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HealthyW8_60+ Pilot

RecruitingNAAges 60 Years - anyAllLuxembourg Institute of Health
NCT06816147 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This pilot study will focus on men and women aged ≥60 years for a period of 3 months during which each participant will use the HLRS. The primary purpose is to study whether the HLRS, reflecting a multi-component intervention, is well accepted by the participant, has a decent adherence (i.e., user time of the app). In addition, investigators will study the feasibility of the design, i.e. whether the overall design is well suited to the participants, in order to improve their lifestyle, e.g., dietary habits and PA, among others. Secondary outcomes related to the feasibility approach include dietary habits, PA patterns, and selected plasma and urinary endpoints. This pilot study will be of longitudinal design without a control group. A later trial that is planned for the following year will focus further on biological endpoints and will be randomized. In this present pilot study, investiga

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📋 Eligibility rules (as published)
Inclusion Criteria: Individuals aged 60 or older: * both males/females, general free-living population, * residing in Luxembourg, * having normal weight or being overweight, i.e., with a BMI between 18.5 ; 30 kg/m², which is considered a risk factor for developing obesity, * owning a smartphone. Exclusion Criteria: * With known manifest chronic diseases that prohibits participation in the study (e.g., cancer, Parkinson's), * Persons with cognitive diseases (Alzheimer's) or those who are not able to lead an independent life, * Persons following a strict diet (on their own or advised by their physician), * Particular population groups, such as prisoners, the mentally disabled, or groups whose ability to give voluntary informed consent may be in question.
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What it tests

  • Investigators will evaluate the acceptance and adherence to a healthy lifestyle recommender solution (HLRS), a digital app, among participants
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Where

1 site
Clinical and Epidemiological Investigation Center CIEC- LCTR
Luxembourg, Luxembourg
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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