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CompletedNCT06949501Updated Apr 30, 2026

The Effectiveness of Virtual Patient Simulation Versus Peer Simulation in Providing Sexual Counseling During Pregnancy

An interventional study of virtual patient simulation and peer simulation conducted in a virtual environment in Pregnancy and Sexuality, sponsored by Ankara University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-04-30.

Sponsored by Ankara University · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
51
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The aim of this study is to compare, in a multidimensional manner, the effectiveness of different educational methods-virtual patient simulation and peer simulation-in improving sexual counseling skills during pregnancy among nursing faculty students.

The study will evaluate three different training methods: virtual patient simulation, peer simulation conducted in a virtual environment, and face-to-face peer simulation. To determine the effectiveness of peer simulation and virtual patient simulation in sexual health counseling, multimodal data collection and analysis methods will be used. These methods will contribute to the development of counseling skills by examining in detail the verbal and non-verbal communication elements exhibited by participants during their interactions with virtual patients and peers. Throughout the research process, students' demographic characteristics, sexual attitudes and beliefs, sexual counseling skills, learning satisfaction and self-confidence levels, opinions on system usability, eye-tracking data, and body movements will be analyzed.

02

Conditions studied

  • Pregnancy
  • Sexuality

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03

Who can participate

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

Inclusion criteria

  • Having the ability to provide care for pregnant women - Providing informed consent to participate in the study

Exclusion criteria

Exclusion Criteria:

  • Having suspended enrollment or taken a leave of absence from education.
  • Having received formal education aimed at developing sexual counseling skills.
  • Wearing glasses (as it may interfere with the use of wearable eye-tracking systems).
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Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
51 participants (actual)

Study arms

  • Experimental
    virtual patient simulation group

    Other: virtual patient simulation

  • Experimental
    peer simulation conducted in a virtual environment group

    Other: peer simulation conducted in a virtual environment

  • Experimental
    face-to-face peer simulation group

    Other: face-to-face peer simulation

Interventions

  • Othervirtual patient simulation

    Students in this group are expected to provide sexual counseling to a virtual patient model following theoretical training. In this context, a virtual patient model has been developed with whom the students will engage for the counseling process.

  • Otherpeer simulation conducted in a virtual environment

    Students in this group are expected to provide sexual counseling to their peers in a virtual environment following theoretical training. In the virtual peer simulation, students will see the same background displayed in the virtual patient simulation; however, instead of interacting with a virtual patient, they will connect with a peer via an online platform to conduct the counseling session.

  • Otherface-to-face peer simulation

    Students in this group are expected to provide sexual counseling to their peers following theoretical training. In the peer simulation, students will conduct their sessions in a communication skills laboratory designed to resemble a clinical consultation room.

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What researchers measure

Primary outcomes

  1. Sexual Attitudes and Beliefs

    Students' sexual attitudes and beliefs will be assessed using the the sexual attitudes and belief survey. This scale is a six-point Likert-type scale, with scores ranging from a minimum of 12 to a maximum of 72. Higher scores indicate more negative attitudes and beliefs toward sexual care.

    Time frame: immediately before the training-immediately after the training

  2. Learning Satisfaction and Self-Confidence

    Learning satisfaction and self-confidence will be measured using the Student Satisfaction and Self-Confidence in Learning Scale. This scale is a five-point Likert-type scale, with responses ranging from 1 (strongly disagree) to 5 (strongly agree). Higher scores reflect greater student satisfaction and self-confidence in learning.

    Time frame: immediately after the training

  3. Sexual Counseling Skills

    Students' sexual counseling skills will be assessed using the Sexual Counseling Skills Assessment Form. This form is developed based on the BETTER, PLISSIT, Ex-PLISSIT, and One-to-One models, and it covers the entire counseling process from initiation to conclusion. Each item is scored as 0 (not demonstrated) or 1 (demonstrated). The total score ranges from 0 to 34, with higher scores indicating a higher level of skill. The form will be completed while students simulate their counseling skills.

    Time frame: During simulation

  4. System Usability Opinions

    Students' opinions regarding system usability will be assessed using the System Usability Scale (SUS). The SUS is a 10-item instrument scored on a five-point Likert scale. Scores range from a minimum of 10 to a maximum of 100. Higher scores indicate higher perceived usability of the system.

    Time frame: immediately after the training

  5. Eye Tracking

    Eye tracking parameters in the study will be assessed using a wearable eye-tracking system. This device will analyze the areas of focus during students' interactions with virtual patients and peers. The analysis of gaze points and eye movements will help evaluate the distribution of attention during communication.

    Time frame: During simulation

  6. Body Movements

    Body movements will be evaluated using a motion tracking device. These motion detection systems will analyze body language to assess participants' capacity to establish effective connections with virtual patients and peers. This method aims to evaluate participants' ability to use gestures and body language effectively to build strong relationships with patients.

    Time frame: During simulation

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Study locations

1 site
  • Ankara University Faculty of Nursing
    Ankara, Altındağ 06230, Turkey (Türkiye)
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT06949501
Lead sponsor
Ankara University
Collaborators
University of Delaware
Responsible party
NESLİHAN YILMAZ SEZER (ASSOCIATE PROFESSOR, Ankara University) — Principal investigator
First posted
Apr 29, 2025
Start date
Apr 28, 2025
Primary completion
Jun 27, 2025
Completion
Jun 27, 2025
Last update
Apr 30, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
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