Cancer pain
Conditions
Interventions
Intervention group:Questionnaires are sent to patients' mobile phones via the platform to collect self-reported data on pain intensity, pain interference, physical function, sleep-related disturbances
Control group:The conventional telephone follow-up method is adopted, which involves follow-up calls at 1 week and 3 weeks after discharge. Nurses in the ward, who have undergone unified training, con
Sponsors
The Fourth Affiliated Hospital, Zhejiang University School of Medicine
Eligibility
Sex/Gender
All
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: 1. Aged >=18 years; 2. Histologically confirmed cancer with pain that requires analgesic medication; 3. Clear consciousness, without psychiatric diseases or cognitive impairments; 4.Basic comprehension ability, with normal vision and hearing, and basic literacy and writing skills; 5.The patient or the primary caregiver is proficient in using a smartphone, willing to accept follow-up via the cloud platform, and committed to participating throughout the program; 6.Informed consent and voluntary participation.
Exclusion criteria
Exclusion criteria: 1.Patients with severe mental disorders; 2.Patients with advanced cancer who are too frail to participate and cooperate fully throughout the program.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Patient-reported outcomes (PROs); | — |
Secondary
| Measure | Time frame |
|---|---|
| Medication compliance;Patient satisfaction; | — |
Countries
China
Contacts
Public ContactYe Chenxi
The Fourth Affiliated Hospital, Zhejiang University School of Medicine
Outcome results
None listed