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Construction and validation of a health education platform for stoma patients based on a VR interactive storytelling game

Construction and validation of a health education platform for stoma patients based on a VR interactive storytelling game

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114137
Enrollment
Unknown
Registered
2025-12-08
Start date
2026-01-30
Completion date
Unknown
Last updated
2025-12-15

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

Conditions

Cancer

Interventions

Experimental group:Using a health education platform based on VR interactive storytelling games
Control group:Routine health education
Interview group:Routine health education

Sponsors

Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Colostomy patients: patients aged >18 years; diagnosed with CRC by clinical and pathological diagnosis and who had undergone enterostomy; with clear vision, hearing, consciousness, good communication and expression skills; aware of their condition; volunteered to participate in the study and signed an informed consent form. 2.Healthcare professionals: healthcare professionals working in gastrointestinal surgery, oncology, and stoma-related roles; volunteered to participate in this study.

Exclusion criteria

Exclusion criteria: 1.Colostomy patients: people with diagnosed cognitive impairment or other disorders that impede understanding and who are unable to communicate effectively; people with severe poppy disease in Hopi who are unable to co-operate; vulnerable groups, including people with mental illness, cognitive impairment, critically ill patients, pregnant women, illiterate people, and so on. 2.Healthcare professionals: trainees or interns; vulnerable groups other than employees of the research unit or subordinates of the researcher, including: mentally ill, cognitively impaired, critically ill, pregnant women, illiterate, etc.

Design outcomes

Primary

MeasureTime frame
Patient self-care capacity;

Secondary

MeasureTime frame
Safety assessment;Quality of life;Basic information;Satisfaction;Platform usage;Usability assessment;

Countries

China

Contacts

Public ContactXuemei Xian

Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University

xianxuemei@zju.edu.cn+86 571 86002140

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026