Clinical Trials in Brazil / NCT07162311
Enrolling by invitation Not applicable

Effect of Home-Based Transcranial Direct Current Stimulation on Pain in Patients With Rheumatoid Arthritis With Low Inflammatory Activity

NCT07162311 · tracked via the Priya Life Science Brazil tracker
Phase
Not applicable
Started
2024-01-01
Last updated
2025-09-09

Condition(s) studied

Rheumatic ArthritisChronic Pain

Investigational drug(s) / intervention(s)

tDCS

tDCS: Home-Based Transcranial Direct Current Stimulation

Study summary

Rheumatoid arthritis (RA) is a highly complex inflammatory autoimmune disease. Several drugs have been developed in recent decades to target the immune components of inflammation. However, even with effective anti-inflammatory and immunosuppressive therapies for controlling RA, many patients still report significant levels of chronic pain due to CNS neuroplasticity, perpetuating physical disability, psychosocial problems, decreased work activity, and poor quality of life. In addition, chronic pain can lead to increased public spending due to the need for more medical visits, ineffective drug treatments, and financial disability benefits. Transcranial stimulation (a noninvasive neural stimulation technique with minimal adverse effects and easy home use) has been a promising adjunct tool in the treatment of chronic pain and psychological disorders in diseases that affect the central nervous system in the long term. Thus, exploring transcranial direct current stimulation in RA patients with low levels of inflammation could impact on improving pain, functionality, psychological aspects and overall quality of life, as well as reducing healthcare costs for society.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
70 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Participants aged 18-70 with RA. * Participants with generalized pain ≥ 40 mm on the VAS-Pain scale, lasting over 3 months, and not of mechanical or inflammatory origin, as assessed by a certified rheumatologist. * Evidence of low inflammatory markers, including with C-reactive protein (CRP) \<10 mg/dL and sedimentation rate (ESR) \<20 mm/h, and stable treatment for PsA for at least 6 months prior to study enrollment. Exclusion Criteria: * History of brain surgery, traumatic brain injury, stroke, previous intracranial metal implantation, pregnancy, or breastfeeding. * Previous history of autoimmune diseases other than RA. * History of neurological diseases. * Previous history of neoplasia. * History of any other uncompensated clinical disease. * Use of illicit drugs within the past 6 months.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Hospital de Clínicas de Porto Alegre Porto Alegre Rio Grande do Sul

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07162311 on ClinicalTrials.gov ↗ ← All trials in Brazil