FITBIR_DATA_ACCESS_support_stmt_a_6-14-13

FITBIR_DATA_ACCESS_support_stmt_a_6-14-13.doc

National Institute of Neurological Disorders and Stroke FITBIR Data Access Request

OMB: 0925-0677

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Supporting Statement A for





National Institute of Neurological Disorders and Stroke

FITBIR Data Access Request



(June 14, 2013)












Office of Science Policy and Planning

National Institute of Neurological Disorders and Stroke

31 Center Drive, Room 8A03

Bethesda, Maryland 20892

Phone: 301-496-9271

Fax: 301-480-9172

Email: Rebecca.Frederick@nih.gov



Table of contents


A. JUSTIFICATION

A.1 Circumstances Making the Collection of Information Necessary

A.2. Purpose and Use of the Information COLLECTION

A.3 Use of Information Technology and Burden Reduction

A.4 Efforts to Identify Duplication and Use of Similar Information

A.5 Impact on Small Businesses or Other Small Entities

A.6 Consequences of Collecting the Information Less Frequently

A.7 Special Circumstances Relating to the Guidelines of 5 CFR 1320.5

A.8 Comments in Response to the Federal Register Notice and Efforts to Consult Outside Agency

A.9 Explanation of Any Payment of Gift to Respondents

A.10 Assurance of Confidentiality Provided to Respondents

A.11 Justification for Sensitive Questions

A.12 Estimates of Hour Burden Including Annualized Hourly Costs

A.13 Estimate of Other Total Annual Cost Burden to Respondents or Record

keepers

A.14 Annualized Cost to the Federal Government

A.15 Explanation for Program Changes or Adjustments

A.16 Plans for Tabulation and Publication and Project Time Schedule

A.17 Reason(s) Display of OMB Expiration Date is Inappropriate

A.18 Exceptions to Certification for Paperwork Reduction Act Submissions














A.1 Circumstances Making the Collection of Information Necessary

The National Institutes of Health (NIH) created the Federal Interagency Traumatic Brain Injury Research Informatics System, an informatics system and central data repository, housed at the NIH Center for Information Technology, to support and accelerate research on traumatic brain injuries (TBI). FITBIR collects a wide range of data types, including phenotypic and clinical data as well as medical images, derived from individuals who participate in TBI research, regardless of the source of funding. FITBIR provides the infrastructure to store, search across, retrieve, analyze, and share these varied types of data.


The potential for public benefit to be achieved through sharing TBI research data is significant. However, genotype and phenotype information generated about individuals, such as data related to the circumstances of injury and outcomes may be sensitive. Therefore, protecting the privacy of the research participants and the confidentiality of their data is critically important. Risks to individuals, groups, or communities should be balanced carefully with potential benefits of the knowledge to be gained through FITBIR.


The information requested from the investigator seeking access to FITBIR data, as part of the Data Access Request, may be made public in part or in whole for tracking and reporting purposes. The Data Access Request provides a Privacy Act Notification pursuant to Public Law 93-579, Privacy Act of 1974, 5 U.S.C. Section 552a. Authority for the collection of the information requested from the recipient investigators comes from the authorities regarding the establishment of the National Institutes of Health, its general authority to conduct and fund research and to provide training assistance, and its general authority to maintain records in connection with these and its other functions (42 U.S.C. 203, 241, 289l-1 and 44 U.S.C. 3101), and Section 301 and 493 of the Public Health Service Act. These records will be maintained in accordance with the Privacy Act System of Record Notice 09-25-0156, (http://oma.od.nih.gov/ms/privacy/pa-files/0156.htm) covering “Records of Participants in Programs and Respondents in Surveys Used to Evaluate Programs of the Public Health Service, HHS/PHS/NIH/OD.” The NIH System of Record Notice was previously published in the Federal register on September 26, 2002, Volume 67, No 187, page 60742.


A.2 Purpose and Use of the Information Collection

The primary uses of this information are to document, track, monitor, and evaluate the use of the FITBIR datasets, as well as to notify interested recipients of updates, corrections, or other changes to the database. As part of the current Data Access Request process, NIH asks investigators to complete specific items on the Grants.gov SF 424 Form (OMB number 4040-0001, Expiration: 06/30/2011). The use of this previously OMB-approved information collection form was an expedient measure to jumpstart the use of the database in its infancy. As data submission and access procedures are maturing, NIH is interested in developing a Data Access Request Form more tailored to the unique needs of FITBIR. The type of information requested in the new FITBIR Data Access Request Form satisfies the terms and conditions of the FITBIR Data Sharing Policy. The new form contains a section wherein investigators can provide a description of the research project they are proposing to perform with FITBIR data. The form also reminds investigators to provide an annual summary of research accomplishments from using FITBIR in an updated biographical sketch or CV. As investigators typically update their sketches and CVs on a regular basis, this is unlikely to be an undue burden when requested. This valuable information will help NIH understand and evaluate the use of FITBIR in the TBI research community. 


A.3 Use of Information Technology and Burden Reduction

To gain access to FITBIR data, an investigator must obtain FITBIR data access privileges. To obtain these privileges, an investigator must complete, sign, scan, and upload the Data Access Request to the FITBIR web portal. Thus, the process for obtaining access to data within FITBIR is designed to be both electronic (information may be typed into the form and the form is uploaded via a web portal) and mechanical (signatures are requested on the form, which is then scanned and uploaded):

The FITBIR Data Access Request form requests the following pieces of information:

  • The title and a brief summary/abstract of the Research Project for which FITBIR data are sought. A single paragraph is sufficient.

  • Contact information for the investigator seeking access (the FITBIR Data Recipient).

  • Signature from the Recipient Investigator certifying that they will abide by the DUC and the NIH principles, policies and procedures for the use of FITBIR. Investigators also acknowledge that they have shared the Data Access Agreement document and the NIH policies and procedures with any research staff who will participate in the use of FITBIR. 

Once completed, the request package is then sent for adjudication to the Data Access and Quality Committee (DAQ) established to oversee access to the FITBIR shared data. When the investigator's request is approved, the investigator is notified by e-mail and explained the conditions under which the approval is granted.

A privacy impact assessment (PIA) for the FITBIR Informatics System is underway.


A.4 Efforts to Identify Duplication and Use of Similar Information

To protect and assure the confidentiality and privacy of all research participants whose data have been submitted to FITBIR, investigators who seek access to these data are expected to adhere to the specifications of the principles outlined the FITBIR Data Sharing Policy (see https://fitbir.nih.gov/assets/FITBIR_Data_Sharing_Policy.pdf , section entitled, “Data Access”). Furthermore, each research project is unique, and collecting information about these projects, through the new FITBIR Data Access Request Form, will enable NIH to document, track, monitor, and evaluate the use of the FITBIR datasets, as well as to notify interested recipients of updates, corrections, or other changes to the database.


Due to the sensitive nature of the data contained in FITBIR, and in accordance with existing NIH policies, such as that for FITBIR and genome-wide association studies (GWAS, see http://grants.nih.gov/grants/gwas/index.htm), FITBIR data access approvals are granted for one year and may be renewed thereupon.

A.5 Impact on Small Businesses or Other Small Entities

No small businesses will be involved in this study.

A.6 Consequences of Collecting the Information Less Frequently

The information requested in the FITBIR Data Access Request does not ask investigators to generate any new information, because the type of information being requested is fundamental to conducting any research study. The data are collected on a needed basis. We anticipate no more than once a year per researcher/investigator request.


Additionally, the FITBIR Data Access Request states that data recipients may be asked to provide an annual summary of research accomplishments from using FITBIR in an updated biographical sketch or CV (as noted above, FITBIR data access approvals are granted for one year and may be renewed thereupon).  As investigators typically update their sketches and CVs on a regular basis, this is unlikely to be an undue burden when requested.


As stated before, protecting the privacy of the research participants and the confidentiality of their data is critically important. Essential aspects of that protection are careful screening who may obtain access to the database, and ongoing monitoring of the use of those data.

A.7 Special Circumstances Relating to the Guidelines of 5 CFR 1320.5

Not Applicable.

A.8 Comments in Response to the Federal Register Notice and Efforts to Consult Outside Agency


A Federal Register Notice was published on February 22, 2013, Vol 78 FR 04130 (http://regulations.justia.com/regulations/fedreg/2013/02/22/2013-04130.html). No public comments were received.

The Data Access Request has been reviewed and approved by the FITBIR Data Access and Quality Committee (DAQ). The DAQ represents a subset of members of the FITBIR Data Policy Committee and includes NIH and DOD scientific and programmatic staff. Both the DAQ and the FITBIR Data Policy Committee contributed their input during the development of the Data Access Request Form.


A.9 Explanation of Any Payment of Gift to Respondents

No payment or gift will be provided to respondents.

A.10 Assurance of Confidentiality Provided to Respondents


The Federal Privacy Act protects the confidentiality of the Recipient’s NIH records. The NIH and any sites that are provided access to the datasets will have access to the data collected from the Recipient for the purposes described above. In addition, the Act allows the release of some information in the Recipient’s records without his/her permission; for example, if it is required by members of Congress or other authorized individuals. The information requested is voluntary, but necessary for obtaining access to data. 


The information requested from the investigator seeking access to FITBIR data, as part of the Data Access Request, may be made public in part or in whole for tracking and reporting purposes. The Data Access Request provides a Privacy Act Notification pursuant to Public Law 93-579, Privacy Act of 1974, 5 U.S.C. Section 552a. Authority for the collection of the information requested from the recipient investigators comes from the authorities regarding the establishment of the National Institutes of Health, its general authority to conduct and fund research and to provide training assistance, and its general authority to maintain records in connection with these and its other functions (42 U.S.C. 203, 241, 289l-1 and 44 U.S.C. 3101), and Section 301 and 493 of the Public Health Service Act. These records will be maintained in accordance with the Privacy Act System of Record Notice 09-25-0156, September 26, 2002, 67 FR 60742-60794 (http://oma.od.nih.gov/ms/privacy/pa-files/0156.htm) covering “Records of Participants in Programs and Respondents in Surveys Used to Evaluate Programs of the Public Health Service, HHS/PHS/NIH/OD.”


Although the FITBIR data will be coded and the NIH will not hold direct identifiers to individuals within the NIH FITBIR data repository, the agency recognizes the personal and potentially sensitive nature of the genotype-phenotype data. Investigators and institutions seeking access to data or images from FITBIR are expected to meet data security measures and to submit a Data Access Request, including a Data Use Certification, signed by the investigator (see: https://fitbir.nih.gov/jsp/access/index.jsp). The FITBIR Data Access and Quality Control Committee reviews and approves all submission and access requests (see https://fitbir.nih.gov/jsp/contribute/index.jsp).

A.11 Justification for Sensitive Questions

The Federal Interagency Traumatic Injury Research Informatics System does not ask any questions of a sensitive nature, such as sexual behavior and attitudes, religious beliefs, and other matters that are commonly considered private; and therefore, does no need to provide a justification for this type of information.


Upon submission of data, FITBIR staff performs a quality control review to ensure that no personally identifiable information (PII) is contained in the dataset or supporting documentation. Only data that have undergone a quality control review are approved for sharing with the research community.

A.12 Estimates of Hour Burden Including Annualized Hourly Costs

There are two scenarios for completing the form. Sometimes the Principal Investigator completes the whole document, and other times he/she has a Research Assistant complete it (after which the Investigator reviews and signs it). 


OMB approval is requested for 3 years. There are no costs to respondents other than their time. The total estimated annualized burden hours are 63.




  1. Estimates Annual Burden Hours


Form

Estimated Number of Respondents

Estimated Frequency of Response

Average time per response (in hours)

Estimated Total Annual Burden Hour Requested

FITBIR Data Access Request


40

1

95/60

63


Total


40



63


  1. Estimates of Total Annual Cost Burden

Form

Estimate Total Annual Burden Hours

Wage rate

Total Costs

FITBIR Data Access Request

63

$ 91.00

$ 5,733




A.13 Estimate of Other Total Annual Cost Burden to Respondents or Record Keepers


There are no additional costs other than the respondents’ burden given in A12.


A.14 Annualized Cost to the Federal Government

Staff

FITBIR Operations Time

BFITBIR Operations Cost*

FITBR Operations Staff Tier 1

1 hour

$17.50

FITBIR Operations Staff Tier 2

1.25 hour

$87.50

Data Access Committee Staff

1.25 hour

$106.25

Total per Data Access Request Form


$211.25

Annual # of Data Access Requests


40

Total Annualized Cost


$8,450.00




Estimated salaries*



FITBIR (T1) = $17.50/hr



FITBIR (T2) = $70/hr



DAC = $85/hr




A.15 Explanation for Program Changes or Adjustments

This is a new data collection.

A.16 Plans for Tabulation and Publication and Project Time Schedule

There is no specific plan to publish the data collected from this form. These data are for internal monitoring purposes.

A.17 Reason(s) Display of OMB Expiration Date is Inappropriate

Not applicable.

A.18 Exceptions to Certification for Paperwork Reduction Act Submissions

Not applicable.

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File Typeapplication/msword
File TitleSupporting Statement 'A' Preparation - 04/05/2011
SubjectSupporting Statement 'A' Preparation - 04/05/2011
AuthorOD/USER
Last Modified Bycurriem
File Modified2013-06-17
File Created2013-06-17

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