Face-to-Face Versus Distance Learning of Basic Suturing Skills
NCT ID: NCT05275829
Last Updated: 2022-03-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
118 participants
OBSERVATIONAL
2021-01-04
2021-05-19
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
A prospective randomized controlled trial involving 118 pre-medical and medical students with no previous experience in suturing was conducted. Participants were randomized into two groups for learning simple interrupted suturing: F-F and DL groups (59 students in each group) . Evaluation was conducted by two independent assessors. Agreement between the assessors was calculated, and performance scores of the participants were compared between the two groups.
All the participants demonstrated their ability to place three interrupted sutures, with no significant difference in the performance between the two groups. All the respondents positively rated the teaching sessions, found them useful and enjoyable.
Distance learning of basic suturing is as effective as the face-to-face approach in novice learners
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Online vs. In-Person Suturing Training: A Non-Inferiority Randomized Controlled Trial in a Low-Resource Setting
NCT07038525
Optimizing Resource Utilization During Proficiency-based Training of Suturing Skills to Medical Students
NCT03650959
Comparing Proficiency of Laparoscopic Vaginal Cuff Suturing After Laparoscopic Training in Surgically Naive Students
NCT04524988
A Gamified Network for Surgical Education During COVID-19: A Randomized Controlled Trial
NCT04425499
A Pilot Study on Training Simulator Efficacy
NCT05436899
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
In this study, the investigators aimed to compare the effectiveness and retention of distance learning to the traditional face-to-face learning of basic (simple interrupted) suturing in novice learners. This study entails a prospective randomized trial involving two arms (traditional face-to-face versus distance learning of basic simple interrupted suturing) in pre-medical students as well as first and second year medical students at the American University of Beirut (AUB). Immediately after the teaching session as part of research, two independent surgeons assessed the students' simple interrupted suturing performance using a validated checklist and OSATS global rating.
The difference in performance was used to determine the effectiveness of distance learning of basic suturing as compared to the traditional instructional method. In addition, the students in both groups were asked to complete a questionnaire (immediately after the teaching session) to investigate their satisfaction and confidence.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Control group: Face-to-Face learning of simple interrupted suturing
* The students watched a video demonstrating simple interrupted suturing, with the instructor commenting on the steps.
* The students then watched the video again.
* The instructor then demonstrated the procedure for the students.
* The students then practiced suturing with immediate and specific feedback provided by the instructor until he and the students were satisfied with the performance.
No interventions assigned to this group
Study group: Distance learning (tele simulation) of simple interrupted suturing
* The instructor ran the interactive tele simulation sessions utilising web-based video-conferencing technology (WebEx platform). The students used their personal smartphones or laptops with audio-video capabilities. The instructor ran the session through his smartphone.
* The instructor shared a video demonstrating simple interrupted suturing while commenting on the steps (the same video used in the control group).
* The instructor then ran the video again for the students.
* The instructor then demonstrated the skill for the students by turning on his camera.
* The students then practiced suturing, and periodically turned on their cameras to receive live and specific feedback from the instructor on their performance, until the instructor and the students were satisfied.
* No face-to-face interactions between the students and the instructor.
Tele simulation
Interactive tele simulation sessions utilising web-based video-conferencing technology (WebEx platform).
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Tele simulation
Interactive tele simulation sessions utilising web-based video-conferencing technology (WebEx platform).
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
25 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
American University of Beirut Medical Center
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Dr. Ahmad Zaghal
Assistant Professor of Clinical Speciality
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Ahmad Zaghal, MD, MSc, FACS, FEBPS
Role: PRINCIPAL_INVESTIGATOR
American University of Beirut Medical Center ; Department of Surgery
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
American University of Beirut Medical Center
Beirut, , Lebanon
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
SBS-2020-0378
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.