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Clinical Trials/NCT01111617
NCT01111617CompletedNot Applicable

Applications of Realtime fMRI Phase II

Stanford University2 sites in 1 country400 target enrollmentStarted: January 2014Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
400
Locations
2
Primary Endpoint
Pain reduction as measured by visual analog scale (VAS) pain report

Study Overview

Brief Summary

The goal of this research program is to determine the potential effectiveness of real-time fMRI training in improving mental control over pain.

Detailed Description

A research study that looks at pain and how you experience pain. This research project aims to use virtual reality-based real-time functional Magnetic Resonance Imaging (rtfMRI) to assess brain activation during the experience of pain and while subjects attempt to mentally control their pain response.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Age 18-65
  • Chronic Pain patient or healthy control
  • Ability to perform the experimental task

Exclusion Criteria

  • MRI contraindication (metal implants, claustrophobia, pregnant or planning to become pregnant)
  • History of psychiatric disorder (at the discretion of the investigator as to whether it interferes with the experimental task)
  • History of Blistering

Outcomes

Primary Outcomes

Pain reduction as measured by visual analog scale (VAS) pain report

Time Frame: Within the 2 hour feedback session

Secondary Outcomes

  • Control of brain activity as measured by fMRI analysis(Within the 2 hour feedback session)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Sean Mackey

Assistant Professor

Stanford University

Study Sites (2)

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