Virtual Reality for Mindfulness and Anxiety Reduction in Fertility Procedures

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

500 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-07-10

Study Completion Date

2025-12-30

Brief Summary

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This study aims to evaluate the effectiveness of a Virtual Reality (VR)-based mindfulness and meditation intervention in reducing anxiety among patients undergoing fertility-related surgical procedures. Anxiety is a common challenge in fertility treatments, often leading to emotional distress and increased pain perception. By incorporating a non-invasive VR intervention, the investigators seek to improve patient experience, minimize preoperative anxiety, and potentially reduce postoperative discomfort and recovery times. This randomized controlled trial (RCT) will compare standard care with a VR intervention in a clinical setting, measuring key outcomes such as anxiety levels, pain perception, recovery duration, and overall patient satisfaction. The findings may contribute to more patient centered fertility care, offering an innovative, scalable, and cost-effective approach to anxiety management in reproductive medicine.

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Detailed Description

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This study examines the effectiveness of a Virtual Reality (VR) mindfulness intervention in reducing anxiety for patients undergoing fertility surgeries. The trial will compare VR with standard care, measuring outcomes like anxiety, pain, recovery time, and patient satisfaction. The results could provide a cost-effective, patient-centered approach to managing anxiety in fertility treatments.

Conditions

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Virtual Reality Patient Experience

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Control Group (No VR intervention)

Patients will receive standard care without the VR intervention. Anxiety levels will be measured using the State-Trait Anxiety Inventory (STAI) before the procedure (baseline) and after the procedure.

Group Type NO_INTERVENTION

No interventions assigned to this group

Intervention Group (Virtual Reality Intervention)

Patients will experience the VR mindfulness intervention using the Tripp App or comparable applications.

Anxiety levels will be measured using the STAI before the VR experience, immediately after the VR experience, and after the procedure.

Group Type EXPERIMENTAL

Intervention Group (Virtual Reality intervention)

Intervention Type DEVICE

Patients will experience the VR mindfulness intervention using the Tripp App or comparable applications.

Anxiety levels will be measured using the STAI before the VR experience, immediately after the VR experience, and after the procedure.

Interventions

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Intervention Group (Virtual Reality intervention)

Patients will experience the VR mindfulness intervention using the Tripp App or comparable applications.

Anxiety levels will be measured using the STAI before the VR experience, immediately after the VR experience, and after the procedure.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Patients aged 18-50.
* Scheduled for fertility-related surgical procedures.
* Able to provide informed consent.

Exclusion Criteria

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

Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes