Condition: Chemotherapy Induced Peripheral Neuropathy · Sponsor: University of Miami
The purpose of this study is to determine the feasibility of using a portable device at home to self-administer transcutaneous auricular vagus nerve stimulation (taVNS). This handheld device has two small electrodes that are placed on specific areas of the outer ear. This device delivers a mild electrical stimulation to the vagus nerve through the ear. This study will explore how taVNS may affect symptoms of chemotherapy-induced peripheral neuropathy (CIPN). Participants will be assigned to one of two cohorts based on the presence of chemotherapy-induced peripheral neuropathy (CIPN). Participants with CIPN will be placed in the intervention cohort (n=24) and will complete a 2-week trial of daily self-applied taVNS. Participants without CIPN will be placed in the registry cohort (n=12) and will complete study measurements without receiving the intervention. The registry cohort will not receive the taVNS intervention but will undergo identical physiological assessments at baseline and at a 2 week follow up to control for testing effects and biological variability.
This description comes directly from the study's public registry record.
Richard L Martinez, MSPH · 3052842359 · rxm1388@med.miami.edu
Marlon L Wong, PT, PhD · 3052842670 · mwong2@miami.edu
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| University of Miami, Plumer Building | Coral Gables, Florida, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07596030