AI chatbot may calm nerves after a prostate cancer diagnosis
NCT ID NCT07804030
First seen Sep 04, 2026 · Last updated Sep 04, 2026
Summary
This trial tests whether an AI-powered support tool, accessed through a WeChat Mini Program, can reduce anxiety in men recently diagnosed with metastatic prostate cancer. Participants are randomly assigned to use the platform with the AI agent or without it for the first two weeks. The AI agent answers questions about the disease and its management using clinician-reviewed materials. Researchers measure changes in anxiety, illness perception, sleep quality, and patient satisfaction over four weeks.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- AI agent-assisted patient-centered support delivered through a WeChat Mini Program
- What this could lead to
- If it works, this AI-based support could become a scalable way to reduce anxiety and improve quality of life for people facing a new cancer diagnosis.
- What could go wrong
- The trial is small and early, and the AI agent's responses may not always be accurate or helpful. Benefits are measured over just a few weeks, so any effect may be short-lived.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 160 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 80 years
- Sex
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Male participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Newly diagnosed prostate adenocarcinoma confirmed by histopathology or cytopathology; 2. Metastatic disease confirmed by imaging or pathology; 3. Diagnosis of metastatic prostate cancer within 2 weeks before enrollment; 4. Aged 18-80 years; 5. A GAD-7 score of 5 or higher at screening; 6. Adequate cognitive ability to understand and participate in the study; 7. Adequate language comprehension and ability to complete the study questionnaires independently; 8. Access to a smartphone and an internet connection required to use the study platform; 9. Provision of written informed consent. Exclusion Criteria: 1. An acute or unstable psychiatric disorder, such as severe depressive or anxiety disorder, or severe insomnia requiring urgent specialist care; 2. History of or current cognitive impairment, such as intellectual disability or Alzheimer's disease; 3. A requirement for emergency surgery within 72 hours after enrollment; 4. Planned prostate cancer-directed radiotherapy, surgery, or chemotherapy during the study period; 5. Current participation in another interventional clinical trial; 6. A request from the participant's family to withhold the diagnosis or disease-related information from the participant.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
4 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Fudan University Shanghai Cancer Center
Shanghai, Shanghai Municipality, 200032, China
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Fujian Cancer Hospital
Fuzhou, Fujian, 350011, China
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The First Affiliated Hospital of Wenzhou Medical University
Wenzhou, Zhejiang, 325000, China
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Yunnan Cancer Hospital
Kunming, Yunnan, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a common diabetes drug slow prostate cancer progression?
- Chemo combo vs. radioactive drug: which tames aggressive prostate cancer?
- Can a blood filtering technique reveal more about prostate cancer spread?
- Can a vaccine plus immune booster tackle resistant prostate cancer?
- Can a smart drug deliver a toxic payload to prostate cancer cells?
- Can a blast of testosterone shrink hard-to-treat prostate cancer?