Viabilidad del Programa Integrado de Salud, Nutrición y Bienestar Renal (THINK-Well)

Experimental: PIENSA-Bien

Educación nutricional práctica híbrida (presencial y virtual) con personas que viven con enfermedad renal. Las sesiones grupales permitirán el apoyo social de otras personas con enfermedad renal, facilitarán el establecimiento de objetivos y la resolución de problemas individualizada, discutirán un enfoque integrado de la nutrición para personas con múltiples condiciones de salud y desarrollarán habilidades culinarias básicas mientras se fomenta una dieta saludable para el corazón basada en alimentos integrales. Los participantes también recibirán asistencia financiera para comprar productos y asesoramiento nutricional individual 1:1 opcional.

Conductual: THINK-Well

Seven hybrid (online or in-person) group nutrition education sessions paired with food bucks and one individual consultation with a dietitian over 12-20 weeks.

Comparador activo: Enhanced Usual Care

The enhanced usual care group will receive two virtual nutrition education sessions led by a trained educator over 12-20 weeks.

Otro: Cuidado Habitual Mejorado

Dos sesiones educativas virtuales de nutrición en grupo proporcionadas por un educador capacitado.

Viabilidad del Reclutamiento

La viabilidad del reclutamiento se evaluará mediante métricas de cribado, elegibilidad y inscripción. Se registrará el número total de pacientes cribados para la elegibilidad del estudio. La tasa de elegibilidad se calculará como el número de pacientes que cumplen los criterios de elegibilidad del estudio dividido por el número total de pacientes cribados. La tasa de inscripción se calculará como el número de pacientes inscritos dividido por el número de pacientes elegibles y se expresará como un porcentaje mensual.

Participant retention

Retention will be assessed as the proportion of enrolled participants who complete the 12-week THINK-Well program and the end-of-study assessment. Retention rate will be calculated as the number of participants who complete the final study assessment divided by the total number of participants enrolled, expressed as a percentage. Monthly dropout rate and reason for dropout

Intervention adherence

Intervention adherence will be assessed by participant attendance at scheduled program sessions. Adherence will be calculated as the number of sessions attended divided by the total number of planned sessions for each participant and summarized as the mean percentage of sessions attended across participants.

Participant satisfaction

Participant satisfaction with the THINK-Well program will be assessed using a post-intervention questionnaire administered at the end of the intervention. The survey will assess participants' perceptions of the usefulness, relevance, and overall satisfaction with the program content, delivery format (virtual and in-person sessions), and program activities. Satisfaction will be summarized using descriptive statistics, including mean scores and the proportion of participants reporting high satisfaction.

Cambio en la composición corporal (porcentaje de grasa corporal)

La composición corporal se evaluará mediante análisis de impedancia bioeléctrica (BIA) con un analizador de composición corporal. El BIA estima la composición corporal midiendo la impedancia eléctrica a través de los tejidos corporales e incorporando las características del participante (por ejemplo, edad, sexo, altura y peso) en ecuaciones de predicción.

Las siguientes medidas de composición corporal se medirán y obtendrán del BIA:

Porcentaje de grasa corporal (%): La proporción del peso corporal total compuesta por tejido graso, expresada como un porcentaje que va del 0 al 100%.

Porcentaje de masa muscular (%): La proporción del peso corporal total compuesta por tejido muscular, expresada como un porcentaje que va del 0 al 100%.

Las reducciones en el porcentaje de grasa corporal y el aumento en el porcentaje de masa muscular representan mejoras en la composición corporal.

Change from Baseline in Life's Essential 8 score at 12-weeks

Life's Essential 8 score is a composite cardiovascular health (CVH) score developed by the American Heart Association (AHA) to quantify and track an individual's heart- and brain-health based on eight key lifestyle behaviors and clinical health factors (healthy diet, physical activity, nicotine exposure, sleep health, body mass index, lipids, glucose and blood pressure). The score ranges from 0 to 100 points, with higher scores indicating better overall cardiovascular health.

Interpretation of the composite score usually follows these general categories:

0-49: Low cardiovascular health 50-79: Moderate cardiovascular health 80-100: High (optimal) cardiovascular health

Change from Baseline in Self-Efficacy for Managing Chronic Disease (SEMCD) at 12-weeks

Self-efficacy will be assessed using the Chronic Disease Self-Efficacy Scale (Self-Efficacy for Managing Chronic Disease 6-Item Scale). This instrument measures an individual's confidence in their ability to manage symptoms, fatigue, emotional distress, and health tasks associated with chronic disease.

The scale includes 6 items, each rated on a 10-point numeric scale ranging from 1 ("not at all confident") to 10 ("totally confident").

Scores are calculated as the mean of the six items, producing a final score ranging from 1 to 10.

Higher scores indicate greater confidence in the ability to manage chronic disease-related health challenges.

Change from Baseline Patient Activation Measure, 13-item version (PAM-13) at 12-weeks

Patient activation will be measured using the Patient Activation Measure-13 (PAM-13), which assesses an individual's knowledge, skills, and confidence in managing their health and healthcare.

The PAM-13 consists of 13 statements rated on a 4-point Likert scale (strongly disagree to strongly agree) with an additional "not applicable" option.

Responses are summed and converted using a proprietary scoring algorithm to a standardized activation score ranging from 0 to 100.

Higher scores indicate greater patient activation.

Change from Baseline Kidney Disease Quality of Life - 36 at 12-weeks

KDQOL is a kidney disease-specific quality-of-life instrument that combines a generic core with targeted modules to measure how CKD and its treatments impact patients' well-being across physical, emotional, and social dimensions.

The instrument contains five subscales:

1. Symptoms and Problems of Kidney Disease (12 items)
2. Effects of Kidney Disease on Daily Life (8 items)
3. Burden of Kidney Disease (4 items)
4. Physical Component Summary (PCS) derived from the Short Form-12
5. Mental Component Summary (MCS) derived from the Short Form-12

Each subscale is scored on a 0-100 scale after standard scoring transformation according to KDQOL-36 scoring guidelines. Higher scores indicate better quality of life or fewer symptoms/burdens. The KDQOL-36 does not produce a single total score; results are reported for each subscale.

Change from Baseline in Mediterranean Diet adherence at 12-weeks

Diet quality will be assessed using the Mediterranean Eating Pattern for Americans (MEPA) tool, which is an instrument developed to assess how closely a person's diet aligns with the Mediterranean dietary pattern adapted for U.S. populations. Total scores are summed to produce a composite Mediterranean diet adherence score. Higher scores indicate closer alignment with the Mediterranean Eating Pattern.

The screener consists of 16 items assessing frequency or quantity of consumption of key Mediterranean diet components including fruits, vegetables, whole grains, legumes, nuts, fish, olive oil, and red or processed meats.

Each item contributes 0 or 1 point based on whether the recommended intake threshold is met. Scores are summed to produce a total score ranging from 0 to 16.

Change from baseline in Body Composition at 12-weeks

Using a bioimpedence scale, we will measure and collect body composition data. This will include: Fat Mass (measured in kilograms), Muscle Mass (measured in kilograms), Percent Fat Mass (measured as a percentage), and Percent Muscle Mass (measured as a percentage).

Change in Body Mass Index (BMI)

Body Mass Index (BMI) will be calculated from two anthropometric measures, body weight and reported height. These two measures will be collected using standardized measurement procedures. The following measures will be assessed: Body weight (kg): Body weight will be measured in kilograms using a calibrated digital scale with participants wearing light clothing and no shoes. Reported height will be taken from an average of the patient's three most recent electronic medical record heights.

Body mass index (BMI) (kg/m²): BMI will be calculated as weight in kilograms divided by reported height in meters squared.

Change in Waist-to-Hip Ratio

Waist-to-hip ratio measures will be collected using standardized measurement procedures and measured in centimeters. Waist circumference and hip circumference will be measured in centimeters using a flexible measuring tape. Waist circumference will be measured at the midpoint between the lower rib and the iliac crest. Hip circumference will be measured at the widest portion of the buttocks. Waist-to-hip ratio will be calculated as waist circumference (cm) divided by hip circumference (cm).

Change in Body Composition (Fat Mass)

Body composition will be assessed using bioelectrical impedance analysis (BIA) with a body composition analyzer. BIA estimates body composition by measuring electrical impedance through body tissues and incorporating participant characteristics (e.g., age, sex, height, and weight) into prediction equations.

The following body composition measures will be collected:

Fat mass (kg): Estimated total body fat mass measured in kilograms.

Reductions in fat mass represent improvements in body composition.

Change in Body Composition (Muscle Mass)

Body composition will be assessed using bioelectrical impedance analysis (BIA) with a body composition analyzer. BIA estimates body composition by measuring electrical impedance through body tissues and incorporating participant characteristics (e.g., age, sex, height, and weight) into prediction equations.

The following body composition measures will be collected:

Muscle mass (kg): Estimated total skeletal muscle mass measured in kilograms.

Increases in muscle mass represent improvements in body composition.

Change in Body Composition (Percent Muscle Mass)

Body composition will be assessed using bioelectrical impedance analysis (BIA) with a body composition analyzer. BIA estimates body composition by measuring electrical impedance through body tissues and incorporating participant characteristics (e.g., age, sex, height, and weight) into prediction equations.

The following body composition measures will be calculated: Percent muscle mass (%): The proportion of total body weight composed of skeletal muscle tissue, expressed as a percentage ranging from 0-100%. Percent Muscle Mass will be calculated from two collected measures: Body Mass (kg), and Muscle Mass (kg).

Increases in muscle mass and percent muscle mass represent improvements in body composition.