Skip to content

Randomized controlled trial of intervention effect of fatty liver data analysis and management software on non-alcoholic fatty liver disease

Randomized controlled trial of intervention effect of fatty liver data analysis and management software on non-alcoholic fatty liver disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069763
Enrollment
Unknown
Registered
2023-03-24
Start date
2023-04-01
Completion date
Unknown
Last updated
2023-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nonalcoholic fatty liver disease

Interventions

Intervention group:Fatty liver Data Analysis and Intervention Software was used to manage the intervention group
Control group:Health education and lifestyle guidance are provided by professional clinicians and dietitians/health managers via phone and wechat

Sponsors

Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: ? The diagnosis of NAFLD is consistent with the diagnosis of NAFLD; ? the age range is from 18 to 65 years old. 24kg/m2=BMI=35kg/m2; (3) Patients had smart phones in line with the operating environment of the software program of this study, and had the ability to use the software program of this study through guidance; ? The patients agreed to participate in the study, receive review and follow-up on time, and sign the informed consent.

Exclusion criteria

Exclusion criteria: ? Genetic metabolic or autoimmune liver disease with hepatophil virus and non-hepatophil virus infection drug/poison/alcohol/biliary liver injury, cirrhosis or any end-stage liver disease; ? Liver or extrahepatic malignancies; ? Diabetic patients with unstable blood glucose control (patients treated with insulin, HbA1C > 9%); ? Pregnant and lactating women; (5) suffering from other major cardiovascular and cerebrovascular diseases, liver and kidney diseases; (6) Patients with severe respiratory, heart, brain and other diseases who cannot complete diet and exercise intervention and need other treatment; ? Concomitant mental illness, including anxiety or depression; ? Researchers believe that there are objects that are not suitable for inclusion factors.

Design outcomes

Primary

MeasureTime frame
Weight loss rate;

Secondary

MeasureTime frame
Liver fat attenuation paramete;Liver stiffness value (LSM);Body mass index (BMI);Waist to hip ratio;Liver function (AST, ALT);Fasting plasma glucose;Fasting insulin;glycosylated hemoglobin;Adverse/serious adverse event rates;

Countries

china

Contacts

Public ContactSun Chao

Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

csun7682@163.com13818676775

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026