Clinical trial · Interventional
Using Mini Program for Self-management VS Conventional Pharmaceutical Care for Cancer Pain
Comparison of Cancer Pain Patients With or Without Mini Program
NCT04844645CI-TRIAL-00051267unknownN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
With the existing medical system and insufficient medical resources in China, we developed a mini program. a pain management mini app can be useful and appreciated by patients and health care professionals, making it a good choice for the management of cancer pain in our country . our study want to develop and test the mini program for pain management among Chinese cancer patients in or discharged from hospital treatment.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cancer Pain | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| conventional pharmaceutical care | Other | — | UNRESOLVED |
| mini program | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- a mini program trial group
- description
- Pharmacists conducted a standardized education session to teach the participants how to operate the mobile phone, use mini program, assess pain. The participants in the trial group were asked to complete initial and final pain assessment questionnaires and Medication compliance on the mobile phones provided to them. Participants were encouraged to use mini program as much as possible to record their pain status.
- interventionNames
- Other: mini program
- type
- SHAM_COMPARATOR
- label
- a control group
- description
- The control group received conventional pharmaceutical care. Initial and final pain and Medication compliance data were collected. Before the patient was discharged from the hospital, the clinical pharmacist conducted detailed medication education (including medication methods, prevention and treatment of adverse reactions, and precautions) and asked the patient to attempt to maintain a paper version of the pain diary.
- interventionNames
- Other: conventional pharmaceutical care
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
Inclusion Criteria: * Patients aged 18 years or older; * Be able to read Chinese and use a mobile phone; * Histologically or cytologically confirmed solid tumor; * Diagnosed chronic cancer pain * Could understand the study process and evaluation, agreed to participate in the trial, and signed the informed consent form. Exclusion Criteria: * Illiterate person; * Incompetence; * Inability to complete the pain assessment; * Participation in any other therapies or other study protocols that may have an impact on pain intensity, which were the main outcomes of this study;
References
Publications (0)
Data not yet available
No reference posted for this study.