fatty liver non-alcoholic fatty liver disease
Conditions
Interventions
The intervention in the app group consists of asking people to use this
application during their follow-up time.
Sponsors
Universiteit Maastricht
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: • Aged 18 years or older • Diagnosed with NAFLD by CAPTM (>215 dB/m) as measured by the FibroScan® device and VCTE
Exclusion criteria
Exclusion criteria: • Not proficient in the Dutch language • Already in a weight-loss/management project included (e.g., weight watchers, dietitian guidance).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main study parameter/endpoint: a *5% reduction in weight measured in kg. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary study parameters/endpoints: 1) Reduction of NAFLD (as measured by the FibroScan®). 2) Acceptability and satisfaction of the Happi liver mobile application. 3) An increase in knowledge concerning NAFLD. 4) Quality of life improvement. | — |
Countries
Netherlands
Outcome results
None listed