Submission for OMB Review; Comment Request; Interactive Diet and Activity Tracking in AARP (iDATA): Biomarker Based Validation Study (NCI), 28052-28054 [2011-11824]

Download as PDF 28052 [FR Doc. 2011–11746 Filed 5–12–11; 8:45 am] BILLING CODE 4160–01–C DEPARTMENT OF HEALTH AND HUMAN SERVICES mstockstill on DSKH9S0YB1PROD with NOTICES National Institutes of Health Submission for OMB Review; Comment Request; Interactive Diet and Activity Tracking in AARP (iDATA): Biomarker Based Validation Study (NCI) Under the provisions of Section 3507(a)(1)(D) of the Paperwork Reduction Act of 1995, the National Cancer Institute (NCI), the National Institutes of Health (NIH), has submitted SUMMARY: VerDate Mar<15>2010 17:22 May 12, 2011 Jkt 223001 PO 00000 Frm 00067 Fmt 4703 Sfmt 4703 to the Office of Management and Budget (OMB) a request to review and approve the information collection listed below. This proposed information collection was previously published in the Federal Register on March 14, 2011 (76 FR 13647) and allowed 60-days for public comment. There were no public comments in response to the notice. The purpose of this notice is to allow an additional 30 days for public comment. The National Institutes of Health may not conduct or sponsor, and the respondent is not required to respond to, an information collection that has E:\FR\FM\13MYN1.SGM 13MYN1 EN13MY11.012</GPH> Federal Register / Vol. 76, No. 93 / Friday, May 13, 2011 / Notices Federal Register / Vol. 76, No. 93 / Friday, May 13, 2011 / Notices been extended, revised, or implemented on or after October 1, 1995, unless it displays a currently valid OMB control number. Proposed Collection: Title: Interactive Diet and Activity Tracking in AARP (iDATA): Biomarker Based Validation Study. Type of Information Collection Request: New. Need and Use of Information Collection: The AARPbased study is one component of a multi-center biomarker validation study project involving two other large cohorts in the United States. The iDATA study involves large cohorts and provides the necessary sample size to evaluate the measurement error structure of the diet and physical activity assessment instruments and the heterogeneity of the measurement error structure across multiple and diverse study populations. The iDATA study will include 1,500 participants from the NIH–AARP Diet and Health Study and current AARP membership. The data collection instruments adhere to The Public Health Service Act, which provides authority to the Risk Factor Monitoring and Methods Branch in the Division of Cancer Control and Population Sciences and the Division of Cancer Epidemiology and Genetics. Both divisions work to reduce cancer in the U.S. population by establishing and supporting programs for the detection, diagnosis, prevention 28053 and treatment of cancer; and by collecting, identifying, analyzing and disseminating information on cancer research, diagnosis, prevention and treatment. Dietary and physical activity data will be gathered using the instruments as detailed below. In addition, biospecimen and clinic data will be also gathered. Frequency of Response: Monthly. Affected Public: Individuals. Type of Respondents: U.S. adults (persons aged 50–74). The annual reporting burden is provided for each study component as shown in the table below. There are no Capital Costs, Operating Costs, and/or Maintenance Costs to report. TABLE 1—ESTIMATES OF ANNUAL BURDEN HOURS Study component Number of respondents Instrument Average time per response (Minutes/Hour) Frequency of response Annual burden hours Type of Respondents for All Instruments: Adult Participants, 50–74 Years of Age Screening ........... Clinical Components. Dietary Questionnaires. mstockstill on DSKH9S0YB1PROD with NOTICES Physical Activity Questionnaires. Home Collections VerDate Mar<15>2010 Pre-Screening Telephone Interview (Attachment 1). Clinic Eligibility Screening Interview (Attachment 3). NHANES III Anthropometry (Attachment 13). Resting Metabolic rate—Main (Attachment 7). Resting Metabolic Rate—Subsample (Attachment 7). Fasting Blood Protocol and Form (Attachment 5). Fitness test Protocol and Form (Attachment 10). Physical Activity Readiness Questionnaires—PAR–Q or PARmedX (Attachments 11A–11B). Doubly Labelled Water—Main (Attachment 6). Doubly Labelled Water—Subsample (Attachment 6). Automated Self-Administered 24hour Dietary Recall (ASA24) (Attachment 32). 4–Day Food Record (Attachment 17). Diet History Questionnaire (DHQ*Web-II) (Attachment 33). 7–Day Food Checklist (Attachment 16). Activities Completed over Time in 24 Hours (ACT24) (Attachment 34). Community Healthy Activities Model Program for Seniors (CHAMPS) (Attachment 19). Harvard Lifestyle Validation Study Physical Activity Questionnaire (Attachment 18). Sedentary Behaviors Questionnaire (Attachment 21). Stanford physical activity Survey (Attachment 22). NIH–AARP physical activity questions (Attachment 20). 24 Hour Urine Collection Log (Attachment 14). 17:22 May 12, 2011 Jkt 223001 PO 00000 Frm 00068 1,334 15/60 (.25) 334 742 1 10/60 (.167) 124 742 3 10/60 (.167) 371 742 1 30/60 (.50) 371 34 1 30/60 (.50) 17 742 2 10/60 (.167) 247 742 1 15/60 (.25) 186 742 1 5/60 (.083) 62 742 1 40/60 (.667) 495 34 1 40/60 (.667) 23 742 6 30/60 (.50) 2,227 742 2 60/60 (1.0) 1,485 742 2 45/60 (.75) 1,114 742 2 60/60 (1.0) 1,485 742 6 30/60 (.50) 2,227 742 2 15/60 (.25) 371 742 2 10/60 (.167) 247 742 2 20/60 (.33) 495 742 2 8/60 (.133) 198 742 2 10/60 (.167) 247 742 Fmt 4703 1 2 60/60 (1.0) 1,485 Sfmt 4703 E:\FR\FM\13MYN1.SGM 13MYN1 28054 Federal Register / Vol. 76, No. 93 / Friday, May 13, 2011 / Notices TABLE 1—ESTIMATES OF ANNUAL BURDEN HOURS—Continued Study component Number of respondents Instrument Average time per response (Minutes/Hour) Frequency of response Annual burden hours Saliva Protocol and Form (Attachment 15). Heart Rate Monitor Log (Attachment 8). Physical Activity Monitor Log (Accelerometer/Inclinometer) (Attachment 12). mstockstill on DSKH9S0YB1PROD with NOTICES Total ............ 742 3 10/60 (.167) 371 34 1 35/60 (.583) 20 742 2 35/60 (.583) 866 ......................................................... ................................ ................................ ................................ 15,060 Request for Comments: Written comments and/or suggestions from the public and affected agencies should address one or more of the following points: (1) Evaluate whether the proposed collection of information is necessary for the proper performance of the function of the agency, including whether the information will have practical utility; (2) Evaluate the accuracy of the agency’s estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; (3) Enhance the quality, utility, and clarity of the information to be collected; and (4) Minimize the burden of the collection of information on those who are to respond, including the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology. Direct Comments to OMB: Written comments and/or suggestions regarding the item(s) contained in this notice, especially regarding the estimated public burden and associated response time, should be directed to the Attention: NIH Desk Officer, Office of Management and Budget, at OIRA_submission@omb.eop.gov or by fax to 202–395–6974. To request more information on the proposed project or to obtain a copy of the data collection plans and instruments, contact Heather Bowles, Risk Factor Monitoring and Methods Branch, Division of Cancer Control and Population Sciences, National Cancer Institute, 6130 Executive Blvd. MSC 7344, Bethesda, MD 20892–7335 or call non-toll-free number 301–496–7344 or e-mail your request, including your address to: bowleshr@mail.nih.gov. Comments Due Date: Comments regarding this information collection are best assured of having their full effect if received within 30 days of the date of this publication. VerDate Mar<15>2010 17:22 May 12, 2011 Jkt 223001 Dated: May 9, 2011. Vivian Horovitch-Kelley, NCI Project Clearance Liaison, National Institutes of Health. [FR Doc. 2011–11824 Filed 5–12–11; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute of Neurological Disorders and Stroke; Notice of Meetings Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), notice is hereby given of meetings of the National Advisory Neurological Disorders and Stroke Council. The meetings will be open to the public as indicated below, with attendance limited to space available. Individuals who plan to attend and need special assistance, such as sign language interpretation or other reasonable accommodations, should notify the Contact Person listed below in advance of the meeting. The meetings will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: National Advisory Neurological Disorders and Stroke Council, Clinical Trials Subcommittee. Date: May 25, 2011. Closed: 6:30 p.m. to 8 p.m. Agenda: To review and evaluate grant applications. PO 00000 Frm 00069 Fmt 4703 Sfmt 4703 Place: Hyatt Regency Bethesda, One Bethesda Metro Center, 7400 Wisconsin Avenue, Bethesda, MD 20814. Open: 8 p.m. to 8:30 p.m. Agenda: To discuss clinical trials policy. Place: Hyatt Regency Bethesda, One Bethesda Metro Center, 7400 Wisconsin Avenue, Bethesda, MD 20814. Contact Person: Petra Kaufmann, MD, Director, Office of Clinical Research—NINDS, National Institutes of Health, Neuroscience Center—Room 2216, 6001 Executive Blvd., Bethesda, MD 20892, 301–496– 9135,Kaufmanp2@ninds.nih.gov. This notice is being published less than 15 days prior to the meeting due to timing limitations imposed by the review funding cycle. Name of Committee: National Advisory Neurological Disorders and Stroke Council, Basic and Preclinical Programs Subcommittee. Date: May 26, 2011. Open: 8 a.m. to 9 a.m. Agenda: To discuss basic and preclinical programs policy. Place: National Institutes of Health, Building 31, C Wing, Conference Room 10, Bethesda, MD 20892. Closed: 9 a.m. to 9:30 a.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, Building 31, C Wing, Conference Room 10, Bethesda, MD 20892. Contact Person: Walter Joseph Koroshetz, MD, Deputy Director, NINDS, Building 31, Room 8A52, 31 Center Drive, MSC 2540, 301–496–3167, Koroshetzw@ninds.nih.gov. This notice is being published less than 15 days prior to the meeting due to timing limitations imposed by the review funding cycle. Name of Committee: National Advisory Neurological Disorders and Stroke Council Training, Career Development, and Special Programs Subcommittee. Date: May 26, 2011. Open: 9:30 a.m. to 10:30 a.m. Agenda: To discuss the training plan of the institute. Place: National Institutes of Health, Building 31, C Wing, Conference Room 10, Bethesda, MD 20892. Contact Person: Stephen J. Korn, PhD, Training and Special Programs Officer, National Institute of Neurological Disorders and Stroke, National Institutes of Health, E:\FR\FM\13MYN1.SGM 13MYN1

Agencies

[Federal Register Volume 76, Number 93 (Friday, May 13, 2011)]
[Notices]
[Pages 28052-28054]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-11824]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Submission for OMB Review; Comment Request; Interactive Diet and 
Activity Tracking in AARP (iDATA): Biomarker Based Validation Study 
(NCI)

SUMMARY: Under the provisions of Section 3507(a)(1)(D) of the Paperwork 
Reduction Act of 1995, the National Cancer Institute (NCI), the 
National Institutes of Health (NIH), has submitted to the Office of 
Management and Budget (OMB) a request to review and approve the 
information collection listed below. This proposed information 
collection was previously published in the Federal Register on March 
14, 2011 (76 FR 13647) and allowed 60-days for public comment. There 
were no public comments in response to the notice. The purpose of this 
notice is to allow an additional 30 days for public comment. The 
National Institutes of Health may not conduct or sponsor, and the 
respondent is not required to respond to, an information collection 
that has

[[Page 28053]]

been extended, revised, or implemented on or after October 1, 1995, 
unless it displays a currently valid OMB control number.
    Proposed Collection: Title: Interactive Diet and Activity Tracking 
in AARP (iDATA): Biomarker Based Validation Study. Type of Information 
Collection Request: New. Need and Use of Information Collection: The 
AARP-based study is one component of a multi-center biomarker 
validation study project involving two other large cohorts in the 
United States. The iDATA study involves large cohorts and provides the 
necessary sample size to evaluate the measurement error structure of 
the diet and physical activity assessment instruments and the 
heterogeneity of the measurement error structure across multiple and 
diverse study populations. The iDATA study will include 1,500 
participants from the NIH-AARP Diet and Health Study and current AARP 
membership. The data collection instruments adhere to The Public Health 
Service Act, which provides authority to the Risk Factor Monitoring and 
Methods Branch in the Division of Cancer Control and Population 
Sciences and the Division of Cancer Epidemiology and Genetics. Both 
divisions work to reduce cancer in the U.S. population by establishing 
and supporting programs for the detection, diagnosis, prevention and 
treatment of cancer; and by collecting, identifying, analyzing and 
disseminating information on cancer research, diagnosis, prevention and 
treatment. Dietary and physical activity data will be gathered using 
the instruments as detailed below. In addition, biospecimen and clinic 
data will be also gathered. Frequency of Response: Monthly. Affected 
Public: Individuals. Type of Respondents: U.S. adults (persons aged 50-
74). The annual reporting burden is provided for each study component 
as shown in the table below. There are no Capital Costs, Operating 
Costs, and/or Maintenance Costs to report.

                                                        Table 1--Estimates of Annual Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
                                                                                                                   Average time per
            Study component                         Instrument                 Number of         Frequency of     response  (Minutes/    Annual burden
                                                                              respondents          response              Hour)               hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
                                     Type of Respondents for All Instruments: Adult Participants, 50-74 Years of Age
--------------------------------------------------------------------------------------------------------------------------------------------------------
Screening..............................  Pre-Screening Telephone                       1,334                   1         15/60 (.25)                 334
                                          Interview (Attachment 1).
                                         Clinic Eligibility Screening                    742                   1        10/60 (.167)                 124
                                          Interview (Attachment 3).
Clinical Components....................  NHANES III Anthropometry                        742                   3        10/60 (.167)                 371
                                          (Attachment 13).
                                         Resting Metabolic rate--Main                    742                   1         30/60 (.50)                 371
                                          (Attachment 7).
                                         Resting Metabolic Rate--                         34                   1         30/60 (.50)                  17
                                          Subsample (Attachment 7).
                                         Fasting Blood Protocol and Form                 742                   2        10/60 (.167)                 247
                                          (Attachment 5).
                                         Fitness test Protocol and Form                  742                   1         15/60 (.25)                 186
                                          (Attachment 10).
                                         Physical Activity Readiness                     742                   1         5/60 (.083)                  62
                                          Questionnaires--PAR-Q or
                                          PARmed-X (Attachments 11A-11B).
                                         Doubly Labelled Water--Main                     742                   1        40/60 (.667)                 495
                                          (Attachment 6).
                                         Doubly Labelled Water--                          34                   1        40/60 (.667)                  23
                                          Subsample (Attachment 6).
Dietary Questionnaires.................  Automated Self-Administered 24-                 742                   6         30/60 (.50)               2,227
                                          hour Dietary Recall (ASA24)
                                          (Attachment 32).
                                         4-Day Food Record (Attachment                   742                   2         60/60 (1.0)               1,485
                                          17).
                                         Diet History Questionnaire                      742                   2         45/60 (.75)               1,114
                                          (DHQ*Web-II) (Attachment 33).
                                         7-Day Food Checklist                            742                   2         60/60 (1.0)               1,485
                                          (Attachment 16).
Physical Activity Questionnaires.......  Activities Completed over Time                  742                   6         30/60 (.50)               2,227
                                          in 24 Hours (ACT24)
                                          (Attachment 34).
                                         Community Healthy Activities                    742                   2         15/60 (.25)                 371
                                          Model Program for Seniors
                                          (CHAMPS) (Attachment 19).
                                         Harvard Lifestyle Validation                    742                   2        10/60 (.167)                 247
                                          Study Physical Activity
                                          Questionnaire (Attachment 18).
                                         Sedentary Behaviors                             742                   2         20/60 (.33)                 495
                                          Questionnaire (Attachment 21).
                                         Stanford physical activity                      742                   2         8/60 (.133)                 198
                                          Survey (Attachment 22).
                                         NIH-AARP physical activity                      742                   2        10/60 (.167)                 247
                                          questions (Attachment 20).
Home Collections.......................  24 Hour Urine Collection Log                    742                   2         60/60 (1.0)               1,485
                                          (Attachment 14).

[[Page 28054]]

 
                                         Saliva Protocol and Form                        742                   3        10/60 (.167)                 371
                                          (Attachment 15).
                                         Heart Rate Monitor Log                           34                   1        35/60 (.583)                  20
                                          (Attachment 8).
                                         Physical Activity Monitor Log                   742                   2        35/60 (.583)                 866
                                          (Accelerometer/Inclinometer)
                                          (Attachment 12).
                                        ----------------------------------------------------------------------------------------------------------------
    Total..............................  ...............................  ..................  ..................  ..................              15,060
--------------------------------------------------------------------------------------------------------------------------------------------------------

    Request for Comments: Written comments and/or suggestions from the 
public and affected agencies should address one or more of the 
following points: (1) Evaluate whether the proposed collection of 
information is necessary for the proper performance of the function of 
the agency, including whether the information will have practical 
utility; (2) Evaluate the accuracy of the agency's estimate of the 
burden of the proposed collection of information, including the 
validity of the methodology and assumptions used; (3) Enhance the 
quality, utility, and clarity of the information to be collected; and 
(4) Minimize the burden of the collection of information on those who 
are to respond, including the use of appropriate automated, electronic, 
mechanical, or other technological collection techniques or other forms 
of information technology.
    Direct Comments to OMB: Written comments and/or suggestions 
regarding the item(s) contained in this notice, especially regarding 
the estimated public burden and associated response time, should be 
directed to the Attention: NIH Desk Officer, Office of Management and 
Budget, at OIRA_submission@omb.eop.gov or by fax to 202-395-6974. To 
request more information on the proposed project or to obtain a copy of 
the data collection plans and instruments, contact Heather Bowles, Risk 
Factor Monitoring and Methods Branch, Division of Cancer Control and 
Population Sciences, National Cancer Institute, 6130 Executive Blvd. 
MSC 7344, Bethesda, MD 20892-7335 or call non-toll-free number 301-496-
7344 or e-mail your request, including your address to: 
bowleshr@mail.nih.gov.
    Comments Due Date: Comments regarding this information collection 
are best assured of having their full effect if received within 30 days 
of the date of this publication.

    Dated: May 9, 2011.
Vivian Horovitch-Kelley,
NCI Project Clearance Liaison, National Institutes of Health.
[FR Doc. 2011-11824 Filed 5-12-11; 8:45 am]
BILLING CODE 4140-01-P
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