Effectiveness of Gestaverso Virtual Reality Birth Preparation in Women With Previous Negative Birth Experiences

NCT ID
NCT07846306
Registry status
Not yet recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
Fundación de investigación HM
Conditions
Childbirth-Related Anxiety, Fear of Childbirth

Overview

ClinicalTrials.gov lists this study as Not yet recruiting.

Official title: Effectiveness of Gestaverso Versus Usual Childbirth Preparation in Pregnant Women With Previous Negative Birth Experiences: A Multicenter Randomized Controlled Trial

Enrollment: 124 participants (Estimated).

What is being studied

  • Behavioral: Control group
  • Intervention: Control Groups
  • Intervention: Epidemiologic Methods
  • Intervention: Epidemiologic Research Design
  • Behavioral: Gestaverso
  • Intervention: Investigative Techniques
  • Intervention: Methods
  • Intervention: Research Design

Who may be eligible

Ages
18 Years to no maximum
Sex
Female
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: * Pregnant women aged 18 years or older. * Pregnant women at or beyond 32 weeks of gestation. * Having experienced at least one previous childbirth. * Reporting a previous negative childbirth experience, defined by an affirmative response to the question: "Was there any moment during your previous childbirth that you found distressing or traumatic?" * Ability to read and understand the language in which the childbirth preparation program is delivered. * Willingness to participate voluntarily and provide written informed consent. Exclusion Criteria: * Women who have never given birth before (primiparous women). * Previous psychiatric diagnosis or anxiety disorder requiring active treatment. * Multiple pregnancies, high-risk pregnancies, or obstetric complications that may limit participation. * Cognitive or sensory impairments that prevent the use of virtual reality.

Study locations

No study locations are listed in the registry data.

Study details

Start date
November 1, 2026
Primary completion date
June 30, 2027
Completion date
July 1, 2027
First posted
September 29, 2026

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07846306
Registry last updated
September 29, 2026
QualifiedStudies registry data refreshed
October 5, 2026
QualifiedStudies record fetched
October 5, 2026

View NCT07846306 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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