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Smartphone App for Non-alcoholic Fatty Liver Disease (AppLiver)

Primary Purpose

Non-Alcoholic Fatty Liver Disease

Status
Not yet recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Smartphone app use
Standard of care
Sponsored by
The University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Non-Alcoholic Fatty Liver Disease focused on measuring non-alcoholic fatty liver disease, telemedicine, mobile health, self-management

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • known NAFLD
  • able to read and understand Chinese
  • owns a compatible smartphone
  • without major cognitive impairment.

Exclusion Criteria:

  • on SGLT-2 inhibitors, GLP-1 agonists, or thiazolidinediones
  • patients with cirrhosis
  • patients who are pregnant
  • patients on special diet or with special dietary requirement (e.g. vegan, gluten free)
  • patients with heavy alcohol use (≥20 grams/ day for women or ≥30 grams/ day for men)
  • history of HCC or LT

Sites / Locations

  • The University of Hong Kong

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Other

Arm Label

Smartphone app arm

Standard of care

Arm Description

Use the dedicated smartphone app for NAFLD patients

Standard of care

Outcomes

Primary Outcome Measures

Change in body weight
Body weight of the participants will be measured at baseline and 12 months

Secondary Outcome Measures

Reduction in hepatic steatosis
Hepatic steatosis will be quantified by transient elastography as expressed by controlled attenuation parameter (CAP)
ALT normalization
ALT as part of liver biochemistry will be measured at baseline and 12 months
Reversal of sarcopenia
Skeletal muscle mass will be quantified by bioelectrical analysis. Sarcopenia is common among subjects with NAFLD and is defined according to international guidelines.
Changes in lipid profile
Fasting lipid profile will be measured at baseline and 12 months
Changes in glucose levels
Fasting glucose levels will be measured at baseline and 12 months
Visceral fat reduction
Visceral fat will be assessed using bioelectrical analysis machine at baseline and 12 months

Full Information

First Posted
December 1, 2021
Last Updated
May 8, 2023
Sponsor
The University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT05180760
Brief Title
Smartphone App for Non-alcoholic Fatty Liver Disease
Acronym
AppLiver
Official Title
Effectiveness of a Smartphone App in Promoting Weight Loss in Patients With Non-alcoholic Fatty Liver Disease: a Pilot Multi-centre Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
July 1, 2023 (Anticipated)
Primary Completion Date
December 31, 2025 (Anticipated)
Study Completion Date
December 31, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The University of Hong Kong

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Non-alcoholic fatty liver disease (NAFLD) is a disease spectrum that encompasses excessive liver deposition of fat (NAFL), non-alcoholic steatohepatitis (NASH), and NASH cirrhosis. NAFLD is regarded as the hepatic manifestation of metabolic syndrome and is currently the most common etiology for chronic liver disease worldwide, affecting 25% of the adult population globally. It is estimated that cirrhosis and liver-related death occur in 20% and 12%, respectively, over a 10-year period in patients with NAFLD. The incidence of decompensated cirrhosis and hepatocellular carcinoma (HCC) due to NAFLD are increasing with time. In United States, the number of patient listing for liver transplantation (LT) due to NAFLD has surpassed that of from chronic viral hepatitis and is currently the second leading cause for LT waitlist overall. Locally, the prevalence of NAFLD is estimated to be 42% according to a health census in healthy blood donors in Hong Kong, and up to 13.5% healthy subjects will develop new onset NAFLD in 3-5 years of follow-up. Clearly, NAFLD is a chronic liver disease with alarmingly high prevalence that warrants attention. Despite the high prevalence and potential to develop serious liver-related morbidity, there are currently no approved drugs for patients with NAFLD. To achieve resolution of steatohepatitis and improvement of liver fibrosis, weight loss appears to be the only effective means. This study is aimed to evaluate the effectiveness of a self-developed smartphone app for achieving weight loss in Chinese adults with non-alcoholic fatty-liver disease (NAFLD) at 12 months. Endorsed by the WHO, mobile technology is being increasingly used to promote health. There is a lack of research on the use of mobile technology for promoting weight loss in Chinese NAFLD patients.
Detailed Description
The Investigators formed a multi-disciplinary team consisting of hepatologist, computer scientist, dietitian and endocrinologist. The investigators hypothesize that NAFLD subjects who use the dedicated smartphone app will achieve more weight loss than subjects who are managed with standard of care (SOC) without smartphone app. The present study is a multi-center, two-arm randomized, placebo-controlled, 1:1 trial to examine the effectiveness of a self-developed simple-to-use smartphone app for NAFLD patients. The smartphone app consists of elements that track health data, provide health education, estimate calorie intake and energy expenditure. Anthropometric measurements, blood tests, transient elastography, and bioelectrical impedance analysis will be performed at baseline and 12 months. The intervention is either Smartphone app vs SOC. The main outcome measures will include changes in body weight, liver fat, liver enzyme, muscle mass, lipid and glucose profile.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-Alcoholic Fatty Liver Disease
Keywords
non-alcoholic fatty liver disease, telemedicine, mobile health, self-management

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
260 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Smartphone app arm
Arm Type
Active Comparator
Arm Description
Use the dedicated smartphone app for NAFLD patients
Arm Title
Standard of care
Arm Type
Other
Arm Description
Standard of care
Intervention Type
Behavioral
Intervention Name(s)
Smartphone app use
Intervention Description
Smartphone app use in the active arm
Intervention Type
Behavioral
Intervention Name(s)
Standard of care
Intervention Description
Standard of care
Primary Outcome Measure Information:
Title
Change in body weight
Description
Body weight of the participants will be measured at baseline and 12 months
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Reduction in hepatic steatosis
Description
Hepatic steatosis will be quantified by transient elastography as expressed by controlled attenuation parameter (CAP)
Time Frame
12 months
Title
ALT normalization
Description
ALT as part of liver biochemistry will be measured at baseline and 12 months
Time Frame
12 months
Title
Reversal of sarcopenia
Description
Skeletal muscle mass will be quantified by bioelectrical analysis. Sarcopenia is common among subjects with NAFLD and is defined according to international guidelines.
Time Frame
12 months
Title
Changes in lipid profile
Description
Fasting lipid profile will be measured at baseline and 12 months
Time Frame
12 months
Title
Changes in glucose levels
Description
Fasting glucose levels will be measured at baseline and 12 months
Time Frame
12 months
Title
Visceral fat reduction
Description
Visceral fat will be assessed using bioelectrical analysis machine at baseline and 12 months
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: known NAFLD able to read and understand Chinese owns a compatible smartphone without major cognitive impairment. Exclusion Criteria: on SGLT-2 inhibitors, GLP-1 agonists, or thiazolidinediones patients with cirrhosis patients who are pregnant patients on special diet or with special dietary requirement (e.g. vegan, gluten free) patients with heavy alcohol use (≥20 grams/ day for women or ≥30 grams/ day for men) history of HCC or LT
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lung-Yi Mak, MD
Phone
852 22554704
Email
lungyi@hku.hk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lung-Yi Mak, MD
Organizational Affiliation
The University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
The University of Hong Kong
City
Hong Kong
State/Province
Select A State Or Province
ZIP/Postal Code
0000
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No

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Smartphone App for Non-alcoholic Fatty Liver Disease

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