Using Virtual Reality Technology on Depression, Anxiety, and Stress Among Palestinian Patients Undergoing Breast Biopsy (VR/RCT)

Nablus University for Vocational and Technical Education

Status: Not yet enrolling

Conditions: Depression; Anxiety; Stress

Treatments: Device: Meta Quest 2 VR headset

Study type: Interventional

Funder types: Other

Identifiers

NCT07267741

Nrs.September2025/6

Details and patient eligibility

About

The goal of this randomized controlled trial was to investigate the impact of Virtual Reality (VR) technology on depression, anxiety, and stress levels among Palestinian patients undergoing breast biopsy. The study aimed to evaluate the effectiveness of VR as a non-pharmacological intervention to reduce psychological distress associated with the biopsy procedure.

The main research hypotheses are:

H01: There will be no significant difference in depression levels between patients who receive immersive VR during breast biopsy and those who receive standard care.

H02: There will be no significant difference in anxiety levels between patients who receive immersive VR during breast biopsy and those who receive standard care.

H03: There will be no significant difference in stress levels between patients who receive immersive VR during breast biopsy and those who receive standard care.

Participants will:

Receive either a VR intervention or standard care during their breast biopsy. Wear a VR headset for 15-30 minutes, experiencing a calming virtual environment designed to promote relaxation.

Complete assessments of depression, anxiety, and stress before and after the procedure using validated psychological questionnaires.

Full description

Title: The Impact of Using Virtual Reality Technology on Depression, Anxiety, and Stress Among Palestinian Patients Undergoing Breast Biopsy: A Randomized Controlled Trial

Background:

Breast biopsy is an essential diagnostic procedure for detecting breast abnormalities but often induces significant psychological distress, including depression, anxiety, and stress, which can negatively affect patient wellbeing and procedure outcomes. Virtual Reality (VR) technology provides immersive and calming environments that may help alleviate these emotional burdens without pharmacological intervention. This study aims to assess the effectiveness of VR in reducing depression, anxiety, and stress among Palestinian patients undergoing breast biopsy.

Methods:

A randomized controlled trial will be conducted at a healthcare facility in Palestine, enrolling a total of 80 patients scheduled for breast biopsy. Participants will be randomly assigned to either the VR intervention group (n=40) or the control group receiving standard care (n=40). The VR group will wear a head-mounted VR device for 15 to 30 minutes during the biopsy, immersing themselves in soothing virtual environments such as peaceful natural landscapes with accompanying relaxing music and nature sounds. Psychological assessments measuring depression, anxiety, and stress levels will be administered before and after the procedure using validated questionnaires. The data collection and intervention period will span approximately two months.

Enrollment: 80 estimated patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Female patients scheduled to undergo a breast biopsy.
• Patients older than 18 years.
• Patients who are able to provide informed consent.
• Patients with no prior history of severe psychiatric disorders that could affect the assessment of depression, anxiety, or stress.
• Patients who are willing and able to participate in the VR intervention and complete self-report questionnaires.

Exclusion criteria

• Patients who have a history of severe psychiatric disorders, epilepsy, hypertension, or chronic pain.
• Patients who are mute and cannot read or write, patients with visual, hearing, or cognitive impairment.
• Patients who have implanted hearing aids or cardiac pacemakers.
• Patients who will receive any anxiolytic, sedative, or hypnotic drugs before or during the procedure.
• Patients who may be exposed to complications during the procedure.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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80 participants in 2 patient groups

VR group

Experimental group

Description:

The VR group will utilize a head-mounted VR headset with built-in headphones. Patients will be selected for VR environments from a predefined list of natural scenes. VR will be applied during the procedure, with sessions lasting 15 to 30 minutes.

Treatment:

Device: Meta Quest 2 VR headset

control group

No Intervention group

Description:

Participants will receive only standard care according to the hospital protocol during the procedure.