CyberCycling to Reduce Therapeutic Side Effects and Improve Quality of Life in AYA Cancers



Status:Recruiting
Healthy:No
Age Range:15 - 30
Updated:2/10/2019
Start Date:August 24, 2016
End Date:July 2019
Contact:Nora L Nock, PhD
Email:nln@case.edu
Phone:216-368-5633

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'Rainbow Riders': A Pilot Trial of CyberCycling to Reduce Therapeutic Side Effects and Improve Quality of Life in Adolescent and Young Adults (AYA) Diagnosed With Cancer

Only a few clinical trials evaluating the potential benefits of exercise have been conducted
in adolescents and young adults (AYA) with cancer and, no prior studies have evaluated the
potential effects of 'cybercycling' (exergaming on a stationary bike) in AYA cancer
survivors. Therefore, the study aims to conduct a pilot trial to determine feasibility
(adherence, user acceptance) and to explore potential effects of a 'cybercycling' exercise
program on fitness, body composition, quality of life, sleep and cognition.

Objectives Specific Aim 1: To evaluate the feasibility (adherence; user acceptance: exercise
tolerance, enjoyment and motivation) of performing an adaptive, moderate intensity, aerobic
exercise program on a 'cybercycle' compared to control (stretching/resistance bands) in
adolescent and young adults (AYA) with cancer.

(Exploratory) Aim 2: To explore the effects of an adaptive, moderate intensity aerobic
exercise program using a 'cybercycle' compared to control (stretching/resistance bands) on
changes in fitness, body composition, quality of life (QoL), fatigue, sleep and cognition.

Study Design/Overview:

This study is a randomized trial in 20 adolescent and young adult (AYA) cancer survivors
(15-30 years old) which will comparing two intervention arms: 1) aerobic exercise on a
'cybercycle' (stationary cycling with exergaming/videogaming); and, 2) a
stretching/resistance band 'control' condition.

Inclusion Criteria:

- histologically confirmed cancer

- completed primary treatment

- approved to be contacted by the treating oncologist/nurse practitioner

- meet screening criteria

Exclusion Criteria:

- patients unable to provide informed consent

- patients not available for follow-up testing

- patients with any pre-existing medical conditions that would be a contraindication to
exercise.
We found this trial at
1
site
Cleveland, Ohio 44106
Principal Investigator: Nora L Nock, PhD
Phone: 216-368-5653
?
mi
from
Cleveland, OH
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