[Federal Register Volume 75, Number 145 (Thursday, July 29, 2010)]
[Notices]
[Pages 44796-44798]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2010-18413]
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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.
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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: ``Eisenberg Center Voluntary Customer Survey Generic Clearance
for the Agency for Health Care Research and Quality.'' In accordance
with the Paperwork Reduction Act, 44 U.S.C. 3501-3520, AHRQ invites the
public to comment on this proposed information collection.
This proposed information collection was previously published in
the Federal Register on May 20th, 2010 and allowed 60 days for public
comment. One comment was received. The purpose of this notice is to
allow an additional 30 days for public comment.
DATES: Comments on this notice must be received by August 30, 2010.
ADDRESSES: Written comments should be submitted to: AHRQs OMB Desk
Officer by fax at (202) 395-6974 (attention: AHRQ's desk officer) or by
e-mail at [email protected] (attention: AHRQ's desk
officer).
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
[email protected].
SUPPLEMENTARY INFORMATION:
Proposed Project
Eisenberg Center Voluntary Customer Survey Generic Clearance for
the Agency for Healthcare Research and Quality The Agency for
Healthcare Research and Quality (AHRQ) requests that the Office of
Management and Budget (OMB) renew, under the Paperwork Reduction Act of
1995, AHRQ's Generic Clearance to collect information from users of
work products and services initiated by the John M. Eisenberg Clinical
Decisions and Communications Science Center (Eisenberg Center).
AHRQ is the lead agency charged with supporting research designed
to improve the quality of healthcare, reduce its cost, improve patient
safety, decrease medical errors, and broaden access to essential
services. See 42 U.S.C. 299.
AHRQ's Eisenberg Center is an innovative effort aimed at improving
communication of findings to a variety of audiences (``customers''),
including consumers, clinicians, and health care policy makers. The
Eisenberg Center compiles research results into a variety of useful
formats for customer stakeholders. The Eisenberg Center also conducts
its own program of research into effective communication of research
findings in order to improve the usability and rapid incorporation of
findings into medical practice. The Eisenberg Center is one of three
components of AHRQ's Effective Health Care Program, see 42 U.S.C. 299b-
7. For the period 2005 until September 2008, the Eisenberg Center was
operated through a contractual arrangement with the Oregon Health and
Science University (OHSU), Department of Medicine, located in Portland,
Oregon. In September 2008, the contract for operation of the Eisenberg
Center was awarded to Baylor College of Medicine (BCM), located in
Houston Texas.
The collections proposed under this clearance include activities to
assist in the development of materials to be disseminated through the
Eisenberg Center and to provide feedback to AHRQ on the extent to which
these products meet customer needs. These materials include Summary
Guides that summarize and translate the findings of comparative
effectiveness reviews (CER) and research reports for purposes of
summarizing research findings for various decision-making audiences,
such as consumers, clinicians, or policymakers. The guides are designed
to help these decision makers use research evidence to maximize the
benefits of health care, minimize harm, and optimize the use of health
care resources. In addition, each year of the project the Eisenberg
Center will develop one computerized, interactive decision aid for
those clinical problems identified from selected CERs. The intent is
for the decision aid to increase the patient/consumer's knowledge of
the health condition, options, and risk/benefits, lead to greater
assurance in making a decision, increase the congruence between values
and choices, and enhance involvement in the decision making process.
Information collections conducted under this generic clearance are not
required by regulation and will not be used to regulate or sanction
customers. Surveys will be entirely voluntary, and information provided
by respondents will be combined and summarized so that no individually
identifiable information will be released. The Eisenberg Center will
produce from 17 to a maximum of 33 Summary Guides per audience (i.e.,
clinician, policymaker, consumer) per year, depending on the
information needed for each product with each audience.
In accordance with OMB guidelines for generic clearances for
voluntary customer surveys and Executive Order 12862, AHRQ has
established an independent review process to assure the development,
implementation, and analysis of high quality customer surveys within
AHRQ. Specifically, AHRQ understands that each activity conducted must
be submitted to OMB with a supporting statement and accompanying
instruments. Information collection may not proceed until approved by
OMB.
Method of Collection
Information collections conducted under this clearance will be
collected via the following methods:
Focus Groups. Focus groups may include clinical
professionals, patients or other health care consumers, or health
policy makers. They will be used to provide input regarding the needs
for products and for the development of Decision Aids and Summary
Guides. Focus groups may also be used to test draft products to
determine if intended information and messages are being delivered
through products that are produced and disseminated through the
Eisenberg Center.
In-person or Telephone Interviews. Interviews will be
conducted with individuals from one or more of the three groups
identified above. The purpose of these interviews is to (1) to provide
input regarding the development of Decision Aids and Summary Guides,
(2) to determine if intended information and messages are being
delivered effectively through products that are produced and
disseminated through the Eisenberg Center, and (3) to engage the
subject in cognitive testing to (a) determine if changes in topical
knowledge levels can be identified following exposure to
[[Page 44797]]
Eisenberg Center informational or instructional products, and (b)
identify strengths and weaknesses in products and services for purposes
of making improvements that are practical and feasible.
Customer Satisfaction Survey for the Decision Aids.
Baseline survey data will be collected on both clinician and patient
characteristics, characteristics of the health care condition, and
selected outcome measures such as knowledge and decisional self-
efficacy. Following delivery of the decision aid, a user survey will be
completed to explore subjects' impressions of the tool, including ease
of use, clarity of presentation, length, balance of information, rating
of interactive features, and overall satisfaction. Both clinicians and
patients/consumers will be surveyed. For patients, the customer
satisfaction survey will include decisional outcome measures (e.g.,
decisional conflict, desire for involvement in decision-making),
measures of attitudes and self-efficacy, and indicators of choice
intention or actual choice made. If the aid is evaluated within a
clinical context, measures of physician-patient interaction will also
be considered. Additionally, clinicians may be interviewed about the
impact of the aid on clinical flow.
Customer Satisfaction Surveys for the Summary Guides.
These surveys will be offered to health care professionals, consumers,
and policy makers that use the online Summary Guides. Respondents will
report via Likert-type or numerical response scales how specific
informational or educational products or materials influenced health
care or clinical practice behaviors.
Follow-up CME Surveys. Continuing Medical Education (CME)
credit will be offered to physicians who wish to participate in online
activities developed around the Summary Guides for clinicians. Three
months after completing the educational activity, physicians will be
asked to complete a follow-up survey to assess realized changes in
clinical practice, barriers to making change, and self-assessed impacts
on patient care.
Solicited Topic Nominations. Visitors to the Website will
have the opportunity to provide information about suggested topics that
might be addressed through the research and dissemination efforts of
the EHC program.
Web site Registration. Visitors to the Web site will be
able to register personal contact information (e.g., name, email
address) if wishing to receive updated information and materials as
they become available.
Glossary Feedback Survey. Visitors to the Website who
access the health care glossary will be asked to suggest missing terms
and provide additional comments on definitions or usage sentences, if
desired.
This information will be used to develop, improve and/or maintain
high quality products and services to lay and health professional
publics.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated annualized burden for the
respondents' time to participate in this research. These estimates
assume a maximum of 33 Summary Guides per year and separate Guides for
clinicians, policy makers and consumers and are thus slight
overestimates. Focus groups will be used for needs assessment and will
be conducted with clinicians and consumers for development of the
Summary Guides, and additionally with policymakers for those Guides in
which policy recommendations are applicable. Focus groups will be
conducted with no more than 1,056 persons per year and will last about
1\1/2\ hours.
Once the Summary Guides are developed they will be subjected to in-
person or telephone interviews for purposes of usability and product
testing with clinicians, policy makers and consumers. In-person/
telephone interviews will be conducted twice with about 1,386 persons
annually and will take about 66 minutes on average. Two rounds of
interviews will be conducted with all consumer representatives during
product development, with a second round of interviews conducted
occasionally with clinicians and policy makers, as needed.
Customer satisfaction surveys for the Summary Guides will be
conducted with approximately 6,600 representatives from the audience to
be targeted by the Summary Guides annually (i.e., clinician,
policymaker or consumer) and will take 5 minutes to complete.
Customer satisfaction surveys will also be administered to
approximately 50 clinicians and 500 patients in evaluating the Decision
Aid. These surveys will take about 10 minutes to complete, and will be
administered before and after implementation of the Decision Aid in the
study populations.
Clinicians that have completed CME accrediting requirements and are
requesting CME credit will be asked to complete the follow-up CME
Survey three months following completion of the online activity. This
data collection will be completed with about 1,320 clinicians annually
and will require 5 minutes to complete.
Approximately 2,500 solicited topic nomination forms will be
completed annually by healthcare professional and consumer visitors to
the Website and will require about 5 minutes to complete. Website
Registration will be completed by all persons wanting to stay up-to-
date with the latest information from the Eisenberg Center, about 6,000
annually, and requires about 5 minutes to complete. The Glossary
Feedback Survey will be completed by about 200 persons annually that
access the glossary and takes 5 minutes to complete. The total burden
hours are estimated to be 6,203.
Exhibit 2 shows the estimated annualized cost burden associated
with the respondent's time to participate in this research. The cost
burden is estimated to be $290,227 annually.
Exhibit 1--Estimated Annualized Burden Hours
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Number of
Type of data collection Number of response per Hours per Total burden
respondents respondent response hours
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Focus Groups.................................... 1,056 1 1.5 1,584
In-person/Telephone Interviews.................. 1,386 2 1.1 3,050
Customer Satisfaction Surveys for the Decision 550 2 10/60 184
Aid............................................
Customer Satisfaction Surveys for the Summary 6,600 1 5/60 550
Guides.........................................
Follow-up CME Surveys........................... 1,320 1 5/60 110
Solicited Topic Nominations..................... 2,500 1 5/60 208
Web site Registration........................... 6,000 1 5/60 500
Glossary Feedback Survey........................ 200 1 5/60 17
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[[Page 44798]]
Total....................................... 19,612 na na 6,203
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Exhibit 2--Estimated annualized cost burden
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Number of Total burden Average hourly Total cost
Type of data collection respondents hours wage rate* burden
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Focus Groups.................................... 1,056 1,584 $48.98 $77,584
In-person/Telephone Interviews.................. 1,386 3,050 46.82 142,801
Customer Satisfaction Surveys for the Decision 550 184 25.53 4,698
Aid............................................
Customer Satisfaction Surveys for the Summary 6,600 550 39.55 21,753
Guides.........................................
Follow-up CME Surveys........................... 1,320 110 77.64 8,540
Solicited Topic Nominations..................... 2,500 208 48.07 9,999
Web site Registration........................... 6,000 500 48.07 24,035
Glossary Feedback Survey........................ 200 17 48.07 817
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Total....................................... 19,612 6,203 na 290,227
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* Based upon the mean and weighted mean wages for clinicians (29-1062 family and general practitioners), policy
makers (11-0000 management occupations, 11-3041 compensation & benefits managers, 13-1072 compensation,
benefits & job analysis specialists, 11-9111 medical and health service managers, 13-2053 insurance
underwriters and 15-2011 actuaries) and consumers (00-0000 all occupations). Focus groups include 528
clinicians ($77.64/hr) and 528 consumers ($20.32/hr); in-person/telephone interviews includes 528 clinicians,
330 policy makers ($39.91/hr) and 528 consumers; customer satisfaction surveys for the decision aid includes
50 clinicians and 500 consumers; customer satisfaction surveys for the summary guides includes 1,650
clinicians, 1,650 policy makers and 3,300 consumers; follow-up CME surveys includes 1,320 clinicians;
solicited topic nominations include 1,125 clinicians, 250 policy makers and 1,125 consumers; website
registration includes 2,700 clinicians, 600 policy makers and 2,700 consumers; glossary feedback survey
includes 90 clinicians, 20 policy makers and 90 consumers, National Compensation Survey: Occupational wages in
the United States May 2008, ``U.S. Department of Labor, Bureau of Labor Statistics.''
Estimated Annual Costs to the Federal Government
The maximum cost to the Federal Government is estimated to be
$1,439,003 annually.
Exhibit 3 shows the total and annualized cost by the major cost
components.
Exhibit 3--Estimated Total and Annualized Cost
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Annualized
Cost component Total cost cost
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Project Development........................... $1,019,970 $339,990
Data Collection Activities.................... 735,405 245,135
Data Processing and Analysis.................. 1,889,505 629,835
Project Management............................ 557,380 185,793
Overhead...................................... 114,750 38,250
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Total..................................... 4,317,010 1,439,003
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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.
Dated: July 19, 2010.
Carolyn M. Clancy,
Director.
[FR Doc. 2010-18413 Filed 7-28-10; 8:45 am]
BILLING CODE 4160-90-M