NCT07867418

Brief Summary

The goal of this clinical trial is to learn if using virtual simulations (AP-DESTEK) works to improve family planning counseling education for nursing and midwifery undergraduate students. The main questions it aims to answer are: What are the opinions of subject matter experts and nursing/midwifery students regarding the digital simulations prepared for family planning counseling education? How does the use of virtual simulations in family planning counseling education affect students' academic achievement, satisfaction, and self-confidence in learning? Researchers will compare students using the virtual simulation system (AP-DESTEK) to a control group receiving traditional/standard family planning counseling education to evaluate its effectiveness. Participants will:Complete a pre-test before the educational intervention. Receive family planning counseling education via the AP-DESTEK virtual simulation system or standard educational methods. Complete a post-test, the Student Satisfaction and Self-Confidence in Learning Scale, and the Educational Practices Questionnaire to evaluate achievement, satisfaction, and self-confidence

Trial Health

75
On Track

Trial Health Score

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

Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
1mo left

Started Sep 2026

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress36%
Sep 2026Nov 2026

Study Start

First participant enrolled

September 28, 2026

Completed
7 days until next milestone

First Submitted

Initial submission to the registry

October 5, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

October 9, 2026

Completed
17 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 26, 2026

Expected
6 days until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2026

Last Updated

October 9, 2026

Status Verified

October 1, 2026

Enrollment Period

28 days

First QC Date

October 5, 2026

Last Update Submit

October 5, 2026

Conditions

Keywords

Family planningfamily planning counselingvirtual simulationsnursing educationclinical scenario

Outcome Measures

Primary Outcomes (2)

  • Academic Achievement in Family Planning Counseling

    Knowledge score evaluated through an achievement test on family planning counseling

    Baseline (pre-test) and immediately post-intervention (post-test, at the 4th week)

  • Counselor Self-Efficacy

    This scale was developed by Johnson et al. to measure the self-efficacy of psychological counselors. The version of the scale adapted into Turkish by Bozkurt Karalı and Özkan (2020) will be used. The Counselor Self-Efficacy Scale (CSES) was adapted into Turkish by Bozkurt Karalı and Özkan (2020), involving validity and reliability analyses. Following the establishment of the scale's linguistic validity, exploratory and confirmatory factor analyses were conducted to examine its construct validity. The analyses resulted in a reliability coefficient (Cronbach's alpha) of 0.985 for the 33 items.

    Baseline (pre-test) and immediately post-intervention (post-test, at the 4th week)

Secondary Outcomes (2)

  • Student Perception of Educational Practices

    Immediately post-intervention (at the 4th week / post-test)

  • Student Satisfaction and Self-Confidence in Learning

    Immediately post-intervention (at the 4th week / post-test)

Study Arms (2)

Experiment

EXPERIMENTAL

AP-DESTEK Virtual Simulation Training

Behavioral: AP-DESTEK Virtual Simulation Training

Control

ACTIVE COMPARATOR

Standard Family Planning Counseling Education

Behavioral: Standard Family Planning Counseling Education

Interventions

Family planning counseling training delivered through interactive virtual simulations (AP-DESTEK).

Also known as: experiment
Experiment

Standard/traditional theoretical curriculum on family planning counseling.

Also known as: control
Control

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Being an undergraduate student currently enrolled in the Nursing or Midwifery Department at Sakarya University Faculty of Health Sciences.
  • Taking the Family Planning Counseling course during the study period.
  • Volunteering to participate in the study and providing written informed consent.

You may not qualify if:

  • Students who do not consent to participate in the study.
  • Students who have previously taken a formal course or professional training specifically on family planning counseling prior to the current academic semester.
  • Students who fail to complete all required training sessions or evaluation questionnaires (pre-test/post-test).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sakarya University

Sakarya, Serdivan, 54050, Turkey (Türkiye)

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: A randomized controlled trial with a 2x2 mixed (split-plot) pretest-posttest design will be used. Participants will be randomly allocated into two parallel groups: an intervention group receiving family planning counseling training supported by the AP-DESTEK virtual simulation system, and a control group receiving standard theoretical education. Outcome measures (academic achievement, learning satisfaction, and self-confidence) will be evaluated before and after the intervention in both groups.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assoc. Prof. Dr. Zeliha Demir-Kaymak

Study Record Dates

First Submitted

October 5, 2026

First Posted

October 9, 2026

Study Start

September 28, 2026

Primary Completion (Estimated)

October 26, 2026

Study Completion (Estimated)

November 1, 2026

Last Updated

October 9, 2026

Record last verified: 2026-10

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be made publicly available to protect participant privacy. De-identified aggregate data and study results will be published in scientific journals and presented at academic conferences.

Locations