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Cross-sectional Study of Chinese Liver Cancer Patients

Anxiety, Depression, Immune Function and Quality of Life Among Chinese Liver Cancer Patients in the COVID-19 Pandemic Era

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05872828
Enrollment
120
Registered
2023-05-24
Start date
2023-04-01
Completion date
2024-04-30
Last updated
2023-11-22

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

Conditions

Liver Cancer

Brief summary

The goal of this cross-sectional study is to investigate the prevalence and risk factors of anxiety and depression and their relationships with immune functions and quality of life among liver cancer patients in the COVID-19 pandemic era. The objectives of this study are: 1. To examine the prevalence of anxiety and depression among patients with liver cancer during the COVID-19 pandemic. 2. To identify risk factors associated with anxiety and depression among these patients. 3. To determine the association between anxiety, depression, immune function, and quality of life among liver cancer patients. Participants will be asked to fill a digital questionnaire.

Interventions

OTHERNo intervention

Observational study. No intervention will be adopted.

Sponsors

The Nethersole School of Nursing
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Participants must meet all the following criteria for study entry: 1. Aged 18 or older. 2. Participants have a confirmed diagnosis of liver cancer in the medical records. 3. Participants are able to communicate with Chinese.

Exclusion criteria

Participants who meet any of the following criteria will be excluded from study entry: 1. Participant has multiple organ failure which makes him/her incapable to comply with the study protocol. 2. Participant has hepatic encephalopathy or severe mental disorder which makes him/her incapable of understanding the meanings of the questionnaires.

Design outcomes

Primary

MeasureTime frameDescription
Anxiety scoreBaselineParticipants' anxiety status with HADS
Depression scoreBaselineParticipants' depression status with HADS

Secondary

MeasureTime frameDescription
Immune variables 1BaselineWhite blood cell counts (WBC). Collected from daily medical records.
Immune variables 2BaselineTotal neutrophil count. Collected from daily medical records.
Immune variables 3BaselineTotal lymphocyte count. Collected from daily medical records.
Immune variables 4BaselineTotal monocyte count. Collected from daily medical records.
Quality of life score (The EORTC QLQ-C30)BaselineThe European Organization for Research and Treatment of Cancer(EORTC) Quality of Life Questionnaire results. Scores range from 0 to 100. A higher score represents a higher (better) level of functioning, or a higher (worse) level of symptoms.
Immune variables 6BaselinePercentage of lymphocytes. Collected from daily medical records.
Immune variables 7BaselineMonocyte percentage. Collected from daily medical records.
Immune variables 8BaselineC-reactive protein (CRP). Collected from daily medical records.
Immune variables 5BaselineNeutrophilic granulocyte percentage. Collected from daily medical records.
Quality of life score (The EORTC QLQ-HCC18)BaselineThe Hepatocellular Carcinoma Module of The European Organization for Research and Treatment of Cancer Quality of Life Questionnaire. Scores range from 0 to 100. A higher score represents a high level of symptomatology or problems.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026