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Clinical Trial Summary

The purpose of this research study is to evaluate how exercise and surgical weight loss affect how likely an individual is to develop peripheral neuropathy and other neurologic complications.


Clinical Trial Description

The length of this study, including screening is approximately 24 months. Patients in the Adult Bariatric Surgery Clinic at the University of Michigan will be recruited for this study. Both patients that decide to undergo bariatric surgery, and those that do not undergo surgery will be enrolled. Patients will be randomized to either a high intensity interval training (HIIT) or standard exercise regimen after eligibility is confirmed and the baseline visit is complete. All patients will complete follow-up appointments at 3 month, 12 months and 24 months. Patients that are randomized to the HIIT program will compete 2 supervised and 1 unsupervised training sessions a week for 24 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03617185
Study type Interventional
Source University of Michigan
Contact Ericka Chant, MPH
Phone 734-936-8770
Email echant@med.umich.edu
Status Recruiting
Phase N/A
Start date July 12, 2018
Completion date June 30, 2023

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