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N/A Completed N=208 Randomized Quadruple-blind Treatment

Home-based tDCS and Mindfulness-based Meditation for Self-management of Clinical Pain and Symptoms

Osteo Arthritis Knee
Source: ClinicalTrials.gov NCT04375072 ↗
Enrolled (actual)
208
Serious AEs
0.0%
Results posted
Nov 2025
Primary outcomePrimary: Change in Numeric Rating Score (NRS) of Pain — -19.41; -7.16; -16.78; -6.20 units on a scale

Summary

This clinical trial aims to evaluate whether a 2 week regimen of transcranial direct current stimulation (tDCS) paired with mindfulness-based meditation (MBM) can improve pain modulation, reduce clinical pain, and alleviate osteoarthritis (OA)-related symptoms in patients with knee OA.

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in Numeric Rating Score (NRS) of Pain
-19.41; -7.16; -16.78; -6.20
SECONDARY
Change in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC).
-6.98; -7.90; -8.08; -4.50

Eligibility Criteria

Inclusion Criteria

  • have symptomatic knee OA based on American College of Rheumatology clinical criteria
  • have had knee OA pain in the past 3 months with an average of at least 30 on a 0-100 NRS for pain,
  • can speak and read English
  • have no plan to change medication regimens for pain throughout the trial

Exclusion Criteria

  • history of brain surgery, brain tumor, seizure, stroke, or intracranial metal implantation
  • systemic rheumatic disorders, including rheumatoid arthritis,systemic lupus erythematosus, and fibromyalgia
  • alcohol/substance abuse
  • diminished cognitive function that would interfere with understanding study procedures (i.e., Mini-Mental Status Exam score ≤ 23)
  • pregnancy or lactation
  • prosthetic knee replacement or non-arthroscopic surgery to the affected knee
  • hospitalization within the preceding year for psychiatric illness
  • no access to a device that can be used for secure videoconferencing for real-time remote supervision.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04375072). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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