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Clinical Trial Summary

The primary objective of this study is to determine whether the UpRight Go posture trainer reduces the symptoms of cubital tunnel syndrome in patients who have not had corrective surgery, as determined by improvements in VAS scores for pain, numbness, and weakness.


Clinical Trial Description

This is a randomized controlled, non-blinded trial. All patients who are eligible to participate and who consent to participate will be randomized to either receive standard of care treatment alone, or standard of care treatment with the additional intervention of posture training. The nature of the intervention prevents blinding. All patients will be followed for 6 weeks and evaluated for symptom improvement or resolution. All patients aged 18 and older who present to clinic with cubital tunnel syndrome of any severity and who have not previously undergone surgical intervention for this condition will be eligible to participate in this study. All participants must be amenable to conservative management of CuTS, wearing a posture training device daily, completing the accompanying questionnaires throughout the study, and returning for follow-up. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06095011
Study type Interventional
Source Yale University
Contact Elspeth Hill, MBChB, PhD, MRes, MRCS
Phone 314-827-7307
Email elspeth.hill@yale.edu
Status Recruiting
Phase N/A
Start date December 15, 2023
Completion date May 2025

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