Smart VR Mindfulness for Breast Cancer: Integrating Biofeedback and Evaluating Chemotherapy Effectiveness

Recruiting now · Not applicable

Conditions studied: Breast Cancer, Chemotherapy, Virtual Reality, Mindfulness

In brief

Breast cancer patients undergoing chemotherapy often face significant physical and emotional symptoms, with stress contributing to symptom severity. This study investigates the effectiveness of a mindfulness-based virtual reality (VR) intervention in reducing stress and symptom severity. A total of 60 participants will be stratified and randomized into three groups: mindfulness-based VR, mindfulness-based audio, and control. Data will be analyzed using generalized estimating equations and machine learning. The goal is to improve understanding and quality of care for cancer patients by evaluating the potential benefits of mindfulness-based VR interventions.

Key facts

Study ID

NCT06541587

Run by

Hsin Yi Lu

People needed

60

Starts

2024-03-01

Expected to finish

2025-03-30

Last updated by the study team

2024-08-07

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Age above 18 years.
• Diagnosed with breast cancer stages I to III, with diagnostic codes C50, C79.81, C84.7A, D03.52, D05, D24, D48, or D49; there are no restrictions on tumor type, receptor subtype, or whether breast tumor removal surgery has been performed.
• Undergoing the first inpatient preoperative or postoperative chemotherapy, without restrictions on the type of medication or treatment cycles.
• Able to communicate in Mandarin and literate; without cognitive impairments, psychiatric disorders, motion sickness, epilepsy, or a history of drug or alcohol addiction.
• No prior experience with mindfulness-based interventions. Understanding of the research procedures, agreement to participate, and signing of the informed consent form; owning a smartphone capable of installing the required research applications and able to operate independently.

You may not qualify if…

• individuals with blindness or visual impairments that preclude the identification of on-screen visuals
• individuals with auditory impairments preventing the recognition of sounds through headphones.

Where it is running

• Tri-Service General Hospital — Taipei, Neihu Distinct, Taiwan (enrolling)

Full record on ClinicalTrials.gov

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