2016-09313. Submission for OMB Review; 30-Day Comment Request; The Framingham Heart Study (NHLBI)  

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    SUMMARY:

    Under the provisions of Section 3507(a)(1)(D) of the Paperwork Reduction Act of 1995, 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 12/31/2015, pages 81830-81832. No comment s were received. The purpose of this notice is to allow an additional 30 days for public comment. The National Heart, Lung and Blood Institute (NHLBI), 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 currently valid OMB control number.

    Direct Comments to OMB: Written comments and/or suggestions regarding the 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, OIRA_submission@omb.eop.gov or by fax to 202-395-6974, Attention: NIH Desk Officer.

    Comment 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.

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    FOR FURTHER INFORMATION CONTACT:

    To obtain a copy of the data collection plans and instruments, submit comments in writing, or request more information on the proposed project, contact: Ms. Deshiree Belis, National Heart, Lung, and Blood Institute, National Institutes of Health, 6705 Rockledge Dr., Suite 6185A, Bethesda, MD 20892, or call non-toll-free number 301-435-1032, or Email your request, including your address to deshiree.belis@nih.gov. Formal requests for additional plans and instruments must be requested in writing.

    Proposed Collection: The Framingham Heart Study, 0925-0216, Revision, National Heart, Lung, and Blood Institute (NHLBI), the National Institutes of Health (NIH).

    Need and Use of Information Collection: This proposal is to extend the Framingham Study to examine the Generation Three Cohort, New Offspring Spouses and Omni Group 2 Cohort, as well as to continue to monitor the morbidity and mortality which occurs in all Framingham Cohorts. The contractor, with the collaborative assistance of NHLBI Intramural staff, will invite study participants, schedule appointments, administer examinations and testing, enter information into computer databases for editing, and prepare scientific reports of the information for publication in appropriate scientific journals. All participants have been examined previously and thus the study deals with a stable, carefully described group. Data are collected in the form of an observational health examination involving such components as blood pressure measurements, venipuncture, electrocardiography and a health interview, including questions about lifestyles and daily living situations. The National Heart, Lung, and Blood Institute uses the results of the Framingham Study to: (1) Characterize risk factors for cardiovascular and lung diseases so that national prevention programs can be designed and implemented; (2) evaluate trends in cardiovascular diseases and risk factors over time to measure the impact of overall preventive measures; and (3) understand the etiology of cardiovascular and lung diseases so that effective treatment and preventive modalities can be developed and tested. Most of the reports of study results have been published in peer reviewed medical journals and books.

    OMB approval is requested for 3 years. There are no costs to respondents other than their time. The total estimated annualized burden hours are 8,382.

    Estimated Annualized Burden HoursStart Printed Page 23736

    Table A.12-1.1—Estimate of Respondent Burden, Original Cohort Annualized

    Type of respondentNumber of respondentsNumber of responses per respondentAverage time per response (in hours)Total annual burden hour
    I. Participant Components Annual Follow-Up:
    a. Records Request (Attach #5)30115/608
    b. Health Status Update (Attach #3)30115/608
    Sub-Total: Participant Components* 3015
    II. Non-Participant Components:
    A. Informant Contact (Pre-exam and Annual Follow-up) (Attach #3—pages 3-7)15110/603
    B. Health Care Provider Records Request (Annual follow-up) (Attach #5)30115/608
    Sub-Total: Non-Participant Components4510
    Total: Participant and Non-Participant Components757525
    * Number of participants as reflected in Row I.b. above.

    Table A.12-1.2—Estimate of Respondent Burden, Offspring Cohort and OMNI Group 1 Cohort Annualized

    Type of respondentNumber of respondentsNumber of responses per respondentAverage time per response (in hours)Total annual burden hour
    I. Participant Components Annual Follow-Up:
    a. Records Request (Attach #5)1500115/60375
    b. Health Status Update (Attach #3)1700115/60425
    Sub-Total: Participant Components*1700800
    II. Non-Participant Components:
    A. Informant contact (Pre-exam and Annual Follow-up) (Attach #3-pages 3-7)150110/6025
    B. Health Care Provider Records Request (Annual follow-up) (Attach #5)1500115/60375
    Sub-Total: Non-Participant Components1650400
    Total: Participant and Non-Participant Components335033501200
    * Number of participants as reflected in Row I.b. above.

    Table A.12—1.3—Estimate of Respondent Burden, Generation 3 Cohort, NOS and OMNI Group 2 Cohort Annualized

    Type of respondentNumber of respondentsNumber of responses per respondentAverage time per response (in hours)Total annual burden hour
    I. Participant Components:
    A. Pre-Exam
    1.Telephone contact for appointment1,450110/60242
    2. Exam appointment, scheduling, reminder and instructions (Attach #6)1,270135/60741
    B. Exam Cycle 3
    1. Exam at study center (Attach #1)1,200190/601,800
    2. Consent (Attach #10)1,200120/60400
    2. Home or nursing home visit (Attach #1—partial as respondent is capable)351135
    C. Post-Exam
    eFHS Mobile Technology for Collection of CVD Risks (Attach #2)1,100189/602,970
    D. Annual Follow—Up
    1. Records Request (Attach #5)1,200115/60300
    2. Health Status Update (Attach #3)1,400115/60350
    Sub-Total: Participant Components* 2,8506,830
    II. Non-Participant Components-Annual Follow-Up:
    A. Informant Contacts (Attach #3—pages 3-7)180110/6030
    B. Health Care Provider Record Request (Attach #5)1,155115/60289
    Sub-Total: Non-Participant Components1,335319
    Total: Participant and Non-Participant Components4,18528,8907,157
    * Number of participants as reflected in Rows I.A.1 and I.D.2 above.
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    Estimates of annualized total hour burden are summarized in Table A.12-1.4 Below.

    Type of respondentNumber of respondentsNumber of responses per respondentAverage time per response (in hours)Total annual burden hour
    Participants4580190/607,653
    Non-Participants3030115/60729
    Totals761028,382
    (Note: reported and calculated numbers differ slightly due to rounding.)
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    Dated: April 18, 2016.

    Valery Gheen,

    NHLBI Project Clearance Liaison, National Institutes of Health.

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    [FR Doc. 2016-09313 Filed 4-21-16; 8:45 am]

    BILLING CODE 4140-01-P

Document Information

Published:
04/22/2016
Department:
National Institutes of Health
Entry Type:
Notice
Document Number:
2016-09313
Dates:
Comments regarding this information collection are best assured of having their full effect if received within 30-days of the date of this publication.
Pages:
23735-23737 (3 pages)
PDF File:
2016-09313.pdf