Construction and Preliminary Validation of Multi sensory Stimulation Comfort Care Technology Package

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2500113350

Enrollment

Unknown

Registered

2025-11-27

Start date

2025-12-05

Completion date

Unknown

Last updated

2025-12-01

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

Conditions

End stage, dying, cancer

Interventions

control group:Conventional Comfort Care

experimental group:Multi sensory stimulation and comfortable care technology

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Diagnosed with cancer through pathological examination, with an expected survival time of less than 6 months; 2. Age >= 18 years old; 3. The patient is aware of the disease situation, has no serious cognitive impairment or symptoms, and can clearly express their feelings; 4. Informed consent of survey subjects, etc.

Exclusion criteria

Exclusion criteria: 1. Individuals with consciousness disorders, confusion, schizophrenia, etc. who are unable to express their feelings clearly; 2. Unable to stimulate individuals.

Design outcomes

Primary

Measure	Time frame
Comfort condition;	—

Secondary

Measure	Time frame
quality of life;anxiety;	—

Countries

China

Contacts

Public ContactZhou Wei

The First Affiliated Hospital of Chongqing Medical University

zw12192021@163.com+86 187 1696 7208

Outcome results

None listed

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