Clinical trial Recruiting at 1 site Interventional Women only

Using Emotional Freedom Techniques and Virtual Reality to Help Pregnant Women Overcome Fear of Childbirth

Official title: The Effect of Emotional Freedom Techniques and Virtual Reality Application Applied to Reduce the Fear of Childbirth on Attachment and Mental Well-being in Primiparous Pregnant Women

Run by Inonu University · NCT06813547 · Data updated 2026-11-12

This study is testing if using Emotional Freedom Techniques and virtual reality can help first-time pregnant women feel less anxious about childbirth and improve their emotional well-being.

More Virtual Reality trials

Quick facts

Study typeInterventional
SexWomen only
Enrollment30 (estimated)
SponsorInonu University
Academic / other
Locations1 site (Malatya)
StatusRecruiting
StartedJanuary 31, 2025
Main results expectedDecember 31, 2025
Study endsMay 30, 2026
Registry record updatedMay 30, 2025
Trial IDNCT06813547 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are first-time pregnant women between 32 and 38 weeks of gestation who do not have psychiatric disorders or obstetric complications.

Probably not a fit

Patients who may not benefit from this study include those with verbal communication issues, psychiatric disorders, or those experiencing early labor.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to address the fear of childbirth in first-time pregnant women by utilizing Emotional Freedom Techniques (EFT) and virtual reality (VR) applications. The approach combines relaxation techniques with immersive simulations to help reduce anxiety and improve mental well-being during pregnancy. Participants will be divided into groups receiving either the intervention or no treatment, allowing for a comparison of outcomes related to maternal attachment and emotional health. The study focuses on women in their late pregnancy stages, specifically between 32 and 38 weeks gestation.

Why it matters

Potential benefit: If successful, this intervention could significantly reduce anxiety and improve the emotional well-being of expectant mothers, fostering better maternal-infant relationships.

How similar studies have gone: Other studies have shown promising results using similar nonpharmacological approaches to reduce anxiety in pregnant women, indicating potential for success in this novel application.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* No verbal communication problems
* Primiparous pregnancy
* 32/0-38/0 weeks of gestation
* Having a single, viable foetus
* No psychiatric disorder
* No obstetric complications
* Absence of scar tissue or an obstacle to touch at the points of EFT application

Exclusion Criteria:

* Not wanting to continue the research
* Early labour

Where it's running

  • Malatya Training and Research Hospital
    Malatya, Turkey (Türkiye)
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.