Actively Recruiting
Personalized Live-remote Exercise Training for Cancer Survivors
Led by UMC Utrecht · Updated on 2026-05-11
350
Participants Needed
1
Research Sites
193 weeks
Total Duration
On this page
Sponsors
U
UMC Utrecht
Lead Sponsor
G
German Cancer Research Center
Collaborating Sponsor
AI-Summary
What this Trial Is About
Background Many people with cancer face ongoing problems from their disease and treatments, like fatigue, reduced physical fitness, feeling anxious or down, and neuropathy. While exercise might help with these problems, most studies did not focus on tailoring exercise to address these specific complaints. Exercise programs under supervision (like with a trainer) seem to work better, but barriers for following such sessions are travel distance and time. Therefore, following an exercise program at home with a trainer guiding via video (live-remote) might be a good solution. But, it is unclear how effective this remote exercise program is for cancer patients. Goal of the study: The main goal of this study is to assess the effectiveness of a personalized, live-remote exercise intervention for cancer survivors on quality of life and the patients' main complaint. The four complaints tackled in this study are: 1) fatigue, 2) reduced physical functioning, 3) anxiety and/or depressive symptoms, and 4) neuropathy. Design of the study In the LION study, 350 cancer patients will be randomly divided into the exercise group or control group. These patients all have at least one of these complaints: 1) fatigue, 2) reduced physical functioning, 3) anxiety and/or depressive symptoms, and/or 4) neuropathy. Patients cannot participate in the study if they are already very active. The exercise group will start a 12-week exercise program right away, and the other group will wait for 12 weeks before starting. The exercise program consists of three sessions per week. Two sessions per week include aerobic training and strength training. These sessions will be followed by all patients; and aim to improve fitness and strength. The third session specifically aims at improvement of the main complaint, for example fatigue. Participants will get an app and a fitness tracker to help them stay on track with their exercises. Furthermore, patients get information on the effects of exercise for cancer patients and why exercise is important for specific complaints. Measurements The main outcomes of this study are quality of life and the main side-effect of the patient. Other measurements include all kind of patient reported outcomes (like sleep problems and pain), physical fitness, muscle strength, balance, anthropometrics, and (inflammatory) markers in blood. Conclusion: This study investigates if personalized exercises done at home, with video guidance, can make cancer survivors feel better and manage their side effects more effectively.
CONDITIONS
Official Title
Personalized Live-remote Exercise Training for Cancer Survivors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years of age or older
- Diagnosed with any type of invasive cancer and treated with systemic chemotherapy
- Completed primary cancer treatment with curative intent 12 weeks to 1 year ago
- No evidence of distant metastatic disease
- ECOG performance status of 2 or less
- Experiencing at least one side-effect: fatigue, low physical functioning, anxiety or depressive symptoms, or chemotherapy-induced peripheral neuropathy
- Access to good quality and stable internet connection
- Able and willing to perform the exercise program and wear the activity tracker
- Able to read, speak, and understand the main country language
You will not qualify if you...
- Physically active over 210 minutes per week or currently in a similar exercise program
- Following or planning to follow a structured psychological intervention during the study
- Participated in an exercise study intervention during cancer treatment
- Unable to complete testing or training sessions or contraindications for exercise
- Severe neurologic or cardiac impairment
- Uncontrolled severe respiratory insufficiency or oxygen dependence
- Uncontrolled pain
- Inability to give informed consent or adhere to study requirements
- Unable to attend training sessions for more than 1 week during the intervention
AI-Screening
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Trial Site Locations
Total: 1 location
1
University Medical Center Utrecht
Utrecht, Netherlands
Actively Recruiting
Research Team
E
Evelyn Monninkhof, PhD
CONTACT
A
Anne May, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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