University of Campania Luigi Vanvitelli
Naples, Campania, 80138, Italy
NCT Number: NCT07366463
Metabolic dysfunction associated Steatotic Liver Disease (MASLD) is frequently complicated by cardiometabolic (CMR) comorbidities, and prognosis is substantially influenced by acute cardiovascular events (ACE). Although several pharmacological approaches target CMR risk factors, lifestyle modification remains the cornerstone of management. However, adherence to dietary behavioral prescriptions is often poor, and the influence of sociodemographic determinants on compliance remains unclear. Moreover, the long-term real-life impact of behavioral and motivational support in MASLD is insufficiently characterized.
This randomized controlled trial aims to evaluate the effectiveness of a multidisciplinary management (including Hepatological counseling, Nutrition intervention, and Psychological support) in improving clinical MASLD outcomes, by increasing adherence to specialist-tailored recommendations.
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Notify Me40 year–79 year
All sexes
Interventional
Not applicable
Naples, Campania, 80138, Italy
Metabolic dysfunction-associated Steatotic Liver disease (MASLD) represents a predominant hepatopathy worldwide, as well as a complex systemic condition complicated by various extra-hepatic dysmetabolic manifestations.
Among these, acute cardiovascular events represent a serious burden, drastically increasing mortality rates, emphasizing the absolute need for holistic and multidisciplinary treatment strategies.
Even though several pharmacological approaches have been proposed, targeting the different dysmetabolic manifestations, lifestyle changes remain the paramount intervention for patients with simple steatosis. However, adherence to dietary and behavioral recommendations is often poor. Growing evidence highlights the importance of cognitive behavioral therapy (CBT) in supporting these recommendations. However, the real benefits of providing motivational support to individuals with MASLD remain largely unexplored in real-world applications.
This randomized controlled trial aims to evaluate the effectiveness of a multidisciplinary approach (integrating Hepatological counseling, Nutrition intervention, and Psychological support) in improving long-term clinical MASLD outcomes, by increasing adherence to specialist-tailored recommendations, as well as to investigate the social determinants impacting on the loss of compliance with this strategy.
MASLD patients will be consecutively enrolled and randomized into three Groups:
Groups A and B represent the "standard of care" cohort, while Group B represents the "experimental" cohort.
Baseline anthropometric, biochemical, clinical, liver stiffness (LSM), controlled attenuation parameter (CAP), lifestyle habits (including dietary and physical exercise), and body composition values will be recorded.
Along 18 months:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Hepatologic counseling will be offered every six months to individuals belonging to all study groups. These specialists-provided check-ups consisted of recording, at baseline, demographics and, at baseline and every six months, collecting anthropometrical, biochemical, clinical (including the assessment of previous cardiovascular events and the determination of individual cardiovascular risk), and body composition data, as well as evaluating the liver disease progression by using Noninvasive tools (NITs) (Fibroscan CAP).
Moreover, at baseline, the hepatologist, after assessing the initial compliance of each individual with the Mediterranean diet and active physical exercise, by respectively adopting the MDS questionnaire and the IPAQ-SF score questionnaire, also recommended, for the entire duration of the study, generic lifestyle changes, including a Mediterranean diet style, and proper physical activity (> 150 min/week of moderate - or 75 min/week of vigorous physical activity).
Nutritional counseling by a specialist will be provided on a semestral basis, scheduled on the same day as the hepatology follow-up visits, although conducted separately and after the hepatology consultation, and was offered exclusively to patients in Groups B and C. In these occasions, specialised anamnesis will be performed (including the investigation of general dietary habits, food allergies, and taste preferences), as well as the multicompartmental BIA-assessed body composition results will be properly interpreted to design, and eventually dynamically change along the duration of the study, a personalised dietary plan with a tailored physical activity strategy (integrating the generic recommendations received by the hepatologists), as well as to establish, and periodically revaluate, individual body composition outcomes.
The psychological intervention will be structured in sequential phases to enhance disease awareness, coping skills, and adherence to lifestyle changes. The first 90-minute session will include a comprehensive personal, familial, and physiological assessment, with systematic evaluation of social determinants of health using a dedicated CRF. The psychologist will assess disease awareness, quality of life, motivation for change, and treatment expectations. Emotional and cognitive components will be explored through interviews and standardized tools (BAI, BDI-II). Individualized therapeutic goals will be jointly defined. Weekly 60-minute sessions over six months will address previous behavioural change attempts, barriers, facilitators, and strategy refinement. Motivation will be continuously monitored according to the Transtheoretical Model. Semiannual follow-up sessions will reassess progress and address emotional or situational challenges.
Other names: Cognitive behavioral therapy
Time frame: From enrollment to the end of intervention at 18 months
The primary endpoint of this study was to highlight a significantly higher proportion (at least > 15%) of patients obtaining (intermediate time-point, i.e., after 12 months), and maintaining (end of the study, i.e., after 18 months), a reduction of at least 10% in body weight in the experimental cohort compared with the standard of care
Time frame: From enrollment to the end of intervention at 18 months
After 18 months, at the end of the study, in the experimental cohort compared with the standard of care, to report a statistically significant improvement of Body Mass Index (BMI) and Waist-to-hip ratio (WHR)].
Time frame: From enrollment to the end of intervention at 18 months
In the experimental cohort compared with the standard of care, to highlight significant changes in cardiovascular risk by using the Atherosclerotic Cardiovascular Disease (ASCVD) risk score, adopting the calculator available online on the American College of Cardiology website (https://tools.acc.org/ascvd-risk-estimator-plus) (accessed on 4th June 2024), considering > 7.5% the threshold defining a significant risk.
Time frame: From enrollment to the end of intervention at 18 months
After the 18 months, at the end of the study, in the experimental cohort compared with the standard of care, to report a statistically significant improvement of Homeostatic Model Assessment for Insulin Resistance (HOMA-IR),
Time frame: From enrollment to the end of intervention at 18 months
After the 18 months, at the end of the study, in the experimental cohort compared with the standard of care, to report a statistically significant improvement of high-density lipoprotein cholesterol (HDL)],
Time frame: From enrollment to the end of intervention at 18 months
After 18 months, at the end of the study, in the experimental cohort compared with the standard of care, to report a statistically significant improvement of body composition parameters [free-fat mass (FFM) and fat mass (FM)].
Time frame: From enrollment to the end of intervention at 18 months
After the 18 months, at the end of the study, in the experimental cohort compared with the standard of care, to report a statistically significant improvement of Liver Stiffness Measurement (LSM).
Time frame: From enrollment to the end of intervention at 18 months
After the 18 months, at the end of the study, in the experimental cohort compared with the standard of care, to report a statistically significant improvement of Controlled Attenuation Parameter (CAP).
Time frame: From enrollment to the end of intervention at 18 months
To reveal a significant correlation between anxiety levels [Beck Anxiety Inventory (BAI) questionnaire] and levels of compliance with the assigned intervention.
Note: Adherence to the assigned behavioral intervention is assessed using a 4-item questionnaire specifically developed for this study. The tool is conceptually informed by general adherence principles but is independently created, with original items and scoring, and does not reproduce or rely on the proprietary MMAS-4.
University of Campania Luigi Vanvitelli
Other
Integrating Hepatological, Nutritional, and Cognitive Behavioral Therapy-based Psychological Support is an Effective Multidisciplinary Approach to Improve Long-term Clinical Outcomes in the Management of MASLD Patients: a Randomized Clinical Trial [The "CoCoNut" Study]
Acronym: CoCoNut
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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