AI decodes the mystery of persistent pain in rheumatoid arthritis
NCT ID NCT07769619
First seen Aug 18, 2026 · Last updated Aug 19, 2026 · Updated 1 time
Summary
This observational study aims to understand why some people with rheumatoid arthritis (RA) continue to experience chronic pain even when their inflammation is well-controlled. Researchers will compare two groups of RA patients—those with active disease and those in remission without significant pain—using clinical assessments, blood tests, and optional brain activity monitoring. By analyzing genetic, molecular, and neurophysiological data with artificial intelligence, the study hopes to identify distinct pain-related subtypes and uncover biomarkers that predict persistent pain. The ultimate goal is to pave the way for more personalized, mechanism-based pain treatments in rheumatology.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to better ways to predict and treat chronic pain in rheumatoid arthritis, even when inflammation is under control.
- What could go wrong
- This is an observational study, so it won't test any new treatment. The findings may not apply to all patients, and the AI models need validation before they can be used in practice.
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.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2026
- Expected to finish
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Jun 2029
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.
Who is studied
Adults with confirmed rheumatoid arthritis recruited during routine clinical care visits at a tertiary rheumatology referral center (4th Military Clinical Hospital with Polyclinic, Wrocław, Poland). The study population includes patients with active RA qualifying for biological therapy and patients in sustained clinical remission under biological therapy.
- Ages
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18 years and older
- Sex
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Anyone
- 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 - Study Group (Active RA) * Age ≥18 years. * Confirmed diagnosis of rheumatoid arthritis according to applicable classification criteria. * Active phase of the disease requiring initiation of biological therapy. * Qualification for treatment under the national drug program B.33: "Treatment of rheumatoid arthritis and juvenile idiopathic arthritis with aggressive course (ICD-10: M05, M06, M08)". * Ability to provide written informed consent. * Willingness to participate in clinical assessments, EEG, biological sample collection, and questionnaire-based evaluation. Exclusion Criteria - Study Group * Contraindications to biological therapy as defined by the Polish Society of Rheumatology recommendations and the National Health Fund (NFZ) requirements under the B.33 drug program. * Inability to provide informed consent. * Any condition that, in the opinion of the investigator, may interfere with study participation or data interpretation. Inclusion Criteria - Control Group (RA in Remission) * Age ≥18 years * Confirmed diagnosis of rheumatoid arthritis. * Ongoing biological therapy with sustained remission for at least 1.5 years and good tolerance of the treatment. * No current chronic pain reported in the clinical interview. * Ability to provide written informed consent. * Willingness to participate in study procedures, including biological sampling, EEG and questionnaire assessments.
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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
1 site. 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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4th Military Clinical Hospital with Polyclinic (4WSzKzP SPZOZ)
RECRUITINGWroclaw, 50-981, Poland
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