Submission for OMB Review; 30-Day Comment Request; Population Assessment of Tobacco and Health (PATH) Study-3rd Wave (NIDA), 34684-34685 [2015-14902]

Download as PDF 34684 Federal Register / Vol. 80, No. 116 / Wednesday, June 17, 2015 / Notices Title X Family Planning Program [‘‘Population Research and Voluntary Family Planning Programs’’ (91)], which was enacted in 1970 as Title X of the Public Health Service Act (Section 1001 of Title X of the Public Health Service Act, 42 United States Code [U.S.C.] 300). resources to Title X centers. Data will be collected through an online data collection tool directly from grantees and from Title X centers. Likely Respondents: This annual reporting requirement is service sites that receive funding (either directly from OPA or through a sub recipient or grantee agency) for family planning services authorized and funded by the long term sustainability of the Title X network. Data collected from this effort will be used to inform the work of the training centers so they can better support the Title X grantees. This data will help OPA better understand challenges affecting Title X centers in order to better work with HHS entities and national stakeholders to provide TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS Number of responses per respondent Number of respondents Average annualized burden per response (hours) Annual total burden (hours) Type of respondent Form name Grantees ........................ Service Sites .................. Sustainability Assessment—Grantees ................ Sustainability Assessment—Sites ....................... 92 4,168 1 1 0.66 0.66 60.72 2750.88 Total ........................ .............................................................................. 4,260 ........................ ........................ 2,811.60 Terry S. Clark, Asst Information Collection Clearance Officer. [FR Doc. 2015–14850 Filed 6–16–15; 8:45 am] BILLING CODE 4150–48–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Submission for OMB Review; 30-Day Comment Request; Population Assessment of Tobacco and Health (PATH) Study—3rd Wave (NIDA) Under the provisions of Section 3507(a)(1)(D) of the Paperwork Reduction Act of 1995, the National Institutes of Health (NIH) has submitted to the Office of Management and Budget (OMB) a request for review and approval of the information collection listed below. This proposed information collection was previously published in the Federal Register on February 11, 2015, pages 7619–7620 and allowed 60days for public comment. One public comment was received. The purpose of this notice is to allow an additional 30 days for public comment. The National Institute on Drug Abuse (NIDA), National Institutes of Health may not conduct or sponsor, and the respondent is not required to respond to, an information collection that has been asabaliauskas on DSK5VPTVN1PROD with NOTICES SUMMARY: (PATH) Study—Third Wave of Data Collection—0925–0664—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 0925–0664, expires 9/30/2016) for the Population Assessment of Tobacco and Health (PATH) Study to conduct the third wave of data collection. 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 assess within-person changes and between-person differences in tobacco-product use behaviors and related health conditions over time. Its longitudinal, population-based data will help to enhance the evidence base that informs FDA’s regulatory actions under the Family Smoking Prevention and Control Act to protect the Nation’s public health and reduce its burden of tobacco-related morbidity and mortality. OMB approval is requested for 3 years. There are no costs to respondents other than their time. The total estimated annualized burden hours are 54,434. extended, revised, or implemented on or after October 1, 1995, unless it displays a currently valid OMB control number. 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: NIH Desk Officer. DATES: Comment 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. FOR FURTHER INFORMATION CONTACT: To obtain a copy of the data collection plans and instruments 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. Proposed Collection: Population Assessment of Tobacco and Health ESTIMATED ANNUALIZED BURDEN HOURS Form or activity name Type of respondent Adult Extended Interview ....................................................... Consent for Adult Extended Interview ................................... Adults .......... Adults .......... VerDate Sep<11>2014 18:47 Jun 16, 2015 Jkt 235001 PO 00000 Frm 00079 Fmt 4703 Number of respondents Sfmt 4703 Number of responses per respondent 25,444 2,046 E:\FR\FM\17JNN1.SGM 1 1 17JNN1 Average burden per response (in hours) 1 4/60 Total annual burden hours 25,444 136 34685 Federal Register / Vol. 80, No. 116 / Wednesday, June 17, 2015 / Notices ESTIMATED ANNUALIZED BURDEN HOURS—Continued Form or activity name Type of respondent Adult Extended Interview (Aged-up) ...................................... Consent for Biological Samples ............................................. Biospecimen Collection: Urine ............................................... Biospecimen Collection: Blood ............................................... Tobacco Use Form ................................................................. Follow-up/Tracking Participant Information Form for Adults .. Youth Extended Interview ...................................................... Assent for Youth Extended Interview ..................................... Youth Extended Interview (Aged-up) ..................................... Parent Interview ..................................................................... Parent Permission and Consent for Parent Interview ........... Parent Interview (Aged-up) .................................................... Verification Interview .............................................................. Validation Interview ................................................................ Follow-up/Tracking Participant Information Form for Youth .. Follow-up/Tracking Participant Information Form for Sample Shadow Youth. Adults .......... Adults .......... Adults .......... Adults .......... Adults .......... Adults .......... Youth ........... Youth ........... Youth ........... Parents ........ Parents ........ Parents ........ Adults .......... Adults .......... Parents ........ Parents ........ Dated: June 12, 2015. Genevieve deAlmeida-Morris, Project Clearance Liaison, NIDA, NIH. [FR Doc. 2015–14902 Filed 6–16–15; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Center for Scientific Review; Notice of Closed Meetings asabaliauskas on DSK5VPTVN1PROD with NOTICES Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), notice is hereby given of the following meetings. 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: Center for Scientific Review Special Emphasis Panel Member Conflict: Neurobiology of Psychiatric Disorders and Addictions. Date: June 24, 2015. Time: 12:00 p.m. to 3:00 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, 6701 Rockledge Drive, Bethesda, MD 20892 (Telephone Conference Call). Contact Person: Boris P. Sokolov, Ph.D., Scientific Review Officer, Center for Scientific Review, National Institutes of VerDate Sep<11>2014 18:47 Jun 16, 2015 Jkt 235001 Number of respondents 1,780 1,780 13,805 765 14,570 27,224 9,625 1,923 1,923 9,818 2,161 1,961 35,564 3,579 11,548 2,282 Health, 6701 Rockledge Drive, Room 5217A, MSC 7846, Bethesda, MD 20892, 301–408– 9115, bsokolov@csr.nih.gov. This notice is being published less than 15 days prior to the meeting due to the timing limitations imposed by the review and funding cycle. Name of Committee: Center for Scientific Review Special Emphasis Panel Small Business: Non HIV Microbial Vaccines and Countermeasures. Date: July 13–14, 2015. Time: 8:00 a.m. to 5:00 p.m. Agenda: To review and evaluate grant applications. Place: Wyndham Grand Chicago Riverfront, 71 E. Wacker Drive, Chicago, IL 60601375. Contact Person: Andrea Keane-Myers, BS, Ph.D., Scientific Review Officer, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 4218, Bethesda, MD 20892, 3014351221, andrea.keane-myers@nih.gov. Name of Committee: Center for Scientific Review Special Emphasis Panel Fellowships: Oncological Sciences. Date: July 13–14, 2015. Time: 8:00 a.m. to 5:00 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, 6701 Rockledge Drive, Bethesda, MD 20892 (Virtual Meeting). Contact Person: Ola Mae Zack Howard, Ph.D., Scientific Review Officer, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Dr., Room 4192, MSC 7806, Bethesda, MD 20892, 301–451–4467, howardz@mail.nih.gov. Name of Committee: Center for Scientific Review Special Emphasis Panel Member Conflict: Vascular Regulation and Diseases. Date: July 16–17, 2015. Time: 10:00 a.m. to 6:00 p.m. Agenda: To review and evaluate grant applications. PO 00000 Frm 00080 Fmt 4703 Sfmt 4703 Number of responses per respondent 1 1 1 1 1 2 1 1 1 1 1 1 1 1 2 2 Average burden per response (in hours) 68/60 5/60 10/60 18/60 5/60 8/60 35/60 3/60 45/60 16/60 5/60 19/60 2/60 4/60 8/60 8/60 Total annual burden hours 2,017 148 2,301 230 1,214 7,260 5,615 96 1,442 2,618 180 621 1,185 239 3,079 609 Place: National Institutes of Health, 6701 Rockledge Drive, Bethesda, MD 20892 (Virtual Meeting). Contact Person: Ai-Ping Zou, MD, Ph.D., Scientific Review Officer, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 4118, MSC 7814, Bethesda, MD 20892, 301–408– 9497, zouai@csr.nih.gov. Name of Committee: Center for Scientific Review Special Emphasis Panel Fellowships: Oncology. Date: July 20–21, 2015. Time: 8:00 a.m. to 5:00 p.m. Agenda: To review and evaluate grant applications. Place: Embassy Suites at the Chevy Chase Pavilion, 4300 Military Road NW., Washington, DC 20015. Contact Person: Juraj Bies, Ph.D., Scientific Review Officer, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Dr., Rm. 4158, MSC 7806, Bethesda, MD 20892, 301 435 1256, biesj@mail.nih.gov. Name of Committee: Center for Scientific Review Special Emphasis Panel Member Conflict: Auditory Mechanisms. Date: July 20–21, 2015. Time: 8:00 a.m. to 6:00 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, 6701 Rockledge Drive, Bethesda, MD (Virtual Meeting). Contact Person: John Bishop, Ph.D., Scientific Review Officer, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 5182, MSC 7844, Bethesda, MD 20892, (301) 408– 9664, bishopj@csr.nih.gov. Name of Committee: Center for Scientific Review Special Emphasis Panel Member Conflict: Topics in Virology. Date: July 21, 2015 Time: 10:00 a.m. to 6:00 p.m. Agenda: To review and evaluate grant applications. E:\FR\FM\17JNN1.SGM 17JNN1

Agencies

[Federal Register Volume 80, Number 116 (Wednesday, June 17, 2015)]
[Notices]
[Pages 34684-34685]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-14902]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Submission for OMB Review; 30-Day Comment Request; Population 
Assessment of Tobacco and Health (PATH) Study--3rd Wave (NIDA)

SUMMARY: Under the provisions of Section 3507(a)(1)(D) of the Paperwork 
Reduction Act of 1995, the National Institutes of Health (NIH) has 
submitted to the Office of Management and Budget (OMB) a request for 
review and approval of the information collection listed below. This 
proposed information collection was previously published in the Federal 
Register on February 11, 2015, pages 7619-7620 and allowed 60-days for 
public comment. One public comment was received. The purpose of this 
notice is to allow an additional 30 days for public comment. The 
National Institute on Drug Abuse (NIDA), 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.
    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: NIH Desk Officer.

DATES: Comment 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.

FOR FURTHER INFORMATION CONTACT: To obtain a copy of the data 
collection plans and instruments 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.
    Proposed Collection: Population Assessment of Tobacco and Health 
(PATH) Study--Third Wave of Data Collection--0925-0664--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 0925-0664, expires 9/30/2016) for the Population Assessment of 
Tobacco and Health (PATH) Study to conduct the third wave of data 
collection. 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 assess 
within-person changes and between-person differences in tobacco-product 
use behaviors and related health conditions over time. Its 
longitudinal, population-based data will help to enhance the evidence 
base that informs FDA's regulatory actions under the Family Smoking 
Prevention and Control Act to protect the Nation's public health and 
reduce its burden of tobacco-related morbidity and mortality.
    OMB approval is requested for 3 years. There are no costs to 
respondents other than their time. The total estimated annualized 
burden hours are 54,434.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                     Number of    Average burden
    Form or activity name           Type of          Number of     responses per   per  response   Total annual
                                   respondent       respondents     respondent      (in hours)     burden hours
----------------------------------------------------------------------------------------------------------------
Adult Extended Interview.....  Adults...........          25,444               1               1          25,444
Consent for Adult Extended     Adults...........           2,046               1            4/60             136
 Interview.

[[Page 34685]]

 
Adult Extended Interview       Adults...........           1,780               1           68/60           2,017
 (Aged-up).
Consent for Biological         Adults...........           1,780               1            5/60             148
 Samples.
Biospecimen Collection: Urine  Adults...........          13,805               1           10/60           2,301
Biospecimen Collection: Blood  Adults...........             765               1           18/60             230
Tobacco Use Form.............  Adults...........          14,570               1            5/60           1,214
Follow-up/Tracking             Adults...........          27,224               2            8/60           7,260
 Participant Information Form
 for Adults.
Youth Extended Interview.....  Youth............           9,625               1           35/60           5,615
Assent for Youth Extended      Youth............           1,923               1            3/60              96
 Interview.
Youth Extended Interview       Youth............           1,923               1           45/60           1,442
 (Aged-up).
Parent Interview.............  Parents..........           9,818               1           16/60           2,618
Parent Permission and Consent  Parents..........           2,161               1            5/60             180
 for Parent Interview.
Parent Interview (Aged-up)...  Parents..........           1,961               1           19/60             621
Verification Interview.......  Adults...........          35,564               1            2/60           1,185
Validation Interview.........  Adults...........           3,579               1            4/60             239
Follow-up/Tracking             Parents..........          11,548               2            8/60           3,079
 Participant Information Form
 for Youth.
Follow-up/Tracking             Parents..........           2,282               2            8/60             609
 Participant Information Form
 for Sample Shadow Youth.
----------------------------------------------------------------------------------------------------------------


    Dated: June 12, 2015.
Genevieve deAlmeida-Morris,
Project Clearance Liaison, NIDA, NIH.
[FR Doc. 2015-14902 Filed 6-16-15; 8:45 am]
 BILLING CODE 4140-01-P
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.