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Clinical Trials in China / NCT06432283
Active, not recruiting Observational

A Machine Learning-based Estimated Survival Model

NCT06432283 · tracked via the Priya Life Science China tracker
Sponsor
Zhao Siyao
Phase
Observational
Started
2024-05-01
Last updated
2024-05-29

Condition(s) studied

Advanced Solid Tumor

Study summary

Malignant tumors are the leading cause of death in elderly patients, and palliative care can improve the quality of life for elderly advanced cancer patients. One of the main reasons why these patients are not included in palliative care is the lack of accurate estimation of their survival period by patients, family members, and doctors. Both doctors and patients tend to be overly optimistic about the survival period of elderly advanced cancer patients, leading to overtreatment. Therefore, assessing the risk of death for these patients and further establishing a survival period estimation model can improve the accuracy of doctors' clinical predictions of patient survival, facilitate early referral to palliative care, and promote rationalization of medical decision-making.

Eligibility

Sex
ALL
Min age
60 Years
Max age
Healthy volunteers
No
Inclusion Criteria:Inclusion criteria for late-stage malignant tumor patients: Must meet Condition 1) and also meet either Condition 2), 3), or 4): 1. Clinical diagnosis of advanced malignant tumor: TNM stage III or IV 2. "Surprise question": If this patient were to die within the next 6 months, it would not be surprising to you. 3. Karnofsky performance status (KPS) score ≤ 50 4. Palliative Performance Scale (PPS) ≤ 50% Exclusion Criteria: 1. Patients who refuse to participate in the study; 2. Patients who, for various reasons, are unable to cooperate and complete the questionnaire survey; 3. Patients who, for various reasons, are unable to cooperate and complete the follow-up.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Siyao Zhao Chengdu Sichuan

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06432283 on ClinicalTrials.gov ↗ ← All trials in China