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NCT01111617 Clinical Trial

Applications of Realtime Functional Magnetic Resonance Imaging (fMRI )

Pain Clinical Trial

Official title:
Applications of Realtime fMRI Phase II

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01111617
Other study ID # SU-11062007-809
Secondary ID 95194
Status Completed
Phase N/A
First received
Last updated
Start date January 2014
Est. completion date November 2023

Study information
Verified date March 2024
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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

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.

Recruitment information / eligibility
Status Completed
Enrollment 400
Est. completion date November 2023
Est. primary completion date November 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Real-time fMRI feedback
Patients receive real-time fMRI biofeedback to modulate pain

Locations
Country Name City State
United States Stanford University School of Medicine Stanford California

Sponsors (1)
Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain reduction as measured by visual analog scale (VAS) pain report Within the 2 hour feedback session
Secondary Control of brain activity as measured by fMRI analysis Within the 2 hour feedback session
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