Refining mUltiple Artificial intelliGence strateGies for Automatic Pain Assessment Investigations: RUGGI Study

Recruiting now · Not applicable

Conditions studied: Chronic Pain, Cancer Pain, Neuropathic Pain, Pain Assessment

In brief

This single-center, non-profit, observational-interventional study aims to develop artificial intelligence (AI) models for the automatic assessment of chronic pain (APA - Automatic Pain Assessment). The study will enroll adult patients with chronic pain of various origins (oncologic and non-oncologic). Participants will undergo multidimensional evaluations that include clinical assessments, self-report questionnaires, bio-signal collection (e.g., EEG, EDA, HRV, GSR, PPG), and facial expression analysis via infrared thermography and video recordings. The primary objective is to calibrate and test machine learning and deep learning models to recognize and predict the presence and severity of pain using multimodal data inputs. Secondary objectives include evaluating the effectiveness of pain treatments, assessing quality of life, and developing a standardized APA dataset for future research. All data collection procedures are non-invasive and safe, and include tools like wearable sensors and standardized neurocognitive tests. The study is approved by the Italian Ethics Committee (Comitato Etico Territoriale Campania 2) and complies with GDPR and EU AI regulations.

Key facts

Study ID

NCT07038434

Run by

Valentina Cerrone

People needed

200

Starts

2025-05-06

Expected to finish

2026-01-01

Last updated by the study team

2025-06-26

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adults (≥18 years old) with chronic pain, defined according to IASP and ICD-11 as pain that persists or recurs for more than three months.
• Diagnosed with either:
• Chronic primary pain (e.g., fibromyalgia, irritable bowel syndrome, chronic headaches)
• Chronic secondary non-cancer pain (e.g., low back pain, osteoarthritis, post-surgical pain)
• Chronic cancer-related pain (due to cancer or its treatment)
• Ability to understand the study procedures and provide written informed consent.

You may not qualify if…

• Current treatment with psychotropic drugs or presence of active psychiatric disorders (e.g., psychosis, major depression).
• Known history of alcohol or substance abuse.
• Pregnancy or breastfeeding.
• Age under 18 years.
• Inability to provide informed consent (e.g., due to cognitive impairment).

Where it is running

• Azienda Ospedaliera Universitaria San Giovanni di Dio e Ruggi d'Aragona — Salerno, Italy, Italy (enrolling)

Full record on ClinicalTrials.gov

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