Interactive AI-based Mental Health Service for the Patients With Cancer
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Interactive Artificial Intelligence.
- Who it may be relevant to
- Registry conditions: Cancer. Basic parameters: from 19 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- South Korea
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Scenario-based Clinical Interview Data Construction and User Experience Evaluation
Overview
The aims of this study are developments of mental health care services for cancer patients based on interactive artificial intelligence. To do these things, survey of unmet medical needs and data collection of clinical interviews will be done, and newly developed assessment and intervention scenarios will be simulated to cancer patients group.
Detailed description
A total of 20 people will be recruited from 3 institutions to investigate unmet medical needs. Based on the needs, we will develop scenarios to assess, classify, explain and conduct supportive interviews. We plan to develop a stress self-management scenario that helps manage lifestyle habits and provides meditation-based cognitive therapy. For moderate to severe distress, we plan to develop scenarios to link medical care and manage suicide risk. We plan to conduct interviews with a total of 300 people to collect clinical interview data for scenario development.
Interventions
- Other Interactive Artificial Intelligence
scenario based AI to assess, classify, explain and conduct supportive interviews
Primary outcome measures
- Distress [Time frame: baseline]
- Quality of life measurement [Time frame: baseline]
- Stress [Time frame: baseline]
- Self-esteem [Time frame: baseline]
- Acceptance of Disability [Time frame: baseline]
- Pain measurement [Time frame: baseline]
- Insomnia [Time frame: baseline]
- Quality of sleep [Time frame: baseline]
- Fatigue [Time frame: baseline]
- Anxiety & Depression [Time frame: baseline]
Eligibility criteria
Inclusion criteria
- Patients diagnosed with malignant tumor and undergoing treatment, or patients undergoing follow-up after completing curative treatment
Exclusion criteria
- Patients unable to consent to research or be interviewed due to cognitive decline
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Other
Study locations
South Korea · 1 center
- Seoul National University Hospital — Seoul
Identifiers
NCT: NCT06415201 · HI23C0315