Effect on Body Weight Reduction of a Behavioral Intervention on Lifestyle Using a Digital Nutritional Program in People Living With HIV and Metabolic Dysfunction-associated Steatotic Liver Disease

Enrolling by invitation · Not applicable

Conditions studied: Metabolic Dysfunction-Associated Steatotic Liver Disease, People Living With HIV, Life Style

In brief

Metabolic dysfunction-associated steatotic liver disease (MASLD) is now the leading cause of chronic liver disease in people living with HIV (PLWH). Currently, there are no approved medications to treat this condition. That's why weight loss through healthy lifestyle changes is the most important way to manage it. This study will test if a digital nutritional program (DNP), using a mobile phone app, can help improve weight loss better than the usual advice on healthy eating and exercise. The study includes people living with HIV, aged 18 and older, with fatty liver (detected by ultrasound or other scans), and on stable HIV treatment. Participants will be randomly assigned to two groups: * Intervention group: Will receive personalized lifestyle support through a mobile app (DNP). * Control group: Will receive general advice on healthy habits. The study will last 12 months, with follow-up visits during and after the program. What Will Be Measured: * Weight, waist size, blood pressure, and body fat. * Blood tests to check cholesterol, sugar levels, liver enzymes, and other markers. * Liver scans to assess fat and stiffness. * Questionnaires on eating habits, exercise, and satisfaction with the program. Goals of the Study: Main goal: To see how many people lose at least 5% of their body weight after 6 months. Other goals: To see the effects on weight after 12 months, and 6 months after stopping the program, and to monitor improvements in liver health. Why This Matters: This study aims to find new ways to help people with HIV improve their liver health and overall well-being through simple, practical tools like a mobile app.

Key facts

Study ID: NCT07456332
Run by: Hospital Universitari de Bellvitge
People needed: 116
Starts: 2025-04-23
Expected to finish: 2028-02-01
Last updated by the study team: 2026-03-10

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

HIV-infected patients
≥ 18 years of age
On stable antiretroviral therapy during the last 6 months
HIV viral load <50 copies/ml for ≥ 6 months
CD4 cell count >200 cells/uL
Diagnosis of liver steatosis on ultrasound or Controlled Attenuation Parameter (CAP) measured by vibration-controlled transient elastography

You may not qualify if…

Body mass index ≤ 23 kg/m2
Presence of a condition that precluded modification of activity or diet behaviour
Known liver disease other tan MASLD including viral, haemochromatosis, Wilson's Disease, alpha-1 antitripsin deficiency, autoimmune hepatitis and cirrhosis
Excessive alcohol consumption (>15 gr/day for women and 30 gr/day for men),
Endocrine disorders: hyperthyroidism or uncontrolled hypothyroidism
Pharmacological treatment with immunosuppressants, cytotoxic agents, systemic corticosteroids, or other drugs that could potentially cause hepatic steatosis (amiodarone, tamoxifen, methotrexate) or alter liver tests
The use of weight modifiers or previous weight loss surgery at any time
Cardiovascular event in the last 6 months
Stage 4 and above kidney disease
Active infection, cancer or autoimmune disease
Inability to use an internet application or not having a Smartphone,
Low command of spanish or illiteracy,
Refusal to give informed consent
Pregnant women or women planning pregnancy

Where it is running

Hospital Universitari de Bellvitge — L'Hospitalet de Llobregat, Barcelona, Spain

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.