Agency information collection activities; proposals, submissions, and approvals,

Federal Register, March 26, 2003 (Nbr. Vol. 68, No. 58)

Notices - National Institutes of Health
Permanent Link: http://regulations.vlex.com/vid/collection-proposals-submissions-approvals-22845852
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Federal Register: March 26, 2003 (Volume 68, Number 58)NoticesPage 14669From the Federal Register Online via GPO Access [wais.access.gpo.gov]

DOCID:fr26mr03-95

DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health

National Heart, Lung, and Blood Institute; Submission for OMB Review; Comment Request, Women's Health Initiative Observational Study

SUMMARY: Under the provisions of section 3507(a)(1)(D) of the Paperwork Reduction Act of 1995, the Office of the Director, the National Heart, Lung, and Blood Institute (NHLBI), 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 September 20, 2002, page 59294 and allowed 60- days for public comment. No public comments were received. The purpose of this notice is to allow an additional 39 days for public comment. The 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 current valid OMB control number.

Proposed Collection: Title: Women's Health Initiative (WHI) Observational Study. Type of Information Collection Request: Revision: OMB No. 0925-0414, expiration date: 05/31/2003. 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. Frequency of Response: On occasion. Affected Public: Individuals and physicians. Type of Respondents: Women, next-of-kin, and physician's office staff. The annual reporting burden is as follows:

Estimated

Estimated Estimated number of Average burden total annual Type of respondents

number of responses per hours per burden hours respondents respondent response

requested

OS Participants.................................

86,886

1.4084

0.17042

20,855 Next-of-kin.....................................

2,916

1

0.0835

243 Physician's Office Staff........................

43

1

0.0835

4

Total.......................................

89,845 .............. ..............

21,102

The annualized cost burden to respondents is estimated at $211,180. There are no Capital Costs, Operating Costs and/or Maintenance Costs to report.

Request for Comments: Written comments and/or suggestions from the public and affected agencies should address one or more of the following points: (1) Evaluate whether the proposed collection is necessary for the proper performance of the function of the agency, including whether the information will have practical utility; (2) evaluate 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) enhance the quality, utility, and clarity of the information to be collected; and (4) 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.

Direct Comments to OMB: Written comments and/or suggestions regarding 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, New Executive Office Building, Room 10235, Washington, DC 20503, Attention: Desk Officer for NIH. To request more information on the proposed project or to obtain a copy of the data collection plan and instruments, contact: Dr. Linda Pottern, Project Officer, Women's Health Initiative Program Office, 6705 Rockledge Drive, 1 Rockledge Centre, Suite 300, MSC 7966, Bethesda, MD 20892-7966, or call (301) 402-2900 or E-mail your request, including your address to: Linda_ Pottern@nih.gov.

Comments 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.

Dated: March 13, 2003. Jacques E. Rossouw, Lead Project Officer, Women's Health Initiative.

FR Doc. 03-7154 Filed 3-25-03; 8:45 amBILLING CODE 4140-01-M

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