Proposed Collection; Comment Request; Women's Health Initiative Observational Study, 3237 [2010-974]

Download as PDF 3237 Federal Register / Vol. 75, No. 12 / Wednesday, January 20, 2010 / Notices (MVPR), 1800 F Street, Room 4041, NW., Washington, DC 20405. FOR FURTHER INFORMATION CONTACT: Mr. Edward Chambers, Contract Policy Branch, GSA, (202) 501–3221 or e-mail at edward.chambers@gsa.gov. SUPPLEMENTARY INFORMATION: A. Purpose FAR Subpart 30.6 and the provision at 52.230–5 include pertinent rules and regulations related to the Cost Accounting Standards along with necessary administrative policies and procedures. These administrative policies require certain contractors to submit cost impact estimates and descriptions in cost accounting practices and also to provide information on CAS-covered subcontractors. B. Annual Reporting Burden Number of Respondents: 644. Responses per Respondent: 2.27. Total Responses: 1,462. Average Burden Hours per Response: 175.00. Total Burden Hours: 255,829. Obtaining Copies of Proposals: Requesters may obtain a copy of the information collection documents from the General Services Administration, Regulatory Secretariat (MVPR), 1800 F Street, Room 4041, NW., Washington, DC 20405, telephone (202) 501–4755. Please cite OMB Control Number 9000– 0129, Cost Accounting Standards Administration, in all correspondence. Al Matera, Director, Acquisition Policy Division. [FR Doc. 2010–994 Filed 1–19–10; 8:45 am] BILLING CODE 6820–EP–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Proposed Collection; Comment Request; Women’s Health Initiative Observational Study SUMMARY: In compliance with the requirement of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, for opportunity for public comment on proposed data collection projects, the National Heart, Lung, and Blood Institute (NHLBI), 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: The Women’s Health Initiative (WHI) Observational Study. Type of Information Collection Request: Revision OMB #0925–0414. Need and Use of Information Collection: This study will be used by the NIH to evaluate risk factors for chronic disease among older women by developing and following a large cohort of postmenopausal women and relating subsequent disease development to baseline assessments of historical, physical, psychosocial, and physiologic characteristics. In addition, the observational study will complement the clinical trial (which has received clinical exemption) and provide additional information on the common causes of frailty, disability and death for postmenopausal women, namely, coronary heart disease, breast and colorectal cancer, and osteoporotic fractures. Continuation of follow-up for ascertainment of medical history update forms will provide essential data for outcomes assessment for this population of aging women. Frequency of Response: Annually. Affected Public: Individuals or households and health care providers. Type of Respondents: Women, next-of-kin, and physician’s office staff. The annual reporting burden is as follows: ESTIMATE OF ANNUAL HOUR BURDEN Type of response Number of respondents Frequency of response Average hours per response Annual hour burden Observational Study Participants .............................................................. Next of Kin 1 ............................................................................................... Health Care Providers 1 ............................................................................. 42,550 941 8 1.12 1 1 .4155 .083 .085 19,800 79 Total .................................................................................................... 43,499 .......................... .......................... 19,880 .63 1 Annual pwalker on DSK8KYBLC1PROD with NOTICES burden is placed on health care providers and respondent relatives/informants through requests for information which will help in the compilation of the number and nature of new fatal and nonfatal events. The annualized cost to respondents is estimated at $397,617, assuming respondents time at the rate of $20 per hour and physician time at the rate of $50 per hour. There are no Capital Costs to report. There are no Operating or Maintenance Costs to report. 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 VerDate Nov<24>2008 16:06 Jan 19, 2010 Jkt 220001 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 to obtain a copy of the data collection plans and instruments, contact Ms. Shari Eason Ludlam, MPH, Project Officer, NIH, NHLBI, 6701 Rockledge Drive, MSC 7913, Bethesda, MD 20892–7934, or call non-toll-free number 301–402–2900 or PO 00000 Frm 00045 Fmt 4703 Sfmt 9990 E-mail your request, including your address to: Ludlams@nhlbi.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: January 4, 2010. Michael S. Lauer, Director, Division of Cardiovascular Science, NHLBI, National Institutes of Health. Dated: January 6, 2010. Suzanne Freeman, Chief, FOIA, NHLBI, National Institutes of Health. [FR Doc. 2010–974 Filed 1–19–10; 8:45 am] BILLING CODE 4140–01–P E:\FR\FM\20JAN1.SGM 20JAN1

Agencies

[Federal Register Volume 75, Number 12 (Wednesday, January 20, 2010)]
[Notices]
[Page 3237]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-974]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Proposed Collection; Comment Request; Women's Health Initiative 
Observational Study

SUMMARY: In compliance with the requirement of Section 3506(c)(2)(A) of 
the Paperwork Reduction Act of 1995, for opportunity for public comment 
on proposed data collection projects, the National Heart, Lung, and 
Blood Institute (NHLBI), 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: The Women's Health Initiative (WHI) Observational Study. 
Type of Information Collection Request: Revision OMB 0925-
0414. Need and Use of Information Collection: This study will be used 
by the NIH to evaluate risk factors for chronic disease among older 
women by developing and following a large cohort of postmenopausal 
women and relating subsequent disease development to baseline 
assessments of historical, physical, psychosocial, and physiologic 
characteristics. In addition, the observational study will complement 
the clinical trial (which has received clinical exemption) and provide 
additional information on the common causes of frailty, disability and 
death for postmenopausal women, namely, coronary heart disease, breast 
and colorectal cancer, and osteoporotic fractures. Continuation of 
follow-up for ascertainment of medical history update forms will 
provide essential data for outcomes assessment for this population of 
aging women. Frequency of Response: Annually. Affected Public: 
Individuals or households and health care providers. Type of 
Respondents: Women, next-of-kin, and physician's office staff. The 
annual reporting burden is as follows:

                                         Estimate of Annual Hour Burden
----------------------------------------------------------------------------------------------------------------
                                                     Number of     Frequency of    Average hours    Annual hour
                Type of  response                   respondents      response      per response       burden
----------------------------------------------------------------------------------------------------------------
Observational Study Participants................          42,550            1.12           .4155       19,800
Next of Kin \1\.................................             941            1              .083            79
Health Care Providers \1\.......................               8            1              .085              .63
                                                 ---------------------------------------------------------------
    Total.......................................          43,499  ..............  ..............       19,880
----------------------------------------------------------------------------------------------------------------
\1\ Annual burden is placed on health care providers and respondent relatives/informants through requests for
  information which will help in the compilation of the number and nature of new fatal and nonfatal events.

    The annualized cost to respondents is estimated at $397,617, 
assuming respondents time at the rate of $20 per hour and physician 
time at the rate of $50 per hour. There are no Capital Costs to report. 
There are no Operating or Maintenance Costs to report.
    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 to obtain a copy of the data collection plans and 
instruments, contact Ms. Shari Eason Ludlam, MPH, Project Officer, NIH, 
NHLBI, 6701 Rockledge Drive, MSC 7913, Bethesda, MD 20892-7934, or call 
non-toll-free number 301-402-2900 or E-mail your request, including 
your address to: Ludlams@nhlbi.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: January 4, 2010.
Michael S. Lauer,
Director, Division of Cardiovascular Science, NHLBI, National 
Institutes of Health.
    Dated: January 6, 2010.
Suzanne Freeman,
Chief, FOIA, NHLBI, National Institutes of Health.
[FR Doc. 2010-974 Filed 1-19-10; 8:45 am]
BILLING CODE 4140-01-P
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