Findings of Research Misconduct, 61361-61362 [2011-25537]
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Federal Register / Vol. 76, No. 192 / Tuesday, October 4, 2011 / Notices
Sherette.funncoleman@hhs.gov, or call
the Reports Clearance Officer on (202)
690–5683. Send written comments and
recommendations for the proposed
information collections within 30 days
of this notice directly to the OS OMB
Desk Officer; faxed to OMB at 202–395–
5806.
FOR FURTHER INFORMATION CONTACT: To
request additional information, please
contact Sherette.funncoleman@hhs.gov,
or call the Reports Clearance Office on
(202) 690–6162.
SUPPLEMENTARY INFORMATION:
Title: FedStrive Employee Wellness
Program Social Media Survey.
Abstract: The information collection
activity will garner qualitative customer
and stakeholder feedback in an efficient,
timely manner, in accordance with the
Administration’s commitment to
improving service delivery. By
qualitative feedback we mean
information that provides useful
insights on perceptions and opinions,
but are not statistical surveys that yield
quantitative results that can be
generalized to the population of study.
This feedback will provide insights into
customer or stakeholder perceptions,
experiences and expectations, provide
an early warning of issues with service,
or focus attention on areas where
communication, training or changes in
operations might improve delivery of
products or services. These collections
will allow for ongoing, collaborative and
actionable communications between the
Agency and its customers and
stakeholders. It will also allow feedback
to contribute directly to the
improvement of program management.
Feedback collected under this generic
clearance will provide useful
information, but it will not yield data
that can be generalized to the overall
population. This type of generic
clearance for qualitative information
will not be used for quantitative
information collections that are
designed to yield reliably actionable
results, such as monitoring trends over
time or documenting program
performance. Such data uses require
more rigorous designs that address: the
target population to which
generalizations will be made, the
sampling frame, the sample design
(including stratification and clustering),
the precision requirements or power
calculations that justify the proposed
sample size, the expected response rate,
methods for assessing potential nonresponse bias, the protocols for data
collection, and any testing procedures
that were or will be undertaken prior
fielding the study. Depending on the
degree of influence the results are likely
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to have, such collections may still be
eligible for submission for other generic
mechanisms that are designed to yield
quantitative results.
The Agency received 0 comments
were received in response to the 60-day
notice published in the Federal Register
of December 22, 2010 (75 FR 80542).
Below we provide the Department of
Health and Human Services, projected
average estimates for the next three
years:1
Current Actions: New collection of
information.
Type of Review: New Collection.
Affected Public: Individuals and
Households, Businesses and
Organizations, State, Local or Tribal
Government.
Average Expected Annual Number of
Activities
Respondents: 3000.
Annual Responses: 3000.
Frequency of Response: Once per
Request.
Average Minutes per Response: 5.
Burden Hours: 250 total.
An agency may not conduct or
sponsor, and a person is not required to
respond to, a collection of information
unless it displays a currently valid
Office of Management and Budget
control number.
Keith Tucker,
Office of the Secretary, Paperwork Reduction
Act Clearance Officer.
[FR Doc. 2011–25143 Filed 10–3–11; 8:45 am]
BILLING CODE P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
Findings of Research Misconduct
Office of the Secretary, HHS.
Notice.
AGENCY:
ACTION:
Notice is hereby given that
the Office of Research Integrity (ORI)
has taken final action in the following
case:
Scott Weber, Ed.D., MSN, University
of Pittsburgh: Based on the letters from
the Research Integrity Officer at the
University of Pittsburgh (UP), ORI’s
SUMMARY:
1 The 60-day notice included the following
estimate of the aggregate burden hours for this
generic clearance federal-wide:
Average Expected Annual Number of Activities:
25,000.
Average Number of Respondents per Activity:
200.
Annual Responses: 5,000,000.
Frequency of Response: Once per Request.
Average Minutes per Response: 30.
Burden Hours: 2,500,000.
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61361
oversight review, and an admission by
the Respondent, ORI found that Dr.
Scott Weber, former Assistant Professor,
Health and Community Systems, School
of Nursing, UP, engaged in research
misconduct by (1) plagiarizing text and
falsifying data from two publications
supported by U.S. Public Health Service
(PHS) funding (P30 MH60570; HS5
SM52671; PHS employee generated
article) in two unpublished
manuscripts, and (2) including
significant portions of that plagiarized
text in two grant applications to the
National Institutes of Health (NIH) (1
L30 NR010444–01; 1 R03 HD062761–
01).
ORI found that the Respondent
engaged in research misconduct by
plagiarizing text, falsifying data and
references, and fabricating data from
two publications (Mufson, L., Dorta,
K.P., Wickramaratne, P., Nomura, Y.,
Olfson, M., Weissman, M.M. ‘‘A
randomized effectiveness trial of
interpersonal psychotherapy for
depressed adolescents.’’ Arch Gen
Psychiatry 61(6):577–84, 2004 June;
hereafter referred to as ‘‘Mufson et al.
´
2004;’’ and Cho, M.J., Moscicki, E.K.,
Narrow, W.E., Rae, D.S., Locke, B.Z.,
Regier, D.A. ‘‘Concordance between two
measures of depression in the Hispanic
Health and Nutrition Examination
Survey.’’ Soc Psychiatry Psychiatr
Epidemiol. 28(4):156–63, 1993 August;
hereafter referred to as ‘‘Cho et al.,
1993’’) supported by PHS in two journal
article submissions. Specifically, ORI
found that the Respondent plagiarized
more than 90 percent of the text from
Mufson et al. 2004 in a manuscript
entitled ‘‘A randomized effectiveness
trial of psychiatric-mental health nurse
practitioner-administered interpersonal
psychotherapy for sexual minority
adolescents with depression in primary
care clinics’’ and submitted to the
Journal of the American Academy of
Nurse Practitioners (JAANP MS).
Furthermore, the Respondent
plagiarized approximately 66 percent of
the text from Cho et al. 1993 in a
manuscript entitled ‘‘Assessing the
diagnostic predictive power of a
screening tool for depression:
Concordance between the CES–D and
DIS in the Parent Identity Survey’’ and
submitted to the Journal of GLBT Family
Studies (JGMS MS).
In both manuscripts, the Respondent
falsified and fabricated tables and
figures by using all or nearly all of the
data in tables and graphs from the
plagiarized articles while altering
numbers and changing text to represent
data as if from another subject
population; he also copied most of the
original bibliographic references but
E:\FR\FM\04OCN1.SGM
04OCN1
61362
Federal Register / Vol. 76, No. 192 / Tuesday, October 4, 2011 / Notices
falsified 35% of the copied references
from JAANP MS and 25% of the copied
references from JGMS MS, by changing
volume numbers and/or publication
years, apparently to hinder detection of
the plagiarism. The data fabrication
occurred when the Respondent altered
or added values to Table 2 in each
manuscript describing the demographic
characteristics of the study population
that was never studied.
ORI also finds that the Respondent
engaged in research misconduct by
plagiarizing text from Cho et al. 1993 in
two NIH grant applications (1 L30
NR010444–01 and 1 R03 HD062761–01)
by copying substantial word-for-word
portions of the text describing the test
instrument to be used in the proposed
study without citing the Cho et al. 1993
paper.
Dr. Weber has voluntarily agreed for
a period of three (3) years, beginning on
September 7, 2011:
(1) To exclude himself from any
contracting or subcontracting with any
agency of the United States Government
and from eligibility or involvement in
nonprocurement programs of the United
States Government referred to as
‘‘covered transactions’’ pursuant to
HHS’ Implementation (2 CFR part 376 et
seq.) of OMB Guidelines to Agencies on
Governmentwide Debarment and
Suspension, 2 CFR part 180 (collectively
the ‘‘Debarment Regulations’’); and
(2) to exclude himself from serving in
any advisory capacity to PHS including,
but not limited to, service on any PHS
advisory committee, board, and/or peer
review committee, or as a consultant.
FOR FURTHER INFORMATION CONTACT:
Director, Division of Investigative
Oversight, Office of Research Integrity,
1101 Wootton Parkway, Suite 750,
Rockville, MD 20852, (240) 453–8800.
John Dahlberg, Ph.D.,
Director, Division of Investigative Oversight,
Office of Research Integrity.
[FR Doc. 2011–25537 Filed 10–3–11; 8:45 am]
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BILLING CODE 4150–31–P
Vital Statistics of the National Center for
Health Statistics, CDC. The collection of
the data is authorized by 42 U.S.C. 242k.
This submission requests approval to
collect the monthly and annually
summary statistics for three years.
The Monthly Vital Statistics Report
forms provide counts of monthly
occurrences of births, deaths, infant
deaths, marriages, and divorces. Similar
data have been published since 1937
and are the sole source of these data at
the National level. The data are used by
the Department of Health and Human
Services and by other government,
academic, and private research and
commercial organizations in tracking
changes in trends of vital events.
Respondents for the Monthly Vital
Statistics Report Form are registration
officials in each State and Territory, the
District of Columbia, and New York
City. In addition, local (county) officials
in New Mexico who record marriages
occurring and divorces and annulments
granted in each county of New Mexico
will use this form. This form is also
designed to collect counts of monthly
occurrences of births, deaths, infant
deaths, marriages, and divorces
immediately following the month of
occurrence.
The Annual Vital Statistics
Occurrence Report Form collects final
annual counts of marriages and divorces
by month for the United States and for
each State. The statistical counts
requested on this form differ from
provisional estimates obtained on the
Monthly Vital Statistics Report Form in
that they represent complete counts of
marriages, divorces, and annulments
occurring during the months of the prior
year. These final counts are usually
available from State or county officials
about eight months after the end of the
data year. The data are widely used by
government, academic, private research,
and commercial organizations in
tracking changes in trends of family
formation and dissolution. Respondents
for the Annual Vital Statistics
Occurrence Report Form are registration
officials in each State and Territory, the
District of Columbia, and New York
City.
There are no costs to respondents
other than their time.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–11–0213]
Proposed Data Collections Submitted
for Public Comment and
Recommendations
In compliance with the requirement
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on
proposed data collection projects, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the
proposed project or to obtain a copy of
data collection plans and instruments,
call the CDC Reports Clearance Officer
on 404–639–5960 or send comments to
Daniel Holcomb, CDC Reports Clearance
Officer, 1600 Clifton Road, MS–D74,
Atlanta, GA 30333 or send an e-mail to
omb@cdc.gov.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology. Written comments should
be received within 60 days of this
notice.
Proposed Project
National Vital Statistics Report Forms
(OMB No. 0920–0213, Expiration Date
April 30, 2012)—Extension—National
Center for Health Statistics (NCHS),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The compilation of national vital
statistics dates back to the beginning of
the 20th century and has been
conducted since 1960 by the Division of
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondent
Form name
State, Territory and New Mexico
County officials.
Monthly Vital Statistics Report .........
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Number of
responses per
respondent
91
E:\FR\FM\04OCN1.SGM
12
04OCN1
Average
burden per
response
(in hours)
10/60
Total burden
hours
182
Agencies
[Federal Register Volume 76, Number 192 (Tuesday, October 4, 2011)]
[Notices]
[Pages 61361-61362]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-25537]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
Findings of Research Misconduct
AGENCY: Office of the Secretary, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: Notice is hereby given that the Office of Research Integrity
(ORI) has taken final action in the following case:
Scott Weber, Ed.D., MSN, University of Pittsburgh: Based on the
letters from the Research Integrity Officer at the University of
Pittsburgh (UP), ORI's oversight review, and an admission by the
Respondent, ORI found that Dr. Scott Weber, former Assistant Professor,
Health and Community Systems, School of Nursing, UP, engaged in
research misconduct by (1) plagiarizing text and falsifying data from
two publications supported by U.S. Public Health Service (PHS) funding
(P30 MH60570; HS5 SM52671; PHS employee generated article) in two
unpublished manuscripts, and (2) including significant portions of that
plagiarized text in two grant applications to the National Institutes
of Health (NIH) (1 L30 NR010444-01; 1 R03 HD062761-01).
ORI found that the Respondent engaged in research misconduct by
plagiarizing text, falsifying data and references, and fabricating data
from two publications (Mufson, L., Dorta, K.P., Wickramaratne, P.,
Nomura, Y., Olfson, M., Weissman, M.M. ``A randomized effectiveness
trial of interpersonal psychotherapy for depressed adolescents.'' Arch
Gen Psychiatry 61(6):577-84, 2004 June; hereafter referred to as
``Mufson et al. 2004;'' and Cho, M.J., Mo[sacute]cicki, E.K., Narrow,
W.E., Rae, D.S., Locke, B.Z., Regier, D.A. ``Concordance between two
measures of depression in the Hispanic Health and Nutrition Examination
Survey.'' Soc Psychiatry Psychiatr Epidemiol. 28(4):156-63, 1993
August; hereafter referred to as ``Cho et al., 1993'') supported by PHS
in two journal article submissions. Specifically, ORI found that the
Respondent plagiarized more than 90 percent of the text from Mufson et
al. 2004 in a manuscript entitled ``A randomized effectiveness trial of
psychiatric-mental health nurse practitioner-administered interpersonal
psychotherapy for sexual minority adolescents with depression in
primary care clinics'' and submitted to the Journal of the American
Academy of Nurse Practitioners (JAANP MS). Furthermore, the Respondent
plagiarized approximately 66 percent of the text from Cho et al. 1993
in a manuscript entitled ``Assessing the diagnostic predictive power of
a screening tool for depression: Concordance between the CES-D and DIS
in the Parent Identity Survey'' and submitted to the Journal of GLBT
Family Studies (JGMS MS).
In both manuscripts, the Respondent falsified and fabricated tables
and figures by using all or nearly all of the data in tables and graphs
from the plagiarized articles while altering numbers and changing text
to represent data as if from another subject population; he also copied
most of the original bibliographic references but
[[Page 61362]]
falsified 35% of the copied references from JAANP MS and 25% of the
copied references from JGMS MS, by changing volume numbers and/or
publication years, apparently to hinder detection of the plagiarism.
The data fabrication occurred when the Respondent altered or added
values to Table 2 in each manuscript describing the demographic
characteristics of the study population that was never studied.
ORI also finds that the Respondent engaged in research misconduct
by plagiarizing text from Cho et al. 1993 in two NIH grant applications
(1 L30 NR010444-01 and 1 R03 HD062761-01) by copying substantial word-
for-word portions of the text describing the test instrument to be used
in the proposed study without citing the Cho et al. 1993 paper.
Dr. Weber has voluntarily agreed for a period of three (3) years,
beginning on September 7, 2011:
(1) To exclude himself from any contracting or subcontracting with
any agency of the United States Government and from eligibility or
involvement in nonprocurement programs of the United States Government
referred to as ``covered transactions'' pursuant to HHS' Implementation
(2 CFR part 376 et seq.) of OMB Guidelines to Agencies on
Governmentwide Debarment and Suspension, 2 CFR part 180 (collectively
the ``Debarment Regulations''); and
(2) to exclude himself from serving in any advisory capacity to PHS
including, but not limited to, service on any PHS advisory committee,
board, and/or peer review committee, or as a consultant.
FOR FURTHER INFORMATION CONTACT: Director, Division of Investigative
Oversight, Office of Research Integrity, 1101 Wootton Parkway, Suite
750, Rockville, MD 20852, (240) 453-8800.
John Dahlberg, Ph.D.,
Director, Division of Investigative Oversight, Office of Research
Integrity.
[FR Doc. 2011-25537 Filed 10-3-11; 8:45 am]
BILLING CODE 4150-31-P