Correlation Between Psychological Stress and Disease Progression in Newly Diagnosed Glioblastoma Patients

Trial Title: Correlation Between Psychological Stress and Disease Progression in Newly Diagnosed Glioblastoma Patients

NCT ID: NCT05515133

Condition: Glioblastoma

Conditions: Official terms:
Glioblastoma
Stress, Psychological

Conditions: Keywords:
glioblastoma
psychological stress
Immune microenvironment

Study type: Observational

Overall status: Not yet recruiting

Study design:

Time perspective: Prospective

Intervention:

Intervention type: Other
Intervention name: stressors
Description: Patients are exposed to stressful situations related to the diagnosis and treatment of the disease
Arm group label: Observation group of newly diagnosed glioblastoma patients with high-level psychological stress

Summary: It is a single-center, prospective, observational，non-randomized study of newly diagnosed glioblastoma patients conducted in a tertiary hospital. The investigators examine the psychological stress, immune biomarker changes, quality of life, and disease progression of patients with glioblastoma at five-time points. The study had two cohorts, a high-stress cohort and a low-stress cohort, which are grouped after initial recruitment. Both groups undergo total resection of tumors and received 3 months of standardized treatment with radiotherapy and chemotherapy. Neither participants nor doctors but the researcher can choose which group participants are in. No one knows if one study group is better or worse than the other.

Detailed description: Glioblastoma (GBM) is the most common and aggressive primary malignant brain tumor affecting adults, with a median survival of 12-16 months after diagnosis. The diagnosis of a malignant tumor has a huge impact on patients' psychology, which is easy to lead to patients in a state of stress. The high-stress level can lead to a change in patients' health behaviors and correlates with the prognosis outcome. In addition, psychological stress can lead to changes in the immune microenvironment, but disease progression and quality of life in glioblastoma have not been adequately demonstrated. Grouping process: 60 patients are expected to be enrolled. After enrollment, participants will receive regular tumor in situ fluid (fluid within the surgical cavity, TISF) sampling for tumor mutation burden（TMB) analysis and recceive regular MRI. Under the standard of care, participants will receive psychological stress assessment after being diagnosed. according to five psychological scales, and the patients were grouped according to the cut-off value of each scale, the psychological stress of the patients is measured by distress thermometer (DT), perceived stress scale (PSS), anxiety/depression (HADS), VAS stress, and fear of disease progression scale（PoP-Q-SF). Primary study objectives: • To evaluate the changes in immune markers of acute and chronic psychological stress in patients with glioblastoma after diagnosis. Secondary study objectives: - To evaluate the quality of life of patients with different psychological stress levels. - To evaluate the progression-free survival of patients with different psychological stress levels. Exploratory objectives: - To evaluate the effect of managing the patient's psychological stress on the patient's immune microenvironment. - To evaluate the incidence of mental illness. - To evaluate the patient treatment compliance.

Criteria for eligibility:

Study pop:
newly diagnosed glioblastoma

Sampling method: Probability Sample
Criteria:
Inclusion Criteria: - age ≥18 years - Karnofsky Performance Score ≥ 70 % - histologically confirmed, previously untreated GBM - receiving a standardized chemoradiotherapy regimen - no previous history of mental illness, drug abuse, or alcohol abuse - ability to communicate and read and write independently - willing and able to comply with the protocol as judged by the investigator's signed informed consent. Exclusion Criteria: - Patients who have any other disease, either metabolic or psychological, or who have any evidence on clinical examination or special investigations (including laboratory findings) which give reasonable suspicion of a condition that interferes with the adequate measurement of the stress axis (e.g. chronic use of corticosteroids ≥ 3 months before study entry for diseases other than glioblastoma, (dexamethasone use in the context of glioblastoma is allowed) Severe, medically treated psychiatric disorder prior to the diagnosis of glioblastoma Participation in a study with investigational drugs. - pregnancy or breast-feeding - Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, neurologic deficits that interfere with the planned walking tests, dementia, or confusional state.

Gender: All

Minimum age: 18 Years

Maximum age: 75 Years

Healthy volunteers: No

Locations:

Facility:
Name: Henan Provincial People's Hospital

Address:
City: Zhengzhou
Zip: 450003
Country: China

Contact:
Last name: Xingyao Bu
Email: xingyaob@zzu.edu.cn

Start date: December 15, 2022

Completion date: December 31, 2025

Lead sponsor:
Agency: Henan Provincial People's Hospital
Agency class: Other

Source: Henan Provincial People's Hospital

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05515133