Submission for OMB Review; 30-Day Comment Request, Questionnaire Cognitive Interviewing and Pretesting (NCI), 22997-22998 [2014-09446]
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mstockstill on DSK4VPTVN1PROD with NOTICES
Federal Register / Vol. 79, No. 80 / Friday, April 25, 2014 / Notices
‘‘[w]ithin 30 days after the Secretary
receives service of any petition filed
under section 2111 the Secretary shall
publish notice of such petition in the
Federal Register.’’ Set forth below is a
list of petitions received by HRSA on
March 1, 2014, through March 31, 2014.
This list provides the name of
petitioner, city and state of vaccination
(if unknown then city and state of
person or attorney filing claim), and
case number. In cases where the Court
has redacted the name of a petitioner
and/or the case number, the list reflects
such redaction.
Section 2112(b)(2) also provides that
the special master ‘‘shall afford all
interested persons an opportunity to
submit relevant, written information’’
relating to the following:
1. The existence of evidence ‘‘that
there is not a preponderance of the
evidence that the illness, disability,
injury, condition, or death described in
the petition is due to factors unrelated
to the administration of the vaccine
described in the petition,’’ and
2. Any allegation in a petition that the
petitioner either:
(a) ‘‘Sustained, or had significantly
aggravated, any illness, disability,
injury, or condition not set forth in the
Vaccine Injury Table but which was
caused by’’ one of the vaccines referred
to in the Table, or
(b) ‘‘Sustained, or had significantly
aggravated, any illness, disability,
injury, or condition set forth in the
Vaccine Injury Table the first symptom
or manifestation of the onset or
significant aggravation of which did not
occur within the time period set forth in
the Table but which was caused by a
vaccine’’ referred to in the Table.
In accordance with Section
2112(b)(2), all interested persons may
submit written information relevant to
the issues described above in the case of
the petitions listed below. Any person
choosing to do so should file an original
and three (3) copies of the information
with the Clerk of the U.S. Court of
Federal Claims at the address listed
above (under the heading FOR FURTHER
INFORMATION CONTACT), with a copy to
HRSA addressed to Director, Division of
Vaccine Injury Compensation Program,
Healthcare Systems Bureau, 5600
Fishers Lane, Room 11C–26, Rockville,
MD 20857. The Court’s caption
(Petitioner’s Name v. Secretary of Health
and Human Services) and the docket
number assigned to the petition should
be used as the caption for the written
submission. Chapter 35 of title 44,
United States Code, related to
paperwork reduction, does not apply to
information required for purposes of
carrying out the Program.
VerDate Mar<15>2010
16:57 Apr 24, 2014
Jkt 232001
Dated: April 19, 2014.
Mary K. Wakefield,
Administrator.
List of Petitions Filed
1. Dawn Somelofski on behalf of A.S.,
Albany, New York, Court of Federal
Claims No: 14–0169V
2. Mikayla Rose Burchill, St. Charles,
Illinois, Court of Federal Claims No:
14–0176V
3. Matthew Andrews, Cincinnati, Ohio,
Court of Federal Claims No: 14–
0181V
4. Thomas and Ashley Saunders on
behalf of T.A.S., Evans, Georgia,
Court of Federal Claims No: 14–
0184V
5. Michelle Schneider, Washington
District of Columbia, DC, Court of
Federal Claims No: 14–0185V
6. Jana Wilkes on behalf of D.N.T., Fort
Worth, Texas, Court of Federal
Claims No: 14–0186V
7. Itza Mejia on behalf of Brenda Mejia,
Deceased, Downey, California,
Court of Federal Claims No: 14–
0189V
8. Andy De’ on behalf of Annapoorna
‘‘Uma’’ De’, Irving, Texas, Court of
Federal Claims No: 14–0190V
9. Kyle and Shannon Carda on behalf of
G.J.C., Sioux Falls, South Dakota,
Court of Federal Claims No: 14–
0191V
10. Bruce McDonald, Riverdale, Georgia,
Court of Federal Claims No: 14–
0192V
11. Miranda Hoffman, Tuscaloosa,
Alabama, Court of Federal Claims
No: 14–0195V
12. Marie Verdier, Georgetown,
Delaware, Court of Federal Claims
No: 14–0196V
13. Martin D. Casper, San Diego,
California, Court of Federal Claims
No: 14–0197V
14. Stephen Wallen, Colorado Springs,
Colorado, Court of Federal Claims
No: 14–0209V
15. Alex Joiner, Guy C. Joiner, Dwain
Joiner, Dorothy Jean Disher, Linda
Guagliardo, and Robbin Thompson,
on behalf of Henrietta Duplessis
Joiner, Deceased, New Orleans,
Louisiana, Court of Federal Claims
No: 14–0211V
16. Caylee Harrington, Tempe, Arizona,
Court of Federal Claims No: 14–
0212V
17. Melodie Rose on behalf of Allison
Rose, Mountain View, California,
Court of Federal Claims No: 14–
0215V
18. Damien Dufour, Lewiston, Maine,
Court of Federal Claims No: 14–
0219V
19. Michael Foy, Mayfield, Kentucky,
Court of Federal Claims No: 14–
0220V
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22997
20. Cynthia Winward on behalf of James
Winward, Yuba City, California,
Court of Federal Claims No: 14–
0223V
21. Paul Drobbin, West Long Branch,
New Jersey, Court of Federal Claims
No: 14–0225V
22. Bridget Sullivan on behalf of James
Sullivan, Granard, County
Longford, Ireland, Court of Federal
Claims No: 14–0226V
23. Krystyn Snyder, Pittsburgh,
Pennsylvania, Court of Federal
Claims No: 14–0227V
24. Janice D. Whitfield, Kentwood,
Michigan, Court of Federal Claims
No: 14–0231V
25. Lisa Brown and Christopher Brown
on behalf of Z.B., Torrington,
Connecticut, Court of Federal
Claims No: 14–0234V
26. Victoria Nifakos, Loxahatchee,
Florida, Court of Federal Claims No:
14–0236V
27. Linda Leggett, Hattiesburg,
Mississippi, Court of Federal
Claims No: 14–0238V
28. James Schutte on behalf of Carolyn
Schutte, Excelsior Springs,
Missouri, Court of Federal Claims
No: 14–0239V
29. Carey Sweet, Sacramento, California,
Court of Federal Claims No: 14–
0240V
30. Brian Lauer, Boston, Massachusetts,
Court of Federal Claims No: 14–
0244V
31. Joaquim Pereira, Boston,
Massachusetts, Court of Federal
Claims No: 14–0246V
32. Michael Askew, Durham, North
Carolina, Court of Federal Claims
No: 14–0252V
33. Charmaine Johnson on behalf of K.J.,
Houston, Texas, Court of Federal
Claims No: 14–0254V
[FR Doc. 2014–09422 Filed 4–24–14; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Submission for OMB Review; 30-Day
Comment Request, Questionnaire
Cognitive Interviewing and Pretesting
(NCI)
Under the provisions of
Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National
Institutes of Health (NIH), has submitted
to the Office of Management and Budget
(OMB) a request for review and
approval of the information collection
listed below. This proposed information
collection was previously published in
SUMMARY:
E:\FR\FM\25APN1.SGM
25APN1
22998
Federal Register / Vol. 79, No. 80 / Friday, April 25, 2014 / Notices
the Federal Register on January 3, 2014,
(Vol. 79, p. 402) and allowed 60-days for
public comment. No public comments
were received. The purpose of this
notice is to allow an additional 30 days
for public comment. The National
Cancer Institute (NCI), National
Institutes of Health, may not conduct or
sponsor, and the respondent is not
required to respond to, an information
collection that has been extended,
revised, or implemented on or after
October 1, 1995, unless it displays a
currently valid OMB control number.
Direct Comments To OMB: Written
comments and/or suggestions regarding
the item(s) contained in this notice,
especially regarding the estimated
public burden and associated response
time, should be directed to the: Office
of Management and Budget, Office of
Regulatory Affairs, OIRA_submission@
omb.eop.gov or by fax to 202–395–6974,
Attention: NIH Desk Officer.
DATES: Comment Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 30-days of the date of
this publication.
FOR FURTHER INFORMATION CONTACT: To
obtain a copy of the data collection
plans and instruments or request more
information on the proposed project
contact: Gordon Willis, Division of
Cancer Control and Population
Sciences, 9609 Medical Center Drive,
Rm 3E358, Bethesda, MD 20892–9762 or
call non-toll-free number 240–276–6788
or Email your request, including your
address to: willis@mail.nih.gov. Formal
requests for additional plans and
instruments must be requested in
writing.
Proposed Collection: Questionnaire
Cognitive Interviewing and Pretesting
(NCI), 0925–0589, Revision, National
Cancer Institute (NCI), National
Institutes of Health (NIH).
Need and Use of Information
Collection: For many surveys and selfreport-based data collection efforts, it is
advantageous to the government if
development follows a pretesting
sequence equivalent to that used at
National Center for Health Statistics or
the Census Bureau. For example, the
Health Information National Trends
Survey (HINTS: OMB No. 0925–0538)
has undergone multiple cycles of
cognitive testing to refine both the
questionnaire, and supporting materials
such as advance letters and brochures.
The types of activities covered by this
Generic request include: (1) Survey
material development and pretesting
based on cognitive interviewing
methodology and use of focus groups,
(2) Research on the cognitive aspects of
survey methodology, (3) Research on
computer-user interface design for
computer-assisted instruments, also
known as Usability Testing, (4) Pilot
Household interviews are pilot tests
(either personal, telephone, or Webbased) conducted with respondents
using professional field interviewers;
and (5) Formative research that depends
on the use of interviewing techniques to
develop products such as research
priorities, or expert consensus on best
practices. Additionally, formative
research has been increasingly used to
develop new data collection
instruments using psychometric
procedures, including Computerized
Adaptive Testing (CAT). Test-retest
reliability testing can also be used as a
type of formative research in the
development of questionnaires, software
applications that depend on self-report,
and other measurement instruments.
OMB approval is requested for 3
years. There are no costs to respondents
other than their time. The total
estimated annualized burden hours are
3,600.
3-YEAR ESTIMATED BURDEN HOURS
Type of
respondents
Number of
respondents
Physicians, Scientists and similar Respondents .............................................
Experts in their Field ........................................................................................
Administrators/Managers .................................................................................
General Public .................................................................................................
Dated: April 21, 2014.
Vivian Horovitch-Kelley,
NCI Project Clearance Liaison, National
Institutes of Health.
[FR Doc. 2014–09446 Filed 4–24–14; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
mstockstill on DSK4VPTVN1PROD with NOTICES
National Institutes of Health
Submission for OMB Review; 30-Day
Comment Request; Next Series of
Tobacco Use Supplements to the
Current Population Survey (TUS–CPS)
(NCI)
Under the provisions of
Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National
Institutes of Health (NIH), has submitted
to the Office of Management and Budget
SUMMARY:
VerDate Mar<15>2010
16:57 Apr 24, 2014
Jkt 232001
1,200
600
600
1,200
(OMB) a request for review and
approval of the information collection
listed below. This proposed information
collection was previously published in
the Federal Register on January 22
(Volume 79, P. 3598) and allowed 60days for public comment. There were a
total of three comments. Two of the
three comments were requests for a
copy of the questionnaire and plans,
which were sent to the requestors. One
of these requestors commented in
support of FDA’s co-sponsorship with
NCI of the TUS–CPS and NCI/NIH
working with sister agencies and HHS to
harmonize and coordinate tobacco use
information across various federal
surveys. It further stated the importance
of this kind of HHS evaluation with
sister agencies, made specific
suggestions what this should include,
and concluded with offering assistance.
Additionally, the third public comment
PO 00000
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Number of
responses per
respondent
1
1
1
1
Average
burden per
response
(in hours)
75/60
75/60
75/60
30/60
Burden hours
1,500
750
750
600
was about spending of tax-payers’
dollars. The purpose of this notice is to
allow an additional 30 days for public
comment. The National Cancer Institute
(NCI), National Institutes of Health, may
not conduct or sponsor, and the
respondent is not required to respond
to, an information collection that has
been extended, revised, or implemented
on or after October 1, 1995, unless it
displays a currently valid OMB control
number.
Direct Comments to OMB: Written
comments and/or suggestions regarding
the item(s) contained in this notice,
especially regarding the estimated
public burden and associated response
time, should be directed to the: Office
of Management and Budget, Office of
Regulatory Affairs, OIRA_submission@
omb.eop.gov or by fax to 202–395–6974,
Attention: NIH Desk Officer.
E:\FR\FM\25APN1.SGM
25APN1
]]>Agencies
[Federal Register Volume 79, Number 80 (Friday, April 25, 2014)]
[Notices]
[Pages 22997-22998]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-09446]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Submission for OMB Review; 30-Day Comment Request, Questionnaire
Cognitive Interviewing and Pretesting (NCI)
SUMMARY: Under the provisions of Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National Institutes of Health (NIH), has
submitted to the Office of Management and Budget (OMB) a request for
review and approval of the information collection listed below. This
proposed information collection was previously published in
[[Page 22998]]
the Federal Register on January 3, 2014, (Vol. 79, p. 402) and allowed
60-days for public comment. No public comments were received. The
purpose of this notice is to allow an additional 30 days for public
comment. The National Cancer Institute (NCI), National Institutes of
Health, may not conduct or sponsor, and the respondent is not required
to respond to, an information collection that has been extended,
revised, or implemented on or after October 1, 1995, unless it displays
a currently valid OMB control number.
Direct Comments To OMB: Written comments and/or suggestions
regarding the item(s) contained in this notice, especially regarding
the estimated public burden and associated response time, should be
directed to the: Office of Management and Budget, Office of Regulatory
Affairs, OIRA_submission@omb.eop.gov or by fax to 202-395-6974,
Attention: NIH Desk Officer.
DATES: Comment Due Date: Comments regarding this information collection
are best assured of having their full effect if received within 30-days
of the date of this publication.
FOR FURTHER INFORMATION CONTACT: To obtain a copy of the data
collection plans and instruments or request more information on the
proposed project contact: Gordon Willis, Division of Cancer Control and
Population Sciences, 9609 Medical Center Drive, Rm 3E358, Bethesda, MD
20892-9762 or call non-toll-free number 240-276-6788 or Email your
request, including your address to: willis@mail.nih.gov. Formal
requests for additional plans and instruments must be requested in
writing.
Proposed Collection: Questionnaire Cognitive Interviewing and
Pretesting (NCI), 0925-0589, Revision, National Cancer Institute (NCI),
National Institutes of Health (NIH).
Need and Use of Information Collection: For many surveys and self-
report-based data collection efforts, it is advantageous to the
government if development follows a pretesting sequence equivalent to
that used at National Center for Health Statistics or the Census
Bureau. For example, the Health Information National Trends Survey
(HINTS: OMB No. 0925-0538) has undergone multiple cycles of cognitive
testing to refine both the questionnaire, and supporting materials such
as advance letters and brochures. The types of activities covered by
this Generic request include: (1) Survey material development and
pretesting based on cognitive interviewing methodology and use of focus
groups, (2) Research on the cognitive aspects of survey methodology,
(3) Research on computer-user interface design for computer-assisted
instruments, also known as Usability Testing, (4) Pilot Household
interviews are pilot tests (either personal, telephone, or Web-based)
conducted with respondents using professional field interviewers; and
(5) Formative research that depends on the use of interviewing
techniques to develop products such as research priorities, or expert
consensus on best practices. Additionally, formative research has been
increasingly used to develop new data collection instruments using
psychometric procedures, including Computerized Adaptive Testing (CAT).
Test-retest reliability testing can also be used as a type of formative
research in the development of questionnaires, software applications
that depend on self-report, and other measurement instruments.
OMB approval is requested for 3 years. There are no costs to
respondents other than their time. The total estimated annualized
burden hours are 3,600.
3-Year Estimated Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per
Type of respondents respondents responses per response (in Burden hours
respondent hours)
----------------------------------------------------------------------------------------------------------------
Physicians, Scientists and similar Respondents.. 1,200 1 75/60 1,500
Experts in their Field.......................... 600 1 75/60 750
Administrators/Managers......................... 600 1 75/60 750
General Public.................................. 1,200 1 30/60 600
----------------------------------------------------------------------------------------------------------------
Dated: April 21, 2014.
Vivian Horovitch-Kelley,
NCI Project Clearance Liaison, National Institutes of Health.
[FR Doc. 2014-09446 Filed 4-24-14; 8:45 am]
BILLING CODE 4140-01-P
