Status:
COMPLETED
Virtual Integrated Environment in Decreasing Phantom Limb Pain
Lead Sponsor:
Henry M. Jackson Foundation for the Advancement of Military Medicine
Collaborating Sponsors:
Johns Hopkins University
Conditions:
Phantom Limb
Eligibility:
All Genders
18-65 years
Brief Summary
The purpose of this study is to determine if observing a virtual arm decreases phantom limb pain (PLP) in upper extremity amputees.
Detailed Description
Nearly all traumatic limb amputees will experience cognizance of a phantom limb and perceive a vivid impression that their lost limb is not only fully present, but also painful. The John Hopkins Unive...
Eligibility Criteria
Inclusion
- Male or female subjects, 18 to 65 years of age, active duty military, beneficiary, or retiree.
- Written informed consent and written authorization for use or release of health and research study information.
- At least one upper-limb amputation (trans radial or trans humeral) at any time prior to enrollment.
- No prior history of vertebral disk disease/condition, sciatica or radiculopathy.
- Normal neurological examination with the exception of limb amputation.
- Ability to follow study instructions and likely to complete all required visits.
- Experiencing PLP at least 3 times a week at an intensity of at least 3 out of 10 at the time of enrollment.
Exclusion
- Presence of mild to severe traumatic brain injury - permanent or temporary impairments of cognitive, physical, and psychosocial functions with an associated diminished or altered state of consciousness - as indicated by neuropsychological screening that is currently performed routinely on patients by the traumatic brain injury (TBI) program at Walter Reed National Military Medical Center (WRNMMC) and noted in the patient's medical record.
- Known uncontrolled systemic disease
- Participation (either concurrently or in the 30 days prior to enrollment) in another study for treatment of PLP
- Any condition or situation that, in the investigator's opinion, may put the subject at significant risk, confound study results, or interfere significantly with the subject's participation in the study.
- Significant Axis I or II diagnosis determined by a neurologist or psychiatrist in the 6 months prior to entry into the study
- Subjects with lack of effort as determined by the neurologist or psychiatrist. Subjects will be screened for effort using the Test of Memory Malingering (TOMM) in order to exclude those with blatant exaggeration or malingering. Subjects who score lower than 42/50 on the TOMM-2 will not continue in the study
Key Trial Info
Start Date :
October 1 2011
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
January 1 2014
Estimated Enrollment :
14 Patients enrolled
Trial Details
Trial ID
NCT01462461
Start Date
October 1 2011
End Date
January 1 2014
Last Update
October 16 2015
Active Locations (1)
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1
Walter Reed National Military Medical Center (WRNMMC)
Bethesda, Maryland, United States, 20889