Cancer pain
Conditions
Interventions
Regular Group:Timed telephone follow-up
Wechat follow-up group: reinforced education and guidance with Wechat
Sponsors
First Affiliated Hospital, School of Medicine, Zhejiang University
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Subjects voluntarily signed the informed consent for the clinical observation; 2. Digital score of persistent pain (=4) and (or) number of outbreaks of pain (=3 times per day); 3. Pain is mainly caused by physical factors, not mental and psychological factors; 4. Subjects must understand the research process and evaluation, be able to describe symptoms objectively; 5. Subjects or caregivers can use Wechat skillfully.
Exclusion criteria
Exclusion criteria: 1. Subjects had a history of alcohol abuse, drug abuse and/or opium abuse; 2. New antineoplastic drugs or new radiotherapy schemes were used during clinical observation; 3. Cognitive deficits or mental disorders, patients with consciousness disorders; 4. Used opioid analgesia in the past; 5. Any other reasons are not suitable for clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Titration time; | — |
Secondary
| Measure | Time frame |
|---|---|
| Compliance;satisfaction;Side effects;Quality of Life;sleep; | — |
Countries
China
Contacts
Public ContactZhiyou Peng
First Affiliated Hospital, School of Medicine, Zhejiang University
Outcome results
None listed