Agency Information Collection Activities; Proposed Collection; Public Comment Request, 15725-15726 [2013-05609]

Download as PDF mstockstill on DSK4VPTVN1PROD with NOTICES Federal Register / Vol. 78, No. 48 / Tuesday, March 12, 2013 / Notices mobile devices, awareness and use of content labeling and rating systems, and awareness and use of parental controls for mobile content. Similar questions will be posed to the adult respondents’ children. Likely Respondents: With the assistance of a consumer research firm (hereafter the Contractor), the FTC will develop a draft questionnaire for use in a nationally representative online survey of parents and (with parental permission) their children ages 8–16 years who watch movies, listen to music, and/or play game apps on a mobile device that runs either the Apple iOS or Android operating system. To the extent feasible, the adult panel shall consist of 100 adult respondents for each of the nine child age groups between ages 8 and 16, inclusive (900 total adult respondents). The child survey shall be conducted as an adjunct to the parents’ survey, i.e., by surveying each child about whom the adult respondents answered their survey questions (900 total child respondents). Estimated Annual Hours Burden: Approximately 417 hours (117 hours for the adult screener + 300 hours for the parent and child surveys). • Screening Questions: The screening questions will be asked of approximately 7,000 adult respondents to provide a large enough random sample for the surveys. Cumulatively, screening should require a maximum of 117 hours (7,000 total respondents × 1 minute for each). Because the adult respondents will be pre-screening the 900 child respondents, the Commission does not anticipate any burden on children related to screening. • Survey Questions: Answering the surveys will impose a burden per adult respondent of approximately 10 minutes, totaling 150 hours for all respondents to the surveys (900 respondents × 10 minutes per survey). Similarly, answering the surveys will impose a burden per child respondent of approximately 10 minutes, totaling 150 hours for all respondents to the surveys (900 respondents × 10 minutes per survey). Estimated annual cost burden: $0. The cost per respondent should be negligible. Participation is voluntary, and will not require any labor expenditures by respondents. There are no capital, start-up, operation, maintenance, or other similar costs to the respondents. Request for Comment: You can file a comment online or on paper. For the Commission to consider your comment, we must receive it on or before April 11, 2013. Write ‘‘Entertainment Industry Study: FTC File No. P994511’’ on your VerDate Mar<15>2010 17:21 Mar 11, 2013 Jkt 229001 comment. Your comment—including your name and your state—will be placed on the public record of this proceeding, including, to the extent practicable, on the public Commission Web site, at http://www.ftc.gov/os/ publiccomments.shtm. As a matter of discretion, the Commission tries to remove individuals’ home contact information from comments before placing them on the Commission Web site. Because your comment will be made public, you are solely responsible for making sure that your comment does not include any sensitive personal information, like anyone’s Social Security number, date of birth, driver’s license number or other state identification number or foreign country equivalent, passport number, financial account number, or credit or debit card number. You are also solely responsible for making sure that your comment does not include any sensitive health information, like medical records or other individually identifiable health information. In addition, do not include any ‘‘[t]rade secret or any commercial or financial information * * * which is privileged or confidential.’’ See Section 6(f) of the FTC Act, 15 U.S.C. 46(f), and FTC Rule 4.10(a)(2), 16 CFR 4.10(a)(2). In particular, do not include competitively sensitive information such as costs, sales statistics, inventories, formulas, patterns, devices, manufacturing processes, or customer names. If you want the Commission to give your comment confidential treatment, you must file it in paper form, with a request for confidential treatment, and you have to follow the procedure explained in FTC Rule 4.9(c), 16 CFR 4.9(c). Your comment will be kept confidential only if the FTC General Counsel, in his or her sole discretion, grants your request in accordance with the law and the public interest. Postal mail addressed to the Commission is subject to delay due to heightened security screening. As a result, we encourage you to submit your comments online, or to send them to the Commission by courier or overnight service. To make sure that the Commission considers your online comment, you must file it at https:// ftcpublic.commentworks.com/ftc/ mobileappssurveypra2, by following the instructions on the web-based form. If this Notice appears at http:// www.regulations.gov, you also may file a comment through that Web site. If you file your comment on paper, write ‘‘Entertainment Industry Study: FTC File No. P994511’’ on your comment and on the envelope, and mail PO 00000 Frm 00046 Fmt 4703 Sfmt 4703 15725 or deliver it to the following address: Federal Trade Commission, Office of the Secretary, Room H–113 (Annex J), 600 Pennsylvania Avenue NW., Washington, DC 20580. If possible, submit your paper comment to the Commission by courier or overnight service. Visit the Commission Web site at http://www.ftc.gov to read this Notice. The FTC Act and other laws that the Commission administers permit the collection of public comments to consider and use in this proceeding as appropriate. The Commission will consider all timely and responsive public comments that it receives on or before April 11, 2013. You can find more information, including routine uses permitted by the Privacy Act, in the Commission’s privacy policy, at http://www.ftc.gov/ftc/privacy.shtm. Comments on the information collection requirements subject to review under the PRA should also be submitted to OMB. If sent by U.S. mail, address comments to: Office of Information and Regulatory Affairs, Office of Management and Budget, Attention: Desk Officer for the Federal Trade Commission, New Executive Office Building, Docket Library, Room 10102, 725 17th Street NW., Washington, DC 20503. Comments sent to OMB by U.S. postal mail, however, are subject to delays due to heightened security precautions. Thus, comments instead should be sent by facsimile to (202) 395–5167. David C. Shonka, Acting General Counsel. [FR Doc. 2013–05630 Filed 3–11–13; 8:45 am] BILLING CODE 6750–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Office of the Secretary [Document Identifier: OS–19060–60D] Agency Information Collection Activities; Proposed Collection; Public Comment Request Office of the Secretary, HHS. Notice. AGENCY: ACTION: In compliance with section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, the Office of the Secretary(OS), Department of Health and Human Services, announces plans to submit a new Information Collection Request (ICR), described below, to the Office of Management and Budget (OMB). Prior to submitting that ICR to OMB, OS seeks comments from the SUMMARY: E:\FR\FM\12MRN1.SGM 12MRN1 15726 Federal Register / Vol. 78, No. 48 / Tuesday, March 12, 2013 / Notices public regarding the burden estimate, below, or any other aspect of the ICR. Comments on the ICR must be received on or before May 13, 2013. DATES: Submit your comments to Information.CollectionClearance@ hhs.gov or by calling (202) 690–6162. ADDRESSES: FOR FURTHER INFORMATION CONTACT: Information Collection Clearance staff, Information.CollectionClearance@ hhs.gov or (202) 690–6162. When submitting comments or requesting information, please include the document identifier HHS–OS–19060– 60D for reference. SUPPLEMENTARY INFORMATION: women forty years and over. Evaluation of the initiative will address the following questions: (1) Does a healthy weight intervention based on the individual and the social environment improve health and reduce weight of older lesbian and bisexual women; and, (2) If the intervention does improve health and/or reduce weight, what attributes of the intervention contributed to this success? Information will be gathered and analyzed in an effort to identify and understand the effects of this healthy weight intervention and to inform the applicability of the intervention to other sites across the United States. The project is scheduled for one year. Information Collection Request Title: Living Healthier, Living Longer Program Evaluation. Abstract: The Department of Health and Human Services (HHS), the Office of Women’s Health, (OWH) Coordinating Committee on Lesbian, Gay, Bi-sexual and Transgender (LGBT) Issues has prioritized the collection of health data on LGBT populations. In response, OWH funded an initiative to ‘‘identify and test effective and innovative ways of reducing obesity in lesbian and bisexual women’’ (HHS, 2012). This initiative will include nutritional and physical activity counseling and activities, and will be implemented in New York City. It will be tailored to bisexual and lesbian TOTAL ESTIMATED ANNUALIZED BURDEN HOURS Average burden per response (in hours) Number of responses per respondent Number of respondents Form name Total burden hours Baseline Survey ............................................................................................... Study Completion Survey ................................................................................ Pedometer Profile ............................................................................................ Health Screen (physical measurement) .......................................................... Health History Questionnaire ........................................................................... Intervention Experience Study Mid-Point) ....................................................... Intervention Experience ( Study Completion) .................................................. 40 40 40 40 40 40 40 1 1 1 3 1 1 1 15/60 15/60 2/60 10/60 12/60 1 1 10 10 1 20 8 40 hours 40 hours Total .......................................................................................................... ........................ ........................ ........................ 129 hours OS specifically requests comments on (1) The necessity and utility of the proposed information collection for the proper performance of the agency’s functions, (2) the accuracy of the estimated burden, (3) ways to enhance the quality, utility, and clarity of the information to be collected, and (4) the use of automated collection techniques or other forms of information technology to minimize the information collection burden. Keith A. Tucker, Information Collection Clearance Officer. [FR Doc. 2013–05609 Filed 3–11–13; 8:45 am] BILLING CODE 4150–33–P DEPARTMENT OF HEALTH AND HUMAN SERVICES mstockstill on DSK4VPTVN1PROD with NOTICES Food and Drug Administration [Docket No. FDA–2013–N–0001] Cellular, Tissue and Gene Therapies Advisory Committee; Notice of Meeting AGENCY: Food and Drug Administration, HHS. ACTION: Notice. VerDate Mar<15>2010 17:21 Mar 11, 2013 Jkt 229001 This notice announces a forthcoming meeting of a public advisory committee of the Food and Drug Administration (FDA). At least one portion of the meeting will be closed to the public. Name of Committee: Cellular, Tissue and Gene Therapies Advisory Committee. General Function of the Committee: To provide advice and recommendations to the Agency on FDA’s regulatory issues. Date and Time: The meeting will be held by teleconference on April 17, 2013, from 1:30 p.m. to 5 p.m. Location: Rockwall II Building, 5515 Security Lane, Conference Room 1033, Rockville, MD 20852. The public is welcome to attend the meeting at the specified location where a speakerphone will be provided. Public participation in the meeting is limited to the use of the speakerphone in the conference room. Contact Person: Gail Dapolito (301– 827–1289) or Rosanna Harvey (301– 827–1297), Food and Drug Administration, 1401 Rockville Pike (HFM–71), Rockville, MD 20852, or FDA Advisory Committee Information Line, 1–800–741–8138 (301–443–0572 in the Washington, DC area). A notice in PO 00000 Frm 00047 Fmt 4703 Sfmt 4703 the Federal Register about last minute modifications that impact a previously announced advisory committee meeting cannot always be published quickly enough to provide timely notice. Therefore, you should always check the Agency’s Web site at http://www.fda. gov/AdvisoryCommittees/default.htm and scroll down to the appropriate advisory committee meeting link, or call the advisory committee information line to learn about possible modifications before coming to the meeting. Agenda: On April 17, 2013, the committee will meet by teleconference. In open session, the committee will hear updates of research programs in the Laboratory of Chemistry, Division of Therapeutic Proteins, Office of Biotechnology Products, Center for Drug Evaluation and Research, FDA. FDA intends to make background material available to the public no later than 2 business days before the meeting. If FDA is unable to post the background material on its Web site prior to the meeting, the background material will be made publicly available at the location of the advisory committee meeting, and the background material will be posted on FDA’s Web site after the meeting. Background material is E:\FR\FM\12MRN1.SGM 12MRN1

Agencies

[Federal Register Volume 78, Number 48 (Tuesday, March 12, 2013)]
[Notices]
[Pages 15725-15726]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-05609]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Office of the Secretary

[Document Identifier: OS-19060-60D]


Agency Information Collection Activities; Proposed Collection; 
Public Comment Request

AGENCY: Office of the Secretary, HHS.

ACTION: Notice.

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

SUMMARY: In compliance with section 3506(c)(2)(A) of the Paperwork 
Reduction Act of 1995, the Office of the Secretary(OS), Department of 
Health and Human Services, announces plans to submit a new Information 
Collection Request (ICR), described below, to the Office of Management 
and Budget (OMB). Prior to submitting that ICR to OMB, OS seeks 
comments from the

[[Page 15726]]

public regarding the burden estimate, below, or any other aspect of the 
ICR.

DATES: Comments on the ICR must be received on or before May 13, 2013.

ADDRESSES: Submit your comments to 
Information.CollectionClearance@hhs.gov or by calling (202) 690-6162.

FOR FURTHER INFORMATION CONTACT: Information Collection Clearance 
staff, Information.CollectionClearance@hhs.gov or (202) 690-6162.

SUPPLEMENTARY INFORMATION: When submitting comments or requesting 
information, please include the document identifier HHS-OS-19060-60D 
for reference.
    Information Collection Request Title: Living Healthier, Living 
Longer Program Evaluation.
    Abstract: The Department of Health and Human Services (HHS), the 
Office of Women's Health, (OWH) Coordinating Committee on Lesbian, Gay, 
Bi-sexual and Transgender (LGBT) Issues has prioritized the collection 
of health data on LGBT populations. In response, OWH funded an 
initiative to ``identify and test effective and innovative ways of 
reducing obesity in lesbian and bisexual women'' (HHS, 2012). This 
initiative will include nutritional and physical activity counseling 
and activities, and will be implemented in New York City. It will be 
tailored to bisexual and lesbian women forty years and over. Evaluation 
of the initiative will address the following questions: (1) Does a 
healthy weight intervention based on the individual and the social 
environment improve health and reduce weight of older lesbian and 
bisexual women; and, (2) If the intervention does improve health and/or 
reduce weight, what attributes of the intervention contributed to this 
success? Information will be gathered and analyzed in an effort to 
identify and understand the effects of this healthy weight intervention 
and to inform the applicability of the intervention to other sites 
across the United States. The project is scheduled for one year.

                                     Total Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                      Average
                                                     Number of       Number of      burden per     Total burden
                    Form name                       respondents    responses per   response (in        hours
                                                                    respondent        hours)
----------------------------------------------------------------------------------------------------------------
Baseline Survey.................................              40               1           15/60              10
Study Completion Survey.........................              40               1           15/60              10
Pedometer Profile...............................              40               1            2/60               1
Health Screen (physical measurement)............              40               3           10/60              20
Health History Questionnaire....................              40               1           12/60               8
Intervention Experience Study Mid-Point)........              40               1               1        40 hours
Intervention Experience ( Study Completion).....              40               1               1        40 hours
                                                 ---------------------------------------------------------------
    Total.......................................  ..............  ..............  ..............       129 hours
----------------------------------------------------------------------------------------------------------------

    OS specifically requests comments on (1) The necessity and utility 
of the proposed information collection for the proper performance of 
the agency's functions, (2) the accuracy of the estimated burden, (3) 
ways to enhance the quality, utility, and clarity of the information to 
be collected, and (4) the use of automated collection techniques or 
other forms of information technology to minimize the information 
collection burden.

Keith A. Tucker,
Information Collection Clearance Officer.
[FR Doc. 2013-05609 Filed 3-11-13; 8:45 am]
BILLING CODE 4150-33-P