Agency Information Collection Activities: Proposed Collection; Comment Request, 4908-4910 [2011-1544]
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4908
Federal Register / Vol. 76, No. 18 / Thursday, January 27, 2011 / Notices
on public conduct during advisory
committee meetings.
Dated: January 21, 2011.
Barbara Smith,
Associate Director, Consumer Operated and
Oriented Plan Program, Office of Consumer
Information and Insurance Oversight.
[FR Doc. 2011–1690 Filed 1–24–11; 4:15 pm]
BILLING CODE 4150–03–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Agency for Healthcare Research
and Quality, HHS.
ACTION: Notice.
AGENCY:
This notice announces the
intention of the Agency for Healthcare
Research and Quality (AHRQ) to request
that the Office of Management and
Budget (OMB) approve the proposed
information collection project:
‘‘Understanding Development Methods
from Other Industries to Improve the
Design of Consumer Health IT.’’ In
accordance with the Paperwork
Reduction Act, 44 U.S.C. 3501–3520,
AHRQ invites the public to comment on
this proposed information collection.
DATES: Comments on this notice must be
received by March 28, 2011.
ADDRESSES: Written comments should
be submitted to: Doris Lefkowitz,
Reports Clearance Officer, AHRQ, by email at doris.lefkowitz@AHRQ.hhs.gov.
Copies of the proposed collection
plans, data collection instruments, and
specific details on the estimated burden
can be obtained from the AHRQ Reports
Clearance Officer.
FOR FURTHER INFORMATION CONTACT:
Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427–1477, or by
e-mail at
doris.lefkowitz@AHRQ.hhs.gov.
SUMMARY:
SUPPLEMENTARY INFORMATION:
mstockstill on DSKH9S0YB1PROD with NOTICES
Proposed Project
Understanding Development Methods
from Other Industries to Improve the
Design of Consumer Health IT
Consumer health information
technology (IT) is the collection of tools,
technologies, and artifacts that
individuals can use to support their
health care management tasks (Agarwal
and Khuntia, 2009). Consumer health IT
can play an important role in patients’
efforts to coordinate their care and in
VerDate Mar<15>2010
17:51 Jan 26, 2011
Jkt 223001
ensuring that their personal values and
interests help guide all clinical
decisions. In order to accomplish this,
consumer health IT solutions must take
into account the particular needs of the
consumer.
Useful consumer health IT products
may enhance the quality of health care
by empowering individual consumers to
take a more active, effective, and
collaborative role in their own personal
health care. These products could
provide the following capabilities to
consumers:
• Information storage, archiving, and
retrieval: The capabilities to search
results of past examinations or lab tests,
to interact with electronic versions of
their health records, and identify when
to seek health care services.
• Health monitoring: The capability
to report data (e.g., blood pressure,
weight) from various locations.
• Information seeking and searching:
The capability to interactively search for
a wealth of health-related information.
Despite the potential power of
consumer health IT, consumers have not
adopted these technologies to the same
degree that they have adopted
technology products marketed from
other consumer product industries. One
reason for slow adoption is that the
marketplace lacks robust tools that
allow for the complexity and diversity
of personal health information
management (PHIM) practices. These
types of practices are influenced by a
variety of user and contextual factors,
including demographics, personal
attitudes, the goals and objectives of
users, and the broad range of tasks that
users wish to perform. There is no
comprehensive list of problems that
users encounter as they collect and
reflect on personal information; this
creates a barrier for design of consumer
health IT tools.
New practices for the development of
consumer-facing digital tools are
emerging in a variety of industries. The
success of information management
tools in other industries offers much to
be learned and applied to the health
care field.
In July of 2009, AHRQ held the
Building Bridges: Consumer Needs and
the Design of Health Information
Technology workshop. The workshop
brought together leaders from multiple
disciplines, including health
informatics, health sciences,
information science, consumer health
IT, and human factors to discuss the
diverse needs of different consumer
groups in managing their personal
health information, and how these
needs could be incorporated into the
design of consumer health IT solutions.
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Fmt 4703
Sfmt 4703
The outcome of the workshop was a
framework to further the design of
consumer health IT systems, based on
an understanding of practices that
consumers use in their PHIM. The final
report also included a set of
recommendations for additional work in
the health IT field related to research
and industry and policy. Recognizing
that design plays a key role in consumer
use of personal tools, one researchrelated recommendation that resulted
from the workshop was to investigate
the application of design methodologies
used in other industries to consumer
health IT design.
This project has the following goals:
(1) To investigate the product
development approaches, methods, and
philosophies from a variety of industries
in order to identify promising design
and development techniques that will
be most applicable to consumer health
IT.
(2) To disseminate the project
findings and recommendations to
vendors and developers of consumer
health IT products to assist them in
developing health IT products that are
consumer-focused. This study is being
conducted by AHRQ through its
contractors, Westat and the University
of Wisconsin, pursuant to AHRQ’s
statutory authority to conduct and
support research (1) on health care and
on systems for the delivery of such care,
including activities with respect to
health care technologies, 42 U.S.C.
299a(a)(5), and (2) to advance the use of
computer-based health records, 42
U.S.C. 299b–3(a)(6).
Method of Collection
To achieve the goals of this project the
following activities will be
implemented:
(1) Semi-structured interviews will be
conducted with key informants
identified as being experts in the design,
management, and/or marketing of
consumer products that are relevant to
consumer health IT products. The
purpose of these interviews is to gather
information related to their experiences
in developing consumer products,
focusing on the design processes that
their company uses, how they segment
the market, the role of users in testing
during the various product development
phases, and the factors that affect the
success of their product development
approaches.
(2) The final report will be provided
in PDF format for easy download from
the AHRQ National Resource Center for
Health IT Web site.
Information collected by the study
will support the development of
recommendations for those developers
E:\FR\FM\27JAN1.SGM
27JAN1
4909
Federal Register / Vol. 76, No. 18 / Thursday, January 27, 2011 / Notices
and vendors who design, develop, and
market consumer health IT products.
The ultimate goal is to improve
consumer health IT design and impact
the adoption of this technology by
consumers. This project will identify
principles that led to the success of
other consumer products, so that they
can be evaluated for extension to the
design and development of consumer
health IT.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated
annualized burden hours for the
respondents’ time to participate in this
research. Semi-structured interviews
will be conducted with no more than 15
individuals representing a variety of
consumer-focused industries. The
average burden will be 90 minutes per
interview. The total annual burden is
estimated to be 23 hours.
Exhibit 2 shows the estimated annual
cost burden associated with the
respondent’s time to participate in this
research. The total annual cost burden
is estimated to be $1,770.
EXHIBIT 1—ESTIMATED ANNUALIZED BURDEN HOURS
Number of
technical
experts
Form name
Number of
responses per
expert
Hours per
response
Total burden
hours
Semi-structured interviews ..............................................................................
15
1
1.50
23
Total ..........................................................................................................
15
1
1.50
23
EXHIBIT 2—ESTIMATED ANNUALIZED COST BURDEN
Number of
technical
experts
Form name
Total burden
hours
Average
hourly wage
rate *
Total cost
burden
Semi-structured interviews ..............................................................................
15
23
$76.94
$1,770
Total ..........................................................................................................
15
23
76.94
1,770
* Wage rates calculations were not possible using data from the U.S. Department of Labor, Bureau of Labor Statistics, National Occupational
Employment and Wage Estimates for the United States, Occupational Employment Statistics (OES). The OES categories are too broad to determine a wage rate for a ‘‘Director of Product Development.’’ Instead wage rate calculations are based on information from the Web site
www.salary.com which has a tool providing a range of salaries for a variety of specific job titles. The salary for a ‘‘Product Development Director’’
generally ranges from $130,313 (25th percentile) to $189,771 (75th percentile) with an anticipated median of $160,042. Assuming 2,080 hours
per year (40 hours per week), the resulting median hourly rate is $76.94.
Estimated Annual Costs to the Federal
Government
Exhibit 3 shows the estimated total
and annualized cost to the Federal
Government for this research project.
Since this project’s activities will span
a single year the total and annualized
costs are identical. The estimated total
cost is $409,388.
EXHIBIT 3—ESTIMATED TOTAL AND ANNUAL COST * TO THE FEDERAL GOVERNMENT
Cost component
Total cost
Annualized
cost
Administration and Coordination Activities ..............................................................................................................
Technical Expert Panel ............................................................................................................................................
Environmental Scan and Grey Literature Review ...................................................................................................
OMB Submission Package ......................................................................................................................................
Interviews with Study Participants ...........................................................................................................................
Recommendations for Health IT Vendors and Developers ....................................................................................
Dissemination Activities ...........................................................................................................................................
508 Compliance .......................................................................................................................................................
$91,673
74,217
58,413
11,574
102,018
48,612
14,325
8,556
$91,673
74,217
58,413
11,574
102,018
48,612
14,325
8,556
Total ..................................................................................................................................................................
409,388
409,388
* Costs are fully loaded including overhead, G&A and fees.
mstockstill on DSKH9S0YB1PROD with NOTICES
Request for Comments
In accordance with the above-cited
Paperwork Reduction Act legislation,
comments on AHRQ’s information
collection are requested with regard to
any of the following: (a) Whether the
proposed collection of information is
necessary for the proper performance of
AHRQ healthcare research and
healthcare information dissemination
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functions, including whether the
information will have practical utility;
(b) the accuracy of AHRQ’s estimate of
burden (including hours and costs) of
the proposed collection(s) 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 upon the
respondents, including the use of
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Sfmt 4703
automated collection techniques or
other forms of information technology.
Comments submitted in response to
this notice will be summarized and
included in the Agency’s subsequent
request for OMB approval of the
proposed information collection. All
comments will become a matter of
public record.
E:\FR\FM\27JAN1.SGM
27JAN1
4910
Federal Register / Vol. 76, No. 18 / Thursday, January 27, 2011 / Notices
Dated: January 14, 2011.
Carolyn M. Clancy,
Director.
[FR Doc. 2011–1544 Filed 1–26–11; 8:45 am]
BILLING CODE 4160–90–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–11–0768]
Agency Forms Undergoing Paperwork
Reduction Act Review
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 the CDC Reports Clearance
Officer at (404) 639–5960 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
The Outcome Evaluation of the CDC
National Prevention Information
Network (NPIN, formerly known as the
National AIDS Clearinghouse, OMB No.
0920–0768) -— Revision—National
Center for HIV/AIDS, Viral Hepatitis,
STD, and TB Prevention (NCHHSTP),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
NCHHSTP has the primary
responsibility within the CDC and the
U.S. Public Health Service for the
prevention and control of HIV infection,
viral hepatitis, sexually transmitted
diseases (STDs), and tuberculosis (TB),
as well as for community-based HIV
prevention activities, syphilis, and TB
elimination programs. NPIN serves as
the U.S. reference, referral, and
distribution service for information on
HIV/AIDS, viral hepatitis, STDs, and
TB, supporting NCHHSTP’s mission to
link Americans to prevention,
education, and care services. NPIN is a
critical member of the network of
government agencies, community
organizations, businesses, health
professionals, educators, and human
services providers that educate the
American public about the grave threat
to public health posed by HIV/AIDS,
viral hepatitis, STDs, and TB. NPIN
provides the most comprehensive listing
of HIV/AIDS, viral hepatitis, STD, and
TB resources and services for
prevention partners and the American
public throughout the country and
makes it available on the NPIN Web site.
More than 29 million hits to the Web
site are recorded annually.
To accomplish CDC’s goal of
consistently improving NPIN’s Web site,
and NPIN’s other products and services,
and meet the ever-growing needs of the
prevention professionals, prevention
partners, and the general public, it is
necessary to collect feedback from
visitors to the NPIN Web site and the
users of NPIN’s products and services
on a on-going basis. Every effort has
been made to minimize the burden on
prevention professionals and the general
public.
Evaluation Method and Recruitment
The evaluation will be accomplished
by survey data collection from two
groups—users of the NPIN Web site and
users of NPIN products and services.
Respondents for each survey will
include representatives from
government agencies, community-based
organizations, advocacy organizations,
various other organizations involved in
the prevention and/or treatment of HIV/
AIDS, STDs, TB, and/or viral hepatitis,
and the general public. The NPIN Web
site user survey will be conducted on an
ongoing basis via the Web site and a
blast e-mail reminder will be sent out
annually. The NPIN products and
services user survey will be conducted
on a bi-annual basis with a blast email
sent out every 6 months. When
appropriate, NPIN will distribute the
surveys at conferences and via social
networks. Some of the NPIN Web site
user surveys and the NPIN products and
services surveys will be conducted over
the phone as needed, which will be kept
to an absolute minimum.
The information collected from the
surveys is not intended to provide
statistical data for publication. The
purpose of this activity is solely to
obtain user feedback that will help
identify opportunities to improve the
services and products provided to the
public by NPIN and to ultimately allow
NPIN to fulfill its mission.
Collecting the information described
in this package allows NPIN to:
• Acquire accurate, up-to-date
information from users of the NPIN Web
site, and other products and services on
a regular basis and in a timely manner.
• Identify the service needs of NPIN
users and implement new features to
meet those needs.
• Identify the strengths and
weaknesses of the NPIN Web site, and
others products and services.
• Collect data using a consistent
format.
• Comply with requirements under
the Public Health Service Act, Executive
Order 12862, and GPRA.
• Provide the highest quality
products and services to NPIN users.
Without this information collection,
CDC will be hampered in successfully
carrying out its mission of providing
quality products and services to
populations served. Failure to continue
with our data collection effort would
compromise efforts to meet the
legislative requirement of being as
responsive as possible to the public who
consistently seek information about the
prevention and treatment of HIV/AIDS,
STDS, TB, and viral hepatitis. Moreover,
it would diminish NPIN’s value to the
public in terms of usability and
credibility as a comprehensive Federal
information and education resource.
The total estimated annualized burden
hours are 342.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
mstockstill on DSKH9S0YB1PROD with NOTICES
Type of respondent
Form name
NPIN Web Site User .......................................
NPIN Products and Services User .................
NPIN Web site User Survey ..........................
NPIN Products and Services User Survey ....
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Sfmt 4703
E:\FR\FM\27JAN1.SGM
500
500
27JAN1
Average
burden per
response
(in hours)
Responses
per
respondent
1
2
15/60
13/60
]]>Agencies
[Federal Register Volume 76, Number 18 (Thursday, January 27, 2011)]
[Notices]
[Pages 4908-4910]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-1544]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Agency for Healthcare Research and Quality
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Agency for Healthcare Research and Quality, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces the intention of the Agency for
Healthcare Research and Quality (AHRQ) to request that the Office of
Management and Budget (OMB) approve the proposed information collection
project: ``Understanding Development Methods from Other Industries to
Improve the Design of Consumer Health IT.'' In accordance with the
Paperwork Reduction Act, 44 U.S.C. 3501-3520, AHRQ invites the public
to comment on this proposed information collection.
DATES: Comments on this notice must be received by March 28, 2011.
ADDRESSES: Written comments should be submitted to: Doris Lefkowitz,
Reports Clearance Officer, AHRQ, by e-mail at
doris.lefkowitz@AHRQ.hhs.gov.
Copies of the proposed collection plans, data collection
instruments, and specific details on the estimated burden can be
obtained from the AHRQ Reports Clearance Officer.
FOR FURTHER INFORMATION CONTACT: Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427-1477, or by e-mail at
doris.lefkowitz@AHRQ.hhs.gov.
SUPPLEMENTARY INFORMATION:
Proposed Project
Understanding Development Methods from Other Industries to Improve
the Design of Consumer Health IT Consumer health information technology
(IT) is the collection of tools, technologies, and artifacts that
individuals can use to support their health care management tasks
(Agarwal and Khuntia, 2009). Consumer health IT can play an important
role in patients' efforts to coordinate their care and in ensuring that
their personal values and interests help guide all clinical decisions.
In order to accomplish this, consumer health IT solutions must take
into account the particular needs of the consumer.
Useful consumer health IT products may enhance the quality of
health care by empowering individual consumers to take a more active,
effective, and collaborative role in their own personal health care.
These products could provide the following capabilities to consumers:
Information storage, archiving, and retrieval: The
capabilities to search results of past examinations or lab tests, to
interact with electronic versions of their health records, and identify
when to seek health care services.
Health monitoring: The capability to report data (e.g.,
blood pressure, weight) from various locations.
Information seeking and searching: The capability to
interactively search for a wealth of health-related information.
Despite the potential power of consumer health IT, consumers have
not adopted these technologies to the same degree that they have
adopted technology products marketed from other consumer product
industries. One reason for slow adoption is that the marketplace lacks
robust tools that allow for the complexity and diversity of personal
health information management (PHIM) practices. These types of
practices are influenced by a variety of user and contextual factors,
including demographics, personal attitudes, the goals and objectives of
users, and the broad range of tasks that users wish to perform. There
is no comprehensive list of problems that users encounter as they
collect and reflect on personal information; this creates a barrier for
design of consumer health IT tools.
New practices for the development of consumer-facing digital tools
are emerging in a variety of industries. The success of information
management tools in other industries offers much to be learned and
applied to the health care field.
In July of 2009, AHRQ held the Building Bridges: Consumer Needs and
the Design of Health Information Technology workshop. The workshop
brought together leaders from multiple disciplines, including health
informatics, health sciences, information science, consumer health IT,
and human factors to discuss the diverse needs of different consumer
groups in managing their personal health information, and how these
needs could be incorporated into the design of consumer health IT
solutions. The outcome of the workshop was a framework to further the
design of consumer health IT systems, based on an understanding of
practices that consumers use in their PHIM. The final report also
included a set of recommendations for additional work in the health IT
field related to research and industry and policy. Recognizing that
design plays a key role in consumer use of personal tools, one
research-related recommendation that resulted from the workshop was to
investigate the application of design methodologies used in other
industries to consumer health IT design.
This project has the following goals:
(1) To investigate the product development approaches, methods, and
philosophies from a variety of industries in order to identify
promising design and development techniques that will be most
applicable to consumer health IT.
(2) To disseminate the project findings and recommendations to
vendors and developers of consumer health IT products to assist them in
developing health IT products that are consumer-focused. This study is
being conducted by AHRQ through its contractors, Westat and the
University of Wisconsin, pursuant to AHRQ's statutory authority to
conduct and support research (1) on health care and on systems for the
delivery of such care, including activities with respect to health care
technologies, 42 U.S.C. 299a(a)(5), and (2) to advance the use of
computer-based health records, 42 U.S.C. 299b-3(a)(6).
Method of Collection
To achieve the goals of this project the following activities will
be implemented:
(1) Semi-structured interviews will be conducted with key
informants identified as being experts in the design, management, and/
or marketing of consumer products that are relevant to consumer health
IT products. The purpose of these interviews is to gather information
related to their experiences in developing consumer products, focusing
on the design processes that their company uses, how they segment the
market, the role of users in testing during the various product
development phases, and the factors that affect the success of their
product development approaches.
(2) The final report will be provided in PDF format for easy
download from the AHRQ National Resource Center for Health IT Web site.
Information collected by the study will support the development of
recommendations for those developers
[[Page 4909]]
and vendors who design, develop, and market consumer health IT
products. The ultimate goal is to improve consumer health IT design and
impact the adoption of this technology by consumers. This project will
identify principles that led to the success of other consumer products,
so that they can be evaluated for extension to the design and
development of consumer health IT.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated annualized burden hours for the
respondents' time to participate in this research. Semi-structured
interviews will be conducted with no more than 15 individuals
representing a variety of consumer-focused industries. The average
burden will be 90 minutes per interview. The total annual burden is
estimated to be 23 hours.
Exhibit 2 shows the estimated annual cost burden associated with
the respondent's time to participate in this research. The total annual
cost burden is estimated to be $1,770.
Exhibit 1--Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Number of
Form name technical responses per Hours per Total burden
experts expert response hours
----------------------------------------------------------------------------------------------------------------
Semi-structured interviews...................... 15 1 1.50 23
---------------------------------------------------------------
Total....................................... 15 1 1.50 23
----------------------------------------------------------------------------------------------------------------
Exhibit 2--Estimated Annualized Cost Burden
----------------------------------------------------------------------------------------------------------------
Number of
Form name technical Total burden Average hourly Total cost
experts hours wage rate * burden
----------------------------------------------------------------------------------------------------------------
Semi-structured interviews...................... 15 23 $76.94 $1,770
---------------------------------------------------------------
Total....................................... 15 23 76.94 1,770
----------------------------------------------------------------------------------------------------------------
* Wage rates calculations were not possible using data from the U.S. Department of Labor, Bureau of Labor
Statistics, National Occupational Employment and Wage Estimates for the United States, Occupational Employment
Statistics (OES). The OES categories are too broad to determine a wage rate for a ``Director of Product
Development.'' Instead wage rate calculations are based on information from the Web site www.salary.com which
has a tool providing a range of salaries for a variety of specific job titles. The salary for a ``Product
Development Director'' generally ranges from $130,313 (25th percentile) to $189,771 (75th percentile) with an
anticipated median of $160,042. Assuming 2,080 hours per year (40 hours per week), the resulting median hourly
rate is $76.94.
Estimated Annual Costs to the Federal Government
Exhibit 3 shows the estimated total and annualized cost to the
Federal Government for this research project. Since this project's
activities will span a single year the total and annualized costs are
identical. The estimated total cost is $409,388.
Exhibit 3--Estimated Total and Annual Cost * to the Federal Government
------------------------------------------------------------------------
Annualized
Cost component Total cost cost
------------------------------------------------------------------------
Administration and Coordination $91,673 $91,673
Activities.............................
Technical Expert Panel.................. 74,217 74,217
Environmental Scan and Grey Literature 58,413 58,413
Review.................................
OMB Submission Package.................. 11,574 11,574
Interviews with Study Participants...... 102,018 102,018
Recommendations for Health IT Vendors 48,612 48,612
and Developers.........................
Dissemination Activities................ 14,325 14,325
508 Compliance.......................... 8,556 8,556
-------------------------------
Total............................... 409,388 409,388
------------------------------------------------------------------------
* Costs are fully loaded including overhead, G&A and fees.
Request for Comments
In accordance with the above-cited Paperwork Reduction Act
legislation, comments on AHRQ's information collection are requested
with regard to any of the following: (a) Whether the proposed
collection of information is necessary for the proper performance of
AHRQ healthcare research and healthcare information dissemination
functions, including whether the information will have practical
utility; (b) the accuracy of AHRQ's estimate of burden (including hours
and costs) of the proposed collection(s) 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 upon the respondents, including the use of automated
collection techniques or other forms of information technology.
Comments submitted in response to this notice will be summarized
and included in the Agency's subsequent request for OMB approval of the
proposed information collection. All comments will become a matter of
public record.
[[Page 4910]]
Dated: January 14, 2011.
Carolyn M. Clancy,
Director.
[FR Doc. 2011-1544 Filed 1-26-11; 8:45 am]
BILLING CODE 4160-90-M
