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Effect of virtual reality based intervention model on anxiety and pain in patients with ovarian cancer undergoing intraperitoneal chemotherapy

Effect of virtual reality based intervention model on anxiety and pain in patients with ovarian cancer undergoing intraperitoneal chemotherapy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069808
Enrollment
Unknown
Registered
2023-03-27
Start date
2023-03-27
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Intraperitoneal chemotherapy for ovarian cancer

Interventions

experence group:Virtual reality technology combined with mindfulness meditation
control group:Listen to music with headphones

Sponsors

Peking Universiy International Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: (1) According to the psychological stage of cancer patients, cancer patients with "acceptance period" were selected: 18= age =60 years old; (2) Residual lesions 50ml/min, transaminase > 100u/L, consistent with abdominal chemotherapy; (4) no serious cardiovascular and cerebrovascular diseases or other co-existing diseases; (5) Sign informed consent and voluntarily cooperate with clinical researchers; (6) have not received psychological counseling and treatment before seeing a doctor; (7) Have normal Chinese communication and understanding ability; (8) Self-care Ability Scale: complete self-care, score =60-100 points

Exclusion criteria

Exclusion criteria: Exclusion criteria: (1) Active infection or open wound on face or eye; (2) Eye diseases: visual impairment, glaucoma, cataract, flying mosquito disease, visual defect; (3) People who are allergic to skin or dizzy due to contact with headphones and VR glasses; (4) Have serious hearing impairment; (6) Have a history of mental illness, such as dementia, acrophobia, claustrophobia, epilepsy, etc.

Design outcomes

Primary

MeasureTime frame
Pain score;

Secondary

MeasureTime frame
Monitor heart rate and blood pressure;State-trait anxiety scale;Fear questionnaire;

Countries

China

Contacts

Public Contactchenwenduo

Peking University International Hospital

chenwenduo@pkuih.edu.cn18600578992

Outcome results

None listed

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