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Dietary Intervention and Exercise Training (DIET) in Moderate to Severe Chronic Kidney Disease

Primary Purpose

Chronic Kidney Disease

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
low-impact aerobic exercise
low-calorie (low-fat) diet
Sponsored by
Vanderbilt University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Kidney Disease

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients with Stage III-IV (estimated GFR 20-59 min/ml) chronic kidney disease measured by MDRD formula.
  2. BMI ≥ 30 kg/m2
  3. Age > 18 or < 65 years.
  4. Life expectancy greater than one year.
  5. Ability to understand and provide informed consent for participation in the study.

Exclusion Criteria:

  1. Active inflammatory disease such as: AIDS (HIV seropositivity is not an exclusion criteria), active hepatitis C or B, active gout, other active inflammatory diseases.
  2. Active malignancy excluding basal or squamous cell carcinoma of the skin.
  3. Patients suffering from Type I Diabetes Mellitus
  4. Patients with reduced daily caloric intake at baseline (≤ 2000 kcal/day) or malnutrition.
  5. Patients who are already on a consistent and rigorous exercise regimen.
  6. Gastrointestinal dysfunction requiring parental nutrition.
  7. History of functional kidney transplant < 6 months prior to study entry.
  8. Anticipated live donor kidney transplant over study duration.
  9. Patients taking anti-inflammatory medication except aspirin < 325mg/day over the past 30 days.
  10. Patients taking Vitamin E supplements > 60 IU/day, vitamin C > 500mg/day over the past 30days.
  11. Patients taking any prednisone therapy.
  12. Hospital admission within the last 30 days.
  13. On experimental drug protocols.
  14. Significant cardiac or vascular disease (symptomatic disease; CV event(s) within the last year; significant occlusive atherosclerotic disease or ischemic disease on non-invasive or invasive diagnostic procedures).
  15. Significant physical disability or immobility (joint disease, joint replacement, muscular disorders).

Sites / Locations

  • Vanderbilt University Medical Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

No Intervention

Arm Label

1

2

3

Arm Description

low-impact aerobic exercise group

dietary restriction group

control group

Outcomes

Primary Outcome Measures

a statistically significant decrease in plasma F2-isoprostanes, a specific oxidative stress marker
a statistically significant decrease in hs-CRP, a specific inflammatory marker

Secondary Outcome Measures

significant changes in additional markers of oxidative stress and inflammation
significant changes in insulin resistance and adipocytokines
a significant improvement in endothelial function as measured by brachial artery FMD
a significant improvement in quality of life scores

Full Information

First Posted
December 18, 2007
Last Updated
November 1, 2010
Sponsor
Vanderbilt University
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1. Study Identification

Unique Protocol Identification Number
NCT00581269
Brief Title
Dietary Intervention and Exercise Training (DIET) in Moderate to Severe Chronic Kidney Disease
Official Title
Dietary Intervention and Exercise Training (DIET) in Moderate to Severe Chronic Kidney Disease
Study Type
Interventional

2. Study Status

Record Verification Date
November 2010
Overall Recruitment Status
Terminated
Why Stopped
the Fellow conducting the study left the institution in 2009
Study Start Date
December 2007 (undefined)
Primary Completion Date
April 2009 (Actual)
Study Completion Date
April 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Vanderbilt University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The oxidative stress and inflammatory state is known to contribute to the pathogenesis of atherosclerosis, and is predictive of cardiovascular events and mortality rates in the general population and patients with chronic kidney disease (CKD), particularly in patients with end stage renal disease (ESRD) on dialysis therapy 1. Increased oxidative stress and inflammation has been identified in all stages of CKD, ranging from moderate renal insufficiency to ESRD. However, the pathophysiology of increased oxidative stress and inflammation associated with the development of CKD is currently poorly understood. There is also concern about the epidemic of obesity in the United States, as the overall health status of the general population is adversely affected by increasing adiposity. Recent studies indicate a strong relationship between adiposity and incident CKD. Furthermore, the presence of an elevated body mass index (BMI) is an independent predictor for progression to ESRD, even after additional adjustments for baseline blood pressure and the presence or absence of diabetes mellitus. Limited data in the general population show that healthy lifestyle interventions, such as exercise and dietary caloric restriction, either alone or in combination, reduce the inflammatory and oxidative stress burden seen in obese subjects. The impact of healthy lifestyle modifications on inflammation and oxidative stress has not been investigated in the obese CKD population. Based on the foregoing observations, the purpose of this investigation will be to determine whether healthy lifestyle interventions in the form of low-impact aerobic exercise and dietary calorie restriction in obese subjects (BMI ≥ 30kg/m2) with moderate to severe (Stage III-IV) CKD [estimated glomerular filtration rate (GFR) 20-59 ml/min] will improve oxidative stress, inflammation, insulin resistance, adipocytokines, endothelial dysfunction, and quality of life.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
3 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
low-impact aerobic exercise group
Arm Title
2
Arm Type
Active Comparator
Arm Description
dietary restriction group
Arm Title
3
Arm Type
No Intervention
Arm Description
control group
Intervention Type
Behavioral
Intervention Name(s)
low-impact aerobic exercise
Intervention Description
subjects will undergo supervised physical activity for a maximum of 30-60 minutes, every other day, 3 days per week for 3 months; to offer variety in the exercise prescription, subjects will alternately use a treadmill, an elliptical trainer, a Nu-Step cross-trainer and a recumbent stationary bicycle
Intervention Type
Dietary Supplement
Intervention Name(s)
low-calorie (low-fat) diet
Intervention Description
subjects will undergo a 20% reduction in total daily calories from their usual daily energy consumption every day for 3 months
Primary Outcome Measure Information:
Title
a statistically significant decrease in plasma F2-isoprostanes, a specific oxidative stress marker
Time Frame
3 months
Title
a statistically significant decrease in hs-CRP, a specific inflammatory marker
Time Frame
3 months
Secondary Outcome Measure Information:
Title
significant changes in additional markers of oxidative stress and inflammation
Time Frame
3 months
Title
significant changes in insulin resistance and adipocytokines
Time Frame
3 months
Title
a significant improvement in endothelial function as measured by brachial artery FMD
Time Frame
3 months
Title
a significant improvement in quality of life scores
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with Stage III-IV (estimated GFR 20-59 min/ml) chronic kidney disease measured by MDRD formula. BMI ≥ 30 kg/m2 Age > 18 or < 65 years. Life expectancy greater than one year. Ability to understand and provide informed consent for participation in the study. Exclusion Criteria: Active inflammatory disease such as: AIDS (HIV seropositivity is not an exclusion criteria), active hepatitis C or B, active gout, other active inflammatory diseases. Active malignancy excluding basal or squamous cell carcinoma of the skin. Patients suffering from Type I Diabetes Mellitus Patients with reduced daily caloric intake at baseline (≤ 2000 kcal/day) or malnutrition. Patients who are already on a consistent and rigorous exercise regimen. Gastrointestinal dysfunction requiring parental nutrition. History of functional kidney transplant < 6 months prior to study entry. Anticipated live donor kidney transplant over study duration. Patients taking anti-inflammatory medication except aspirin < 325mg/day over the past 30 days. Patients taking Vitamin E supplements > 60 IU/day, vitamin C > 500mg/day over the past 30days. Patients taking any prednisone therapy. Hospital admission within the last 30 days. On experimental drug protocols. Significant cardiac or vascular disease (symptomatic disease; CV event(s) within the last year; significant occlusive atherosclerotic disease or ischemic disease on non-invasive or invasive diagnostic procedures). Significant physical disability or immobility (joint disease, joint replacement, muscular disorders).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alp Ikizler, MD
Organizational Affiliation
Vanderbilt University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vanderbilt University Medical Center
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37232
Country
United States

12. IPD Sharing Statement

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Dietary Intervention and Exercise Training (DIET) in Moderate to Severe Chronic Kidney Disease

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