Proposed Collection; Comment Request; Methodological Studies for the Population Assessment of Tobacco and Health (PATH) Study, 70451 [2012-28575]

Download as PDF 70451 Federal Register / Vol. 77, No. 227 / Monday, November 26, 2012 / Notices a disability, please contact Lee L. Zwanziger at least 7 days in advance of the meeting. FDA is committed to the orderly conduct of its advisory committee meetings. Please visit our Web site at https://www.fda.gov/Advisory Committees/AboutAdvisoryCommittees/ ucm111462.htm for procedures on public conduct during advisory committee meetings. Notice of this meeting is given under the Federal Advisory Committee Act (5 U.S.C. app. 2). Dated: November 19, 2012. Jill Hartzler Warner, Acting Associate Commissioner for Special Medical Programs. [FR Doc. 2012–28462 Filed 11–23–12; 8:45 am] BILLING CODE 4160–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Proposed Collection; Comment Request; Methodological Studies for the Population Assessment of Tobacco and Health (PATH) Study 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 National Institute on Drug Abuse (NIDA), the National Institutes of Health (NIH) will publish periodic summaries of proposed projects to be submitted to the Office of Management and Budget (OMB) for review and approval. Proposed Collection: Title: Methodological Studies for Population Assessment of Tobacco and Health (PATH) Study. Type of Information Collection Request: New. Need and Use of Information Collection: The PATH study will establish a population-based framework for monitoring and evaluating the behavioral and health impacts of regulatory provisions SUMMARY: implemented as part of the Family Smoking Prevention and Tobacco Control Act (FSPTCA) by the Food and Drug Administration (FDA). NIDA is requesting generic approval from OMB for methodological studies to improve the PATH study instrumentation and data collection procedures. These methodological studies will support ongoing assessment and refinement of the PATH study’s design, and highlight ways to improve study implementation and techniques for retention and followup. Data collection methods to be used in these methodological studies include: in-person and telephone surveys; web and smartphone/mobile phone surveys; and focus group and individual in-depth qualitative interviews. Biospecimens may also be collected from adults. Frequency of Response: Annual [As needed on an on-going and concurrent basis]. Affected Public: Individuals. Type of Respondents: Youth (ages 12– 17) and Adults (ages 18+). Annual Reporting Burden: See Table 1. The annualized cost to respondents is estimated at: $227,562. There are no capital, operating or maintenance costs. TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN SUMMARY—METHODOLOGICAL STUDIES FOR THE PATH STUDY Type of respondent In-person and telephone surveys ............................................ Adults ........ Youth ......... Adults ........ Youth ......... Adults ........ Youth ......... 3,000 2,000 3,000 2,000 800 800 1 1 1 1 1 1 11⁄2 11⁄2 11⁄2 11⁄2 2 2 4,500 3,000 4,500 3,000 1,600 1,600 ................... 11,600 ........................ ........................ 18,200 Web and smartphone/mobile phone surveys .......................... Focus groups and individual in-depth qualitative interviews ... mstockstill on DSK4VPTVN1PROD with NOTICES Total .................................................................................. Request for Comments: Written comments and/or suggestions from the public and affected agencies are invited on one or more of the following points: (1) 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) 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) 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 those who are to respond, including the use of appropriate automated, electronic, mechanical, or other technological VerDate Mar<15>2010 16:24 Nov 23, 2012 Jkt 229001 Number of respondents Responses per respondent Data collection activity collection techniques or other forms of information technology. To request more information on the proposed project or to obtain a copy of the data collection plans contact Kevin P. Conway, Ph.D., Deputy Director, Division of Epidemiology, Services, and Prevention Research, National Institute on Drug Abuse, 6001 Executive Blvd., Room 5185; Rockville, MD 20852, or call non-toll free number 301–443–8755 or email your request, including your address to: PATHprojectofficer@mail. nih.gov. Comments Due Date: Comments regarding this information collection are best assured of having their full effect if received within 60-days of the date of this publication. FOR FURTHER INFORMATION CONTACT: PO 00000 Frm 00040 Fmt 4703 Sfmt 4703 Hours per response Annual hour burden Dated: November 14, 2012. Glenda J. Conroy, Executive Officer (OM Director), NIDA. [FR Doc. 2012–28575 Filed 11–23–12; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Report of the Evidence-Based Methodology Workshop on Polycystic Ovary Syndrome—Request for Comments The National Institutes of Health (NIH) will place in the docket for public review and comment a report resulting from the NIH Evidence-Based Methodology Workshop on Polycystic Ovary Syndrome, to be held December SUMMARY: E:\FR\FM\26NON1.SGM 26NON1

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[Federal Register Volume 77, Number 227 (Monday, November 26, 2012)]
[Notices]
[Page 70451]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-28575]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Proposed Collection; Comment Request; Methodological Studies for 
the Population Assessment of Tobacco and Health (PATH) Study

SUMMARY: 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 National Institute on Drug 
Abuse (NIDA), the National Institutes of Health (NIH) will publish 
periodic summaries of proposed projects to be submitted to the Office 
of Management and Budget (OMB) for review and approval.
    Proposed Collection: Title: Methodological Studies for Population 
Assessment of Tobacco and Health (PATH) Study. Type of Information 
Collection Request: New. Need and Use of Information Collection: The 
PATH study will establish a population-based framework for monitoring 
and evaluating the behavioral and health impacts of regulatory 
provisions implemented as part of the Family Smoking Prevention and 
Tobacco Control Act (FSPTCA) by the Food and Drug Administration (FDA). 
NIDA is requesting generic approval from OMB for methodological studies 
to improve the PATH study instrumentation and data collection 
procedures. These methodological studies will support ongoing 
assessment and refinement of the PATH study's design, and highlight 
ways to improve study implementation and techniques for retention and 
followup. Data collection methods to be used in these methodological 
studies include: in-person and telephone surveys; web and smartphone/
mobile phone surveys; and focus group and individual in-depth 
qualitative interviews. Biospecimens may also be collected from adults.
    Frequency of Response: Annual [As needed on an on-going and 
concurrent basis]. Affected Public: Individuals. Type of Respondents: 
Youth (ages 12-17) and Adults (ages 18+). Annual Reporting Burden: See 
Table 1. The annualized cost to respondents is estimated at: $227,562. 
There are no capital, operating or maintenance costs.

          Table 1--Estimated Annual Reporting Burden Summary--Methodological Studies for the PATH Study
----------------------------------------------------------------------------------------------------------------
                                     Type of         Number of     Responses per     Hours per      Annual hour
   Data collection activity        respondent       respondents     respondent       response         burden
----------------------------------------------------------------------------------------------------------------
In-person and telephone         Adults..........           3,000               1          1\1/2\           4,500
 surveys.
                                Youth...........           2,000               1          1\1/2\           3,000
Web and smartphone/mobile       Adults..........           3,000               1          1\1/2\           4,500
 phone surveys.
                                Youth...........           2,000               1          1\1/2\           3,000
Focus groups and individual in- Adults..........             800               1               2           1,600
 depth qualitative interviews.
                                Youth...........             800               1               2           1,600
                                                 ---------------------------------------------------------------
    Total.....................  ................          11,600  ..............  ..............          18,200
----------------------------------------------------------------------------------------------------------------

    Request for Comments: Written comments and/or suggestions from the 
public and affected agencies are invited on one or more of the 
following points: (1) 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) 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) 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 those who are to 
respond, including the use of appropriate automated, electronic, 
mechanical, or other technological collection techniques or other forms 
of information technology.

FOR FURTHER INFORMATION CONTACT: To request more information on the 
proposed project or to obtain a copy of the data collection plans 
contact Kevin P. Conway, Ph.D., Deputy Director, Division of 
Epidemiology, Services, and Prevention Research, National Institute on 
Drug Abuse, 6001 Executive Blvd., Room 5185; Rockville, MD 20852, or 
call non-toll free number 301-443-8755 or email your request, including 
your address to: PATHprojectofficer@mail.nih.gov.
    Comments Due Date: Comments regarding this information collection 
are best assured of having their full effect if received within 60-days 
of the date of this publication.

    Dated: November 14, 2012.
Glenda J. Conroy,
Executive Officer (OM Director), NIDA.
[FR Doc. 2012-28575 Filed 11-23-12; 8:45 am]
BILLING CODE 4140-01-P
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