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Clinical Trial Summary

This is a single-site interventional open label pilot study of a non-significant risk medical device on patients with defined peripheral neuropathy secondary to chemotherapy (N=10). Patients who have received chemotherapy and have evidence of neuropathy will be seen at MD Anderson. Their severity of neuropathy will be documented and assessed by physical therapy, occupational therapy and based on self-reported activities of daily living (ADL) impairment.


Clinical Trial Description

Primary Objective: To assess the effect of a vibrating device applied to selected muscles on the step Secondary Objectives: - To summarize the adverse events of different levels from using the vibrator device in oncologic AYA patients visiting the outpatient clinic. - To summarize the irritation, pain, and sensation of the application of vibration by the AYA patients, as determined by the survey during the application ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05061238
Study type Interventional
Source M.D. Anderson Cancer Center
Contact David McCall
Phone 713) 792-6604
Email [email protected]
Status Recruiting
Phase N/A
Start date October 4, 2021
Completion date April 15, 2022

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