Proposed Data Collections Submitted for Public Comment and Recommendations, 13057-13058 [2014-04972]
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13057
Federal Register / Vol. 79, No. 45 / Friday, March 7, 2014 / Notices
SEARCH Phase 3 has completed visits
for 1,839 cohort study participants.
CDC plans to continue information
collection for two additional years, with
minor changes. Participants in the
registry study will continue to complete
a Medication Inventory and an Initial
Participant Survey; however, the inperson study examination will be
discontinued. This change will result in
a decrease in burden per respondent.
CDC estimates that each clinical site
will identify and register an average of
255 cases per year, for a total 1,275
cases across all sites.
No data collection changes are
planned for the cohort study. CDC
estimates that each clinical site will
conduct follow-up on an average of 142
cases per year, for a total of 710 cases
across all sites. The items collected for
each case include a Health
Questionnaire (Youth version), an
additional Health Questionnaire (Parent
version), Center for Epidemiologic
Study-Depression, Quality of Care,
Pediatric Quality of Life Survey (Peds
QL), SEARCH Michigan Neuropathy
Screening Instrument, Diabetes Eating
Survey, Low Blood Sugar Survey,
Supplemental Survey, Tanner Stage,
Retinal Photo, Family Conflict Survey,
Pediatric Diabetes Quality of Life Scale,
Physical Exam, Specimen Collection,
and Food Frequency Questionnaire.
Findings from the registry study will
be used to estimate the incidence of
diabetes in youth in the U.S. Findings
from the cohort study will be used to
estimate the prevalence and incidence
of risk factors and complications
associated with diabetes in youth,
including chronic microvascular
complications (retinopathy,
nephropathy, and autonomic
neuropathy) and selected markers of
macrovascular complications
(hypertension, arterial stiffness) of
diabetes.
Participation is voluntary and there
are no costs to respondents other than
their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden per
response
(in hr)
Number of
responses per
respondent
Type of
respondents
Form name
SEARCH Registry Study Participants .....
Medication Inventory ..................
Initial Participant Survey ............
Health Questionnaire-Youth ......
Health Questionnaire-Parent .....
CES-Depression ........................
Quality of Care ...........................
Peds QL .....................................
SEARCH MNSI Neuropathy ......
Diabetes Eating Survey .............
Low Blood Sugar Survey ...........
Supplemental Survey .................
Tanner Stage .............................
Retinal Photo .............................
Family Conflict Survey ...............
Pediatric Diabetes QOL Scale ...
Physical Exam ...........................
Specimen Collection ..................
Food Frequency Questionnaire
1,275
1,275
710
710
710
710
710
710
710
710
710
710
710
710
710
710
710
710
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
5/60
10/60
15/60
15/60
4/60
13/60
5/60
10/60
5/60
5/60
10/60
5/60
15/60
5/60
5/60
3
20/60
20/60
106
213
178
178
47
154
59
118
59
59
118
59
178
59
59
2,130
237
237
....................................................
........................
........................
........................
4,248
SEARCH Cohort Study Participants .......
Total .................................................
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2014–04974 Filed 3–6–14; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
mstockstill on DSK4VPTVN1PROD with NOTICES
[30Day–14–0138]
Proposed Data Collections Submitted
for Public Comment and
Recommendations
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
18:39 Mar 06, 2014
Jkt 232001
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call (404) 639–7570 or send an
email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC 20503 or by fax to (202) 395–5806.
Written comments should be received
within 30 days of this notice.
Proposed Project
Centers for Disease Control and
Prevention
VerDate Mar<15>2010
Number of
respondents
Pulmonary Function Testing Course
Approval Program, 29 CFR 1910.1043
(OMB No. 0920–0138, Expiration 8/31/
2014)—Revision—The National Institute
for Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention (CDC).
PO 00000
Frm 00023
Fmt 4703
Sfmt 4703
Total burden
(in hr)
Background and Brief Description
NIOSH has the responsibility under
the Occupational Safety and Health
Administration’s Cotton Dust Standard,
29 CFR 1920.1043, for approving
courses to train technicians to perform
pulmonary function testing in the cotton
industry. Successful completion of a
NIOSH-approved course is mandatory
under the standard.
To carry out its responsibility, NIOSH
maintains a Pulmonary Function
Testing Course Approval Program. The
program consists of an application
submitted by potential sponsors
(universities, hospitals, and private
consulting firms) who seek NIOSH
approval to conduct courses, and if
approved, notification to NIOSH of any
course or faculty changes during the
approval period, which is limited to five
years. The application form and added
materials, including an agenda,
E:\FR\FM\07MRN1.SGM
07MRN1
13058
Federal Register / Vol. 79, No. 45 / Friday, March 7, 2014 / Notices
curriculum vitae, and course materials
are reviewed by NIOSH to determine if
the applicant has developed a program
which adheres to the criteria required in
the standard. Following approval, any
subsequent changes to the course are
submitted by course sponsors via letter
or email and reviewed by NIOSH staff
to assure that the changes in faculty or
course content continue to meet course
requirements.
Course sponsors also voluntarily
submit an annual report to inform
NIOSH of their class activity level and
any faculty changes. Sponsors who elect
to have their approval renewed for an
additional 5 year period submit a
renewal application and supporting
documentation for review by NIOSH
staff to ensure the course curriculum
meets all current standard requirements.
Approved course sponsors that elect
to offer NIOSH-Approved Spirometry
Refresher Courses must submit a
separate application and supporting
documents for review by NIOSH staff.
Institutions and organizations
throughout the country voluntarily
submit applications and materials to
become course sponsors and carry out
training. Submissions are required for
NIOSH to evaluate a course and
determine whether it meets the criteria
in the standard and whether technicians
will be adequately trained as mandated
under the standard. NIOSH will
disseminate a one-time customer
satisfaction survey to course directors
and sponsor representatives to evaluate
our service to courses, the effectiveness
of the program changes implemented
since 2005, and the usefulness of
potential Program enhancements.
The annualized figures slightly overestimate the actual burden, due to
rounding of the number of respondents
for even allocation over the three-year
clearance period. The estimated annual
burden to respondents is 201 hours.
There are no costs to respondents other
than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Potential Sponsors ..........................................
Leroy Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2014–04972 Filed 3–6–14; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10518]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, HHS.
ACTION: Notice.
AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995 (the
PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
mstockstill on DSK4VPTVN1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
18:39 Mar 06, 2014
Jkt 232001
NIOSH-Approved Spirometry Testing Course
Application.
Annual Report ................................................
NIOSH-Example of email request for course
change.
NIOSH-Approved Spirometry Course Sponsorship Renewal Application.
NIOSH-Approved
Spirometry
Refresher
Course Application.
One-Time Customer Satisfaction Survey ......
information (including each proposed
extension or reinstatement of an existing
collection of information) and to allow
60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
burden estimates or any other aspect of
this collection of information, including
any of the following subjects: (1) The
necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions;
(2) the accuracy of the estimated
burden; (3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and (4) the use of
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
Comments must be received by
May 6, 2014.
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number (OCN). To be
assured consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
DATES:
PO 00000
Frm 00024
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
Number of
respondents
Form name
Average
burden per
response
(in hours)
3
1
3.5
35
12
1
1
30/60
45/60
13
1
6
10
1
8
23
1
12/60
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number lll, Room C4–26–
05, 7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
1. Access CMS’ Web site address at
https://www.cms.hhs.gov/
PaperworkReductionActof1995.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at
(410) 786–1326.
FOR FURTHER INFORMATION CONTACT:
Reports Clearance Office at (410) 786–
1326
SUPPLEMENTARY INFORMATION:
E:\FR\FM\07MRN1.SGM
07MRN1
]]>Agencies
[Federal Register Volume 79, Number 45 (Friday, March 7, 2014)]
[Notices]
[Pages 13057-13058]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-04972]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-14-0138]
Proposed Data Collections Submitted for Public Comment and
Recommendations
The Centers for Disease Control and Prevention (CDC) publishes a
list of information collection requests under review by the Office of
Management and Budget (OMB) in compliance with the Paperwork Reduction
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call
(404) 639-7570 or send an email to omb@cdc.gov. Send written comments
to CDC Desk Officer, Office of Management and Budget, Washington, DC
20503 or by fax to (202) 395-5806. Written comments should be received
within 30 days of this notice.
Proposed Project
Pulmonary Function Testing Course Approval Program, 29 CFR
1910.1043 (OMB No. 0920-0138, Expiration 8/31/2014)--Revision--The
National Institute for Occupational Safety and Health (NIOSH), Centers
for Disease Control and Prevention (CDC).
Background and Brief Description
NIOSH has the responsibility under the Occupational Safety and
Health Administration's Cotton Dust Standard, 29 CFR 1920.1043, for
approving courses to train technicians to perform pulmonary function
testing in the cotton industry. Successful completion of a NIOSH-
approved course is mandatory under the standard.
To carry out its responsibility, NIOSH maintains a Pulmonary
Function Testing Course Approval Program. The program consists of an
application submitted by potential sponsors (universities, hospitals,
and private consulting firms) who seek NIOSH approval to conduct
courses, and if approved, notification to NIOSH of any course or
faculty changes during the approval period, which is limited to five
years. The application form and added materials, including an agenda,
[[Page 13058]]
curriculum vitae, and course materials are reviewed by NIOSH to
determine if the applicant has developed a program which adheres to the
criteria required in the standard. Following approval, any subsequent
changes to the course are submitted by course sponsors via letter or
email and reviewed by NIOSH staff to assure that the changes in faculty
or course content continue to meet course requirements.
Course sponsors also voluntarily submit an annual report to inform
NIOSH of their class activity level and any faculty changes. Sponsors
who elect to have their approval renewed for an additional 5 year
period submit a renewal application and supporting documentation for
review by NIOSH staff to ensure the course curriculum meets all current
standard requirements.
Approved course sponsors that elect to offer NIOSH-Approved
Spirometry Refresher Courses must submit a separate application and
supporting documents for review by NIOSH staff. Institutions and
organizations throughout the country voluntarily submit applications
and materials to become course sponsors and carry out training.
Submissions are required for NIOSH to evaluate a course and determine
whether it meets the criteria in the standard and whether technicians
will be adequately trained as mandated under the standard. NIOSH will
disseminate a one-time customer satisfaction survey to course directors
and sponsor representatives to evaluate our service to courses, the
effectiveness of the program changes implemented since 2005, and the
usefulness of potential Program enhancements.
The annualized figures slightly over-estimate the actual burden,
due to rounding of the number of respondents for even allocation over
the three-year clearance period. The estimated annual burden to
respondents is 201 hours. There are no costs to respondents other than
their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
NIOSH-Approved 3 1 3.5
Spirometry Testing
Course Application.
Potential Sponsors.................... Annual Report........... 35 1 30/60
NIOSH-Example of email 12 1 45/60
request for course
change.
NIOSH-Approved 13 1 6
Spirometry Course
Sponsorship Renewal
Application.
NIOSH-Approved 10 1 8
Spirometry Refresher
Course Application.
One-Time Customer 23 1 12/60
Satisfaction Survey.
----------------------------------------------------------------------------------------------------------------
Leroy Richardson,
Chief, Information Collection Review Office, Office of Scientific
Integrity, Office of the Associate Director for Science, Office of the
Director, Centers for Disease Control and Prevention.
[FR Doc. 2014-04972 Filed 3-6-14; 8:45 am]
BILLING CODE 4163-18-P
