84 FR 134 pgs. 33270-33272 - Proposed Collection; 60-Day Comment Request Application and Impact of Clinical Research Training on Healthcare Professionals in Academia and Clinical Research (Office of the Director)
Type: NOTICEVolume: 84Number: 134Pages: 33270 - 33272
Pages: 33270, 33271, 33272FR document: [FR Doc. 2019-14821 Filed 7-11-19; 8:45 am]
Agency: Health and Human Services Department
Sub Agency: National Institutes of Health
Official PDF Version: PDF Version
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Proposed Collection; 60-Day Comment Request Application and Impact of Clinical Research Training on Healthcare Professionals in Academia and Clinical Research (Office of the Director)
AGENCY:
National Institutes of Health, HHS.
ACTION:
Notice.
SUMMARY:
[top] In compliance with the requirement of the Paperwork
DATES:
Comments regarding this information collection are best assured of having their full effect if received within 60 days of the date of this publication.
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: Dr. Anne Zajicek, M.D., Pharm.D., Deputy Director, Office of Clinical Research, NIH Office of the Director, Building 1, Room 208A, MSC-0155, Bethesda, Maryland 20892 or call non-toll-free number (301) 480-9913 or Email your request, including your address to: zajiceka@mail.nih.gov. Formal requests for additional plans and instruments must be requested in writing.
SUPPLEMENTARY INFORMATION:
Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995 requires: Written comments and/or suggestions from the public and affected agencies are invited to address 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 minimizes 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.
Proposed Collection Title: Application and Impact of Clinical Research Training on Healthcare Professionals in Academia and Clinical Research, Office of Clinical Research, (OCR), 0925-NEW, expiration date XX/XX/XXXX, National Institutes of Health (NIH), Office of the Director (OD).
Need and Use of Information Collection: The purpose of this survey is to assess the long-term impact and outcomes of clinical research training programs provided by the Office of Clinical Research located in the NIH Office of the Director (OD) over a ten-year follow-up period. The information received from respondents will provide insight on the following: Impact of the courses on (a) promotion of professional competence, (b) research productivity and independence, and (c) future career development within clinical, translational and academic research settings. These surveys will provide preliminary data and guidance in (1) developing recommendations for collecting outcomes to assess the effectiveness of the training courses, and (2) tracking the impact of the curriculum on participants' ability to perform successfully in academic, non-academic, research, and non-research settings.
OMB approval is requested for 3 years. There are no costs to respondents other than their time. The total estimated annualized burden hours are 1,589.
| Form name | Type of respondents | Estimated number of respondents | Number of responses per respondent | Average time per response (in hours) | Total annual burden hours |
|---|---|---|---|---|---|
| OCR Learning Portal Registration | Healthcare Professionals | 2,000 | 1 | 10/60 | 333 |
| Students | 1,000 | 1 | 10/60 | 167 | |
| General Public | 500 | 1 | 10/60 | 83 | |
| IPPCR Lecture Evaluation | Healthcare Professionals | 750 | 1 | 10/60 | 125 |
| Students | 500 | 1 | 10/60 | 83 | |
| General Public | 250 | 1 | 10/60 | 42 | |
| IPPCR Final Course Evaluation | Healthcare Professionals | 750 | 1 | 10/60 | 125 |
| Students | 500 | 1 | 10/60 | 83 | |
| General Public | 250 | 1 | 10/60 | 42 | |
| PCP Lecture Evaluation | Healthcare Professionals | 750 | 1 | 10/60 | 125 |
| Students | 500 | 1 | 10/60 | 83 | |
| General Public | 250 | 1 | 10/60 | 42 | |
| PCP Final Course Evaluation | Healthcare Professionals | 750 | 1 | 10/60 | 125 |
| Students | 500 | 1 | 10/60 | 83 | |
| General Public | 250 | 1 | 10/60 | 42 | |
| NIH Summer Course in Clinical and Translational Research Course Evaluation | Healthcare Professionals | 20 | 1 | 10/60 | 3 |
| Sabbatical in Clinical Research Management Course Evaluation | Healthcare Professionals | 20 | 1 | 10/60 | 3 |
| Total | 9,540 | 1,589 |
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Lawrence A. Tabak,
Principal Deputy Director, National Institutes of Health.
[FR Doc. 2019-14821 Filed 7-11-19; 8:45 am]
BILLING CODE 4140-01-P