Skip to content

Virtual Reality vs. Music Relaxation for Reducing Anxiety and Pain During Breast Biopsies

Virtual Reality vs. Music Relaxation for Reducing Anxiety and Pain During Breast Biopsies

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07310004
Enrollment
600
Registered
2025-12-30
Start date
2026-01-20
Completion date
2027-12-01
Last updated
2026-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Breast Biopsy, Pain

Keywords

Breast Biopsy, Virtual Reality, Mindfulness, Pain Reduction, Anxiety Reduction

Brief summary

This study aims to compare the effectiveness of a Virtual Reality (VR) application computer simulation \[(CS) VR Mindful Meditation App')\] versus music relaxation in reducing anxiety and pain in women undergoing breast biopsies. Participants will be randomized into three groups: VR, music relaxation, or standard care. Anxiety and pain will be measured using validated scales, and an optional physiological marker may be collected to assess stress levels. Participants will also be asked about their satisfaction with the intervention received, along with procedure-specific questions.

Interventions

OTHERVirtual Reality (VR) Mindful App

Patients will wear a Virtual Reality (VR) headset and use an application called CS VR Mindful Meditation App.

OTHERStandard Calming Music

Patients will listen to standard calming music played in the room.

Sponsors

Jonsson Comprehensive Cancer Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

This is a randomized controlled trial with three parallel groups: VR intervention, music relaxation, and standard care. Participants will be randomized in a 1:1:1 ratio, and interventions will last for the duration of the biopsy procedure.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Females aged 18 years or older. * Scheduled for an ultrasound-guided or stereotactic breast biopsy. * Capable of understanding and providing informed consent.

Exclusion criteria

* Individuals with a history of epilepsy, motion sickness, or severe cognitive impairment (for the VR group). * Use of anxiolytic medication immediately prior to the biopsy.

Design outcomes

Primary

MeasureTime frameDescription
Anxietyperioperatively/periprocedurallyPre- and post-procedure anxiety will be measured using the State-Trait Anxiety Inventory (STAI). The scale uses a four point Likert scale ranging from "not at all" to "very much so." The score range is from 20-80 with a higher score indicating more anxiety. The change in anxiety scores (pre- to post-procedure) will be compared across the three groups (VR, music relaxation, and control).
Pain Levelperioperatively/periprocedurallyPain will be measured using the Visual Analog Scale (VAS) before and after the procedure. The scale is a subjective measure where individuals mark pain intensity on a 100mm line. typically from "no pain" (0) to "wort possible pain" (100). Higher score is worse. The change in pain scores (pre- to post-procedure) will be analyzed. The

Secondary

MeasureTime frameDescription
Physiological MarkersDuring BiopsyHeart Rate Variability (RR intervals) may be recorded during the biopsy as an objective marker of anxiety and stress. This will be an optional measure and will require the patient to wear either a Polar H10 Heart Rate Sensor below the breast or a Heart Rate Sensor on the arm during the procedure.
Satisfaction Scoresimmediately after the intervention/procedure/surgeryFor participants in the VR and music relaxation groups, a 5-point Likert scale will measure their satisfaction with the intervention. The "Intervention Satisfaction Question" asks "How satisfied were you with the intervention you received?", with 1 being "Not at all satisfied" and 5 being "Extremely satisfied". In this scale, a higher score means a better outcome. There is also the option for "I received no intervention."

Countries

United States

Contacts

CONTACTTaylor L Johnson
taylorjohnson@mednet.ucla.edu310-889-4607
CONTACTAntonia Petruse
apetruse@mednet.ucla.edu

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026