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Dietary Intervention Trial Targeting Metabolic Syndrome After Kidney Transplantation (DIETTX)

Primary Purpose

Kidney Transplant; Complications

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
high-protein, carbohydrate-reduced diet
Dutch Nutritional Guidelines
Sponsored by
University Medical Center Groningen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Kidney Transplant; Complications focused on measuring kidney transplantation, metabolic syndrome, high-protein diet, dietary intervention

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18 years or older.
  • Given informed consent.
  • At least 6 months after kidney transplantation.
  • Stable renal function with an estimated glomerular filtration rate (eGFR) > 30 mL/min.
  • Raised systolic blood pressure (≥130 mmHg) and at least two more features of metabolic syndrome: central obesity (waist circumference ≥102 for men and ≥88cm for women), elevated triglycerides (≥ 1.7 mmol/L), reduced HDL-C (< 1.0 mmol/L for men and < 1.3 mmol/L for women) or on drug treatment for reduced HDL, elevated plasma glucose (≥ 5.6 mmol/L) or on drug treatment for elevated glucose9.
  • Approval by nephrologist for participation in the study.

Exclusion Criteria:

  • Active medical illness, including rejection of the graft.
  • Psychopathology or serious cognitive impairment.
  • Necessity to follow specific dietary measures for health purposes that conflict with the study diets.
  • Use of insulin or sulfonylurea (SU)-derivates.
  • Language barrier.
  • Pregnancy or lactating.
  • Serum potassium > 5.0 mmol/L that requires dietary measures.
  • Moderate or severe malnutrition (Patient-Generated Subjective Global Assessment (PG-SGA) stage B or C). In this case, patient will be referred to a renal dietician.
  • Participation in other intervention trials.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    high-protein, carbohydrate-reduced diet

    Dutch Nutritional Guidelines

    Arm Description

    Outcomes

    Primary Outcome Measures

    Systolic blood pressure
    Change in systolic blood pressure (in mmHg)

    Secondary Outcome Measures

    Cardio-metabolic risk factors (lipids)
    change in circulating triglyceride concentrations, low-density lipoprotein cholesterol (LDL-C) and HDL-C (in fasting serum levels) in mmol/L.
    Cardio-metabolic risk factors (diastolic blood pressure)
    Change in diastolic blood pressure (in mmHg)
    Cardio-metabolic risk factors (waist circumference)
    change in waist circumference (WC) in cm
    Cardio-metabolic risk factors (insulin resistance)
    change in insulin resistance measuring by the homeostatic model assessment of insulin resistance (HOMA-IR index, fasting glucose, insulin)
    Body composition
    change in fat and muscle mass measured by multi-frequency bio-electrical impedance analysis (BIA) BMI, weight
    Anthropometric measures
    Change in weight in kilograms
    Anthropometric measures II
    Change in Body Mass Index (BMI) in kilograms per square meter
    Body composition II
    change in fat and muscle mass measured by multi-frequency bio-electrical impedance analysis (BIA)
    Quality of life (QoL)
    change in QoL, 12-item short form health survey (SF-12)
    Fatigue
    change in fatigue (measured by Dutch Checklist Individual Strength (CIS-20) questionnaire)
    Physical functioning
    change in Hand Grip Strength (HSG)
    Physical functioning II
    change in the five time sit to stand (FTSTS) test
    Nutritional intake
    change in nutritional intake measured by a 3-day food diary
    Nutritional intake II
    change in nutritional intake measured by nutritional intake biomarkers from 24-hour urine measurements (sodium, potassium, and urea excretion for calculating the protein intake by use of the Maroni equation)

    Full Information

    First Posted
    December 23, 2020
    Last Updated
    January 5, 2021
    Sponsor
    University Medical Center Groningen
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04698408
    Brief Title
    Dietary Intervention Trial Targeting Metabolic Syndrome After Kidney Transplantation
    Acronym
    DIETTX
    Official Title
    Dietary Intervention Trial Targeting Metabolic Syndrome After Renal Transplantation
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2021
    Overall Recruitment Status
    Unknown status
    Study Start Date
    January 2021 (Anticipated)
    Primary Completion Date
    June 2022 (Anticipated)
    Study Completion Date
    October 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University Medical Center Groningen

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Kidney transplant recipients (KTR) have a considerably lower life expectancy as compared with the general population, primarily due to a high prevalence of cardiovascular diseases. KTR often develop an unfavourable cardio-metabolic risk profile characterized by weight gain, metabolic syndrome and post-transplantation diabetes mellitus (PTDM). In general, nutrition plays a key role in both the prevention and treatment of these cardio-metabolic derangements. However, in KTR most RCT's with a dietary intervention, failed to show significant improvement in cardio-metabolic health. This at least questions the efficacy of the diets of these intervention, which relied on general or diabetes guidelines, after kidney transplantation. KTR not only face a high cardio-metabolic risk, but also have a high risk for malnutrition and muscle mass depletion. More knowledge is required to determine the optimal diet and macronutrient composition for improvement of the cardio-metabolic risk factors in the context of the high malnutrition risk. In this regard, observational studies point towards the needs for a higher protein intake for better patient outcomes. Therefore, in this study, the investigators will examine if a high-protein, carbohydrate-reduced diet is more effective than a diet in line with the Dutch Dietary Guidelines for improvement of cardio-metabolic risk factors and for improvement of the body composition in KTR.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Kidney Transplant; Complications
    Keywords
    kidney transplantation, metabolic syndrome, high-protein diet, dietary intervention

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Crossover Assignment
    Masking
    Outcomes Assessor
    Allocation
    Randomized
    Enrollment
    30 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    high-protein, carbohydrate-reduced diet
    Arm Type
    Experimental
    Arm Title
    Dutch Nutritional Guidelines
    Arm Type
    Active Comparator
    Intervention Type
    Other
    Intervention Name(s)
    high-protein, carbohydrate-reduced diet
    Intervention Description
    the high-protein, carbohydrate-reduced diet will consist of 1.2-1.4 g/kg/d protein, 26-20en% carbohydrates and +/- 50en% fatty acids, with mainly unsaturated fatty acids. This diet consist of mainly unprocessed, fresh nutrient-dense food-products. Ultra-processed foods and alcoholic beverages will be totally avoided. Salt consumption will not exceed 5-6 g/d. The diet is ad libitum and caloric restriction will not be applied. The diet will be followed for 6 weeks.
    Intervention Type
    Other
    Intervention Name(s)
    Dutch Nutritional Guidelines
    Intervention Description
    the diet according to the Dutch Nutritional Guidelines will consist of a protein intake of 0.8-1.0 g/kg/d and 50-60en% carbohydrates, and +/-30en% fatty acids, with restriction of saturated fatty acids <10en%. This diet consist of mainly unprocessed, fresh nutrient-dense food-products. Ultra-processed foods and alcoholic beverages will be totally avoided. Salt consumption will not exceed 5-6 g/d. The diet is ad libitum and caloric restriction will not be applied. The diet will be followed for 6 weeks.
    Primary Outcome Measure Information:
    Title
    Systolic blood pressure
    Description
    Change in systolic blood pressure (in mmHg)
    Time Frame
    before and after experimental diet (high-protein, carbohydrate-reduced diet - 6 weeks) / before and after active comparator (Dutch Nutritional Guidelines - 6 weeks) / wash-out period in between (6 weeks)
    Secondary Outcome Measure Information:
    Title
    Cardio-metabolic risk factors (lipids)
    Description
    change in circulating triglyceride concentrations, low-density lipoprotein cholesterol (LDL-C) and HDL-C (in fasting serum levels) in mmol/L.
    Time Frame
    before and after experimental diet (high-protein, carbohydrate-reduced diet - 6 weeks) / before and after active comparator (Dutch Nutritional Guidelines - 6 weeks) / wash-out period in between (6 weeks)
    Title
    Cardio-metabolic risk factors (diastolic blood pressure)
    Description
    Change in diastolic blood pressure (in mmHg)
    Time Frame
    before and after experimental diet (high-protein, carbohydrate-reduced diet - 6 weeks) / before and after active comparator (Dutch Nutritional Guidelines - 6 weeks) / wash-out period in between (6 weeks)
    Title
    Cardio-metabolic risk factors (waist circumference)
    Description
    change in waist circumference (WC) in cm
    Time Frame
    before and after experimental diet (high-protein, carbohydrate-reduced diet - 6 weeks) / before and after active comparator (Dutch Nutritional Guidelines - 6 weeks) / wash-out period in between (6 weeks)
    Title
    Cardio-metabolic risk factors (insulin resistance)
    Description
    change in insulin resistance measuring by the homeostatic model assessment of insulin resistance (HOMA-IR index, fasting glucose, insulin)
    Time Frame
    before and after experimental diet (high-protein, carbohydrate-reduced diet - 6 weeks) / before and after active comparator (Dutch Nutritional Guidelines - 6 weeks) / wash-out period in between (6 weeks)
    Title
    Body composition
    Description
    change in fat and muscle mass measured by multi-frequency bio-electrical impedance analysis (BIA) BMI, weight
    Time Frame
    before and after experimental diet (high-protein, carbohydrate-reduced diet - 6 weeks) / before and after active comparator (Dutch Nutritional Guidelines - 6 weeks) / wash-out period in between (6 weeks)
    Title
    Anthropometric measures
    Description
    Change in weight in kilograms
    Time Frame
    before and after experimental diet (high-protein, carbohydrate-reduced diet - 6 weeks) / before and after active comparator (Dutch Nutritional Guidelines - 6 weeks) / wash-out period in between (6 weeks)
    Title
    Anthropometric measures II
    Description
    Change in Body Mass Index (BMI) in kilograms per square meter
    Time Frame
    before and after experimental diet (high-protein, carbohydrate-reduced diet - 6 weeks) / before and after active comparator (Dutch Nutritional Guidelines - 6 weeks) / wash-out period in between (6 weeks)
    Title
    Body composition II
    Description
    change in fat and muscle mass measured by multi-frequency bio-electrical impedance analysis (BIA)
    Time Frame
    before and after experimental diet (high-protein, carbohydrate-reduced diet - 6 weeks) / before and after active comparator (Dutch Nutritional Guidelines - 6 weeks) / wash-out period in between (6 weeks)
    Title
    Quality of life (QoL)
    Description
    change in QoL, 12-item short form health survey (SF-12)
    Time Frame
    before and after experimental diet (high-protein, carbohydrate-reduced diet - 6 weeks) / before and after active comparator (Dutch Nutritional Guidelines - 6 weeks) / wash-out period in between (6 weeks)
    Title
    Fatigue
    Description
    change in fatigue (measured by Dutch Checklist Individual Strength (CIS-20) questionnaire)
    Time Frame
    before and after experimental diet (high-protein, carbohydrate-reduced diet - 6 weeks) / before and after active comparator (Dutch Nutritional Guidelines - 6 weeks) / wash-out period in between (6 weeks)
    Title
    Physical functioning
    Description
    change in Hand Grip Strength (HSG)
    Time Frame
    before and after experimental diet (high-protein, carbohydrate-reduced diet - 6 weeks) / before and after active comparator (Dutch Nutritional Guidelines - 6 weeks) / wash-out period in between (6 weeks)
    Title
    Physical functioning II
    Description
    change in the five time sit to stand (FTSTS) test
    Time Frame
    before and after experimental diet (high-protein, carbohydrate-reduced diet - 6 weeks) / before and after active comparator (Dutch Nutritional Guidelines - 6 weeks) / wash-out period in between (6 weeks)
    Title
    Nutritional intake
    Description
    change in nutritional intake measured by a 3-day food diary
    Time Frame
    before and after experimental diet (high-protein, carbohydrate-reduced diet - 6 weeks) / before and after active comparator (Dutch Nutritional Guidelines - 6 weeks) / wash-out period in between (6 weeks)
    Title
    Nutritional intake II
    Description
    change in nutritional intake measured by nutritional intake biomarkers from 24-hour urine measurements (sodium, potassium, and urea excretion for calculating the protein intake by use of the Maroni equation)
    Time Frame
    before and after experimental diet (high-protein, carbohydrate-reduced diet - 6 weeks) / before and after active comparator (Dutch Nutritional Guidelines - 6 weeks) / wash-out period in between (6 weeks)

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age 18 years or older. Given informed consent. At least 6 months after kidney transplantation. Stable renal function with an estimated glomerular filtration rate (eGFR) > 30 mL/min. Raised systolic blood pressure (≥130 mmHg) and at least two more features of metabolic syndrome: central obesity (waist circumference ≥102 for men and ≥88cm for women), elevated triglycerides (≥ 1.7 mmol/L), reduced HDL-C (< 1.0 mmol/L for men and < 1.3 mmol/L for women) or on drug treatment for reduced HDL, elevated plasma glucose (≥ 5.6 mmol/L) or on drug treatment for elevated glucose9. Approval by nephrologist for participation in the study. Exclusion Criteria: Active medical illness, including rejection of the graft. Psychopathology or serious cognitive impairment. Necessity to follow specific dietary measures for health purposes that conflict with the study diets. Use of insulin or sulfonylurea (SU)-derivates. Language barrier. Pregnancy or lactating. Serum potassium > 5.0 mmol/L that requires dietary measures. Moderate or severe malnutrition (Patient-Generated Subjective Global Assessment (PG-SGA) stage B or C). In this case, patient will be referred to a renal dietician. Participation in other intervention trials.

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

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