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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05736627
Enrollment
240
Registered
2023-02-21
Start date
2022-01-01
Completion date
2027-12-31
Last updated
2023-02-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Online Learning

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.

Interventions

OTHEROnline

Online research course delivered live digitally at a distance.

Sponsors

Copenhagen Academy for Medical Education and Simulation
CollaboratorOTHER
University of Copenhagen
CollaboratorOTHER
Bispebjerg Hospital
Lead SponsorOTHER

Study design

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

Sex/Gender
ALL
Age
18 Years to No maximum
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

Design outcomes

Primary

MeasureTime frameDescription
Theoretical learningUp to 3 monthsKnows or Knows how according to Miller's Pyramid of Competence measured by MCQ

Secondary

MeasureTime frameDescription
Academic achievementUp to 25 monthsMeasured by Google Scholar Profile (number of publications, number of citations, H-index and i10-index
MotivationUp to 3 monthsIntrinsic Motivation Inventory
Self-efficacyUp to 3 monthsWilliams and Smith's single item measure of self-efficacy

Countries

Denmark

Contacts

Primary ContactRie Raffing
rie.raffing@regionh.dk+4538163841
Backup ContactHanne Tønnesen
hanne.tonnesen@regionh.dk+4538163840

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026