Actively Recruiting
The Effect of a Combined Lifestyle Intervention for Patients With Cancer on Quality of Life
Led by UMC Utrecht · Updated on 2025-08-08
244
Participants Needed
1
Research Sites
88 weeks
Total Duration
On this page
Sponsors
U
UMC Utrecht
Lead Sponsor
T
Tilburg University
Collaborating Sponsor
AI-Summary
What this Trial Is About
A growing number of people are living with the (long-term) consequences of cancer and its treatment, which can negatively affect their quality of life. This study aims to assess the effect of a combined lifestyle intervention for patients with cancer on quality of life.
CONDITIONS
Official Title
The Effect of a Combined Lifestyle Intervention for Patients With Cancer on Quality of Life
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with invasive or hematological cancer and either within five years post-primary treatment with curative intent or having advanced stage IV cancer with a prolonged life expectancy
- Report a reduced health-related quality of life with low scores on at least 2 functioning scales or fatigue symptom scale of the EORTC-QLQ-30
- Be 40 years of age or older
- Be able to speak and understand Dutch
You will not qualify if you...
- Currently following or planning to follow a combined lifestyle intervention during the study period
- Being in the terminal phase with life expectancy less than 3 months
- Having mental or behavioral problems that prevent participation in group lifestyle coaching
- Any condition that impedes giving informed consent or following study requirements as judged by the study team or physician
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
UMC Utrecht
Utrecht, Netherlands
Actively Recruiting
Research Team
A
Anna Manshanden, MSc
CONTACT
E
Evelyn Monninkhof, 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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