NCT06926114

Brief Summary

This Quasi-Experimental Study evaluated whether microlearning a strategy delivering brief, focused learning units enhances knowledge acquisition and retention among fifth-year medical students studying pediatric spinal deformities compared to a traditional block-format module. Methods: twenty-four students will be included into two groups. The microlearning group will receive sequential daily learning units over ten days, while the traditional group will engage in a comprehensive two-day self-learning module. Pretest, immediate post-test, and one-month post-intervention assessments will be performed using standardized MCQ and SAQ instruments. Learner engagement, time investment, and content clarity were additionally evaluated via structured surveys.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
24

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Apr 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 25, 2025

Completed
13 days until next milestone

Study Start

First participant enrolled

April 7, 2025

Completed
6 days until next milestone

First Posted

Study publicly available on registry

April 13, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 31, 2025

Completed
7 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 7, 2025

Completed
Last Updated

May 29, 2025

Status Verified

April 1, 2025

Enrollment Period

2 months

First QC Date

March 25, 2025

Last Update Submit

May 27, 2025

Conditions

Keywords

MicrolearningMedical EducationDigital NativesHyperconnectivitySpinal deformities

Outcome Measures

Primary Outcomes (1)

  • knowledge acquisition : Short and long-term retention

    Immediatly post intervention score and one month post intervention score and the difference between pre and immediate post intervention score

Study Arms (2)

Microlearning group

EXPERIMENTAL

thirteen students will be included into the microlearning group

Device: Microlearning intervention

Traditional block-format module group

ACTIVE COMPARATOR

eleven students will be included into traditional block-format module group

Device: Traditional block-format module group

Interventions

thirteen students will be included into the microlearning group will receive sequential daily learning units over ten days, . Pretest, immediate post-test, and one-month post-intervention assessments will be performed using standardized MCQ and SAQ instruments. Learner engagement, time investment, and content clarity will be additionally evaluated via structured surveys.

Microlearning group

eleven students will be inclued into the self block module group will engage in a comprehensive two-day self-learning module. Pretest, immediate post-test, and one-month post-intervention assessments will be performed using standardized MCQ and SAQ instruments. Learner engagement, time investment, and content clarity will be additionally evaluated via structured surveys.

Traditional block-format module group

Eligibility Criteria

Age24 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Currently enrolled fifth-year medical students Registered for the optional module in Physical Medicine and Rehabilitation Access to a personal computer, tablet, or smartphone with internet connectivity Ability to access the institutional Modular Object-Oriented Dynamic Learning Environment (Moodle) learning management system (LMS) Voluntary oral informed consent Commitment to complete both pre-assessment and post-assessment evaluations Willingness to participate in either learning modality (microlearning or traditional block-format) as determined by randomization

You may not qualify if:

  • Failure to complete the pretest assessment Non-completion of the pre and post-test assessment Withdrawal of consent at any point during the study Development of circumstances that would render continued participation burdensome to the participant

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

TUN

Sousse, 4000, Tunisia

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

March 25, 2025

First Posted

April 13, 2025

Study Start

April 7, 2025

Primary Completion

May 31, 2025

Study Completion

June 7, 2025

Last Updated

May 29, 2025

Record last verified: 2025-04

Data Sharing

IPD Sharing
Will not share

Locations