← Eichor
Study identifier: NCT06819982 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Autonomous At Home with Occupational Therapy Support and Assistive Devices

Condition: Frailty · Aging · Home Care Services  ·  Sponsor: Université Catholique de Louvain

PhaseNA
Planned participants3900
Who can joinAll sexes, 65 Years to no upper limit
Healthy volunteersNo

About this study

The aim of the AUDACE study is to evaluate the 'Bien chez Moi 2.0' programme, to assess how, for whom and why do assistive devices, integrated with occupational therapy support, enable older people to remain at home, and under what conditions? The study assesses the impact on areas such as the degree of autonomy, the extent to which life goals are taken into account, the feeling of security at home, the use of hospital emergency services and the postponement of definitive institutionalisation in a nursing home. The expected results of this study are to be able to robustly describe the impact of the 'Bien chez moi 2.0' programme in the areas listed above.

This description comes directly from the study's public registry record.

Talk to the study team

Thérèse Van Durme  ·  +32 (0)2 764 30 99  ·  therese.vandurme@uclouvain.be

Always discuss trial participation with your own doctor first.

Locations (1)

Ergo2.0Yvoir, BelgiumRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06819982