[Federal Register Volume 76, Number 5 (Friday, January 7, 2011)]
[Notices]
[Pages 1168-1169]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2011-85]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2011-N-0001]
Agency Information Collection Activities; Proposed Collection;
Comment Request; Health and Diet Survey
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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SUMMARY: The Food and Drug Administration (FDA) is announcing an
opportunity for public comment on the proposed collection of certain
information by the Agency. Under the Paperwork Reduction Act of 1995
(the PRA), Federal Agencies are required to publish notice in the
Federal Register concerning each proposed collection of information,
including each proposed extension of an existing collection of
information, and to allow 60 days for public comment in response to the
notice. This notice solicits comments on FDA's Health and Diet Survey.
DATES: Submit either electronic or written comments on the collection
of information by March 8, 2011.
ADDRESSES: Submit electronic comments on the collection of information
to http://www.regulations.gov. Submit written comments on the
collection of information to the Division of Dockets Management (HFA-
305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061,
Rockville, MD 20852. All comments should be identified with the docket
number found in brackets in the heading of this document.
FOR FURTHER INFORMATION CONTACT: Denver Presley, Jr., Office of
Information Management, Food and Drug Administration, 1350 Piccard Dr.,
PI50-400B, Rockville, MD 20850, 301-796-3793.
SUPPLEMENTARY INFORMATION: Under the PRA (44 U.S.C. 3501-3520), Federal
Agencies must obtain approval from the Office of Management and Budget
(OMB) for each collection of information they conduct or sponsor.
``Collection of information'' is defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes Agency requests or requirements that members of
the public submit reports, keep records, or provide information to a
third party. Section 3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A))
requires Federal Agencies to provide a 60-day notice in the Federal
Register concerning each proposed collection of information, including
each proposed extension of an existing collection of information,
before submitting the collection to OMB for approval. To comply with
this requirement, FDA is publishing notice of the proposed collection
of information set forth in this document.
With respect to the following collection of information, FDA
invites comments on these topics: (1) Whether the proposed collection
of information is necessary for the proper performance of FDA's
functions, including whether the information will have practical
utility; (2) the accuracy of FDA's estimate of the burden of the
proposed collection of information, including the validity of the
methodology and assumptions used; (3) ways to enhance the quality,
utility, and clarity of the information to be collected; and (4) ways
to minimize the burden of the collection of information on respondents,
including through the use of automated collection techniques, when
appropriate, and other forms of information technology.
Health and Diet Survey (OMB Control Number 0910-0545--Extension)
FDA is seeking extension of OMB approval for the Health and Diet
Survey, which is a voluntary consumer survey
[[Page 1169]]
intended to gauge and track consumer attitudes, awareness, knowledge,
and behavior regarding various topics related to health, nutrition and
physical activity. The authority for FDA to collect the information
derives from FDA's Commissioner of Food and Drugs authority provided in
section 903(d)(2) of the Federal Food, Drug, and Cosmetic Act (21
U.S.C. 393(d)(2)).
The survey consists of two independent data collection activities.
One collection, entitled ``Health and Diet Survey--General Topics,''
tracks a broad range of consumer attitudes, awareness, knowledge, and
self-reported behaviors related to key diet and health issues. The
other collection, entitled ``Health and Diet Survey--Dietary Guidelines
Supplement,'' will provide FDA with updated information about consumer
attitudes, awareness, knowledge, and behavior regarding various
elements of nutrition and physical activity based on the key
recommendations of the Dietary Guidelines for Americans, which are
jointly issued by the Department of Health and Human Services and the
U.S. Department of Agriculture every 5 years.
The information to be collected with the Health and Diet Survey--
General Topics will include: (1) Awareness of diet-disease
relationships, (2) food and dietary supplement label use, (3) dietary
practices including strategies to lose or maintain weight, and (4)
awareness and knowledge of dietary fats. This survey has been repeated
approximately every 3 years over the course of the past several years
for the purpose of tracking changes and trends in public opinions and
consumer behavior, with some new questions added or omitted or
partially modified each iteration in response to current events. In the
next 3 years, FDA plans to field the Health and Diet Survey--General
Topics in 2012 and anticipates that it might have the need for
additional iterations in 2014. The information to be collected with the
Health and Diet Survey--Dietary Guidelines Supplement will include: (1)
Awareness and sources of information, (2) attitudes toward diet and
physical activity, and (3) practice and knowledge related to
recommended behaviors. The survey will also ask about perceptions and
use of Federal nutrition information, special diet, weight status,
health status, and demographics. In the next 3 years, FDA anticipates
to field the Health and Diet Survey--Dietary Guidelines Supplement in
2011-2012.
FDA and other Federal Agencies will use the information from the
Health and Diet Survey to evaluate and develop strategies and programs
to encourage and help consumers adopt healthy lifestyles. The
information will also help FDA and other Federal Agencies evaluate and
track consumer awareness and behavior as outcome measures of their
achievement in improving public health.
Description of Respondents: The respondents are adults, age 18 and
older, drawn from the 50 States and the District of Columbia.
Participation will be voluntary.
FDA estimates the burden of this collection of information as
follows:
Table 1--Estimated Annual Reporting Burden \1\
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Annual
Activity Number of frequency per Total annual Hours per Total hours
respondents response responses response
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General Topics: Pretest......... 27 1 27 0.25 7
General Topics: Screener........ 10,000 1 10,000 0.02 200
General Topics: Survey.......... 3,000 1 3,000 0.25 750
Dietary Guidelines Supplement: 4,000 1 4,000 0.02 80
Screener.......................
Dietary Guidelines Supplement: 1,200 1 1,200 0.22 264
Survey.........................
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Total....................... .............. .............. .............. .............. 1,301
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\1\ There are no capital costs or operating and maintenance costs associated with this collection of
information.
FDA bases its estimate of the number of respondents and the hours
per response on its experience with previous Health and Diet Surveys.
Prior to the administration of the Health and Diet Survey--General
Topics, the Agency plans to conduct a pretest to identify and resolve
potential problems. The pretest will be conducted with 27 participants;
we estimate that it will take a respondent 15 minutes (0.25 hours) to
complete the pretest, for a total of 6.75 hours, rounded to 7. The
Agency will use a screener to select an eligible adult respondent in
each household to participate in the survey. For the Health and Diet
Survey--General Topics data collection activity, a total of 10,000
individuals in the 50 States and the District of Columbia will be
screened by telephone. We estimate that it will take a respondent 1.2
minutes (0.02 hours) to complete the screening, for a total of 200
hours. We estimate that 3,000 eligible adults will participate in the
survey, each taking 15 minutes (0.25 hours), for a total of 750 hours.
For the Health and Diet Survey--Dietary Guidelines Supplement data
collection activity, 4,000 individuals in the 50 States and the
District of Columbia will be screened by telephone. We estimate that it
will take a respondent 1.2 minutes (0.02 hours) to complete the
screening questions, for a total of 80 hours. Of these respondents,
1,200 will complete the survey. We estimate that it will take a
respondent 13 minutes (0.22 hours) to complete the entire survey, for a
total of 264 hours. Thus, the total estimated burden is 1,301 hours.
Dated: January 3, 2011.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2011-85 Filed 1-6-11; 8:45 am]
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