Study details
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Optimizing Accelerated TMS for Chronic Pain With Thompson Sampling
University of Minnesota
NCT IDNCT07103135ClinicalTrials.gov data as of Apr 2026
Phase
Phase 1
Ages
18+
Locations
1 site in MN
About this study
This Phase 1 study is focused on people with chronic pain. The primary outcome being measured is Change in pain intensity.
Based on ClinicalTrials.gov records.
PhasePhase 1
Primary goalChange in pain intensity
Participation effort
Estimated from trial records. Details can vary by site.
Time + visits
Low10%
Logistics
Moderate50%
Logistics difficulty varies by site location and availability.
Trial highlights
Treatment details
Auto-extracted from trial records to preview treatments and outcomes.
Endpoints
Primary: Change in pain intensity
Secondary: Adherence to the protocol and the tolerability of the study visits/procedures, Change in pain intensity, PROMIS Emotional Distress Score, Pain Catastrophizing Scale Score, Pain interference score on the Brief Pain Inventory (BPI), Pain vigilance and awareness questionnaire (PVAQ)
Devices
therapeutic