RecruitingNot ApplicableNCT05819346

Digital Lifestyle Intervention for Lung Cancer Survivors

Effect of a Digital Lifestyle Intervention on Health-Related Quality of Life in Non-Small Cell Lung Cancer Survivors (QUALUCA): a Multicenter Randomized Controlled Trial


Sponsor

Kai-Uwe Schmitt, PhD, MEng, ICID

Enrollment

88 participants

Start Date

Aug 1, 2023

Study Type

INTERVENTIONAL

Summary

The aim of this study is to assess the efficacy of a digital lifestyle intervention in non-small cell lung cancer (NSCLC) survivors on health-related quality of life (HRQoL) over three months.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests a digital lifestyle program designed to help lung cancer survivors stay active, eat well, and manage stress using a smartphone app. The program is tailored to people recovering from lung cancer treatment, with the goal of improving their quality of life and long-term health. **You may be eligible if...** - You are 18 or older - You have been diagnosed with non-small cell lung cancer (NSCLC) - Your life expectancy is at least 6 months - You are currently in rehabilitation, or you finished surgery, chemotherapy, or radiation within the past 24 weeks - You can read and understand German - You have access to a smartphone or tablet **You may NOT be eligible if...** - You have serious mental illness or physical limitations that would prevent participation - You do not have access to a mobile device - You do not understand German Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALLifestyle

Participants assigned to the intervention group receive access to a lifestyle mobile application for three months after rehabilitation or treatment has finished. The digital program is target group-specific and includes personalization and interactive elements without face-to-face appointments during the intervention. One virtual appointment at the beginning of the intervention with the study staff ensures that participants familiarize themselves with the mobile application and that they are assigned to a suitable program level. The intervention is mainly based on the following behavior change technique (BCT) clusters: goals and planning, feedback and monitoring, shaping knowledge, and comparison of behavior.


Locations(4)

Klinik Barmelweid AG

Barmelweid, Switzerland

Zürcher RehaZentren | Klinik Davos

Davos, Switzerland

Berner Reha Zentrum AG

Heiligenschwendi, Switzerland

Zürcher RehaZentren | Klinik Wald

Wald, Switzerland

View Full Details on ClinicalTrials.gov

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NCT05819346