ClinicalTrials.gg
Enrolling by invitationNCT07867418Updated Oct 9, 2026

The Use of Virtual Simulations in Family Planning Counseling Training

An interventional study of AP-DESTEK Virtual Simulation Training and Standard Family Planning Counseling Education in Family Planning Counseling, Nursing Education and Virtual Simulation in Education, sponsored by Sakarya University. Enrolling by invitation at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-09.

Sponsored by Sakarya University · Not applicable, Interventional, and Other

Updated Oct 9, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study 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

Read the detailed description

Family planning is essential for both individual and societal well-being, playing a critical role in preventing unintended pregnancies, improving maternal and child health, and supporting social welfare. In healthcare systems, nurses and midwives provide vital family planning counseling services. However, traditional undergraduate training often faces time constraints in theoretical delivery, which may limit practical preparation. To address these limitations, this study utilizes a Design-Based Research (DBR) approach to develop and evaluate the AP-DESTEK virtual simulation system. DBR bridges theory and practice by contextualizing educational interventions in real-world settings. The primary objective of this randomized controlled study is to evaluate the impact of integrating interactive virtual simulations into the family planning counseling curriculum for undergraduate nursing and midwifery students. The intervention group will receive family planning counseling education supported by interactive AP-DESTEK simulations, while the control group will undergo standard curriculum instruction. The evaluation aims to examine how virtual simulation integration influences student academic achievement, satisfaction with learning, and self-confidence, while also collecting qualitative feedback from subject matter experts and participating students regarding the digital scenarios.

02

Conditions studied

  • Family Planning Counseling
  • Nursing Education
  • Virtual Simulation in Education

Keywords

  • Family planning
  • family planning counseling
  • virtual simulations
  • nursing education
  • clinical scenario
03

In context

Lead sponsor

Sakarya University is the lead sponsor of 183 studies on the registry; 51 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 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.

Exclusion criteria

Exclusion Criteria:

  • 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).
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
100 participants (estimated)

Study arms

  • Experimental
    Experiment

    AP-DESTEK Virtual Simulation Training

    Behavioral: AP-DESTEK Virtual Simulation Training

  • Active comparator
    Control

    Standard Family Planning Counseling Education

    Behavioral: Standard Family Planning Counseling Education

Interventions

  • BehavioralAP-DESTEK Virtual Simulation Training

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

    Also known as: experiment

  • BehavioralStandard Family Planning Counseling Education

    Standard/traditional theoretical curriculum on family planning counseling.

    Also known as: control

06

What researchers measure

Primary outcomes

  1. Academic Achievement in Family Planning Counseling

    Knowledge score evaluated through an achievement test on family planning counseling

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

  2. 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.

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

Secondary outcomes

  1. Student Perception of Educational Practices

    easured using the Educational Practices Questionnaire (Jeffries \& Rizzolo, 2006). The questionnaire consists of 16 items covering 4 factors: Active Learning, Collaboration, Diverse Ways of Learning, and High Expectations. Items are rated on a 5-point Likert scale from 1 (not important) to 5 (very important). Higher scores reflect higher importance/perception of educational practices

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

  2. Student Satisfaction and Self-Confidence in Learning

    Measured using the Student Satisfaction and Self-Confidence in Learning Scale (NLN). The scale consists of 13 items with two subscales: "Satisfaction with Learning" and "Self-Confidence in Learning". Items are rated on a 5-point Likert scale, with total scores ranging from 17 to 61. Higher scores indicate higher satisfaction and self-confidence.

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

07

Study locations

1 site
  • Sakarya University
    Sakarya, Serdivan 54050, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No — 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.

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 9, 2026
Show all 1 update
  1. Oct 9, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07867418
Lead sponsor
Sakarya University
Collaborators
The Scientific and Technological Research Council of Turkey
Responsible party
zeliha demir kaymak (Assoc. Prof. Dr. Zeliha Demir-Kaymak, Sakarya University) — Principal investigator
First posted
Oct 9, 2026
Start date
Sep 28, 2026
Primary completion
Oct 26, 2026 (estimated)
Completion
Nov 2026 (estimated)
Last update
Oct 9, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

No contact was published for this record. The registry link below has the sponsor’s details.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion