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Improvement of Patient Experience and Healthcare Providers' Productivity Using Virtual Reality in the Field of Radiation Therapy

Improvement of Patient Experience and Healthcare Providers' Productivity Using Virtual Reality in the Field of Radiation Therapy

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04141943
Enrollment
196
Registered
2019-10-28
Start date
2020-03-13
Completion date
2021-10-31
Last updated
2020-11-18

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

Conditions

Breast Cancer

Keywords

Breast cancer, radiotherapy, virtual reality

Brief summary

The purpose of this study is to investigate the effect of providing information about radiotherapy using virtual reality and to see whether it would improve the productivity of medical staff, improve patient experience and satisfaction, and reduce patient's anxiety prior to radiotherapy.

Detailed description

All patients enrolled in this study will receive the same routine explanation all radiotherapy patients receive currently. However, prior to the routine explanation, additional detailed information regarding radiotherapy (from simulation to treatment) will be given in two different ways. VR arm: The patients who are allocated to the VR arm will receive information about radiotherapy via virtual reality. Printed document arm: The patients who are allocated to the Printed document arm will receive information about radiotherapy via printed document. Patients will answer the questionnaire related to the anxiety scale related to radiotherapy and measure the vital signs such as blood pressure, pulse rate, and the respiratory rate. Also, patients will answer the questions about radiotherapy to assess the understanding of radiotherapy and questionnaire on hospital satisfaction.

Interventions

OTHERVirtual reality

The patients who are allocated to the VR arm will receive information about radiotherapy via virtual reality.

Sponsors

Yonsei University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

1. Breast cancer patients who received curative surgery and are planned to receive radiotherapy 2. Patients with cognitive abilities to receive virtual reality information 3. Patients who are 20 years old or older

Exclusion criteria

1. Patients who have vision or hearing problems to receive information 2. Patients who do not agree to this study 3. Pregnancy, Fetuses / Newborns, Minors, and Deficient Patients 4. 65 years old or older 5. Patients who have been treated for dizziness within the last 6 months 6. Patients who have experienced severe dizziness within the last 6 months when using electronic devices

Design outcomes

Primary

MeasureTime frameDescription
Amsterdam Preoperative Anxiety and Information Scale (APAIS)Prior to receiving the radiotherapy information via VR or printed documentChanges in APAIS Before and After Providing Virtual Reality or Printed Document Information \- APAIS: scale from 1 (not worried at all) to 5 (extremely worried, most anxious)

Secondary

MeasureTime frameDescription
State-Trait Anxiety Inventory (STAI)Prior to receiving the radiotherapy information via VR or printed documentChanges in STAI Before and After Providing Virtual Reality or Printed Document Information

Countries

South Korea

Contacts

Primary ContactYong Bae Kim
ybkim3@yuhs.ac+82-2228-8095

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026