Training Program Title

Bedside Nursing

CTSA Hub Administered

no

Contact Information

Contact us by email at office@socra.org or by phone at 215-822-8644

Training Program Description

This online course will provide information on the purpose and components of a research protocol and helpful strategies for writing a protocol draft with an Institutional Review Board reviewer’s perspective in mind. Three steps to writing an abstract, the difference between a study purpose and research question, and how to synthesize a review of literature that includes justification for conducting a study will be described. Other information will include: description of a critical thinking path for selecting appropriate data collection methodologies, describing risks and benefits to human subjects, and inclusion of a dissemination plan in study design.

This is a 60 minute internet media player video of a presentation with speaker and slides. A quiz concluding the presentation will summarize the topic and evaluate your understanding of the material.

Competency Keywords

IRB, Protocol

Digital Commons Disciplines

Medical Education

Public

yes

Cost to Access

yes

Competency Domains

Scientific Concepts and Research Design; Ethical and Participant Safety Considerations; Clinical Trials Operations; Study and Site Management

Learning Objectives

At the completion of the webinar, participants should be able to:

  1. Describe an outline of required elements when drafting a protocol for Institutional Review Board submission.

Delivery Method

Online

Target Learners

Clinical Research Professionals (other than PI)

Learning Level

Skilled

Onboarding

no

Frequency

On demand

Time Needed

60 minutes

Associated Assessment

yes

Assessment Methods

Learning outcomes

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