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Clinical Trial Summary

Examination of the effects of short-term use of TENS and t-NMES on passive pain-free ROM of the painful post-stroke shoulder. Treatments are compared with no stimulation.


Clinical Trial Description

Single cohort, cross-over study. Subjects undergo passive pain-free ROM of the painful post-stroke shoulder under 3 stimulation conditions. The stimulation was delivered by a trained occupational therapist under three conditions: 10 seconds of TENS, 10 seconds of t-NMES, and 10 seconds of no stimulation. Each subject was exposed to each of the three stimulation conditions three times in a computer-generated random sequence for each outcome measure with a 5-minute wash-out period between each stimulation. This protocol is repeated for each of the two passive movements tested, shoulder abduction and shoulder external rotation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03683901
Study type Interventional
Source MetroHealth Medical Center
Contact
Status Completed
Phase N/A
Start date December 27, 2010
Completion date May 1, 2011

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