Pain Clinical Trial
Official title:
A Pilot Study to Assess the Efficacy of Mirror-Box and Mental Visualization Treatments on Phantom Limb Pain
The researchers propose to conduct a pilot study on the efficacy of mirror-box and mental
visualization treatments on phantom limb pain. The trial will last for 4 months and during
the first month, data will be gathered daily on the number of episodes of phantom limb pain,
the average length of episodes, average intensity of pain, and worst intensity of pain. In
addition, the rapidity of pain relief, the length of therapy needed to sustain long-lasting
pain relief, and whether use of these two treatment methods during rehabilitation can
provide sustained and/or permanent pain relief will be determined. Cognitive testing will
also be performed to determine the effect of limb amputation on cognition and mood with
results being compared to an on-going study of similar effects in patients with chronic (> 3
months) limb amputation.
The inclusion of subjects with phantom limb pain in upper extremity amputations has recently
been approved.
A total of forty-eight (48) subjects with be enrolled - twenty-four (24) with any unilateral lower limb amputation and twenty-four (24) with any unilateral upper limb amputation. Subjects will be randomized for assignment into three treatment conditions: eight (8) lower and eight (8) upper limb subjects (50% with left-sided amputations) will use mental visualization of foot or hand movements, eight (8) lower and eight (8) upper limb subjects (50% with left-sided amputations) will use an open mirror- box to visualize the reflected image of their intact foot or hand, and eight (8) lower and eight (8) upper limb subjects (50% with left-sided amputations) will use a closed mirror- box (unable to visualize a reflected image). Subjects will use their assigned therapy for 20 minutes daily. Subjects using the closed mirror-box or mental visualization treatments will be switched to mirror therapy if they have not significantly improved following 4 weeks. The subjects for this study will be recruited from the Walter Reed Army Medical Center Amputee clinic. Up to sixty (60) subjects will be recruited and screened according to the inclusion and exclusion criteria since we expect that some may not qualify or drop-out sooner than the scheduled 4-month completion time. ;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Treatment
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