Skip to content

A Survey Study on Cognitive Function, Pain Threshold and Quality of Life in Patients with Cancer Pain

A Survey Study on Cognitive Function, Pain Threshold and Quality of Life in Patients with Cancer Pain

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600122720
Enrollment
Unknown
Registered
2026-04-16
Start date
2025-04-01
Completion date
Unknown
Last updated
2026-04-20

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

Conditions

cancer pain

Interventions

Cancer Pain Group Without Cognitive Dysfunction:N/A
Cancer pain patients with cognitive dysfunction:N/A

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Subjects voluntarily signed the informed consent form. 2. Age = 18 years. 3. Patients with pathologically confirmed malignant tumor. 4. NRS score = 1. 5. Diagnosed with cancer pain by two or more pain specialists. 6. Able to actively cooperate in the study and answer questions objectively.

Exclusion criteria

Exclusion criteria: 1. Pain caused by other definite causes (e.g., diabetes, herpes zoster, etc.). 2. Patients with severe cardiopulmonary diseases or severe hepatic and renal dysfunction. 3. Patients diagnosed with severe anxiety, depression, schizophrenia or other mental illnesses before the onset of cancer pain. 4. Patients with a prior diagnosis of dementia, epilepsy, Parkinson’s disease, cerebral ischemia, brain injury or other neurological diseases. 5. Patients with cognitive dysfunction caused by specific organic causes. 6. Patients with intracranial metastasis of malignant tumors.

Design outcomes

Primary

MeasureTime frame
Cognitive Dysfunction;Inflammatory indicators (including IL-6, IL-8, IL-10, CRP, PCT, TNF-a);

Countries

China

Contacts

Public ContactLi Song

West China Hospital of Sichuan University

song_li76@163.com+86 28 8542 2114

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 23, 2026