Effect of a Specialized Oral Supplement on Nutritional Status and Quality of Life in Non-dialysis CKD
- Conditions
- Protein-Energy MalnutritionChronic Kidney Diseases
- Interventions
- Dietary Supplement: Nutritious ShakeBehavioral: Nutritional counseling
- Registration Number
- NCT06576479
- Lead Sponsor
- NIN Institute
- Brief Summary
In patients whit chronic kidney disease (CKD) there is a high prevalence of nutritional disorders and negative changes in body composition, which is strongly associated with an increased risk of morbidity and mortality.
- Detailed Description
Epidemiological studies have reported that between 30 and 50% of patients with kidney disease show signs of malnutrition and that specifically in patient with CKD in stages 4-5 without replacement therapy, the prevalence of protein energy wasting (PEW) can be up to 45%.
Many factors influence the development of PEW, however, one main factor is insufficient intake of energy and macronutrients. The main obstacle that prevents the patient from meeting their nutritional requirements is the presence of gastrointestinal symptoms. In addition to this, dietary restrictions, lack of adherence to eating plans and the presence of digestive and psychological abnormalities of the patient, contribute directly to the patient directly contribute to insufficient energy and protein intake. Therefore, there is a need for evidence-based nutritional treatment strategies that facilitate the patient's achievement of their nutritional requirements and maintain or improve their nutritional supplements in patients with CKD has been shown to be a good treatment strategy.
Specifically in patients with CKD without replacement therapy, it has been observed that the use of specialized nutritional supplements can contribute to increasing their energy, fat, and fiber intake, while at the same time achieving a decrease in protein intake without causing any change in serum minerals or electrolytes.
This project will provide practical information for the validation of the therapeutic effect of a new specialized food supplement on the nutritional status and quality of life in patients with CKD without replacement therapy, which will be useful both for health professionals and for the patients themselves.
MAIN OBJETIVE To assess the effect and safety of the use of a specialized food supplement on the nutritional status and quality of life of patients with CKD and PEW without replacement therapy.
STUDIO DESING Randomized, blinded clinical trial with an intervention period of 4 months.
PROCESS Recruitment - Nephrologist
Identify those patients who are candidates to participate in the clinical trial.
Review the inclusion and exclusion criteria.
Invite identified patients to participate in the clinical trial.
Share the abstract and invite your treating physician to participate to confirm your approval.
Pre - Nutritional wash out appointment - nutritionist
Evaluate inclusion criteria.
Review and sign the informed consent.
Perform evaluation to indicate a personalized meal plan.
Deliver a meal plan.
Schedule in 30 days for your next nutritional appointment.
0 - Full Assessment Nutritional Appointment - Nutritionist
Evaluate adherence to the meal plan (percentage of adequacy of energy and protein consumption from 70% to 130%).
Assign an intervention group randomly (sealed envelope).
Perform an evaluation of nutritional status, quality of life and body composition.
Offer nutritional treatment according to the assigned intervention group.
Schedule an immediate appointment for laboratory tests of blood and urine.
Schedule in 30 days for your next nutritional appointment.
1. - Nutritional monitoring appointment - nutritionist
Evaluate adherence to the eating plan.
Offer nutritional treatment according to the assigned intervention group.
Schedule in 30 days for your next nutritional appointment.
Make an appointment a few days before your next nutritional appointment to perform blood and urine lab tests.
2. - Full Assessment Nutritional Appointment - Nutritionist
Perform an evaluation of nutritional status, quality of life and body composition.
Offer nutritional treatment according to the assigned intervention group.
Schedule in 30 days for your next nutritional appointment.
3. - Nutritional monitoring appointment - nutritionist
Evaluate adherence to the eating plan.
Offer nutritional treatment according to the assigned intervention group.
Schedule in 30 days for your next nutritional appointment.
3 - Nutritional monitoring appointment - nutritionist
Evaluate adherence to the eating plan.
Offer nutritional treatment according to the assigned intervention group.
Schedule in 30 days for your next nutritional appointment.
Schedule a few days before your nutritional appointment for blood and urine lab tests.
4 - Full Assessment Nutritional Appointment - Nutritionist
Perform an evaluation of nutritional status, quality of life and body composition.
Offer nutritional treatment according to the assigned intervention group.
SAMPLE SIZE 50 participants
STATISTIC ANALYSIS For the comparison of proportions between the groups, it will be done with X2 or Fisher's exact test and to compare quantitative variables, Student's T or Mann-Whitney U will be used. For the intra-group comparisons, Mc Nemar will be used for the qualitative variables and Anova for repeated samples or Friedman's Anova for the quantitative variables. For the analysis of the interaction or intervening variables, a stratified statistical analysis will be carried out, using contingency tables and the Mantel-Haenszel method. The results will be considered statistically significant if the value of p \<0.05.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 50
- Patients over 18 years of age
- Patients with diabetic kidney with eGFR <60 ml / min / 1.73m2 and ≥15 ml / min / 1.73m2, (stage G3a, G3b and G4 respectively)
- Patients with protein energy expenditure (defined by serum albumin < 3.8 g/dl)
- Patients with protein energy expenditure (defined by 24-hour recall less than a dietary protein intake <0.6 g/kg/d or have a consumption <25 kcal/kg/d
- Patients who can read and write (or primary caregiver)
- Domicile within the metropolitan area
- Previous hospitalizations in the last month
- Patients with serious complications (chronic infection, septicemia, cancer, HIV, Alzheimer's, uncontrolled heart failure, liver failure, cerebrovascular syndrome, malabsorption syndrome, or allergy to any ingredient in the nutritional supplement)
- Patients with actual consumption of food supplements and / or keto analogues.
Elimination Criteria:
- Failure to attend nutritional assessment and biochemical testing at baseline, 2 months, and end of the study.
- Failure to take the supplement >10% (>12 failed doses).
- Diagnosis of any comorbidity during the intervention period.
- Initiation of replacement therapy.
- Identification of adverse effects.
- Withdrawal of voluntary participation by the patient.
- Death.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- FACTORIAL
- Arm && Interventions
Group Intervention Description Arm Intervention Nutritious Shake Intervention group: The specialized oral supplement is provided, with the consumption of 1 serving (70g-dissolved in 237 ml natural water) per day in conjunction with individualized nutritional counseling. For 4 months Arm no Intervention Nutritional counseling Control group: They receive specialized nutrition considering the recommendations of the clinical practice guidelines for CKD. For 4 months
- Primary Outcome Measures
Name Time Method Serum Albumin (g/dl) baseline intervention and 4 months Changes in serum albumin (g/dl) for all the patients at baseline and month 4.
Dietary intake (kcal/kg/day) baseline intervention and 4 months Changes in dietary caloric intake of patients at baseline and month 4.
- Secondary Outcome Measures
Name Time Method Adherence to nutritional treatment baseline intervention and 4 months Number of patients who manage to adhere correctly to the treatment, applying a Likert scale.
Adverse effects baseline intervention and 4 months Number of patients who present adverse effects during the intervention, considering frequency and intensity by applying SAS (symptom assessment scale) and Bristol Scale.
Trial Locations
- Locations (1)
Hospital Civil Fray Antonio Alcalde
🇲🇽Guadalajara, Jalisco, Mexico