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Clinical Effects of Symptom Monitoring Management Based on Electronic Patient-Reported Outcomes (ePRO) on Improving Survival Prognosis in Advanced Cancer Patients: A Single-Center, Prospective, Randomized Controlled Clinical Trial

Clinical Effects of Symptom Monitoring Management Based on Electronic Patient-Reported Outcomes (ePRO) on Improving Survival Prognosis in Advanced Cancer Patients: A Single-Center, Prospective, Randomized Controlled Clinical Trial - Symptom Monitoring and Management for Late-Stage Cancer Patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081247
Enrollment
Unknown
Registered
2024-02-27
Start date
2024-03-19
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

Cancer

Interventions

Intervention group:The symptom management team provides specialized symptom management and intervention for cancer patients based on the ePRO system

Sponsors

Peking University Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Age =18 years; outpatient, diagnosed with advanced/late-stage cancer, currently receiving non-curative/palliative systemic anticancer treatment, including chemotherapy, targeted therapy, or immunotherapy; expected survival greater than 3 months, eligible for enrollment at any point during treatment, i.e., at any point in the treatment process or treatment cycle; able to independently complete ePRO system symptom reporting (via WeChat Mini Program) or with assistance from a family member; willing to participate in the study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: Individuals with comorbid severe mental disorders (such as severe depression, schizophrenia, etc.) or cognitive impairment who are unable to cooperate with researchers; patients receiving curative treatment (such as adjuvant chemotherapy for breast cancer); hormonal therapy as the sole treatment modality (e.g., androgen deprivation therapy for prostate cancer); indolent/slow-progressing lymphomas; non-solid tumors, including leukemia, gliomas, etc.; those currently participating in other clinical trials; subjects for whom the researcher believes other conditions could potentially interfere with the effectiveness assessment.

Design outcomes

Primary

MeasureTime frame
Overall survival;

Secondary

MeasureTime frame
EORTC QLQ-C30 physical functioning score;EORTC QLQ-C30 Global Quality of Life scale score;EORTC QLQ-C30 symptom burden score;Changes in EORTC QLQ-C30;THE PATIENTS HEALTH QUESTIONNAIRE-9 (PHQ-9);GENERAL ANXIETY DISORDER-7 (GAD-7);Completion status of chemotherapy;Emergency treatment frequency;Intervention compliance;Weekly eRPO report completion status;

Countries

China

Contacts

Public ContactLILII TANG

Peking University Cancer Hospital

tanglili_cpos@126.com+86 135 2192 0552

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026