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Behavioural Intervention

Group A for Spinal Cord Injury

Phase < 1
Waitlist Available
Research Sponsored by Kessler Foundation
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up immediately post-training session (1 day)
Awards & highlights

Study Summary

This trial is testing how changes in brain activity relate to the intensity and unpleasantness of neuropathic pain in people with SCI.

Eligible Conditions
  • Spinal Cord Injury
  • Neuropathic Pain

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~immediately post-training session (1 day)
This trial's timeline: 3 weeks for screening, Varies for treatment, and immediately post-training session (1 day) for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Brain activity
Secondary outcome measures
Exit Interview
Pain Intensity
Pain Unpleasantness

Trial Design

2Treatment groups
Experimental Treatment
Group I: Group BExperimental Treatment1 Intervention
Participants will be shown information about brain activity while trying different thinking strategies to change their experience of pain. Both groups will be shown brain activity, but the source of the brain activity information will differ between the groups.
Group II: Group AExperimental Treatment1 Intervention
Participants will be shown information about brain activity while trying different thinking strategies to change their experience of pain. Both groups will be shown brain activity, but the source of the brain activity information will differ between the groups.

Find a Location

Who is running the clinical trial?

Kessler FoundationLead Sponsor
173 Previous Clinical Trials
10,678 Total Patients Enrolled
University of SurreyOTHER
117 Previous Clinical Trials
785,337 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~6 spots leftby Apr 2025