77 FR 158 pgs. 48994-48995 - Submission for OMB Review; Comment Request; Population Assessment of Tobacco and Health (PATH) Study
Type: NOTICEVolume: 77Number: 158Pages: 48994 - 48995
FR document: [FR Doc. 2012-20068 Filed 8-14-12; 8:45 am]
Agency: Health and Human Services Department
Sub Agency: National Institutes of Health
Official PDF Version: PDF Version
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Submission for OMB Review; Comment Request; Population Assessment of Tobacco and Health (PATH) Study
SUMMARY:
Under the provisions of Section 3507(a)(1)(D) of the Paperwork Reduction Act of 1995, the National Institute on Drug Abuse (NIDA), 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 May 18, 2012, pages 29667-29668 and allowed 60-days for public comment. Two public comments were received. 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 been extended, revised, or implemented on or after October 1, 1995, unless it displays a currently valid OMB control number.
Proposed Collection: Title: Population Assessment of Tobacco and Health (PATH) Study. Type of Information Collection Request: NEW. Need and Use of Information Collection:
This is a large national longitudinal cohort study on tobacco use behavior and health in the United States conducted under the direction of the National Institutes of Health (NIH) National Institute on Drug Abuse (NIDA) and in partnership with the Food and Drug Administration (FDA). The field test is scheduled to begin in the fall of 2012 and the baseline collection is scheduled to begin in the fall of 2013. Using annual interviews and the collection of biospecimens from adults, the PATH study is designed to establish a population-based framework for monitoring and evaluating the behavioral and health impacts of regulatory provisions by FDA as it meets its mandate under the Family Smoking Prevention and Tobacco Control Act (FSPTCA) to regulate tobacco-product advertising, labeling, marketing, constituents, ingredients, and additives. These regulatory changes are expected to influence tobacco-product risk perceptions, exposures, and use patterns in the short term, and to reduce tobacco-related morbidity and mortality in the long term. By measuring and accurately reporting tobacco product use behaviors and health effects associated with these regulatory changes, this study will provide an empirical evidence base to inform the development, implementation, and evaluation of tobacco-product regulations in the U.S.
Frequency of Response: Annually. Affected Public: Individuals or households. Type of Respondents: Youth (ages 12-17) and Adults (ages 18+). The annual reporting burden for the field test is presented in Table 1, and the annual reporting burden for the baseline data collection is presented in Table 2. The annualized cost to respondents for the field test is estimated at: $22,993; and the annualized cost to respondents for the baseline data collection is: $1,792,156. There are no capital, operating, or maintenance costs.
| Type of respondents | Estimated number of respondents | Estimated number of responses per respondent | Average burden hours per response | Estimated total annual burden hours requested |
|---|---|---|---|---|
| Adults-Household Screener | 1,295 | 1 | 17⁄6 | 367 |
| Adults-Individual Screener | 840 | 1 | 6⁄6 | 84 |
| Adults-Extended Interview | 590 | 1 | 1 9⁄6 | 679 |
| Adults-Biospecimen Collection Forms | 590 | 1 | 9⁄6 | 89 |
| Adults-Tobacco Use Form | 590 | 1 | 2⁄6 | 20 |
| Adults-Followup/Tracking Participant Information Form | 590 | 2 | 6⁄6 | 118 |
| Youth-Extended Interview | 100 | 1 | 35⁄6 | 58 |
| Adult-Parent Interview | 100 | 1 | 19⁄6 | 32 |
| Adults-Followup/Tracking Participant Information Form for Youth (completed by parents) | 100 | 2 | 8⁄6 | 27 |
| Total | 1,446 |
| Type of respondents | Estimated number of respondents | Estimated number of responses per respondent | Average burden hours per response | Estimated total annual burden hours requested |
|---|---|---|---|---|
| Adults-Household Screener | 100,983 | 1 | 17⁄6 | 28,612 |
| Adults-Individual Screener | 63,000 | 1 | 6⁄6 | 6,300 |
| Adults-Extended Interview | 42,730 | 1 | 1 9⁄6 | 49,140 |
| Adults-Biospecimen Collection Forms | 42,730 | 1 | 9⁄6 | 6,410 |
| Adults-Tobacco Use Form | 42,730 | 1 | 2⁄6 | 1,424 |
| Adults-Followup/Tracking Participant Information Form | 42,730 | 2 | 6⁄6 | 8,546 |
| Youth-Extended Interview | 16,857 | 1 | 35⁄6 | 9,833 |
| Adult-Parent Interview | 16,857 | 1 | 19⁄6 | 5,338 |
| Adults-Followup/Tracking Participant Information Form for Youth (completed by parents) | 16,857 | 2 | 8⁄6 | 4,495 |
| Total | 115,602 |
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.
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: Office of Management and Budget, Office of Regulatory Affairs, OIRA_submission@omb.eop.gov or by fax to 202-395-6974, Attention: Desk Officer for NIH. To request more information on the proposed project or to obtain a copy of the data collection plans and instruments, 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; 301-443-8755; email PATHprojectofficer@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: August 7, 2012.
Glenda J. Conroy,
Executive Officer (OM Director) NIDA.
[FR Doc. 2012-20068 Filed 8-14-12; 8:45 am]
BILLING CODE 4140-01-P