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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03079349
Other study ID # CI #20170222001
Secondary ID
Status Completed
Phase N/A
First received March 8, 2017
Last updated March 13, 2017
Start date January 1, 2016
Est. completion date March 1, 2017

Study information

Verified date March 2017
Source Carrick Institute for Graduate Studies
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To test whether the investigator's educational methodology is associated with increasing learning of participants. The investigators second objective is to test the hypothesis that learning in an online classroom would result in similar outcomes as the traditional classroom.


Description:

Subjects will be randomized into a "control" group attending a traditional classroom and a "trial" group of equal numbers participating in an online synchronous Internet streaming classroom.

Main outcome measures: Pre and post multiple choice examinations of Vestibulo-Ocular Reflex (VOR), Movement, Head Turns, Head Tremor, Neurodegeneration, Inferior Olivary Complex, Collateral Projections, Eye Movement Training, Visual Saccades, Head Saccades, Visual Impairment, Walking Speed, Neuroprotection, Autophagy, Hyperkinetic Movement, Eye and Head Stability, Oscilllatory Head Movements, Gaze Stability, Leaky Neural Integrator, Cervical Dystonia, Interstitial Nucleus of Cajal (INC) and Head Tilts, Visual Pursuits, Optokinetic Stimulation, Vestibular Rehabilitation.

Methods: All candidates will take a pretest examination of the subject material. Two 9-hour and one 8-hour sessions over 3 consecutive days will be given live in the classroom or synchronously in the online classroom using the Adobe Connect e-learning platform. Subjects randomized to the online classroom will attend the lectures in a location of their choice and will view the sessions live on the Internet. A posttest examination will be given to all candidates after completion of the course.


Recruitment information / eligibility

Status Completed
Enrollment 274
Est. completion date March 1, 2017
Est. primary completion date July 1, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 75 Years
Eligibility Inclusion Criteria:

- Licensed Health Care Professional, Active Practice

Exclusion Criteria:

- Non Licensed Health Care Professional, Non Active Practice

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Medical Education
All candidates in the Active Comparator: Traditional Classroom will take a pre course test of the subject material followed by two 9-hour and one 8-hour educational sessions given over 3 consecutive days. Following the educational sessions all candidates in the Active Comparator: Traditional Classroom will take a post course test.
Medical Intervention
All candidates in the Experimental: Online Synchronous Classroom will take a pre course test of the subject material followed by two 9-hour and one 8-hour educational sessions given over 3 consecutive days. Following the educational sessions all candidates in theExperimental: Online Synchronous Classroom will take a post course test.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Carrick Institute for Graduate Studies

Outcome

Type Measure Description Time frame Safety issue
Primary Pretest and Posttest scores Pre course test scores compared to Post course test scores 3 days
Secondary Traditional vs Online Classroom Learning Scores Pre course learning scores compared to Post course learning scores compared for traditional classroom and synchronous online learning classroom 3 days
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