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

A

Ankara University

Status

Not yet enrolling

Conditions

Sexuality
Pregnancy

Treatments

Other: virtual patient simulation
Other: face-to-face peer simulation
Other: peer simulation conducted in a virtual environment

Study type

Interventional

Funder types

Other

Identifiers

NCT06949501
03.03.2025/05-87

Details and patient eligibility

About

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.

Enrollment

51 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

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

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).

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

51 participants in 3 patient groups

virtual patient simulation group
Experimental group
Treatment:
Other: virtual patient simulation
peer simulation conducted in a virtual environment group
Experimental group
Treatment:
Other: peer simulation conducted in a virtual environment
face-to-face peer simulation group
Experimental group
Treatment:
Other: face-to-face peer simulation

Trial contacts and locations

0

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Central trial contact

Ankara University Faculty of Nursing

Data sourced from clinicaltrials.gov

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