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Development and Application Effect Research of an AI-Powered Digital Human for Personalized Grief Counseling Integrated with Narrative Medicine

Development and Application Effect Research of an AI-Powered Digital Human for Personalized Grief Counseling Integrated with Narrative Medicine

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112895
Enrollment
Unknown
Registered
2025-11-20
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

Cancer

Interventions

Pilot AI Grief Counseling Intervention Group:All enrolled family members will receive an 8-week grief counseling intervention delivered by the AI-powered digital human. Assessments of the family membe
Qualitative Interview Exploration Group:None

Sponsors

Tianjin Cancer Institute &Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Qualitative Research Interview Phase: 1. Adult family members who lost a relative with advanced cancer within the past 3–12 months; 2.Aged >= 18 years, with clear verbal expression ability; 3. Whose deceased relative received treatment in the Radiation Oncology Department of this hospital; 4. Voluntarily participate in the study and sign the informed consent form. Pilot Study Phase: 1. Primary caregivers of patients who died of advanced cancer, including family members such as spouses, parents, and children; 2. Aged >= 18 years; 3. Within 1–6 months of bereavement; 4. With mild to moderate grief level, as indicated by a score of 11–35 on the PG-13 (Prolonged Grief-13) scale; 5. Having a need for intervention but not reaching the severe level requiring inpatient treatment; 6. Providing informed consent for this study.

Exclusion criteria

Exclusion criteria: Qualitative Research Interview Phase (Exclusion Criteria): 1.Presence of severe mental illness or cognitive impairment; 2.Currently experiencing other major life stressors; 3. Unsuitable for interview due to excessive emotional arousal or emotional instability. Pilot Study Phase (Exclusion Criteria): 1.Currently receiving other formal psychological treatment or grief counseling; 2. Past or current diagnosis of severe mental disorders (e.g., schizophrenia, bipolar affective disorder, major depressive episode); 3. Concurrent experience of other major life stressors (e.g., recent death of another family member, significant financial hardship, diagnosis of a severe physical illness); 4. Pregnant or lactating women; 5. Other circumstances deemed unsuitable for participation by the researchers.

Design outcomes

Primary

MeasureTime frame
Prolonged grief disorder questionnaire,PG-13;

Countries

China

Contacts

Public ContactShuang Yang

Tianjin Cancer Institute &Hospital

yang_shuang86@126.com+86 186 2203 2575

Outcome results

None listed

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