Notices. DEPARTMENT OF HEALTH AND HUMAN SERVICES
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/register/2011/07/08/2011-17201·A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
BILLING CODE 4160-01-P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health New Proposed Collection; Comment Request; Study Logistic Formative Research Methodology Studies for the National Children's 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 Institute of Child Health and Human Development (NIHCD), 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. This proposed information collection was previously published in the **Federal Register** on April 27, 2011, pages 23605-23606, and allowed 60 days for public comment. No comments were received. The purpose of this notice is to allow an additional 30 days for public comment. Proposed Collection *Title:* Study Logistics Formative Research Methodology Studies for the National Children's Study (NCS). *Type of Information Collection Request:* Generic Clearance. *Need and Use of Information Collection:* The Children's Health Act of 2000 (Pub. L. 106-310) states:
(a)PURPOSE.—It is the purpose of this section to authorize the National Institute of Child Health and Human Development* to conduct a national longitudinal study of environmental influences (including physical, chemical, biological, and psychosocial) on children's health and development.
(b)IN GENERAL.—The Director of the National Institute of Child Health and Human Development* shall establish a consortium of representatives from appropriate Federal agencies (including the Centers for Disease Control and Prevention, the Environmental Protection Agency) to—
(1)Plan, develop, and implement a prospective cohort study, from birth to adulthood, to evaluate the effects of both chronic and intermittent exposures on child health and human development; and
(2)Investigate basic mechanisms of developmental disorders and environmental factors, both risk and protective, that influence health and developmental processes.
(c)REQUIREMENT.—The study under subsection
(b)shall—
(1)Incorporate behavioral, emotional, educational, and contextual consequences to enable a complete assessment of the physical, chemical, biological, and psychosocial environmental influences on children's well-being;
(2)Gather data on environmental influences and outcomes on diverse populations of children, which may include the consideration of prenatal exposures; and
(3)Consider health disparities among children, which may include the consideration of prenatal exposures. To fulfill the requirements of the Children's Health Act, the results of formative research will be used to maximize the efficiency (measured by scientific robustness, participant and infrastructure burden, and cost) of new and existing study measures, participant communication techniques, and technologies being utilized, and thereby inform data collection methodologies for the National Children's Study
(NCS)Vanguard and Main Studies. With this submission, the NCS seeks to obtain OMB's generic clearance to conduct formative research relating to instrument design and modality with a view to reduce item and unit non-response to Study instruments while preserving scientific quality. The results from these formative research projects will inform the feasibility (scientific robustness), acceptability (burden to participants and study logistics) and cost of NCS Vanguard and Main Study instrument design and modality in a manner that minimizes public information collection burden compared to burden anticipated if these projects were incorporated directly into either the NCS Vanguard or Main Study. *Frequency of Response:* Annual [As needed on an on-going and concurrent basis]. *Affected Public:* Members of the public, researchers, practitioners, and other health professionals. *Type of Respondents:* Women of child-bearing age, fathers, health care facilities and professionals, public health professional organizations and practitioners, and schools and child care organizations. These include both persons enrolled in the NCS Vanguard Study and their peers who are not participating in the NCS Vanguard Study. *Annual reporting burden:* See Table 1. The annualized cost to respondents is estimated at: $300,000 (based on $10 per hour). There are no Capital Costs to report. There are no Operating or Maintenance Costs to report. Table 1—Estimated Annual Reporting Burden Summary, Study Operations Data collection activity Type of respondent Estimated number of respondents Estimated number of responses per respondent Average burden hours per response Estimated total annual burden hours requested Small, focused survey and instrument design and administration NCS participants 4,000 2 1 8,000 Members of NCS target population (not NCS participants) 4,000 2 1 8,000 Health and Social Service Providers 2,000 1 1 2,000 Community Stakeholders 2,000 1 1 2,000 Focus groups NCS participants 2,000 1 1 2,000 Members of NCS target population (not NCS participants) 2,000 1 1 2,000 Health and Social Service Providers 2,000 1 1 2,000 Community Stakeholders 2,000 1 1 2,000 Cognitive interviews NCS participants 500 1 2 1,000 Members of NCS target population (not NCS participants) 500 1 2 1,000 Total 21,000 30,000 *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 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 Dr. Sarah L. Glavin, Deputy Director, Office of Science Policy, Analysis and Communication, National Institute of Child Health and Human Development, 31 Center Drive Room 2A18, Bethesda, Maryland, 20892, or call non-toll free number
(301)496-1877 or E-mail your request, including your address to *glavins@mail.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: June 21, 2011. Sarah L. Glavin, Deputy Director, Office of Science Policy, Analysis and Communications, National Institute of Child Health and Human Development. [FR Doc. 2011-17201 Filed 7-7-11; 8:45 am]
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Notices
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Pub. L.Pub. L. 106-310
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