Proposed Collection; Comment Request; Recruitment and Screening for the Insight Into Determination of Exceptional Aging and Longevity (IDEAL) Study, 57038-57039 [2010-23263]

Download as PDF 57038 Federal Register / Vol. 75, No. 180 / Friday, September 17, 2010 / Notices Description: The Runaway and Homeless Youth Act, as amended by Public Law 106–71 (42 U.S.C. 5701 et seq.), mandates that the Department of Health and Human Services (HHS) report regularly to Congress on the status of HHS-funded programs serving runaway and homeless youth. Such reporting is similarly mandated by the Government Performance and Results Act. Organizations funded under the Runaway and Homeless Youth program are required by statute (42 U.S.C. 5712, 42 U.S.C. 5714–2) to meet certain data collection and reporting requirements. These requirements include maintenance of client statistical records on the number and the characteristics of the runaway and homeless youth, and youth at risk of family separation, who participate in the project, and the services provided to such youth by the project. Respondents: Public and private, community-based nonprofit, and faithbased organizations receiving HHS funds for services to runaway and homeless youth. ANNUAL BURDEN ESTIMATES Number of respondents Instrument Youth profile ................................................................................................... Street Outreach Report ................................................................................. Brief Contacts ................................................................................................ Turnaways ..................................................................................................... Data Transfer ................................................................................................. wwoods2 on DSK1DXX6B1PROD with NOTICES_PART 1 Estimated Total Annual Burden Hours: 58,480.22. Additional Information: Copies of the proposed collection may be obtained by writing to the Administration for Children and Families, Office of Administration, Office of Information Services, 370 L’Enfant Promenade, SW., Washington, DC 20447, Attn: ACF Reports Clearance Officer. All requests should be identified by the title of the information collection. E-mail address: infocollection@acf.hhs.gov. OMB Comment: OMB is required to make a decision concerning the collection of information between 30 and 60 days after publication of this document in the Federal Register. Therefore, a comment is best assured of having its full effect if OMB receives it within 30 days of publication. Written comments and recommendations for the proposed information collection should be sent directly to the following: Office of Management and Budget, Paperwork Reduction Project, Fax: 202–395–7285, E-mail: OIRA_SUBMISSION@OMB.EOP.GOV, Attn: Desk Officer for the Administration for Children and Families. Dated: September 14, 2010. Robert Sargis, Reports Clearance Officer. [FR Doc. 2010–23253 Filed 9–16–10; 8:45 am] BILLING CODE 4184–01–P 536 141 536 536 536 National Institutes of Health Proposed Collection; Comment Request; Recruitment and Screening for the Insight Into Determination of Exceptional Aging and Longevity (IDEAL) Study Summary: In compliance with the requirement of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, for the opportunity for public comment on proposed data collection projects, the National Institute on Aging (NIA), 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: Recruitment and Screening for the Insight into Determination of Exceptional Aging and Longevity (IDEAL) Study. Type of Information Collection Request: NEW. Need and Use of Information Collection: The purpose of the project for is to conduct recruitment and screening for the IDEAL Study. A multifaceted recruitment approach will be used to reach the target audience in a wide variety of ways. Those who are interested in participating in the IDEAL study will be asked to complete a two stage recruitment process consisting of a telephone interview and a physical Number of respondents Individuals who complete the phone interview .............................................. Individuals who complete the physical exam ................................................ 14:46 Sep 16, 2010 Jkt 220001 PO 00000 Frm 00060 Fmt 4703 Sfmt 4703 Average burden hours per response 153 4,211 305 13 2 DEPARTMENT OF HEALTH AND HUMAN SERVICES Type of respondent VerDate Mar<15>2010 Number of responses per respondent 0.25 0.02 0.15 0.15 0.50 Total burden hours 20,502 11,875.02 24,522 1,045.20 536 exam. The Stage One interview consists of questions concerning demographics, physical ability, health status, and medical conditions. Those who are eligible after completing the telephone interview will be asked to complete the second stage of the screening process. The physical examination is a modified version of the full BLSA assessment protocol consisting of the following components: general appearance; vital signs; chest and heart auscultation; sensory systems including vision, hearing, sensory proprioception, neuropathy and balance; and movement and strength of the upper and lower extremities. In addition the potential participant will also be asked to complete physical performance tests, cognitive exams, an electrocardiogram and a blood draw. Frequency of Response: Once. Affected Public: Individuals or households. Type of Respondents: Healthy individuals who are at least 80 years of age. The annual reporting burden is as follows: Estimated Number of Respondents: 1,500; Estimated Number of Responses per Respondent: 1; Average Burden Hours per Response: 0.833; and Estimated Total Annual Burden Hours Requested: 701. There is no annualized cost to respondents. There are no Capital costs to report. There are no Operating or Maintenance Costs to report. Frequency of response 1,500 * 300 E:\FR\FM\17SEN1.SGM 1 1 17SEN1 Average time per response 0.167 1.5 Annual hour burden 251 450 Federal Register / Vol. 75, No. 180 / Friday, September 17, 2010 / Notices Number of respondents Type of respondent Totals ...................................................................................................... 1,500 Frequency of response Average time per response ........................ 57039 Annual hour burden .......................... 701 * These individuals are included in the 1,500 above. 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 obtain a copy of the data collection plans and instruments, contact Dr. Luigi Ferrucci, Principal Investigator, NIA Clinical Research Branch, Harbor Hospital, 5th Floor, 3001 S. Hanover, Baltimore, MD 21225, or call this non-toll-free number (410) 350–3936 or E-mail your request including your address to: Ferruccilu@grc.nia.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: September 8, 2010. Melissa Fraczkowski, Project Clearance Liason, NIA, National Institutes of health. [FR Doc. 2010–23263 Filed 9–16–10; 8:45 am] wwoods2 on DSK1DXX6B1PROD with NOTICES_PART 1 BILLING CODE 4140–01–P VerDate Mar<15>2010 14:46 Sep 16, 2010 Jkt 220001 FEDERAL TRADE COMMISSION DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare & Medicaid Services [CMS–1356–N] DEPARTMENT OF HEALTH AND HUMAN SERVICES Office of the Inspector General Medicare Program; Workshop Regarding Accountable Care Organizations, and Implications Regarding Antitrust, Physician SelfReferral, Anti-Kickback, and Civil Monetary Penalty (CMP) Laws Federal Trade Commission (FTC), Centers for Medicare & Medicaid Services (CMS), and Office of the Inspector General (OIG), HHS. ACTION: Notice of meeting. AGENCY: This notice announces a public workshop hosted by the Federal Trade Commission (FTC), the Centers for Medicare & Medicaid Services (CMS), and the Office of the Inspector General (OIG) of the Department of Health and Human Services (DHHS). This workshop will include panel discussions and a listening session on certain legal issues related to Accountable Care Organizations (ACOs). Physicians, physician associations, hospitals, health systems, consumers, and all others interested in ACOs are invited to participate, in person or by calling into the teleconference. The meeting is open to the public, but attendance is limited to space and teleconference lines available. An agenda will be posted on the CMS Web site at https://www.cms.gov/center/ physician.asp prior to the session. DATES: Meeting Date: The public workshop will be held on Tuesday, October 5, 2010 from 9 a.m. until 4:30 p.m. Eastern Daylight Time (E.D.T.). Deadline for Meeting Registration and Request for Special Accommodations: Registration opens on September 16, 2010. Registration must be completed by 5 p.m. e.d.t. on September 27, 2010. Requests for special accommodations must be received by 5 p.m. e.d.t. on September 27, 2010. SUMMARY: PO 00000 Frm 00061 Fmt 4703 Sfmt 4703 Deadline for Submission of Written Comments or Statements for Discussion at the Workshop: Written comments or statements to be considered for discussion at the Workshop may be sent via mail or electronically to the address specified in the ADDRESSES section of this notice and must be received by 5 p.m. E.D.T. on September 27, 2010. ADDRESSES: Meeting Location: The public workshop will be held in the main auditorium of the Central Building of the Centers for Medicare & Medicaid Services, 7500 Security Boulevard, Baltimore, MD 21244–1850. Registration and Special Accommodations: Persons interested in attending the meeting in person must register by completing the on-line registration via the CMS Web site at https://www.cms.hhs.gov/apps/events/ event.asp?id=607 Individuals who require special accommodations should send an e-mail request to thomas.carey@hhs.gov or via regular mail to the address specified in the FOR FURTHER INFORMATION CONTACT section of this notice. Information regarding attending via teleconference and Web conference will be posted on the CMS Web site at https://www.cms.gov/center/ physician.asp prior to the session. Written Comments or Statements: Written comments or statements may be sent via e-mail to ACOlegalissues@cms.hhs.gov or sent via regular mail to: Attn: ACO Legal Issues, Mail Stop C5–15–12, Centers for Medicare & Medicaid Services, 7500 Security Boulevard, Baltimore, MD 21244–1850. All persons planning to make a statement in person at the afternoon listening session are urged to submit statements in writing in advance of the listening session and should subsequently submit the information electronically by the timeframe specified in the DATES section of this notice. FOR FURTHER INFORMATION CONTACT: Kristin Bohl at (410) 786–8680, for issues specific to CMS. Elizabeth Jex at (202) 326–3273, for issues specific to FTC. Patrice Drew at (202) 619–1368, for issues specific to OIG. Thomas Carey at (410) 786–4560, for general and logistical issues. You may also send general and logistical inquiries about this workshop via e- E:\FR\FM\17SEN1.SGM 17SEN1

Agencies

[Federal Register Volume 75, Number 180 (Friday, September 17, 2010)]
[Notices]
[Pages 57038-57039]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-23263]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Proposed Collection; Comment Request; Recruitment and Screening 
for the Insight Into Determination of Exceptional Aging and Longevity 
(IDEAL) Study

    Summary: In compliance with the requirement of Section 
3506(c)(2)(A) of the Paperwork Reduction Act of 1995, for the 
opportunity for public comment on proposed data collection projects, 
the National Institute on Aging (NIA), 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: Recruitment and Screening for the 
Insight into Determination of Exceptional Aging and Longevity (IDEAL) 
Study. Type of Information Collection Request: NEW. Need and Use of 
Information Collection: The purpose of the project for is to conduct 
recruitment and screening for the IDEAL Study. A multifaceted 
recruitment approach will be used to reach the target audience in a 
wide variety of ways. Those who are interested in participating in the 
IDEAL study will be asked to complete a two stage recruitment process 
consisting of a telephone interview and a physical exam. The Stage One 
interview consists of questions concerning demographics, physical 
ability, health status, and medical conditions. Those who are eligible 
after completing the telephone interview will be asked to complete the 
second stage of the screening process. The physical examination is a 
modified version of the full BLSA assessment protocol consisting of the 
following components: general appearance; vital signs; chest and heart 
auscultation; sensory systems including vision, hearing, sensory 
proprioception, neuropathy and balance; and movement and strength of 
the upper and lower extremities. In addition the potential participant 
will also be asked to complete physical performance tests, cognitive 
exams, an electrocardiogram and a blood draw. Frequency of Response: 
Once. Affected Public: Individuals or households. Type of Respondents: 
Healthy individuals who are at least 80 years of age. The annual 
reporting burden is as follows: Estimated Number of Respondents: 1,500; 
Estimated Number of Responses per Respondent: 1; Average Burden Hours 
per Response: 0.833; and Estimated Total Annual Burden Hours Requested: 
701. There is no annualized cost to respondents. There are no Capital 
costs to report. There are no Operating or Maintenance Costs to report.

----------------------------------------------------------------------------------------------------------------
                                                     Number of     Frequency of    Average time     Annual hour
               Type of respondent                   respondents      response      per response       burden
----------------------------------------------------------------------------------------------------------------
Individuals who complete the phone interview....           1,500               1           0.167             251
Individuals who complete the physical exam......           * 300               1           1.5               450
                                                 ---------------------------------------------------------------

[[Page 57039]]

 
    Totals......................................           1,500  ..............  ..............             701
----------------------------------------------------------------------------------------------------------------
* These individuals are included in the 1,500 above.

    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 obtain a copy of the data collection plans and 
instruments, contact Dr. Luigi Ferrucci, Principal Investigator, NIA 
Clinical Research Branch, Harbor Hospital, 5th Floor, 3001 S. Hanover, 
Baltimore, MD 21225, or call this non-toll-free number (410) 350-3936 
or E-mail your request including your address to: 
Ferruccilu@grc.nia.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: September 8, 2010.
Melissa Fraczkowski,
Project Clearance Liason, NIA, National Institutes of health.
[FR Doc. 2010-23263 Filed 9-16-10; 8:45 am]
BILLING CODE 4140-01-P
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