Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
Healthy Volunteers
ID07014267

Virtual Reality for Mindfulness and Anxiety Reduction in Fertility Procedures

Led by ART Fertility Clinics LLC · Updated on 2025-07-29

500

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate how a Virtual Reality (VR)-based mindfulness and meditation intervention affects anxiety in patients undergoing fertility-related surgeries. Anxiety during fertility treatments often causes emotional distress and increased pain, so this study compares a VR intervention with standard care to see if it improves patient experience. The trial is a randomized controlled study measuring anxiety, pain perception, recovery time, and patient satisfaction to explore a patient-centered, cost-effective approach to managing anxiety in reproductive medicine. Participants are randomly assigned to one of two groups: a control group receiving standard care without VR, and an intervention group using a VR mindfulness app such as the Tripp App. Anxiety levels are measured using the State-Trait Anxiety Inventory (STAI) before, immediately after, and after the procedure. Both groups undergo fertility-related surgical procedures, with the intervention group experiencing the VR session before surgery. During the study, anxiety is assessed 10 minutes before and after the procedure, along with pain scores immediately post-procedure. The amount of pain medication used and recovery time are recorded 30 minutes after the procedure before discharge. Patient satisfaction is also measured, and effectiveness is evaluated by gender and procedure type over about one year. Participation lasts from screening through completion of all assessments and follow-up.

CONDITIONS

Brief Title

Virtual Reality for Mindfulness and Anxiety Reduction in Fertility Procedures

Who Can Participate

Age: 18Years - 50Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 to 50 years
  • Scheduled for fertility-related surgical procedures
  • Able to provide informed consent
Not Eligible

You will not qualify if you...

  • History of motion sickness or VR-related discomfort
  • Cognitive or psychological conditions affecting participation
  • Procedures requiring emergency intervention

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - Day of the procedure

Participants undergo fertility-related surgical procedures and those in the intervention group experience a Virtual Reality mindfulness intervention to reduce anxiety.

1 visit (in-person)

Post-operative Follow-up

Duration - Up to 1 year

Participants have their pain, recovery time, and satisfaction assessed up to 30 minutes after the procedure, with long-term effectiveness monitored through study completion (about 1 year).

Follow-up assessments immediately post-procedure and periodically through study completion

Trial Site Locations

Total: 1 location

1

ART Fertility Clinics LLC

Abu Dhabi, United Arab Emirates

Actively Recruiting

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Research Team

J

Jonalyn Edades, Research Coordinator

B

Barbara Lawrenz, Research Director

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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