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NCT Number: NCT05618626

Prevention of NAFLD and CVD Through Lifestyle Intervention

Prevention of non-alcoholic fatty liver disease (NAFLD) and cardiovascular disease (CVD) through lifestyle intervention (MAUCO+) is a clinical trial that aims to improve sarcopenia, aerobic capacity, body composition, and lipid profile, insulin resistance, cardiovascular risk, NAFLD, and maintain a healthier lifestyle. Through the implementation of physical activity and nutritional programs.

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Key information

Age range

45 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Centro MAUCO+

Molina, Maule Region, Chile

Location status: Recruiting

Location contact

Laura A Huidobro, MD, PhD

CONTACT

[email protected]

About this study

BACKGROUND. Gallstone disease (GSD), including gallstones and cholecystectomy, is a common digestive disease worldwide, and Chile has one of the highest reported rates of gallstone prevalence. GSD, in particular cholecystectomy, has been associated with nonalcoholic fatty liver disease (NAFLD). In previous studies, investigators confirmed the association of cholecystectomy with a higher risk of NAFLD only in men. Additionally, reasearchers found a higher cardiovascular event risk in 3 years for male gallstone carriers. Investigators aim to step forward toward translational research by evaluating the effectiveness of a risk-reduction strategy customized to our population.

STUDY GOALS. To evaluate a metabolic risk reduction strategy based on: 1. A Physical exercise trial to increase muscle mass and strength, and 2. A nutritional intervention based on an anti-inflammatory diet, sleep hygiene, and prolonged fasting periods.

METHODS. Intensive Lifestyle Intervention, Randomized Controlled Trial: 300 participants will be randomly allocated to control (n=150) or an experimental group (n=150). The control group will receive standard prevention recommendations, personalized advice, educational material regarding lifestyle and metabolic diseases, and follow-up evaluation of physical activity, physical condition, anthropometry, diet, and sleep habits. The intervention group will receive, tailored to each participant: 3.1 An Exercise Program consisting of directly supervised and home-based telehealth sessions emphasizing muscle building, and 3.2. A Nutritional plus Program based on a diet rich in anti-inflammatory components and legumes, low in fat and refined carbohydrates, controlled energy according to BMI, extended nocturnal fasting periods, and healthy sleep habits. The programs will have a 6-month intensive phase of bi-weekly directly supervised exercise sessions in a municipality gym and a weekly telehealth session, followed by six months of telephone support and bi-monthly direct supervision to reinforce adherence and early identification of risk factors for abandonment. Intervention outcomes measured at baseline and years 1 and 2 are changes in non-invasive serum and ultrasound-based biomarkers of NAFLD; improvement in sarcopenia, aerobic capacity, body composition, lipid profile, insulin resistance, and cardiovascular risk; among overweight participants, permanent loss of at least 5% body weight; the decrease of depression symptoms, improvement of quality of life scores, and maintenance of a healthier lifestyle.

EXPECTED RESULTS: is expected that a 12-month intervention of a personalized physical activity program together with a metabolic protective diet will improve markers of metabolic syndrome and NAFLD and decrease CVD risk scores in all participants who adhere to more than 50% of both interventions, with a clear dose-response effect.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • With and without gallstones disease
  • With various degrees of NAFLD (none too severe)

Exclusion criteria

  • Any significant comorbidity or physical limitation to undergo resistance exercise program
  • Use of medications that alter muscle mass (e.g., corticosteroids)
  • History of hepatitis B or C
  • Use of hepatotoxic drugs

Treatment and study plan

Physical exercise and dietary intervention for NAFLD

Other

Investigators will assess the efficiency of the intervention by measuring adherence to physical exercise and nutritional diet.

Primary outcomes

  1. Presence and severity of Non-Alcoholic Fatty liver Disease (NAFLD) at baseline and 12 month later.

    Time frame: 36 months

    It will be measured through the liver steatosis marker "Controlled Attenuation Parameter (CAP)" (dB/m).

Secondary outcomes

  1. Framingham Cardiovascular risk score

    Time frame: 36 months

    It will be measured at baseline and 12 months.

  2. HDL cholesterol (mg/dL)

    Time frame: 36 months

    It will be measured at baseline and 12 months.

  3. Triglycerides (mg/dL)

    Time frame: 36 months

    It will be measured at baseline and 12 months.

  4. Glycemia (mg/dL)

    Time frame: 36 months

    It will be measured at baseline and 12 months.

  5. Insulin (uU/mL)

    Time frame: 36 months

    It will be measured at baseline and 12 months.

  6. HBA1c

    Time frame: 36 months

    It will be measured at baseline and 12 months.

  7. usPCR (mg/L)

    Time frame: 36 months

    It will be measured at baseline and 12 months.

  8. AST:ALT ratio

    Time frame: 36 months

    It will be measured at baseline and 12 months.

  9. Total cholesterol (mg/dL)

    Time frame: 36 months

    It will be measured at baseline and 12 months.

  10. Platelets (#cells/uL)

    Time frame: 36 months

    It will be measured at baseline and 12 months.

  11. HOMA-IR

    Time frame: 36 months

    It will be measured at baseline and 12 months.

  12. Total Bilirrubin (mg/dL)

    Time frame: 36 months

    It will be measured at baseline and 12 months.

  13. Alkaline phosphatase (UI/l)

    Time frame: 36 months

    It will be measured at baseline and 12 months.

  14. Glutamiz oxaloacetic transaminase (GOT) (UI/l)

    Time frame: 36 months

    It will be measured at baseline and 12 months.

  15. Glutamic pyruvic trasaminase (GPT) (UI/l)

    Time frame: 36 months

    It will be measured at baseline and 12 months.

  16. Gamma-glutamyl Transferase (GGT) (UI/l)

    Time frame: 36 months

    It will be measured at baseline and 12 months.

  17. Metabolic syndrome

    Time frame: 36 months

    To be diagnosed with metabolic syndrome it is necessary to meet 3 or more conditions. (abdominal obesity, high triglycerides, low HDL cholesterol, high blood pressure and high fasting glucose). Metabolic syndrome will be measure at baseline and 12 month.

Other outcomes

  1. Muscular mass percentage measure

    Time frame: 36 months

    Muscular mass percentage will be measure by bioimpedance analysis at baseline and 12 month.

  2. Body fat percentage

    Time frame: 36 months

    Body fat percentage will be measure by bioimpedance analysis at baseline and 12 month.

  3. Body Mass Index (BMI) (kg/m^2)

    Time frame: 36 months

    A BMI will considered Underweight, Normal, Overweight or Obesity if it is less than 18.5 kg/m^2, it is between 18.5 and 24.9 kg/m^2, it is between 25 and 29.9 kg/m^2, or it is equal or greater than 30 kg/m^2, respectively.

  4. Aerobic capacity VO2max (ml/kg/min)

    Time frame: 36 months

    Aerobic capacity VO2max will be measure at baseline and 12 month

  5. Waist circumference (cm)

    Time frame: 36 months

    Waist circumference will be measure at baseline and 12 month.

Study contacts

Contact information is provided by the study sponsor or research team.

Catterina Ferreccio, MD

CONTACT

[email protected]

+56 9 95788658

Laura A Huidobro, PhD

CONTACT

[email protected]

+56 9 9219 6618

Sponsors and collaborators

Lead sponsor

Pontificia Universidad Catolica de Chile

Other

Registry information

Official study title

Cardiovascular Diseases (CVD) and Nonalcoholic Fatty Liver Diseases (NAFLD) Among Gallstone and Cholecystectomy Patients and the Impact of a Novel Diet and Muscle Training Program

Acronym: MAUCO+

Important dates

Study start
2021
Primary completion
2025
Study completion
2025
First posted
Nov 16, 2022
Registry last updated
Nov 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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