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NeoplasmAIPSYNCT07751757

Multimodal Artificial Intelligence for Detecting the Psychological State of Cancer Patients

An observational study of Neoplasm, run by Chinese PLA General Hospital at 1 site in China.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

Artificial intelligence (AI) technology is expected to assist clinical doctors in promptly identifying cancer patients at risk of developing psychological issues and to develop preemptive management plans, thereby enhancing their quality of life. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Neoplasm
How many people
1,500 participants
Where
1 siteChina
Study dates
1 Mar 2021to 31 Dec 2028
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients with cancers such as liver cancer, thyroid cancer and lung cancer et al. The demographic and clinical characteristics of tumor patients were collected and included, including age, gender, educational background, monthly income, marital status, ECOG score, liver function stage, Barcelona stage, recurrence frequency, lesion information, biochemical indicators, etc

Who may be able to join

  • Age ≥18 years old
  • Patients with tumors diagnosed by magnetic resonance imaging or contrast-enhanced ultrasound
  • The patient has self-awareness and is able to cooperate with the research
  • Patients who voluntarily undergo psychological assessment tests

Who cannot join

  • Age ≤18 years old
  • Not diagnosed as a tumor patient
  • Lack of autonomy and inability to conduct cooperative research

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

China1 site
  • Chinese PLA Hospital

    Beijing

Other trials in China

About this study

Artificial intelligence (AI) technology is expected to assist clinical doctors in promptly identifying cancer patients at risk of developing psychological issues and to develop preemptive management plans, thereby enhancing their quality of life. Computer vision technology can directly capture and extract subtle changes in skin color from facial images in videos, assess heart rate using signal processing algorithms, and also extract facial expressions to evaluate psychological conditions through facial expression change signal processing algorithms. The accuracy rate can exceed 88%. By leveraging the capabilities of computer vision technology, it can accurately capture subtle movements and expressions of the human body, thereby understanding the internal psychological state and obtaining relevant psychological information

Conditions
Neoplasm
Medical subject headings
Neoplasms

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Area Under the Receiver Operating Characteristic Curve (AUC) of the Multimodal Machine Learning Model for Anxiety and Depression Screening

    The AUC quantifies the overall discriminative ability of the final multimodal machine learning model to distinguish between patients with positive vs. negative anxiety/depression status. The AUC will be calculated on an independent test set that is strictly separated from the training and validation sets and will not be used in any model training or hyperparameter tuning.

    Measured: Data collected at two time points: 1 day pre-operatively and at ≤7 days post-operatively or at discharge, whichever came first

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Aug 2026
  2. Study start1 Mar 2021
  3. Primary completion31 Dec 2028 (estimated)
  4. Study completion31 Dec 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
1,500 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07751757
Sponsor's protocol ID
AIPSY
Other IDs
82030047
Acronym
AIPSY
Status last verified
Aug 2026
First submitted
25 Mar 2026
Last updated
14 Aug 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Neoplasm, run by Chinese PLA General Hospital at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 14 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Area Under the Receiver Operating Characteristic Curve (AUC) of the Multimodal Machine Learning Model for Anxiety and Depression Screening (time frame: Data collected at two time points: 1 day pre-operatively and at ≤7 days post-operatively or at discharge, whichever came first). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Aug 2026.

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