Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07150117

Cycling-Based Aerobic Exercise Intervention for Individuals With Chemotherapy-Induced Peripheral Neuropathy (CIPN)

Led by University of Alberta · Updated on 2026-03-12

30

Participants Needed

1

Research Sites

74 weeks

Total Duration

On this page

Sponsors

U

University of Alberta

Lead Sponsor

C

Cross Cancer Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

CYCLE-CIPN is a proof-of-concept study designed to evaluate whether a prescribed aerobic exercise intervention has the potential to reduce the symptoms and functional impact of CIPN. The small number of participants in the proposed study will allow us to make decisions on the feasibility ("go/no-go") of a future larger-scale trial. The protocol will assess feasibility and acceptability through recruitment, completion, adherence, program satisfaction, and safety. The study will also evaluate CIPN symptoms using both patient-reported and objective outcome measures, as well as fitness and quality of life outcomes. We aim to recruit 30 participants. The Health Research Board of Alberta Cancer Committee has approved this study. Participants will participate in a stationary cycling-based aerobic exercise program biweekly for 12 weeks. Exercise sessions will be supervised and progressive, between 30 and 60 minutes each.

CONDITIONS

Official Title

Cycling-Based Aerobic Exercise Intervention for Individuals With Chemotherapy-Induced Peripheral Neuropathy (CIPN)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years or older
  • Cancer diagnosis stage I to III
  • Mild (grade 1) chemotherapy-induced peripheral neuropathy (CIPN)
  • Currently receiving or have completed chemotherapy treatment for cancer
  • Able to speak, read, and understand English
Not Eligible

You will not qualify if you...

  • Medical conditions causing additional neuropathy symptoms (e.g., diabetes)
  • Any uncontrolled medical conditions
  • Scheduled for surgery or radiation therapy during the study period
  • Currently participating in an aerobic exercise training program
  • Currently involved in another exercise-based research study
  • Unable to provide signed informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Cross Cancer Institute

Edmonton, Alberta, Canada, T6G 1Z2

Actively Recruiting

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Research Team

C

Christopher Sellar, PhD

CONTACT

T

Trei Lindstrom, BSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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