This PDF is the current document as it appeared on Public Inspection on 03/24/2014 at 08:45 am.
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), 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.
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.
To Submit Comments and For Further Information: To obtain a copy of the data collection plans and instruments, submit comments in writing, or request more information on the proposed project, contact: Dr. Larissa Aviles-Santa, 6701 Rockledge, Epidemiology Branch, Program in Prevention and Population Sciences, Division of Cardiovascular Sciences, National Heart, Lung, and Blood Institute, National Institutes of Health, 6701 Rockledge Dr., MSC 7936, Bethesda, MD 20892-7936, or call non-toll-free number 301-435-0450, or Email your request, including your address to email@example.com. Formal requests for additional plans and Start Printed Page 16346instruments must be requested in writing.
Comment 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.
Proposed Collection: The Hispanic Community Health Study/Study of Latinos (HCHS/SOL), Revised, National Heart, Lung and Blood Institute (NHLBI), National Institutes of Health (NIH).
Need and Use of Information Collection: The purpose and use of the information collection for this project is to study the prevalence of cardiovascular and pulmonary disease and other chronic diseases, and their risk and protective factors, understand their relationship to all-cause, cardiovascular and pulmonary morbidity and mortality, and understand the role of sociocultural factors (including acculturation) on the prevalence or onset of disease among over 16,400 Hispanics/Latinos of diverse origins, aged 18-74 years at enrollment, living in four U.S. communities: San Diego, California; Chicago, Illinois; Miami, Florida, and the Bronx, New York. In order to achieve these objectives, the HCHS/SOL had two integrated components:
1. Examination of the cohort following a standardized protocol, which consisted of interviews and clinical measurements to assess physiological and biochemical measurements including DNA/RNA extraction for ancillary genetic research studies.
2. Follow-up of the cohort, which consists of an annual telephone interview to assess vital status, changes in health status and medication intake, and new cardiovascular and pulmonary events (including fatal and non-fatal myocardial infarction and heart failure; fatal and non-fatal stroke; and exacerbation of asthma and chronic obstructive pulmonary disease).
OMB approval is requested for 3 years. There are no costs to respondents other than their time. The total estimated annualized burden hours are 30,940.
|Type of respondents||Survey instrument||Number of respondents||Number of responses per respondent||Average time per response (in hours)||Total burden hours|
|Participants Visit 2 Examination (Appendix 15)||Pre-visit scheduling & safety screening||13,878||1||2/60||463|
|Reception, informed consent, medical releases||13,878||1||20/60||4,626|
|Ppt. safety update and routing||13,878||1||2/60||463|
|Change clothes, urine specimen||13,878||1||10/60||2,313|
|Updated personal information||13,878||1||5/60||1,157|
|Determination of fasting & blood draw||13,878||1||11/60||2,544|
|Determination of blood glucose, OGTT||13,878||1||6/60||1,388|
|2-hour blood draw, snack||13,878||12/60||2,776|
|Personal Medical History||13,878||1||10/60||2,313|
|Reproductive Medical History||9,000||1||9/60||1,350|
|Pregnancy Complications History||9,000||1||4/60||600|
|Health Care Access and Utilization||13,878||1||15/60||3,470|
|Abbreviated Medication Use||13,878||1||4/60||925|
|Participants Annual Follow-Up Interview (Appendix 16)||AFU Year 3||3,146||1||15/60||787|
|AFU Year 4||9,033||1||15/60||2,258|
|AFU Year 5||14,259||1||15/60||3,565|
|AFU Year 6||16,222||1||15/60||4,055|
|AFU Year 7||16,222||1||15/60||4,055|
|AFU Year 8||16,222||1||15/60||4,055|
|AFU Year 9||16,222||1||15/60||4,055|
|AFU Year 10||16,222||1||15/60||4,055|
|AFU Year 11||16,222||1||15/60||4,055|
Dated: March 11, 2014.
Director, DCVS, NHLBI, NIH.
Dated: March 11, 2014.
NHLBI Project Clearance Liaison, National Institutes of Health.
[FR Doc. 2014-06401 Filed 3-24-14; 8:45 am]
BILLING CODE 4140-01-P