Agency Information Collection Activities: Proposed Collection; Comment Request, 49518-49520 [2013-19712]
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49518
Federal Register / Vol. 78, No. 157 / Wednesday, August 14, 2013 / Notices
EXHIBIT 2—ESTIMATED ANNUALIZED COST BURDEN—Continued
Number of
respondents
Form name
Total ..........................................................................................................
Total burden
hours
1,200
300
Average
hourly wage
rate *
n/a
Total cost
burden
25,578
* Based upon the higher of the two means of the hourly wages for general and family practitioners and general pediatricians, National Compensation Survey: ‘‘May 2011 National Occupational Employment and Wage Estimates, United States.’’ U.S. Department of Labor, Bureau of
Labor Statistics.
Request for Comments
In accordance with the Paperwork
Reduction Act, 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 health care
research and health care 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: August 2, 2013.
Carolyn M. Clancy,
AHRQ Director.
[FR Doc. 2013–19724 Filed 8–13–13; 8:45 am]
BILLING CODE 4160–90–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.
tkelley on DSK3SPTVN1PROD with NOTICES
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:
‘‘Collection of Information for Agency
SUMMARY:
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16:16 Aug 13, 2013
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for Healthcare Research and Quality’s
(AHRQ) Consumer Assessment of
Healthcare Providers and Systems
(CAHPS) Health Plan Survey
Comparative Database.’’ In accordance
with the Paperwork Reduction Act, 44
U.S.C. 3501–3521, AHRQ invites the
public to comment on this proposed
information collection.
DATES: Comments on this notice must be
received by October 15, 2013.
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
email at doris.lefkowitz@AHRQ.hhs.gov.
SUPPLEMENTARY INFORMATION:
Proposed Project
Collection of Information for Agency for
Healthcare Research and Quality’s
(AHRQ) Consumer Assessment of
Healthcare Providers and Systems
(CAHPS) Health Plan Survey
Comparative Database
Request for information collection
approval. The Agency for Healthcare
Research and Quality (AHRQ) requests
that the Office of Management and
Budget (OMB) reapprove, under the
Paperwork Reduction Act of 1995,
AHRQ’s collection of information for
the AHRQ Consumer Assessment of
Healthcare Providers and Systems
(CAHPS) Database for Health Plans:
OMB Control number 0935–0165,
expiration July 31, 2013. The CAHPS
Health Plan Database consists of data
from the AHRQ CAHPS Health Plan
Survey. Health plans in the U.S. are
asked to voluntarily submit data from
the survey to AHRQ, through its
contractor, Westat. The CAHPS
Database was developed by AHRQ in
1998 in response to requests from health
plans, purchasers, and the Centers for
Medicare & Medicaid Services (CMS) to
provide comparative data to support
PO 00000
Frm 00075
Fmt 4703
Sfmt 4703
public reporting of health plan ratings,
health plan accreditation and quality
improvement.
Background on the CAHPS Health
Plan Survey. The CAHPS Health Plan
Survey is a tool for collecting
standardized information on enrollees’
experiences with health plans and their
services. The development of the
CAHPS Health Plan Survey began in
1995, when AHRQ awarded the first set
of CAHPS grants to Harvard, RTI, and
RAND. In 1997 the CAHPS 1.0 survey
was released by the CAHPS Consortium.
The CAHPS Consortium refers to the
research organizations involved in the
development, dissemination, and
support of CAHPS products. The
current Consortium includes AHRQ,
CMS, RAND, Yale School of Public
Health, and Westat.
Since that time, the Consortium has
clarified and updated the survey
instrument to reflect field test results;
feedback from industry experts; reports
from health plan participants, data
collection vendors, and other users; and
evidence from cognitive testing and
focus groups. In November 2006, the
CAHPS Consortium released the latest
version of the instrument: the CAHPS
Health Plan Survey 4.0. The
development of this update to the
Health Plan Survey has been part of the
‘‘Ambulatory CAHPS (A–CAHPS)
Initiative,’’ which arose as a result of
extensive research conducted with
users. AHRQ released the CAHPS
Health Plan Survey 4.0, along with
guidance on how to customize and
administer it. The National Quality
Forum endorsed the 4.0 version of the
Health Plan Survey in July 2007.
Rationale for the information
collection. The CAHPS Health Plan
Database uses data from AHRQ’s
standardized CAHPS Health plan survey
to provide comparative results to health
care purchasers, consumers, regulators
and policy makers across the country.
The Database also provides data for
AHRQ’s annual National Healthcare
Quality and National Healthcare
Disparities Reports. Voluntary
participants include public and private
employers, State Medicaid agencies,
State Children’s Health Insurance
E:\FR\FM\14AUN1.SGM
14AUN1
49519
Federal Register / Vol. 78, No. 157 / Wednesday, August 14, 2013 / Notices
Programs (SCHIP), the Centers for
Medicare & Medicaid Services (CMS),
and individual health plans.
This study is being conducted by
AHRQ through its contractor, Westat,
pursuant to AHRQ’s statutory authority
to conduct and support research on
healthcare and on systems for the
delivery of such care, including
activities with respect to: The quality,
effectiveness, efficiency,
appropriateness and value of healthcare
services; quality measurement and
improvement; and database
development. 42 U.S.C. 299a(a)(1), (2),
and (a)(8).
Method of Collection
Each year State Medicaid agencies,
and individual health plans decide
whether to participate in the database
and prepare their materials and dataset
for submission to the CAHPS Health
Plan Database. Participating
organizations are typically State
Medicaid agencies with multiple health
plans. However, individual health plans
are also encouraged to submit their data
to the CAHPS Database. The number of
data submissions per registrant varies
from participant to participant and year
to year because some participants
submit data for multiple health plans,
while others may only submit survey
data for one plan.
Each organization that decides to
participate in the database must have
their point-of-contact (POC) complete a
registration form providing their contact
information for access to the on-line
data submission system, sign and
submit a DUA, and provide health plan
characteristics such as health plan
name, product type, type of population
surveyed, health plan state, and plan
name to appear in the reporting of their
results.
Each vendor that submits files on
behalf of a Medicaid agency or
individual health plan must also
complete the registration form in order
to obtain access to the on-line
submission system. The vendor, on
behalf of their client, may also complete
additional information about survey
administration (CAHPS survey version
used, mode of survey administration,
total enrollment count, description of
how the sample was selected), submit a
copy of the questionnaire used, and
submit one data file per health plan.
Commercial health plan data is received
directly from NCQA. Medicare health
plan data is received from CMS.
Survey data from the CAHPS Health
Plan Database is used to produce four
types of products: (1) An annual
chartbook available to the public on the
CAHPS Database Web site (https://
www.cahpsdatabase.ahrq.gov/
CAHPSIDB/Public/Chartbook.aspx); (2)
individual participant comparative
reports that are confidential and
customized for each participating
organization (e.g., health plan, Medicaid
agency) that submits their data; (3) a
research database available to
researchers wanting to conduct
additional analyses; and (4) data tables
provided to AHRQ for inclusion in the
National Healthcare Quality and
National Healthcare Disparities Reports.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated burden
hours for the respondent to participate
in the database. The burden hours
pertain only to the collection of
Medicaid data from State Medicaid
agencies and individual Medicaid
health plans because those are the only
entities that submit data through the
data submission process (other data are
obtained directly from NCQA and CMS
as noted earlier in Section 2). The 80
POCs in exhibit 1 are a combination of
an estimated 60 State Medicaid agencies
and individual health plans, and 20
estimated vendors.
Each State Medicaid agency, health
plan or vendor will register online for
submission. The online Registration
form will require about 5 minutes to
complete. Each submitter will also
complete a Health Plan information
form of information about each Health
Plan such as the name of the plan, the
product type (e.g., HMO, PPO), the
population surveyed (e.g., adult
Medicaid or child Medicaid), the health
plan State, total enrollment at the time
the sample frame was generated, mode
of survey administration (mail,
telephone, IVR) and how the sample
was selected. The online Health Plan
Information form takes on average 30
minutes to complete per health plan
with each POC completing the form for
4 plans on average. The data use
agreement will be completed by the 60
participating State Medicaid agencies or
individual health plans. Vendors do not
sign or submit DUAs. The DUA requires
about 3 minutes to sign and return by
fax or mail. Each submitter will provide
a copy of their questionnaire and the
survey data file in the required file
format. Survey data files must conform
to the data file layout specifications
provide by the CAHPS Database. Since
the unit of analysis is at the health plan
level, submitters will upload one data
file per health plan. Once a data file is
uploaded the file will be automatically
checked to ensure it conforms to the
specifications and a data file status
report will be produced and made
available to the submitter. Submitters
will review each report and will be
expected to fix any errors in their data
file and resubmit if necessary. It will
take about one hour to submit the data
for each plan, and each POC will submit
data for 4 plans on average. The total
burden is estimated to be 490 hours
annually.
Exhibit 2 shows the estimated
annualized cost burden based on the
respondents’ time to complete one
submission process. The cost burden is
estimated to be $20,202 annually.
EXHIBIT 1—ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents/
POCs
Form name
Number of
responses
per POC
Hours per
response
Total burden
hours
tkelley on DSK3SPTVN1PROD with NOTICES
Registration Form ............................................................................................
Health Plan Information Form .........................................................................
Data Use Agreement .......................................................................................
Data Files Submission .....................................................................................
80
80
60
80
1
4
1
4
5/60
30/60
3/60
1
7
160
3
320
Total ..........................................................................................................
300
NA
NA
490
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E:\FR\FM\14AUN1.SGM
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Federal Register / Vol. 78, No. 157 / Wednesday, August 14, 2013 / Notices
EXHIBIT 2—ESTIMATED ANNUALIZED COST BURDEN
Number of
respondents/
POCs
Form name
Total burden
hours
Average
hourly wage
rate *
Total cost
burden
Registration Form ............................................................................................
Health Plan Information Form .........................................................................
Data Use Agreement .......................................................................................
Data Files Submission .....................................................................................
80
80
60
80
7
160
3
320
a 47.34
c 37.63
$331
7,574
255
12,042
Total ..........................................................................................................
300
490
NA
20,202
a 47.34
b 85.02
* National
Compensation Survey: Occupational wages in the United States May 2012, ‘‘U.S. Department of Labor, Bureau of Labor Statistics.’’
a Based on the mean hourly wage for Medical and Health Services Managers (11–9111).
b Based on the mean hourly wage for Chief Executives (11–1011).
c Based on the mean hourly wages for Computer Programmer (15–1131).
Request for Comments
In accordance with the Paperwork
Reduction Act, 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 health care
research and health care 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: August 8, 2013.
Carolyn M. Clancy,
AHRQ Director.
[FR Doc. 2013–19712 Filed 8–13–13; 8:45 am]
BILLING CODE 4160–90–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
tkelley on DSK3SPTVN1PROD with NOTICES
Agency for Healthcare Research and
Quality
Scientific Information Request on
Imaging Techniques for the
Surveillance, Diagnosis, and Staging
of Hepatocellular Carcinoma
Agency for Healthcare Research
and Quality (AHRQ), HHS.
ACTION: Request for scientific
information submissions.
AGENCY:
VerDate Mar<15>2010
16:16 Aug 13, 2013
The Agency for Healthcare
Research and Quality (AHRQ) is seeking
scientific information submissions from
the public on imaging techniques for the
surveillance, diagnosis, and staging of
hepatocellular carcinoma. Scientific
information is being solicited to inform
our review of Imaging Techniques for
the Surveillance, Diagnosis, and Staging
of Hepatocellular Carcinoma, which is
currently being conducted by the
Evidence-based Practice Centers for the
AHRQ Effective Health Care Program.
Access to published and unpublished
pertinent scientific information on
imaging techniques for the surveillance,
diagnosis, and staging of hepatocellular
carcinoma will improve the quality of
this review. AHRQ is conducting this
comparative effectiveness review
pursuant to Section 1013 of the
Medicare Prescription Drug,
Improvement, and Modernization Act of
2003, Public Law 108–173, and Section
902(a) of the Public Health Service Act,
42 U.S.C. 299a(a).
DATES: Submission Deadline on or
before September 13, 2013.
ADDRESSES:
Online submissions: https://
effectivehealthcare.AHRQ.gov/
index.cfm/submit-scientificinformation-packets/. Please select the
study for which you are submitting
information from the list to upload your
documents.
Email submissions: SIPS@epc-src.org.
Print submissions:
Mailing Address: Portland VA Research
Foundation, Scientific Resource
Center, ATTN: Scientific Information
Packet Coordinator, PO Box 69539,
Portland, OR 97239.
Shipping Address (FedEx, UPS, etc.):
Portland VA Research Foundation,
Scientific Resource Center, ATTN:
Scientific Information Packet
Coordinator, 3710 SW U.S. Veterans
Hospital Road, Mail Code: R&D 71,
Portland, OR 97239.
FOR FURTHER INFORMATION CONTACT:
Robin Paynter, Research Librarian,
SUMMARY:
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Frm 00077
Fmt 4703
Sfmt 4703
Telephone: 503–220–8262 ext. 58652 or
Email: SIPS@epc-src.org.
SUPPLEMENTARY INFORMATION: The
Agency for Healthcare Research and
Quality has commissioned the Effective
Health Care (EHC) Program Evidencebased Practice Centers to complete a
review of the evidence for Imaging
Techniques for the Surveillance,
Diagnosis, and Staging of
Hepatocellular Carcinoma.
The EHC Program is dedicated to
identifying as many studies as possible
that are relevant to the questions for
each of its reviews. In order to do so, we
are supplementing the usual manual
and electronic database searches of the
literature by requesting information
from the public (e.g., details of studies
conducted). We are looking for studies
that report on imaging techniques for
the surveillance, diagnosis, and staging
of hepatocellular carcinoma, including
those that describe adverse events. The
entire research protocol, including the
key questions, is also available online
at: https://www.effectivehealthcare.
AHRQ.gov/search-for-guides-reviewsand-reports/?pageaction
=displayproduct&productID=1600#7839
This notice is to notify the public that
the EHC program would find the
following information on imaging
techniques for the surveillance,
diagnosis, and staging of hepatocellular
carcinoma helpful:
D A list of completed studies your
company has sponsored for this
indication. In the list, indicate whether
results are available on
ClinicalTrials.gov along with the
ClinicalTrials.gov trial number.
D For completed studies that do not
have results on ClinicalTrials.gov, a
summary, including the following
elements: study number, study period,
design, methodology, indication and
diagnosis, proper use instructions,
inclusion and exclusion criteria,
primary and secondary outcomes,
baseline characteristics, number of
patients screened/eligible/enrolled/lost
E:\FR\FM\14AUN1.SGM
14AUN1
Agencies
[Federal Register Volume 78, Number 157 (Wednesday, August 14, 2013)]
[Notices]
[Pages 49518-49520]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-19712]
-----------------------------------------------------------------------
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: ``Collection of Information for Agency for Healthcare Research
and Quality's (AHRQ) Consumer Assessment of Healthcare Providers and
Systems (CAHPS) Health Plan Survey Comparative Database.'' In
accordance with the Paperwork Reduction Act, 44 U.S.C. 3501-3521, AHRQ
invites the public to comment on this proposed information collection.
DATES: Comments on this notice must be received by October 15, 2013.
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 email at
doris.lefkowitz@AHRQ.hhs.gov.
SUPPLEMENTARY INFORMATION:
Proposed Project
Collection of Information for Agency for Healthcare Research and
Quality's (AHRQ) Consumer Assessment of Healthcare Providers and
Systems (CAHPS) Health Plan Survey Comparative Database
Request for information collection approval. The Agency for
Healthcare Research and Quality (AHRQ) requests that the Office of
Management and Budget (OMB) reapprove, under the Paperwork Reduction
Act of 1995, AHRQ's collection of information for the AHRQ Consumer
Assessment of Healthcare Providers and Systems (CAHPS) Database for
Health Plans: OMB Control number 0935-0165, expiration July 31, 2013.
The CAHPS Health Plan Database consists of data from the AHRQ CAHPS
Health Plan Survey. Health plans in the U.S. are asked to voluntarily
submit data from the survey to AHRQ, through its contractor, Westat.
The CAHPS Database was developed by AHRQ in 1998 in response to
requests from health plans, purchasers, and the Centers for Medicare &
Medicaid Services (CMS) to provide comparative data to support public
reporting of health plan ratings, health plan accreditation and quality
improvement.
Background on the CAHPS Health Plan Survey. The CAHPS Health Plan
Survey is a tool for collecting standardized information on enrollees'
experiences with health plans and their services. The development of
the CAHPS Health Plan Survey began in 1995, when AHRQ awarded the first
set of CAHPS grants to Harvard, RTI, and RAND. In 1997 the CAHPS 1.0
survey was released by the CAHPS Consortium. The CAHPS Consortium
refers to the research organizations involved in the development,
dissemination, and support of CAHPS products. The current Consortium
includes AHRQ, CMS, RAND, Yale School of Public Health, and Westat.
Since that time, the Consortium has clarified and updated the
survey instrument to reflect field test results; feedback from industry
experts; reports from health plan participants, data collection
vendors, and other users; and evidence from cognitive testing and focus
groups. In November 2006, the CAHPS Consortium released the latest
version of the instrument: the CAHPS Health Plan Survey 4.0. The
development of this update to the Health Plan Survey has been part of
the ``Ambulatory CAHPS (A-CAHPS) Initiative,'' which arose as a result
of extensive research conducted with users. AHRQ released the CAHPS
Health Plan Survey 4.0, along with guidance on how to customize and
administer it. The National Quality Forum endorsed the 4.0 version of
the Health Plan Survey in July 2007.
Rationale for the information collection. The CAHPS Health Plan
Database uses data from AHRQ's standardized CAHPS Health plan survey to
provide comparative results to health care purchasers, consumers,
regulators and policy makers across the country. The Database also
provides data for AHRQ's annual National Healthcare Quality and
National Healthcare Disparities Reports. Voluntary participants include
public and private employers, State Medicaid agencies, State Children's
Health Insurance
[[Page 49519]]
Programs (SCHIP), the Centers for Medicare & Medicaid Services (CMS),
and individual health plans.
This study is being conducted by AHRQ through its contractor,
Westat, pursuant to AHRQ's statutory authority to conduct and support
research on healthcare and on systems for the delivery of such care,
including activities with respect to: The quality, effectiveness,
efficiency, appropriateness and value of healthcare services; quality
measurement and improvement; and database development. 42 U.S.C.
299a(a)(1), (2), and (a)(8).
Method of Collection
Each year State Medicaid agencies, and individual health plans
decide whether to participate in the database and prepare their
materials and dataset for submission to the CAHPS Health Plan Database.
Participating organizations are typically State Medicaid agencies with
multiple health plans. However, individual health plans are also
encouraged to submit their data to the CAHPS Database. The number of
data submissions per registrant varies from participant to participant
and year to year because some participants submit data for multiple
health plans, while others may only submit survey data for one plan.
Each organization that decides to participate in the database must
have their point-of-contact (POC) complete a registration form
providing their contact information for access to the on-line data
submission system, sign and submit a DUA, and provide health plan
characteristics such as health plan name, product type, type of
population surveyed, health plan state, and plan name to appear in the
reporting of their results.
Each vendor that submits files on behalf of a Medicaid agency or
individual health plan must also complete the registration form in
order to obtain access to the on-line submission system. The vendor, on
behalf of their client, may also complete additional information about
survey administration (CAHPS survey version used, mode of survey
administration, total enrollment count, description of how the sample
was selected), submit a copy of the questionnaire used, and submit one
data file per health plan. Commercial health plan data is received
directly from NCQA. Medicare health plan data is received from CMS.
Survey data from the CAHPS Health Plan Database is used to produce
four types of products: (1) An annual chartbook available to the public
on the CAHPS Database Web site (https://www.cahpsdatabase.ahrq.gov/CAHPSIDB/Public/Chartbook.aspx); (2) individual participant comparative
reports that are confidential and customized for each participating
organization (e.g., health plan, Medicaid agency) that submits their
data; (3) a research database available to researchers wanting to
conduct additional analyses; and (4) data tables provided to AHRQ for
inclusion in the National Healthcare Quality and National Healthcare
Disparities Reports.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated burden hours for the respondent to
participate in the database. The burden hours pertain only to the
collection of Medicaid data from State Medicaid agencies and individual
Medicaid health plans because those are the only entities that submit
data through the data submission process (other data are obtained
directly from NCQA and CMS as noted earlier in Section 2). The 80 POCs
in exhibit 1 are a combination of an estimated 60 State Medicaid
agencies and individual health plans, and 20 estimated vendors.
Each State Medicaid agency, health plan or vendor will register
online for submission. The online Registration form will require about
5 minutes to complete. Each submitter will also complete a Health Plan
information form of information about each Health Plan such as the name
of the plan, the product type (e.g., HMO, PPO), the population surveyed
(e.g., adult Medicaid or child Medicaid), the health plan State, total
enrollment at the time the sample frame was generated, mode of survey
administration (mail, telephone, IVR) and how the sample was selected.
The online Health Plan Information form takes on average 30 minutes to
complete per health plan with each POC completing the form for 4 plans
on average. The data use agreement will be completed by the 60
participating State Medicaid agencies or individual health plans.
Vendors do not sign or submit DUAs. The DUA requires about 3 minutes to
sign and return by fax or mail. Each submitter will provide a copy of
their questionnaire and the survey data file in the required file
format. Survey data files must conform to the data file layout
specifications provide by the CAHPS Database. Since the unit of
analysis is at the health plan level, submitters will upload one data
file per health plan. Once a data file is uploaded the file will be
automatically checked to ensure it conforms to the specifications and a
data file status report will be produced and made available to the
submitter. Submitters will review each report and will be expected to
fix any errors in their data file and resubmit if necessary. It will
take about one hour to submit the data for each plan, and each POC will
submit data for 4 plans on average. The total burden is estimated to be
490 hours annually.
Exhibit 2 shows the estimated annualized cost burden based on the
respondents' time to complete one submission process. The cost burden
is estimated to be $20,202 annually.
Exhibit 1--Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Number of
Form name respondents/ responses per Hours per Total burden
POCs POC response hours
----------------------------------------------------------------------------------------------------------------
Registration Form............................... 80 1 5/60 7
Health Plan Information Form.................... 80 4 30/60 160
Data Use Agreement.............................. 60 1 3/60 3
Data Files Submission........................... 80 4 1 320
---------------------------------------------------------------
Total....................................... 300 NA NA 490
----------------------------------------------------------------------------------------------------------------
[[Page 49520]]
Exhibit 2--Estimated Annualized Cost Burden
----------------------------------------------------------------------------------------------------------------
Number of Average
Form name respondents/ Total burden hourly wage Total cost
POCs hours rate \*\ burden
----------------------------------------------------------------------------------------------------------------
Registration Form............................... 80 7 \a\ 47.34 $331
Health Plan Information Form.................... 80 160 \a\ 47.34 7,574
Data Use Agreement.............................. 60 3 \b\ 85.02 255
Data Files Submission........................... 80 320 \c\ 37.63 12,042
---------------------------------------------------------------
Total....................................... 300 490 NA 20,202
----------------------------------------------------------------------------------------------------------------
\*\ National Compensation Survey: Occupational wages in the United States May 2012, ``U.S. Department of Labor,
Bureau of Labor Statistics.''
\a\ Based on the mean hourly wage for Medical and Health Services Managers (11-9111).
\b\ Based on the mean hourly wage for Chief Executives (11-1011).
\c\ Based on the mean hourly wages for Computer Programmer (15-1131).
Request for Comments
In accordance with the Paperwork Reduction Act, 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 health care research and
health care 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: August 8, 2013.
Carolyn M. Clancy,
AHRQ Director.
[FR Doc. 2013-19712 Filed 8-13-13; 8:45 am]
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