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Upcoming Classes

How to Make the Case for Integrating Health Literacy Throughout Your Organization

Guest Speaker: Alison Caballero, Director of Programs and Services, and Christopher Trudeau, Associate Professor, University of Arkansas for Medical Sciences Center for Health Literacy

Dec 13, 2017
10:00am - 11:00am
Location: Online Region/Office: SCR

Navigating WebEx

Join Annette Parde-Maass (MCR Education and Outreach Coordinator) for a special December Breezing session as she demonstrates how to interact in WebEx using annotation tools, chat, and other resources.

Dec 20, 2017
11:00am - 12:00pm
Location: Online Region/Office: MCR

Keeping up with PubMed- On Demand Online

This class is offered continuously on demand. If you have any registration questions, please contact Ashley Cuffia at acuffia@hshsl.umaryland.edu

Repeats every month until Sun Dec 30 2018.
Nov 14, 2017, Dec 1, 2017, Jan 1, 2018, Feb 1, 2018, Mar 1, 2018, Apr 1, 2018, May 1, 2018, Jun 1, 2018, Jul 1, 2018, Aug 1, 2018, Sep 1, 2018, Oct 1, 2018, Nov 1, 2018, Dec 1, 2018 Location: Online Region/Office: SEA CHIS DIS

2018 MeSH Highlights

On January 5, 2018, join NLM staff for a highlights tour of the 2018 Medical Subject Headings (MeSH). A 20-minute presentation will feature the change of contraindications from subheading to MeSH heading; new publication types; updates to classification of isotopes and radioisotopes; additional terminology for viruses, smoking, and sugars; and restructuring in plant and animal taxonomies.

Jan 5, 2018
1:00pm - 1:30pm
Location: Online Region/Office: NTO CHIS DIS

Bibliometrics, Altmetrics, & the Question of Research Impact

What does it mean for research to be meaningful? How do metrics help and hinder our understanding of research impact? This session addresses the history and evolution of meaningful metrics in higher education.

Jan 17, 2018
1:00pm - 2:00pm
Location: Online Region/Office: PNR CHIS DIS

Moving from Data to Health Equity Action: County Health Rankings and Roadmaps

Join MAR and County Health Rankings and Roadmaps to learn about Moving from Data to Health Equity Action!

Jan 10, 2018
3:30pm - 4:30pm
Location: Online Region/Office: MAR

Keeping up with PubMed- On Demand Online

This class is offered continuously on demand. If you have any registration questions, please contact Ashley Cuffia at acuffia@hshsl.umaryland.edu

Repeats every month until Sun Dec 30 2018.
Nov 14, 2017, Dec 1, 2017, Jan 1, 2018, Feb 1, 2018, Mar 1, 2018, Apr 1, 2018, May 1, 2018, Jun 1, 2018, Jul 1, 2018, Aug 1, 2018, Sep 1, 2018, Oct 1, 2018, Nov 1, 2018, Dec 1, 2018 Location: Online Region/Office: SEA CHIS DIS

Online tutorials, videos, and other instructional materials


Results for: Subjects = ClinicalTrials.gov.

Display 1 to 10 of 10 results.

1. ClinicalTrials.gov: Results Reporting, Unique Evidence, and the Role of Medical Librarians
Description: ClinicalTrials.gov is the openly available federal registry and results database of publicly and privately funded clinical studies conducted in the United States and around the world. ClinicalTrials.gov is a vital resource for researchers, healthcare providers, and health sciences librarians who wish to consult the entire body of evidence on any particular topic. The 4-credit self-paced course is divided into three modules that contain PowerPoint lectures, reading assignments, and discussion assignments.
Format: HTML / Webinar Source Page
Subjects: ClinicalTrials.gov
Archived: No
Date Last Revised: 22-May-2017

2. Finding Studies for Patients and Researchers with New ClinicalTrials.gov Search Tools
Description: Kristina Elliott from the National Center for Biotechnology Information (NCBI) at the National Library of Medicine describes new usability and search enhancements on ClinicalTrials.gov, including changes to default search options, new search filters, and useful tools for managing searches. This presentation was created for the 2017 Medical Library Association annual conference. To try the beta site, see https://clinicaltrials.gov/beta/.
Format: MP4 Video / Video Tutorial
Subjects: ClinicalTrials.gov
Archived: No
Date Last Revised: 18-May-2017

3. ClinicalTrials.gov: New HHS and NIH Trial Reporting Requirements
Description: Rebecca Williams, Assistant Director of ClinicalTrials.gov, will provide an overview of the new clinical trial registration and results information submission requirements that became effective on January 18, 2017. The HHS regulations (42 CFR Part 11) clarify and expand the reporting requirements for clinical trials of FDA-regulated products as initially described in the Food and Drug Administration Amendments Act of 2007. The NIH policy is complementary to the regulations. These requirements are intended to help ensure information about ongoing and completed clinical trials are available to the public. Attendees will gain a better understanding of how these requirements apply to research being conducted at their institution and how to support researchers in understanding the information that must be submitted. Information on the resources available to support institutions and researchers will also be highlighted. Williams will additionally demo the beta version of ClinicalTrials.gov.
Format: HTML / Webinar Source Page
Subjects: ClinicalTrials.gov
Archived: No
Date Last Revised: 08-May-2017

4. Final Rule for Clinical Trials Registration and Results Information Submission Webinar Series
Description: A series of three live webinars provided responsible parties with information about the Final Rule for Clinical Trials Registration and Results Information Submission (42 CFR Part 11).
Format: HTML / Web Page
Subjects: ClinicalTrials.gov
Archived: No
Date Last Revised: 11-Oct-2016

5. Using ClinicalTrials.gov Content for Analysis
Description: Kristina Elliott provides an overview of using ClinicalTrials.gov content for analysis for the 2016 Medical Library Association annual conference. The presentation includes what data are available and how to download. It also includes an overview of the new 'Individual Participant Data' data element, which links to IPD shared on various platforms, critical for meta-analyses by third-party researchers. For more information, see the ClinicalTrials.gov documentation.
Format: MP4 Video / Video Tutorial
Subjects: ClinicalTrials.gov
Archived: No
Date Last Revised: 25-May-2016

6. Linking PubMed and ClinicalTrials.gov (NCBI Minute)
Description: ClinicalTrials.gov is a registry and results database of publicly and privately supported clinical studies. Citations in PubMed that report clinical trial results have links to the original studies in the ClinicalTrials database. You will learn two ways to filter PubMed searches for publications linked to clinical trials in ClinicalTrials.gov.
Format: HTML / Webinar Source Page
Subjects: Clinical Medicine, ClinicalTrials.gov, PubMed
Archived: No
Date Last Revised: 04-May-2016

7. ClinicalTrials.gov Results Database Train-theTrainer Workshop
Description: This workshop, developed for staff at National Institutes of Health (NIH) Clinical and Translational Science Award (CTSA) institutions, focused on the data entry content and format requirements of the results database and provided hands-on tutorials on PRS data entry. The materials on the Web site are from the workshops that were held in June and September 2015. ClinicalTrials.gov is considering offering more workshops, and information will be made available once the dates are confirmed.
Format: HTML / Web Page
Subjects: ClinicalTrials.gov
Archived: No
Date Last Revised: 20-Oct-2015

8. Submitting Results Data to ClinicalTrials.gov (Instructions)
Description: Four presentations provide an overview of each results module, including required data elements, review criteria, and examples of common errors.
Format: Flash Video / Video Tutorial
Subjects: ClinicalTrials.gov
Archived: No
Date Last Revised: 01-Sep-2014

9. Key FDAAA Issues
Description: Deborah A. Zarin, MD, Director, ClinicalTrials.gov, NLM discusses key issues in the Food and Drug Administration Amendments Act (FDAAA) related to registering trials and submitting results.
Format: Flash Video / Webinar
Subjects: ClinicalTrials.gov
Archived: No
Date Last Revised: 01-Oct-2011

10. Overview of ClinicalTrials.gov
Description: Deborah A. Zarin, MD, Director, ClinicalTrials.gov, National Library of Medicine (NLM) Provides an overview of the reasons for registering studies and submitting results, a history of ClinicalTrials.gov, and information on the data submission and review process.
Format: Flash Video / Webinar
Subjects: ClinicalTrials.gov
Archived: No
Date Last Revised: 01-Oct-2011