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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

What this study is about

This Phase 1 study is focused on people with chronic pain. The primary outcome being measured is Change in pain intensity.

Simplified from trial records by PatientMatch.

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Standard assignment

Assignment is predetermined by the study protocol.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

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