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Electronic Patient-Reported Outcomes-Based Symptom Management for Community Cancer Patients: A Quasi-Experimental Study

Electronic Patient-Reported Outcomes-Based Symptom Management for Community Cancer Patients: A Quasi-Experimental Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128935
Enrollment
Unknown
Registered
2026-07-28
Start date
2026-08-10
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Cancer

Interventions

ePRO-MAI Monthly Monitoring and Management Group:Monthly ePRO-based symptom management
ePRO-MAI Weekly Monitoring and Management Group:Weekly ePRO-based symptom management

Sponsors

Yangzhou hospital of Traditional Chinese Medicine(TCM)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Aged =18 years old; 2.Patients with pathologically confirmed cancer or clinically diagnosed cancer via enhanced CT, magnetic resonance imaging (MRI) and other examinations; 3.Patients currently receiving active anti-tumor treatment and presenting with cancer-related clinical symptoms; 4.Permanent residents within the jurisdiction (having resided locally for at least 6 months); 5.Able and willing to complete assessment scales via mobile phones, computers, or assisted by designated monitoring personnel (e.g., village doctors); 6.Capable of complying with scheduled follow-up visits, treatment, examinations and other study procedures, and willing to sign the informed consent form voluntarily;

Exclusion criteria

Exclusion criteria: 1.Cancer patients with long-term stable condition and long survival expectancy; 2.Individuals unable to understand the study content; 3.Patients with current pregnancy; 4.Participation in other ongoing clinical studies; 5.Presence of severe mental illness or cognitive dysfunction; 6.Having any other conditions that may increase the research participation risk or interfere with study outcomes; 7.Any other conditions deemed inappropriate for enrollment by the researchers;

Design outcomes

Primary

MeasureTime frame
6-month primary care first consultation rate;

Secondary

MeasureTime frame
ePRO data completion adherence rate;Improvement rate of life functional burden;Self-efficacy improvement rate;Improvement rate of symptom burden;Timely management rate of symptom alerting;3-month primary care first consultation rate;Medical adherence;Quality of life improvement rate;

Countries

China

Contacts

Public ContactDai Xiaojun

Yangzhou hospital of Traditional Chinese Medicine(TCM)

dxj2319@163.com+86 514 8755 5176

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026