Actively Recruiting

Phase Not Applicable
Age: 40Years +
All Genders
NCT07110753

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

Age: 40Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

UMC Utrecht

Utrecht, Netherlands

Actively Recruiting

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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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