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Research and Application of Multimodal Data-Driven Intelligent Pain Assessment Technology for ICU Patients

Research and Application of Multimodal Data-Driven Intelligent Pain Assessment Technology for ICU Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600128138
Enrollment
Unknown
Registered
2026-07-14
Start date
2026-07-31
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Pain

Interventions

Gold Standard:The CPOT score is used as the gold standard. Nurses conduct CPOT pain assessments on patients every 4 hours as well as at designated event nodes (at rest, daily pain, suctioning, and tur
Index test:Patient facial videos, head posture videos, vocalization status, and physiological parameter data from monitors were collected to develop multimodal data algorithms, thereby establishing a

Sponsors

Beijing Jishuitan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >18 years; 2. Patients admitted to the ICU; 3. Patients capable of pain expression, including verbal communication or non-verbal cues such as eye contact, body movements, and facial expressions.

Exclusion criteria

Exclusion criteria: 1. Patients who were unable or unwilling to cooperate with self-reported pain assessment; 2. Those with quadriplegia, muscle insufficiency, deep sedation (Richmond Agitation-Sedation Scale [RASS] score = -3), or administration of neuromuscular blocking agents; 3. Patients with facial trauma, burns, facial dressings, facial paralysis, or other conditions significantly compromising facial image data acquisition; 4. Patients with a history of dementia, psychiatric illness, or diagnosed delirium; 5. Patients with contraindications to fentanyl administration, including respiratory depression (e.g., obstructive sleep apnea-hypopnea syndrome [OSAHS]), gastrointestinal obstruction, or myasthenia gravis; 6. Patients with incomplete physiological data; 7. Patients who declined to provide informed consent.

Design outcomes

Primary

MeasureTime frame
Sensitivity;Specificity ;

Countries

China

Contacts

Public ContactCui Zhen

Beijing Jishuitan Hospital, Capital Medical University

4563@jst-hosp.com.cn+86 10 57801743

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026