- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01249586
E-learning: Teaching of Blindness Prevention (ELBPS)
November 29, 2010 updated by: Clinica Oftamologica Zona Sul
E-learning as a Complement to Traditional Teaching of Blindness Prevention
E-learning material increases the student knowledge level before the traditional class of blindness prevention and help to fix this information a short period (one month) after the class.
Study Overview
Study Type
Interventional
Phase
- Phase 3
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
São Paulo
-
Campinas, São Paulo, Brazil, 6111
- Clinics Hospital of the State University of Campinas
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 40 years (Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Description
Inclusion Criteria:
- being a medical student matriculated in the course of ophthalmology. This course is taught to fourth-year students at State University of Campinas.
Exclusion Criteria:
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Placebo Comparator: Traditional teaching
A traditional class of blindness prevention.
|
A traditional class of blindness prevention plus an additional e-learning material.
The e-learning material included a PDF article about blindness prevention.
This material was e-mailed one week before the traditional class.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
|---|
|
Immediate pretest score
|
Secondary Outcome Measures
Outcome Measure |
|---|
|
One-month posttest score
|
|
Immediate posttest score.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
February 1, 2010
Primary Completion (Actual)
October 1, 2010
Study Completion (Actual)
October 1, 2010
Study Registration Dates
First Submitted
November 29, 2010
First Submitted That Met QC Criteria
November 29, 2010
First Posted (Estimate)
November 30, 2010
Study Record Updates
Last Update Posted (Estimate)
November 30, 2010
Last Update Submitted That Met QC Criteria
November 29, 2010
Last Verified
November 1, 2010
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ELBPS
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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