80 FR 125 pgs. 37276-37277 - Submission for OMB Review; 60-Day Comment Request; Population Assessment of Tobacco and Health Study
Type: NOTICEVolume: 80Number: 125Pages: 37276 - 37277
Pages: 37276, 37277FR document: [FR Doc. 2015-15844 Filed 6-29-15; 8:45 am]
Agency: Health and Human Services Department
Sub Agency: National Institutes of Health
Official PDF Version: PDF Version
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Submission for OMB Review; 60-Day Comment Request; Population Assessment of Tobacco and Health Study
AGENCY:
National Institute on Drug Abuse (NIDA), the National Institutes of Health (NIH), Department of Health and Human Services.
SUMMARY:
In compliance with the requirements 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.
DATES:
Comment 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:
To Submit Comments and for Further Information: To obtain a copy of the data collection plans and instruments, submit comments in writing, or request more information on the proposed project, contact: Dr. Kevin P. Conway, Deputy Director, Division of Epidemiology, Services, and Prevention Research, NIDA, NIH, 6001 Executive Boulevard, 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. Formal requests for additional plans and instruments must be requested in writing.
SUPPLEMENTARY INFORMATION:
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.
Proposed Collection: Cognitive Interviews and Focus Groups for the Population Assessment of Tobacco and Health (PATH) Study (NIDA), 0925-0663-Revision, National Institute on Drug Abuse (NIDA), National Institutes of Health (NIH), in partnership with the Food and Drug Administration (FDA).
Need and Use of Information Collection: This is a revision request (OMB 0925-0663, expires 11/30/2015) for the Population Assessment of Tobacco and Health (PATH) Study to conduct cognitive interviews and focus groups, to support the development of the Study's questionnaires and other materials. The PATH Study is a national longitudinal cohort study of tobacco use behavior and health among the U.S. household population of adults age 18 and older and youth ages 12 to 17; the Study conducts annual interviews and collects biospecimens from adults to inform FDA's regulatory actions under the Family Smoking Prevention and Control Act. Cognitive interviews and focus groups are qualitative methods to assess how people interpret, process, retrieve, and respond to phrases, questions, response options, and product images that may be used in the development of the PATH Study's questionnaires and other materials. These methods have previously been used to help the PATH Study improve the comprehensibility of its materials for Study participants, and to increase efficiencies in data collection and reduce duplication and its associated burden on participants and the public.
OMB approval is requested for 3 years. There are no costs to respondents other than their time. The total annualized burden hours are 2,400.
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| Activity name | Type of respondent | Number of respondents | Number of responses per respondent | Average burden per response (in hours) | Total annual burden hours |
|---|---|---|---|---|---|
| Completing eligibility screener | Youth | 1,200 | 1 | 10/60 | 200 |
| Adults | 2,400 | 1 | 10/60 | 400 | |
| Examining concepts to be measured in PATH Study | Adults | 200 | 1 | 90/60 | 300 |
| Examining assent forms for participation in PATH Study | Youth | 200 | 1 | 90/60 | 300 |
| Examining consent forms for participation in PATH Study | Adults | 200 | 1 | 90/60 | 300 |
| Examining other forms and materials to support PATH Study data collection | Adults | 200 | 1 | 90/60 | 300 |
| Examining PATH Study questionnaires | Youth | 100 | 1 | 90/60 | 150 |
| Adults | 300 | 1 | 90/60 | 450 |
Dated: June 23, 2015.
Genevieve deAlmeida-Morris,
Project Clearance Liaison, NIDA, NIH.
[FR Doc. 2015-15844 Filed 6-29-15; 8:45 am]
BILLING CODE 4140-01-P