Skip to content

Effects of Mindfulness Based Stress Reduction Intervention in Patients With Non-alcoholic Fatty Liver Disease

Effects of Mindfulness Based Stress Reduction Intervention in Patients With Non-alcoholic Fatty Liver Disease: Beyond the Paradigm of Weight Loss.

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05130346
Enrollment
0
Registered
2021-11-23
Start date
2023-02-28
Completion date
2023-12-31
Last updated
2023-02-08

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

Conditions

Non-Alcoholic Fatty Liver Disease, Fatty Liver, Nonalcoholic, Obesity

Brief summary

The purpose of this research study is to find out about the usefulness of mindfulness for weight loss and improvement of physical and mental health in people who have non-alcoholic fatty liver disease (NAFLD).

Detailed description

Adding mindfulness to lifestyle changes for weight loss may improve fatty liver disease in particular and overall health and well-being in general by helping sustain weight loss and maintain a healthy lifestyle. This study will allow researchers to learn more about it. Non-alcoholic fatty liver disease is a condition where there is accumulation of excess fat in the liver of people who drink little or no alcohol. It is part of the metabolic syndrome characterized by diabetes, or pre-diabetes (insulin resistance), being overweight or obese, elevated blood lipids, as well as high blood pressure, all are risk factors for the disease. In this study, participants will receive usual care, and in addition, they may be asked to participate in a mindfulness-based stress reduction program for 8 weeks. Usual care involves the routine clinic follow up visits and routine lab tests and imaging studies.

Interventions

Participants will be asked to attend group meetings for mindfulness training. Each meeting will last approximately one hour and will take place online via Zoom. The meetings will occur on a weekly basis, over an 8-week period.

Sponsors

Virginia Commonwealth University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Confirmed diagnosis of NAFLD and ALT \>35 U/dl. 2. At least 2 features of Metabolic syndrome (defined by Adult Treatment Panel III (2005 revision)). 3. Age 18-80 years. 4. BMI ≥25 Kg/m2. 5. Capable of providing written or signed informed consent.

Exclusion criteria

1. Any known cause of liver disease other than NAFLD as confirmed by patient's history, laboratory data, and/or histological findings. 2. Decompensated liver cirrhosis based on laboratory data and clinical manifestations (varices, ascites, or encephalopathy). 3. Any previous experimental interventional treatment of NAFLD or NASH within the past 3 months. 4. Pre-existing diseases/conditions that could interfere with the results or the completion of this trial based on the investigator's judgment. 5. Unstable metabolic syndrome and other serious chronic medical conditions. 6. Unstable type 2 diabetes (any of the following): * Requiring medication adjustment within the last 3 months. * Patients requiring GLP-1 agonists treatment. * No more than 10% modification in insulin dose if on insulin. * If on SGLT-2 inhibitors, need to be on stable dose with more than 5% weight loss in the last 3 months. 7. Unable to adhere to out-patient clinic management program. 8. Do not speak English on a daily-user level. 9. Pregnant or planning to become pregnant within the following 6 months. 10. Active substance use disorder. 11. Does not accept follow-ups over 1 year from time of inclusion (T0). 12. Inmates.

Design outcomes

Primary

MeasureTime frameDescription
Change in Fibrosis-4 Index (FIB-4)Baseline to 6 monthsRelative change (%) in FIB-4 at 6 months (T1) from baseline (T0).
Change in Enhanced Liver Fibrosis test (ELF)Baseline to 6 monthsRelative change (%) in ELF at 6 months (T1) from baseline (T0).
Change in Nonalcoholic steatohepatitis related biomarkers score (NIS4)Baseline to 6 monthsRelative change (%) in NIS4 at 6 months (T1) from baseline (T0).
Change in liver stiffnessBaseline to 6 monthsRelative change (%) in liver stiffness as measured by transient elastography at 6 months (T1) from baseline (T0).
Change in hepatic fat depositionBaseline to 6 monthsRelative change (%) in hepatic fat deposition as measured by magnetic resonance imaging (MRI) with proton density fat fraction (PDFF) at 6 months (T1) from baseline (T0).
Change in total body weightBaseline to 6 monthsRelative change (%) in total body weight at 6 months (T1) from baseline (T0).
Change in bilirubinBaseline to 6 monthsRelative change (%) in bilirubin at 6 months (T1) from baseline (T0).
Change in alanine transaminase (ALT)Baseline to 6 monthsRelative change (%) in ALT at 6 months (T1) from baseline (T0).
Change in aspartate transaminase (AST)Baseline to 6 monthsRelative change (%) in AST at 6 months (T1) from baseline (T0).
Change in alkaline phosphatase (ALP)Baseline to 6 monthsRelative change (%) in ALP at 6 months (T1) from baseline (T0).
Change in c-reactive protein (CRP)Baseline to 6 monthsRelative change (%) in CRP at 6 months (T1) from baseline (T0).

Secondary

MeasureTime frameDescription
Change in bilirubinBaseline to 12 monthsRelative change (%) in bilirubin at 1 year (T2) from 6 months (T1) and baseline (T0).
Change in alanine transaminase (ALT)Baseline to 12 monthsRelative change (%) in ALT at 1 year (T2) from 6 months (T1) and baseline (T0).
Change in aspartate transaminase (AST)Baseline to 12 monthsRelative change (%) in AST at 1 year (T2) from 6 months (T1) and baseline (T0).
Change in c-reactive protein (CRP)Baseline to 12 monthsRelative change (%) in CRP at 1 year (T2) from 6 months (T1) and baseline (T0).
Change in Fibrosis-4 Index (FIB-4)Baseline to 12 monthsRelative change (%) in FIB-4 at 1 year (T2) from 6 months (T1) and baseline (T0).
Change in Enhanced Liver Fibrosis test (ELF)Baseline to 12 monthsRelative change (%) in ELF at 1 year (T2) from 6 months (T1) and baseline (T0).
Change in Nonalcoholic steatohepatitis related biomarkers score (NIS4)Baseline to 12 monthsRelative change (%) in NIS4 at 1 year (T2) from 6 months (T1) and baseline (T0).
Change in alkaline phosphatase (ALP)Baseline to 12 monthsRelative change (%) in ALP at 1 year (T2) from 6 months (T1) and baseline (T0).
Change in hepatic fat depositionBaseline to 12 monthsRelative change (%) in hepatic fat deposition as measured by magnetic resonance imaging (MRI) with proton density fat fraction (PDFF) at 1 year (T2) from 6 months (T1) and baseline (T0).
Change in total body weightBaseline to 12 monthsRelative change (%) in total body weight at 1 year (T2) from 6 months (T1) and baseline (T0).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026