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Virtual Reality Application in Chemotherapy

Virtual Reality Application in Chemotherapy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03707210
Enrollment
77
Registered
2018-10-16
Start date
2018-10-11
Completion date
2019-11-30
Last updated
2021-05-28

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

Conditions

Chemotherapy Training

Keywords

virtual reality, chemotherapy

Brief summary

The present study wants to design a training program for chemotherapy with using VR. Then the investigators design a protocol to compare the training effects in the VR program and ISO document.

Detailed description

As technology advances, mobile devices have gradually turned into wearable devices. Furthermore, virtual reality (VR), augmented reality (AR), and mixed reality (MR) are being increasingly applied in medical fields such as medical education and training, surgical simulation, neurological rehabilitation, psychotherapy, and telemedicine. Research results demonstrate the ability of VR, AR, and MR to ameliorate the inconveniences that are often associated with traditional medical care, reduce incidents of medical malpractice caused by unskilled operations, and reduce the cost of medical education and training. What is more, the application of these technologies has enhanced the effectiveness of medical education and training, raised the level of diagnosis and treatment, improved the doctor-patient relationship, and boosted the efficiency of medical execution. The present study wants to design a training program for chemotherapy with using VR. Then the investigators design a protocol to compare the training effects in VR program and ISO document.

Interventions

Use VR software to make a training education program.

Sponsors

Taipei Medical University WanFang Hospital
CollaboratorOTHER
Taipei Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

intervention: VR training; control group: ISO document

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

1. The staffs who require to implement chemotherapy skill in the hospital. 2. Age over 20 years.

Exclusion criteria

1\. Refuse to join the study.

Design outcomes

Primary

MeasureTime frameDescription
The questionnaire about intervention effectAfter intervention 1 week, to perform the test. Including the content design, the convenience, the effectiveness, and promotion.After intervention, the investigator want to know the effect of intervention. A total of 12 questions, using the Likert's scale, very disagree(1) to very agree(5). It will compute a total score, score high means more effective.

Secondary

MeasureTime frameDescription
The questionnaire of Knowledge level for chemotherapy techniqueBefore the intervention, the investigator perform a pretest. After intervention 1 week, the investigator perform the post test.The questionnaire want to understand the Knowledge for chemotherapy operation skill before and after intervention. A total of ten questions, with scores ranging from 0 to 10 points. , score high means more correct.
The questionnaire of Attitude for chemotherapy operationBefore the intervention, the investigator perform a pretest. After intervention 1 week, the investigator perform the post test.The questionnaire want to understand the Attitude for chemotherapy operation skill before and after intervention. A total of ten questions, using the likert's scale, very disagree with 1 point, very agree with 5 points, total scores between 10 points and 50 points. , score high means more active.

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026