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Clinical Trials/NCT05736627
NCT05736627RecruitingNot Applicable

Learning Effect of Onsite vs. Online Education in a Medical Context

Bispebjerg Hospital1 site in 1 country240 target enrollmentStarted: January 1, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
240
Locations
1
Primary Endpoint
Theoretical learning

Study Overview

Brief Summary

The goal of this clinical trial is to learn about the effects of online medical education in PhD students. The main question it aims to answer is:

What is the effect of onsite compared to online research courses on theoretical knowledge of research methodology and motivation for young medical researchers? Participants will join 20 research courses which are computer randomised to be delivered online (intervention) or onsite (control group) with 10-12 PhD students of each course (200-240 participants). Participants will be followed for up to two years after their course. The outcomes are

  • theoretical learning (main)
  • academic achievements
  • motivation
  • self-efficacy

Researchers will compare online and onsite research courses to see if there is a difference in theoretical learning, academic achievements, motivation and self-efficacy.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
Single (Outcomes Assessor)

Masking Description

The randomisation result will be opened for course participants and investigator when sending out the welcome letter about 3 weeks prior to running the course.

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •All PhD students on the courses if they are able to give informed consent

Exclusion Criteria

  • •Declining to participate
  • •Withdrawal of informed consent

Arms & Interventions

Online setting

Experimental

Research course delivered digitally (Zoom or Teams meeting rooms) at a distance.

Intervention: Online (Other)

Onsite setting

No Intervention

Research course delivered physically in educational facilities.

Outcomes

Primary Outcomes

Theoretical learning

Time Frame: Up to 3 months

"Knows" or "Knows how" according to Miller's Pyramid of Competence measured by MCQ

Secondary Outcomes

  • Academic achievement(Up to 25 months)
  • Motivation(Up to 3 months)
  • Self-efficacy(Up to 3 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Hanne Tonnesen

Professor

University Hospital Bispebjerg and Frederiksberg

Study Sites (1)

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