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Brief Title: Portable 3D Visual Material-Supported Simulation Training for Cervical Dilation Assessment

NCT07705503 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 62

Last updated 2026-07-16

No results posted yet for this study

Summary

This randomized controlled trial aimed to evaluate the effectiveness of simulation-based education supported by a portable and mobile three-dimensional (3D) visual material on university students' knowledge of cervical dilation assessment, learning satisfaction, self-confidence in learning, and perceptions of simulation design. Undergraduate health sciences students were randomly assigned to either an intervention group receiving simulation training with the portable 3D material in addition to standard education or a control group receiving standard education alone. The primary outcome was change in knowledge of cervical dilation assessment. Secondary outcomes included student satisfaction, self-confidence in learning, and perceptions of simulation design.

Conditions

  • Assessment, Self
  • Simulation-Based Education

Interventions

BEHAVIORAL

Portable 3D Visual Material-Supported Simulation Training

Simulation-based education supported by a portable and mobile three-dimensional visual educational material designed for cervical dilation assessment. Participants practiced with the material repeatedly throughout the semester in addition to standard education.

BEHAVIORAL

Standard Education

Standard theoretical instruction and laboratory training on cervical dilation assessment delivered as part of the regular curriculum.

Sponsors & Collaborators

  • Marmara University

    lead OTHER

Principal Investigators

  • Aysegul Simsek, PhD · Marmara University

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-01-22
Primary Completion
2024-06-14
Completion
2024-06-14

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07705503 on ClinicalTrials.gov