Home
Search
Study Topics
Glossary
|
|
|
|
|
|
Sponsored by: |
National Institute of Mental Health (NIMH) |
---|---|
Information provided by: | National Institutes of Health Clinical Center (CC) |
ClinicalTrials.gov Identifier: | NCT00623818 |
This study, conducted at the National Institutes of Health (NIH) and at Walter Reed Army Medical Center (WRAMC), will explore the phenomenon of phantom limb pain (a continued feeling of pain in an amputated limb) and will use functional magnetic resonance imaging (fMRI) to investigate the effect of mirror therapy on phantom limb pain.
Right-handed people between 18 and 75 years of age who are in the WRAMC Military Amputee Research Program and healthy control subjects may be eligible for this study. Participants undergo the following procedures:
Amputees
Control Subjects
One group of control subjects undergoes a single fMRI procedure. A second group of control subjects undergoes the same sequence of three fMRIs over the same time period as the amputee subjects. None of the control subjects undergo mirror therapy.
Condition |
---|
Phantom Limb Pain Amputee |
Study Type: | Observational |
Study Design: | Prospective |
Official Title: | fMRI Investigation of Cortical Reorganization and Phantom Limb Pain Following Amputation |
Estimated Enrollment: | 90 |
Study Start Date: | February 2008 |
Objective: The aim of this study is to investigate phantom limb pain (PLP), cortical reorganization and the modulation of PLP by visual input. Mirror therapy (viewing the intact limb in a mirror so that it appears to be the missing limb) has been shown to reduce PLP. This reduction demonstrates that vision can play a key role in modulating PLP. The study proposed here will identify brain regions critical for the success of this therapy using functional magnetic resonance imaging (fMRI).
Study population: Individuals with unilateral amputation of individual limbs and at least three episodes of PLP a week. Additionally, we will study amputees without PLP and healthy control volunteer subjects with no limb amputations.
Design: Amputee subjects with PLP will be scanned using fMRI while they undergo mirror therapy for PLP. During fMRI scans subjects will see images of hands or feet, move their limbs or experience tactile stimulation. Mirror therapy requires four weeks to be effective. Amputee subjects will be scanned prior to starting therapy, two weeks after starting mirror therapy and again after four weeks of mirror therapy. Mirror therapy sessions will be conducted daily and subjects will also complete daily questionnaires (Visual Analogue Scale, or VAS, and Short-Form McGill Pain Questionnaire or SF-MPQ) assessing their level of pain and number of PLP episodes. Amputees without PLP and one group of healthy control subjects will go through the same series of functional imaging scans over the same time period as the amputee subjects, allowing us to identify brain changes that may be associated with repeated scanning (e.g. due to practice of tasks) rather than resulting from the mirror therapy. Another group of control subjects will be scanned once to identify particular brain regions that might be involved in the integration of visual, motor and somatosensory information for use in the analysis of the amputee subject data.
Outcome measures: Changes in fMRI activation during the course of mirror therapy will be compared with data on the number of episodes of PLP, the average length of episodes, and the average intensity of pain assessed using the VAS and SF-MPQ. Analyses will focus on cortical regions known to be involved in visual, tactile and motor representations (including primary motor cortex, primary and secondary somatosensory cortex and regions of visual cortex selectively responsive during the viewing of body parts). Additional brain regions that might be involved in integrating visual, motor and somatosensory information will be identified in control subjects. Direct comparisons will be made between cortical regions (e.g. somatosensory regions) involved in the representation of the amputated limb compared with the intact limb and between amputee subject data and control subject data.
Ages Eligible for Study: | 18 Years to 75 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
For amputee subjects with PLP:
For healthy control subjects:
Ability to follow study instructions and likely to complete all required visits.
EXCLUSION CRITERIA:
For amputee subjects with PLP:
For amputee subjects without PLP:
For healthy control subjects:
Contact: Patient Recruitment and Public Liaison Office | (800) 411-1222 | prpl@mail.cc.nih.gov |
Contact: TTY | 1-866-411-1010 |
United States, District of Columbia | |
Walter Reed Army Medical Center | Recruiting |
Washington, District of Columbia, United States, 20301 | |
United States, Maryland | |
National Institutes of Health Clinical Center, 9000 Rockville Pike | Recruiting |
Bethesda, Maryland, United States, 20892 |
Study ID Numbers: | 080052, 08-M-0052 |
Study First Received: | February 24, 2008 |
Last Updated: | September 9, 2008 |
ClinicalTrials.gov Identifier: | NCT00623818 |
Health Authority: | United States: Federal Government |
Phantom Limb Pain Visual and Motor Integration Cortical Reorganization Amputees Functional Magnetic Resonance Imaging (fMRI) |
Phantom Limb Pain Amputee Healthy Volunteer HV |
Signs and Symptoms Neurologic Manifestations Pain Healthy |
Phantom Limb Neurobehavioral Manifestations Perceptual Disorders |
Nervous System Diseases |