Clinical Trials in Taiwan / NCT07677592
Starting soon Not applicable

Immersive Virtual Reality Training for Stoma Care

NCT07677592 · tracked via the Priya Life Science Taiwan tracker
Phase
Not applicable
Started
2026-06-04
Last updated
2026-07-01

Condition(s) studied

Stoma CareNursing Education

Investigational drug(s) / intervention(s)

immersive virtual reality training programtraditional classroom lecture

immersive virtual reality training program: This training program included (1) Scenario: Hospital ward, 56-year-old female post-rectal cancer surgery with temporary colostomy; (2) Intervention: Ostomy care education via immersive VR; (3) Materials: HTC cloud platform, Insta360 camera, tripod, 2 HMDs; (4) Expert Review: Physician, nursing supervisor, academic faculty, wound/ostomy nurse, nurse practitioner; (5) Training: Two 30 minute VR sessions, one month apart, in a quiet hospital meeting room.

traditional classroom lecture: This group received (1) Intervention: Traditional classroom lecture; (2) Format: Two-hour PowerPoint session; (3) Instructor: Certified wound/ostomy nurse; (4) Location: Meeting room with audiovisual facilities, Yunlin Branch.

Study summary

This study investigates the effectiveness of immersive virtual reality (VR) training in stoma care on nurses' knowledge, skills, self-efficacy, and learning satisfaction.

Using a mixed-method design with convenience sampling, 100 clinical nurses will be recruited and randomly assigned (1:1) to experimental and control groups. The experimental group will receive two VR training sessions one month apart, while the control group will attend a single traditional classroom session. Both groups will follow stoma care replacement procedures established by National Taiwan University Hospital.

Data collection will include demographic information, knowledge/skill tests, and self-efficacy questionnaires administered at three time points: before training, immediately after training, and one month post-training. Learning satisfaction will be assessed immediately after training. Participants reporting adverse VR reactions or scoring below 4 on satisfaction will be invited to one-on-one semi-structured interviews.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Full-time registered nurses employed at the study institution or nursing students currently enrolled in a formal nursing program * Willing to participate in the study and able to provide written informed consent Exclusion Criteria: * Prior participation in virtual reality-based ostomy care training * Self-reported history of significant discomfort during VR use (e.g., dizziness, nausea, or other physical discomfort) * Individuals who consider themselves unable or unwilling to undergo VR training

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
National Taiwn University Hospital Taipei Taiwan

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07677592 on ClinicalTrials.gov ↗ ← All trials in Taiwan