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Virtual patients vs. peers: which better trains nurses for sexual counseling?

NCT ID NCT06949501

Knowledge-focused Sponsor: Ankara University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested two teaching methods—virtual patient simulation and peer simulation—to see which better improves nursing students' attitudes, beliefs, and skills in providing sexual counseling during pregnancy. Fifty-one students participated, and researchers measured outcomes like counseling skills, learning satisfaction, and even eye movements. The goal was to find the most effective way to train future nurses in this sensitive area.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

51 people

The number who actually took part.

Started

Apr 2025

Finished

Jun 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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).

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Conditions

The condition(s) this trial relates to.

Sexuality

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Pregnancy Sexuality

Contacts and locations

Locations

  • Ankara University Faculty of Nursing

    Ankara, Altındağ, 06230, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.