Dynamic study on symptom group of glioma patients and construction of nursing intervention plan based on PRO symptom management

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2500097625

Enrollment

Unknown

Registered

2025-02-21

Start date

2022-03-07

Completion date

Unknown

Last updated

2025-02-24

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

Conditions

glioma tumor

Interventions

intervention group:Evidence based nursing plan

Eligibility

Sex/Gender

All

Age

22 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Voluntarily participate in the experiment and sign the informed consent form; 2. Meet the diagnostic criteria for intracranial tumors, and the pathological results shall prevail; 3. Patients with initial intracranial tumors and no communication barriers

Exclusion criteria

Exclusion criteria: 1. Merge with other tumor patients 2. Patients with underlying diseases that already affect intracranial tumors (such as renal dysfunction) 3. Have received treatment other than surgery 4. Those who have serious data loss in the middle of the process; 5. Those who have serious complications or even death after surgery

Design outcomes

Primary

Measure	Time frame
Anxiety score;	—

Secondary

Measure	Time frame
Subjective well-being;	—

Countries

CHINA

Contacts

Public ContactMENG XIAOJING

Henan Provincial People's Hospital

281859025@qq.com+86 158 3835 0568

Outcome results

None listed

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