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Clinical Trial Summary

The goal of this clinical trial is to learn if the EX-CIPN exercise-based intervention is feasible, acceptable, and safe in participants with persistent chemotherapy-induced peripheral neuropathy (CIPN). It will also give insight on the effectiveness of the exercise intervention in treating CIPN symptoms. The main questions it aims to answer are: - Is EX-CIPN safe, acceptable, and feasible in cancer survivors experiencing persistent CIPN? - Are the study design and methods feasible (recruitment and retention rates, feasibility of data collection and procedures)? Researchers will provide all participants with the exercise-based intervention. Participants will: - Complete assessments at baseline, immediately post-intervention, and 3-months post-intervention - Complete a 10-week remote, individualized exercise program - Receive health coaching calls on weeks 2, 3, 4, 6, and 8 of the intervention - Wear a FitBit throughout the study to track physical activity and promote behaviour change


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06405542
Study type Interventional
Source University Health Network, Toronto
Contact Eric Antonen
Phone 416-581-8453
Email eric.antonen2@uhn.ca
Status Recruiting
Phase Phase 1
Start date April 25, 2024
Completion date July 1, 2025

See also
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