adult.............................. PROMIS SF--Fatigue, SD, 69 1 5/60
SRI, PB, PI.
Adult.............................. Brief Pain Inventory (BPI). 24 1 13/60
Adult.............................. Patient Health 24 1 10/60
Questionnaire (PHQ-8),
Generalized Anxiety
Disorder (GAD-7), CDC
Health-Related Quality of
Life (HRQoL-4).
Adult.............................. CDC HRQoL-4................ 69 1 4/60
Adult.............................. CDC HRQoL-4 with activity 69 1 7/60
limitation questions.
Adult.............................. Self-Rating Depression 24 1 7/60
Scale (SDS).
Adult.............................. Illness Impact 69 1 3/60
Questionnaire.
Adult.............................. Saliva Data Collection 69 1 5/60
Sheet.
Adult.............................. Orthostatic Grading Scale 69 1 5/60
(OGS).
Adult.............................. COMPosite Autonomic Symptom 69 1 7/60
Score 31 (COMPASS-31).
Pediatric.......................... CDC Symptom Inventory: For 36 1 8/60
Baseline Subjects
Pediatrics.
Pediatric.......................... CDC Symptom Inventory: For 29 1 6/60
the Follow-Up Subjects
Pediatrics.
Pediatric.......................... SF-36 Health Survey........ 64 1 5/60
Pediatric.......................... Multidimensional Fatigue 64 1 2/60
Inventory (MFI-20).
Pediatric.......................... Selected Questions from 64 1 5/60
DePaul Pediatric Health
Questionnaire (DPHQ), 19
Questions.
Pediatric.......................... PROMIS Pediatric 64 1 2/60
Instruments (Fatigue &
Pain).
Pediatric.......................... Pediatric Pain 64 1 7/60
Questionnaire (PPQ).
Pediatric.......................... Visual Analogue Scale...... 64 1 6/60
Pediatric.......................... Hospital Anxiety and 64 1 5/60
Depression Scale.
Pediatric.......................... Pediatric Daytime 64 1 2/60
Sleepiness Scale.
Pediatric.......................... Social Participation Form 64 1 7/60
Pediatric.
Pediatric.......................... Sociability Form........... 64 1 3/60
Pediatric.......................... Saliva Collection Form..... 64 1 5/60
Pediatric.......................... CDC Symptom Inventory: For 3 1 20/60
Baseline Subjects
Pediatrics.
Pediatric.......................... CDC Symptom Inventory: For 3 1 9/60
the Follow-Up Subjects
Pediatrics.
Pediatric.......................... SF-36 Health Survey........ 3 1 9/60
Pediatric.......................... Multidimensional Fatigue 3 1 7/60
Inventory (MFI-20).
Pediatric.......................... Selected Questions from 3 1 10/60
DePaul Pediatric Health
Questionnaire (DPHQ), 19
Questions.
Pediatric.......................... PROMIS Pediatric 3 1 3/60
Instruments (Fatigue &
Pain).
Pediatric.......................... Pediatric Pain 3 1 15/60
Questionnaire (PPQ).
Pediatric.......................... Visual Analogue Scale...... 3 1 8/60
Pediatric.......................... Hospital Anxiety and 3 1 7/60
Depression Scale.
Pediatric.......................... Pediatric Daytime 3 1 3/60
Sleepiness Scale.
Pediatric.......................... Social Participation Form 3 1 10/60
Pediatric.
[[Page 7396]]
Pediatric.......................... Sociability Form........... 3 1 5/60
Pediatric.......................... Saliva Collection Form..... 3 1 5/60
Adult.............................. CogState Practice Section.. 109 1 17/60
Adult.............................. CogState Baseline Section.. 109 1 27/60
Adult.............................. WAIS IV DS F+B, TOPF....... 109 1 10/60
Adult.............................. Exercise (Bike) Testing.... 64 1 30/60
Adult.............................. CogState Time 1 Section.... 109 1 22/60
Adult.............................. CogState Time 2 Section.... 109 1 12/60
Adult.............................. CogState Time 3 Section.... 109 1 12/60
Adult.............................. CogState Time 4 Section.... 109 1 12/60
Adult.............................. Visual Analogue Scale for 60 1 8/60
CFS Symptoms.
Adult.............................. EQ-5D-Y Health 60 1 6/60
Questionnaire.
Adult.............................. PROMIS SF v1--Physical 60 1 5/60
Function.
Adult.............................. Physical Fitness and 60 1 2/60
Exercise Activity Levels
of Scale.
Adult.............................. International Physical 60 1 5/60
Activity Questionnaire
(Self-Administered Long
Form).
Adult.............................. Physical Activity Readiness 60 1 5/60
Questionnaire.
Adult.............................. Visual Analogue Scale for 49 1 8/60
CFS Symptoms.
Adult.............................. EQ-5D-Y Health 49 1 6/60
Questionnaire.
Adult.............................. PROMIS SF v1--Physical 49 1 5/60
Function.
Adult.............................. Physical Fitness and 49 1 2/60
Exercise Activity Levels
of Scale.
Adult.............................. International Physical 49 1 5/60
Activity Questionnaire
(Self-Administered Long
Form).
Adult.............................. Physical Activity Readiness 49 1 5/60
Questionnaire.
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2021-01914 Filed 1-27-21; 8:45 am]
BILLING CODE 4163-18-P