Web-based platform for managing cancer pain

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial aims to develop a patient self-reporting applet designed to assist individuals with cancer pain in rural areas of China. The applet will enable participants to report their symptoms and monitor pain levels and medication usage in real-time, facilitating better communication with primary care physicians. By integrating cancer pain management into chronic disease management, the study seeks to enhance healthcare services and improve the quality of life for patients suffering from tumor-related pain. The trial is a Phase 3 interventional study focusing on the effectiveness of this web-based platform.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patients with tumors that are confirmed by pathological findings.
* Presence of tumor-related pain that is moderate or higher and requires intervention with morphine-based pain medication (++).
* Have a life expectancy of more than 6 months.
* Understand and sign a consent to participate in the study, or if the patient is unable to understand the study, his/her direct caregiver must have a good understanding of the study.

Exclusion Criteria:

* Presence of other chronic non-cancer pain/have an unresolved pain-related condition.
* Moderately severe cognitive impairment/cognitive impairment.
* Have schizophrenia or other psychiatric illness.
* Neither the patient nor his/her direct caregiver can understand how to use the Cancer Pain Management applet.
* Being pregnant.

Where it's running

• West China Hospital, Sichuan Universit
  Chengdu, Sichuan, China Recruiting

Study contacts

• Study coordinator: Xingchen Peng
• Email: pxx2014@163.com
• Phone: 18980606753

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.