NCT06484478Completed
A Real-world Wearables Study in Fabry Disease.
A Real-world Monitoring Project Exploring Day-to-day Physical Activity, Sleep, and Quality of Life in Individuals With Fabry Disease.
Source: ClinicalTrials.gov · Last updated 16 Mar 2026
Brief summary (registry, in English)
Despite improvements in Fabry disease care in recent years, many patients still have poor outcomes. In addition to the many physical symptoms that patients can experience, the disease also places individuals at an increased risk of mental health conditions, such as anxiety and depression. Low physical activity levels and increased sedentary time are detrimentally associated with anxiety, depression and quality of life in the general population. Currently, no such research has been conducted in individuals with Fabry disease. Data will consist of: (1) information from hospital medical records, (2) patient reported outcomes collected via questionnaires, and (3) measurements from a clinical-grade wearable device. Individuals with Fabry disease aged 18 years or above will be considered for eligibility screening.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 100 (actual)
- First submitted
- 12 Jun 2024
- Start date
- 5 Nov 2024
- Primary completion date
- 29 May 2025
- Lead sponsor
- Royal Free Hospital NHS Foundation Trust
- Diseases
- Fabry disease
- NCT number
- NCT06484478
What you commit to
- Study type: Observational
- Participants enrolled: 100
- From 5 Nov 2024 to the primary completion date, 29 May 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- A known allergy to any materials in the wearable device.
Other
- Not able to have or use a wearable.
- Taking part in an interventional study which would preclude real-world data collection.
- Unable to communicate in English to a sufficient level to permit engagement in the study.
Who the study is looking for
- Diagnosis of Fabry disease documented by genotyping and/or enzymatic analysis.
- Resident in the UK.
- Aged 18 years and over.
- Capable of providing informed consent.
- Physically able to stand and ambulate independently.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Royal Free London NHS Foundation Trust Coordinator of this site? Confirm its status | London | United Kingdom | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.