Proposed Data Collections Submitted for Public Comment and Recommendations, 11124-11125 [2012-4378]
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11124
Federal Register / Vol. 77, No. 37 / Friday, February 24, 2012 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60-Day–12–0222]
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 404–639–7570 or send comments to
Kimberly Lane, CDC Reports Clearance
Officer, 1600 Clifton Road, MS D–74,
Atlanta, GA 30333 or send an email 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
Questionnaire Design Research
Laboratory (QDRL) 2012–2014, OMB
No. 0920–0222 expiration 3/31/2013)–
Revision–National Center for Health
Statistics (NCHS), Centers for Disease
Control and Prevention (CDC).
srobinson on DSK4SPTVN1PROD with NOTICES
Background and Brief Description
Section 306 of the Public Health
Service (PHS) Act (42 U.S.C. 242k), as
amended, authorizes that the Secretary
of Health and Human Services (DHHS),
acting through NCHS, shall undertake
and support (by grant or contract)
research, demonstrations, and
VerDate Mar<15>2010
18:34 Feb 23, 2012
Jkt 226001
evaluations respecting new or improved
methods for obtaining current data to
support statistical and epidemiological
activities for the purpose of improving
the effectiveness, efficiency, and quality
of health services in the United States.
The Questionnaire Design Research
Laboratory (QDRL) conducts
questionnaire development, pre-testing,
and evaluation activities for CDC
surveys (such as the NCHS National
Health Interview Survey, OMB No.
0920–0214) and other federally
sponsored surveys. NCHS is requesting
3 years of OMB Clearance for this
generic submission.
The QDRL conducts cognitive
interviews, focus groups, usability tests,
field tests/pilot interviews, and
experimental research in laboratory and
field settings, both for applied
questionnaire development and
evaluation as well as more basic
research on response errors in surveys.
QDRL Staff use various techniques to
evaluate interviewer administered, selfadministered, telephone, Computer
Assisted Personal Interviewing (CAPI),
Computer Assisted Self-Interviewing
(CASI), Audio Computer-Assisted SelfInterviewing (ACASI), and web-based
questionnaires.
The most common questionnaire
evaluation method is the cognitive
interview. The interview structure
consists of respondents first answering
a draft survey question and then
providing textual information to reveal
the processes involved in answering the
test question. Specifically, cognitive
interview respondents are asked to
describe how and why they answered
the question as they did. Through the
interviewing process, various types of
question-response problems that would
not normally be identified in a
traditional survey interview, such as
interpretive errors and recall accuracy,
are uncovered. By conducting a
comparative analysis of cognitive
interviews, it is also possible to
determine whether particular
interpretive patterns occur within
particular sub-groups of the population.
Interviews are generally conducted in
small rounds of 20–30 interviews;
ideally, the questionnaire is re-worked
between rounds, and revisions are
tested iteratively until interviews yield
relatively few new insights.
In addition to its traditional QDRL
activities, NCHS is requesting approval
for a large field test that will be
PO 00000
Frm 00062
Fmt 4703
Sfmt 4703
conducted in 2012. This is a 5,000-case
test which involves testing the use of
ACASI in the full National Health
Interview Survey (NHIS). The ACASI
content included in the 5,000-case test
is consistent with the content studied in
two smaller approved tests. The module
includes questions on sexual identity,
alcohol consumption, HIV testing,
mental health, height and weight, sleep,
and financial worries. The objective of
asking a question on sexual identity in
the NHIS is to fill the gaps that exist in
the state of knowledge about the general
health behaviors, health status, and
health care utilization of Lesbian, Gay,
Bisexual, and Transgender (LGBT)
persons.
The 5,000-case test will include one
or more built-in experiments to assess
the impact of ACASI, and components
of ACASI, on prevalence estimates and
data quality. First and foremost, test
cases will be randomly assigned to
receive the above described questions in
either CAPI or ACASI. In particular,
prevalence estimates for the sexual
identity questions will be compared by
mode of administration. Since a
documented advantage of ACASI is the
enhanced level of privacy it affords, we
anticipate higher prevalence estimates
of sexual minorities (Lesbian, Gay,
Bisexual or Transgender persons) from
this mode of administration. Estimates
for sensitive items on mental health,
alcohol consumption, HIV testing,
height and weight, financial worries,
and others will also be compared.
Cognitive interviewing is inexpensive
and provides useful data on
questionnaire performance while
minimizing respondent burden.
Cognitive interviewing offers a detailed
depiction of meanings and processes
used by respondents to answer
questions—processes that ultimately
produce the survey data. As such, the
method offers an insight that can
transform understanding of question
validity and response error.
Documented findings from these studies
represent tangible evidence of how the
question performs. Such documentation
also serves CDC data users, allowing
them to be critical users in their
approach and application of the data.
Similar methodology has been
adopted by other federal agencies, as
well as by academic and commercial
survey organizations. There are no costs
to respondents other than their time.
E:\FR\FM\24FEN1.SGM
24FEN1
11125
Federal Register / Vol. 77, No. 37 / Friday, February 24, 2012 / Notices
ESTIMATED BURDEN TABLE
Number of
responses per
respondent
Number of
respondents
Projects
Average
hours per
response
Response
burden
QDRL Interviews ................................................................................................
Focus groups .....................................................................................................
9000
300
1
1
1
1.5
9000
450
Total ............................................................................................................
........................
........................
......................
9450
Kimberly Lane,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2012–4378 Filed 2–23–12; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60 Day–12–12ET]
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 projects or to obtain a copy of
the data collection plans and
instruments, call 404–639–7570 and
send comments to Kimberly Lane, CDC
Reports Clearance Officer, 1600 Clifton
Road, MS–D74, Atlanta, GA 30333 or
send an email 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
months, and who have a child under age
5, in order to recruit 72 participants for
the focus groups. These focus groups
will be conducted in Atlanta, Georgia
(4) and San Diego, California (4).
Findings from the focus groups will
inform revisions to existing CDC
messages and materials, which will be
further tested in the second information
collection activity, the online survey.
Phase II research will include an online
survey to test the revised messages and
materials. This web survey will: (1)
Examine baseline awareness and
knowledge regarding CMV, (2) assess
baseline CMV prevention behaviors
prior to viewing CMV communication
interventions (factsheet and video), (3)
assess appeal and evaluate the impact of
CMV communication interventions on
their attitudes, beliefs, and behavioral
intentions regarding prevention
behaviors and (4) assess knowledge,
attitudes and behaviors pre- and postinterventions with a larger target
audience sample (N=500). We estimate
that we will screen 3,000 women in
order to recruit 500 respondents for the
online survey.
All survey responses (100%) will be
submitted through a secure survey Web
site established for this project. No
Information in Identifiable Form (IIF)
collected will be transmitted to CDC.
The only IIF being collected (respondent
name, address, and phone number) is to
be used by the focus group facilities to
screen potential respondents to
determine eligibility for the focus
groups. The total estimated annual
burden is 531 hours. There are no costs
to the respondents other than their time.
This request is submitted to obtain
OMB clearance for one year.
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
Communications Research to Inform
Messages and Materials about
Cytomegalovirus (CMV)—NEW—
Prevention Research Branch, National
Center on Birth Defects and
Developmental Disabilities (NCBDDD),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Cytomegalovirus (CMV) is the most
common congenital infection in the
U.S., causing disabilities in more than
5,500 children born each year (CDC,
2010). Disabilities related to congenital
CMV are more common than other wellknown childhood conditions, such as
Down syndrome, fetal alcohol
syndrome, and neural tube defects, and
can include hearing or vision loss,
mental retardation, psychomotor delays,
and speech and language impairment.
This is a multiphase communication
research study that will help inform
CDC’s development materials and
prevention messaging about congenital
CMV. The information collection
activities will consist of focus groups
and an online survey. First, we plan to
conduct 8 focus groups with 9
respondents each to identify potential
messaging frames for communicating
information about congenital CMV to
the target audiences and adopting CMV
preventive guidelines. We estimate that
we will screen 144 women between the
ages of 18–40 who are either pregnant
or plan to get pregnant in the next 12
srobinson on DSK4SPTVN1PROD with NOTICES
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent
Number of
respondents
Form name
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
hours
Phase I: Focus Groups
Women (age 18–40) .........................
VerDate Mar<15>2010
18:34 Feb 23, 2012
Participant Screener .........................
Demographic questionnaire .............
Informed consent form .....................
Jkt 226001
PO 00000
Frm 00063
Fmt 4703
Sfmt 4703
144
72
72
E:\FR\FM\24FEN1.SGM
1
1
1
24FEN1
5/60
15/60
15/60
12
18
18
Agencies
[Federal Register Volume 77, Number 37 (Friday, February 24, 2012)]
[Notices]
[Pages 11124-11125]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-4378]
[[Page 11124]]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60-Day-12-0222]
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 404-639-7570 or send comments to Kimberly Lane,
CDC Reports Clearance Officer, 1600 Clifton Road, MS D-74, Atlanta, GA
30333 or send an email 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
Questionnaire Design Research Laboratory (QDRL) 2012-2014, OMB No.
0920-0222 expiration 3/31/2013)-Revision-National Center for Health
Statistics (NCHS), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
Section 306 of the Public Health Service (PHS) Act (42 U.S.C.
242k), as amended, authorizes that the Secretary of Health and Human
Services (DHHS), acting through NCHS, shall undertake and support (by
grant or contract) research, demonstrations, and evaluations respecting
new or improved methods for obtaining current data to support
statistical and epidemiological activities for the purpose of improving
the effectiveness, efficiency, and quality of health services in the
United States.
The Questionnaire Design Research Laboratory (QDRL) conducts
questionnaire development, pre-testing, and evaluation activities for
CDC surveys (such as the NCHS National Health Interview Survey, OMB No.
0920-0214) and other federally sponsored surveys. NCHS is requesting 3
years of OMB Clearance for this generic submission.
The QDRL conducts cognitive interviews, focus groups, usability
tests, field tests/pilot interviews, and experimental research in
laboratory and field settings, both for applied questionnaire
development and evaluation as well as more basic research on response
errors in surveys.
QDRL Staff use various techniques to evaluate interviewer
administered, self-administered, telephone, Computer Assisted Personal
Interviewing (CAPI), Computer Assisted Self-Interviewing (CASI), Audio
Computer-Assisted Self-Interviewing (ACASI), and web-based
questionnaires.
The most common questionnaire evaluation method is the cognitive
interview. The interview structure consists of respondents first
answering a draft survey question and then providing textual
information to reveal the processes involved in answering the test
question. Specifically, cognitive interview respondents are asked to
describe how and why they answered the question as they did. Through
the interviewing process, various types of question-response problems
that would not normally be identified in a traditional survey
interview, such as interpretive errors and recall accuracy, are
uncovered. By conducting a comparative analysis of cognitive
interviews, it is also possible to determine whether particular
interpretive patterns occur within particular sub-groups of the
population. Interviews are generally conducted in small rounds of 20-30
interviews; ideally, the questionnaire is re-worked between rounds, and
revisions are tested iteratively until interviews yield relatively few
new insights.
In addition to its traditional QDRL activities, NCHS is requesting
approval for a large field test that will be conducted in 2012. This is
a 5,000-case test which involves testing the use of ACASI in the full
National Health Interview Survey (NHIS). The ACASI content included in
the 5,000-case test is consistent with the content studied in two
smaller approved tests. The module includes questions on sexual
identity, alcohol consumption, HIV testing, mental health, height and
weight, sleep, and financial worries. The objective of asking a
question on sexual identity in the NHIS is to fill the gaps that exist
in the state of knowledge about the general health behaviors, health
status, and health care utilization of Lesbian, Gay, Bisexual, and
Transgender (LGBT) persons.
The 5,000-case test will include one or more built-in experiments
to assess the impact of ACASI, and components of ACASI, on prevalence
estimates and data quality. First and foremost, test cases will be
randomly assigned to receive the above described questions in either
CAPI or ACASI. In particular, prevalence estimates for the sexual
identity questions will be compared by mode of administration. Since a
documented advantage of ACASI is the enhanced level of privacy it
affords, we anticipate higher prevalence estimates of sexual minorities
(Lesbian, Gay, Bisexual or Transgender persons) from this mode of
administration. Estimates for sensitive items on mental health, alcohol
consumption, HIV testing, height and weight, financial worries, and
others will also be compared.
Cognitive interviewing is inexpensive and provides useful data on
questionnaire performance while minimizing respondent burden. Cognitive
interviewing offers a detailed depiction of meanings and processes used
by respondents to answer questions--processes that ultimately produce
the survey data. As such, the method offers an insight that can
transform understanding of question validity and response error.
Documented findings from these studies represent tangible evidence of
how the question performs. Such documentation also serves CDC data
users, allowing them to be critical users in their approach and
application of the data.
Similar methodology has been adopted by other federal agencies, as
well as by academic and commercial survey organizations. There are no
costs to respondents other than their time.
[[Page 11125]]
Estimated Burden Table
----------------------------------------------------------------------------------------------------------------
Number of Average
Projects Number of responses per hours per Response
respondents respondent response burden
----------------------------------------------------------------------------------------------------------------
QDRL Interviews................................... 9000 1 1 9000
Focus groups...................................... 300 1 1.5 450
-------------------------------------------------------------
Total......................................... .............. .............. ............ 9450
----------------------------------------------------------------------------------------------------------------
Kimberly Lane,
Reports Clearance Officer, Centers for Disease Control and Prevention.
[FR Doc. 2012-4378 Filed 2-23-12; 8:45 am]
BILLING CODE 4163-18-P