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The Impact of Digital Intelligent Emotion Recognition and Psychological Intervention on Targeted Immunotherapy in Hepatocellular Carcinoma Patients: A Prospective Randomized Controlled Trial

The Impact of Digital Intelligent Emotion Recognition and Psychological Intervention on Targeted Immunotherapy in Hepatocellular Carcinoma Patients: A Prospective Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119897
Enrollment
Unknown
Registered
2026-03-05
Start date
2026-03-10
Completion date
Unknown
Last updated
2026-03-09

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

Conditions

Hepatocellular Carcinoma (HCC)

Interventions

Intervention Group:Intervention Group:Receive targeted immunotherapy + structured mindfulness-based psychological intervention (once every two weeks for 8 weeks). At month 1, month 2, and month 3, fol
Control Group:Control group: Receiving standard targeted immunotherapy, completing GAD-7 and PHQ-9 assessments, as well as multimodal data collection using the "Shouwang" non-contact physiological and

Sponsors

Cancer Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: (1) Aged over 18 years; (2) Diagnosed with hepatocellular carcinoma (HCC) by pathology or clinical criteria; (3) Complete clinical data and medical history; (4) Completed primary school education or above, to ensure the accuracy of questionnaire assessments; (5) All patients and their families signed informed consent prior to treatment, allowing retrospective review and reporting of medical records.

Exclusion criteria

Exclusion criteria: (1) History of mental illness or autoimmune disease; (2) Presence of other malignant tumors; (3) Severe cardiovascular, cerebrovascular, pulmonary, hepatic, renal disease or other organ failure; (4) Previous receipt of similar psychological intervention or targeted immunotherapy; (5) Patients identified with suicidal tendency during psychological screening.

Design outcomes

Primary

MeasureTime frame
Objective Response Rate (ORR);

Secondary

MeasureTime frame
Progression-Free Survival (PFS);Disease-Free Survival (DFS);Overall Survival (OS);Quality of Life (QoL);Effectiveness of psychotherapy;Model Accuracy;

Countries

China

Contacts

Public ContactZeng Hongmei

Cancer Hospital, Chinese Academy of Medical Sciences

hongmeizeng@cicams.ac.cn+86 158 0155 2295

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026