- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05467969
Teleteaching on Clinical Procedural Skills
July 18, 2022 updated by: Theddeus O. H. Prasetyono, Indonesia University
Online Teleteaching and Teleassessment on Clinical Procedural Skills Via Multiscreen Display Layout: A Prospective Observational Cohort Study
This study aims to develop a model of teleteaching and teleassessment for clinical procedural skills, consisted of teleteaching design making and teleteaching intervention was conducted in September 2020 - February 2021 at a tertiary center Dr. Cipto Mangunkusumo Hospital/ Faculty of Medicine Universitas Indonesia.
Study Overview
Status
Completed
Conditions
Detailed Description
Six plastic surgery residents and 12 general practitioners voluntarily participated in 3 different workshops.
Three workshops on different procedural skill sets were conducted by including surgical knotting skills, suturing techniques and basic laparoscopic hand-eye coordination skills.
A group of participants learned the skills on site, while another group joined the workshop synchronously through the online multiscreen display teleconference platform.
The teaching effectiveness was assessed using pre-post written test, OSATS, GRS and self-efficacy.
Online skills teleassessment was also compared to the asynchronous assessment based on pre-recorded videos.
Study Type
Observational
Enrollment (Actual)
18
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
-
-
DKI Jakarta
-
Jakarta Pusat, DKI Jakarta, Indonesia
- Indonesia University
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Medical doctors (General Practitioners or Residents in Plastic Surgery Training)
Description
Inclusion Criteria:
- Medical doctors (General Practitioners or Residents in Plastic Surgery Training) who volunteered to join the workhops
Exclusion Criteria:
- Participants who do not consent to join the workshops
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?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Traditional teaching
A group of participants learned the skills on site
|
|
|
Teleteaching
A group of participant who joined the workshop synchronously through the online multiscreen display teleconference platform
|
Teleteaching of procedural skills include three different techniques through three different workshops.
Each of the workshops was delivered by a respected expert faculty and then accompanied by skills assessment subsequently.
Three different group of learners joined the workshops on knotting skills, suturing skills and laparoscopic hand-eye coordination skills respectively.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Multiscreen display layouts created from multicamera configurations
Time Frame: 2 months
|
A set of configuration of multiscreen display layout was arranged using 3 different cameras to represent 3 different point of views, which accommodated the 1st person view, and two different angles of the 3rd person view
|
2 months
|
|
Pre-post written test scores
Time Frame: Through study completion, an average of 6 weeks
|
Pre-post written tests consisted of questions based on the teaching materials, used specifically to assess participants' knowledge
|
Through study completion, an average of 6 weeks
|
|
Objective Structured Assessment of Technical Skills (OSATS) Score
Time Frame: Through study completion, an average of 6 weeks
|
Checklisted-points which assessed each participants' performance while doing each procedural skills, such as
|
Through study completion, an average of 6 weeks
|
|
Global Rating Scale (GRS)
Time Frame: Through study completion, an average of 6 weeks
|
Consisted of 8 points which assessed each participants' overall performance: professional attitude, timing and movement, correct use of the model, flow, appropriate aseptic techique, overall performance, and final outcome
|
Through study completion, an average of 6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self Efficacy Scale
Time Frame: Through study completion, an average of 6 weeks
|
Consisted of points in which the participants' rated their condifence and performance after doing the procedures
|
Through study completion, an average of 6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Theddeus Prasetyono, M.D, Ph.D, Indonesian Clinical Training and Education Centre (ICTEC), Faculty of Medicine, Universitas Indonesia
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 (Actual)
September 1, 2020
Primary Completion (Actual)
February 28, 2021
Study Completion (Actual)
February 28, 2021
Study Registration Dates
First Submitted
July 4, 2022
First Submitted That Met QC Criteria
July 18, 2022
First Posted (Actual)
July 21, 2022
Study Record Updates
Last Update Posted (Actual)
July 21, 2022
Last Update Submitted That Met QC Criteria
July 18, 2022
Last Verified
July 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- Teleteaching
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.
Clinical Trials on Educational Problems
-
Cairo UniversityRecruitingEducational ProblemsEgypt
-
Gunma PAZ CollegeRecruiting
-
Stanford UniversityWithdrawn
-
The University of Texas Health Science Center at...Genentech, Inc.Active, not recruitingEducational ProblemsUnited States
-
Zeynep YılmazCompleted
-
The Cleveland ClinicActive, not recruitingEducational ProblemsUnited States
-
Stanford UniversityCompleted
-
Balikesir UniversityCompletedEducational ProblemsTurkey
-
The Hong Kong Polytechnic UniversityCompletedEducational ProblemsHong Kong
-
Tokat Gaziosmanpasa UniversityCompleted