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Pathways to Improving Functional Capacity in Older Patients With Chronic Kidney Disease and Cardiovascular Disease (CKD&CAD)

Primary Purpose

Chronic Kidney Disease, Cardiovascular Disease

Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Fish Oil and Bicarbonate
Fish Oil and Bicarbonate Placebo
Fish Oil Placebo and Bicarbonate
Fish Oil Placebo and Bicarbonate Placebo
Sponsored by
Wake Forest University Health Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Chronic Kidney Disease focused on measuring Geriatric, bicarbonate, omega polyunsaturated fatty acids, exercise capacity

Eligibility Criteria

60 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Referred to Cardiac Rehabilitation after acute coronary syndromes or percutaneous intervention
  • Stage III Chronic kidney disease
  • Clinically stable with no mobility conditions that preclude safe walking and able to walk
  • No contraindications that will prevent measurement of physical ability and exercise capacity including severe arthritis or musculoskeletal disorders
  • knee/hip replacement or spinal surgery in past year
  • Approved for participation by Principal Investigator
  • Not involved in any other research study or undergoing physical therapy
  • Able to provide own transportation to study visits and intervention
  • Willing to provide written consent

Exclusion Criteria:

  • Currently taking fish oil supplements
  • Advanced malignancy or other medical condition with life expectancy less than 2 years or undergoing active chemotherapy or radiation therapy
  • Oxygen-dependent chronic obstructive pulmonary disease
  • Normal kidney function or advanced chronic kidney disease (glomerular filtration rate < 20 mL/min/1.73 m2, on dialysis or dialysis anticipated within 6 months)
  • Mini-mental state examination score of ≤ 21 or previously diagnosed dementia or cognitive impairment limiting ability to participate in rehabilitation and follow study protocols
  • Chronic anemia with hemoglobin <10 gm/dl for males, <9 gm/dl for females or acute anemia requiring transfusion
  • Significant impairment from a prior stroke or other neurologic disease or injury that would preclude participation
  • Severe peripheral arterial disease that is the primary limitation to ambulation
  • Medical condition that would limit exercise
  • High risk for non-adherence as determined by screening evaluation
  • Patients who have undergone renal transplantation
  • Currently taking bicarbonate supplementation
  • Current or recent (within the last 3 months) participation in an exercise program
  • Carbon Dioxide level greater than the middle of the normal range i.e. 27mmol/L and thus predisposing to metabolic alkalosis
  • Moderate 2+ or greater lower extremity edema
  • Active congestive heart failure
  • Ejection fraction less than 35%
  • Patients using walkers and canes

Sites / Locations

  • Wake Forest Baptist Health Cardiac Rehab

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Active Comparator

Experimental

Placebo Comparator

Arm Label

Fish Oil and Bicarbonate placebo

Fish Oil Placebo and Bicarbonate

Fish Oil and Bicarbonate

Fish Oil placebo and Bicarbonate placebo

Arm Description

1280mg of fish oil per day and bicarbonate placebo

fish oil placebo and 1mg of bicarbonate per Kg of body weight per day

1280mg of fish oil per day and 1mg of bicarbonate per Kg of body weight per day

Fish oil placebo and Bicarbonate placebo

Outcomes

Primary Outcome Measures

Change from Baseline of VO2 peak at 12 weeks
Treadmill during a graded exercise test to exhaustion using a Ramp protocol

Secondary Outcome Measures

Full Information

First Posted
June 10, 2015
Last Updated
November 3, 2017
Sponsor
Wake Forest University Health Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT02473705
Brief Title
Pathways to Improving Functional Capacity in Older Patients With Chronic Kidney Disease and Cardiovascular Disease
Acronym
CKD&CAD
Official Title
Pathways to Improving Functional Capacity in Older Patients With Chronic Kidney Disease and Cardiovascular Disease
Study Type
Interventional

2. Study Status

Record Verification Date
September 2016
Overall Recruitment Status
Withdrawn
Why Stopped
Unable to find eligible participants to participate in the study.
Study Start Date
January 2016 (undefined)
Primary Completion Date
June 2017 (Anticipated)
Study Completion Date
June 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wake Forest University Health Sciences

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this research study is to study the effect of fish oil and bicarbonate (baking soda) on exercise. In this study fish oil, bicarbonate or both will be compared to placebo to see if study participants increase exercise capacity.
Detailed Description
Patients with chronic kidney disease (CKD) have a high morbidity and mortality from cardiovascular disease (CVD). Both conditions are common in older patients. Reduced exercise capacity predicts poorer outcomes in patients with CVD2 and CKD. Although exercise tolerance is impaired in CKD4 limited improvement in these patients is possible. A critical gap in knowledge is how to optimize exercise capacity in these patients to improve quality and possibly length of life. In CKD, both structure and function of skeletal muscle are deranged. In addition, energy production by mitochondria which falls with age, and various diseases is also reduced in CKD. Recent studies from our group have reported that differences in mitochondrial function are associated with variances in physical ability, exercise capacity, and gait speed. In preliminary data, patients entering our Cardiac Rehabilitation (CR) with Stage III CKD [glomerular filtration rate (GFR) of <60 ml/min/1.73 m2] had a decreased improvement in exercise capacity compared to those with a normal GFR (Δ1.7 vs 2.7 Metabolic Equivalents of Exercise or METs, p<0.05) despite the same degree of adherence. Exercise capacity after CR in patients with a reduced GFR was greater in n-3 polyunsaturated fatty acids (n-3 PUFA) users than in non-users [Δ MET 2.0 (1.4-2.5) vs 1.4 (1.1-1.7), p<0.05], suggesting that n-3 PUFA with exercise may be better than exercise alone. With beneficial clinical effects in CKD, n-3 PUFA are now being extensively investigated in the dialysis population. In other patient populations, including those with chronic obstructive pulmonary disease and dilated cardiomyopathy daily ingestion/use of n-3 polyunsaturated fatty acids (n-3 PUFA) or fish oil improves exercise capacity. This intervention is safe, simple and well-tolerated. Multiple lines of evidence suggest muscle and mitochondrial function improve with exercise and n-3 PUFA supplementation.Such treatment may improve mitochondrial bioenergetics by various mechanisms including up-regulation of mitochondrial biogenesis and genes involved in mitochondrial fatty acid oxidation, as well as increase in mitochondrial content, and function. Flow mediated vasodilation is impaired in CKD. It too may be improved by n-3 PUFA supplementation which could be an alternative mechanism for improved oxygen delivery to muscle in older patients with CAD and CKD as in the non-CKD population. A further possible benefit of n-3 PUFA is suppression of inflammation. Current practice, however, is to enter patients with CAD and CKD into standard CR without prescription of n-3 PUFA. Experimental and epidemiological studies indicate that acidemia and metabolic acidosis are associated with the development and progression of CKD and with increased mortality in these patients. Metabolic acidosis associated with CKD also contributes to skeletal muscle atrophy by activation of the ubiquitin-proteasome axis. Even slight correction of acidosis can improve the anabolic state of muscle by downregulation of the ubiquitin-proteasome system. Clinically, bicarbonate supplementation may improve muscle function. This intervention is also safe, simple and well-tolerated. Given that muscular function is abnormal in CKD and that both n-3 PUFA and bicarbonate supplementation have been shown to improve muscular function and exercise capacity, it is our purpose in this investigation to study the effects of these substances on exercise capacity in patients with CAD and CKD. The investigators propose a double-blind, placebo-controlled, randomized, 2x2 factorial design, pilot study of n-3 PUFA and/or oral bicarbonate use in older (age >60 years) CAD patients with concomitant CKD enrolling in a standard, 3-month CR program. The investigators will assess the effects of this intervention on exercise capacity, markers of inflammation and serum bicarbonate concentration. The investigator's goal is to obtain 8 evaluable patients per group. Exercise capacity will be measured by Oxygen (VO2) peak. Response to bicarbonate will be monitored by serum bicarbonate concentration. Since CKD may adversely affect muscle function both by acidosis and/or mitochondrial function, the investigator's propose that these may be mechanisms for the poorer exercise capacity in these patients. The investigator's overarching hypothesis is that exercise capacity response to CR in older patients with CKD may be modifiable by concomitant n-3 PUFA and/or bicarbonate use to suppress acidosis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Disease, Cardiovascular Disease
Keywords
Geriatric, bicarbonate, omega polyunsaturated fatty acids, exercise capacity

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Fish Oil and Bicarbonate placebo
Arm Type
Active Comparator
Arm Description
1280mg of fish oil per day and bicarbonate placebo
Arm Title
Fish Oil Placebo and Bicarbonate
Arm Type
Active Comparator
Arm Description
fish oil placebo and 1mg of bicarbonate per Kg of body weight per day
Arm Title
Fish Oil and Bicarbonate
Arm Type
Experimental
Arm Description
1280mg of fish oil per day and 1mg of bicarbonate per Kg of body weight per day
Arm Title
Fish Oil placebo and Bicarbonate placebo
Arm Type
Placebo Comparator
Arm Description
Fish oil placebo and Bicarbonate placebo
Intervention Type
Dietary Supplement
Intervention Name(s)
Fish Oil and Bicarbonate
Other Intervention Name(s)
Nordic Naturals - Ultimate Omega
Intervention Description
1280mg of fish oil per day and 1mg of bicarbonate per Kg of body weight per day
Intervention Type
Dietary Supplement
Intervention Name(s)
Fish Oil and Bicarbonate Placebo
Other Intervention Name(s)
Nordic Naturals - Ultimate Omega
Intervention Description
1280mg of fish oil per day and bicarbonate placebo (Methylcellulose)
Intervention Type
Dietary Supplement
Intervention Name(s)
Fish Oil Placebo and Bicarbonate
Intervention Description
Fish oil placebo (soybean oil) and 1mg of bicarbonate per Kg of body weight per day
Intervention Type
Dietary Supplement
Intervention Name(s)
Fish Oil Placebo and Bicarbonate Placebo
Intervention Description
Fish oil placebo (soybean oil) and bicarbonate placebo (Methylcellulose)
Primary Outcome Measure Information:
Title
Change from Baseline of VO2 peak at 12 weeks
Description
Treadmill during a graded exercise test to exhaustion using a Ramp protocol
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Referred to Cardiac Rehabilitation after acute coronary syndromes or percutaneous intervention Stage III Chronic kidney disease Clinically stable with no mobility conditions that preclude safe walking and able to walk No contraindications that will prevent measurement of physical ability and exercise capacity including severe arthritis or musculoskeletal disorders knee/hip replacement or spinal surgery in past year Approved for participation by Principal Investigator Not involved in any other research study or undergoing physical therapy Able to provide own transportation to study visits and intervention Willing to provide written consent Exclusion Criteria: Currently taking fish oil supplements Advanced malignancy or other medical condition with life expectancy less than 2 years or undergoing active chemotherapy or radiation therapy Oxygen-dependent chronic obstructive pulmonary disease Normal kidney function or advanced chronic kidney disease (glomerular filtration rate < 20 mL/min/1.73 m2, on dialysis or dialysis anticipated within 6 months) Mini-mental state examination score of ≤ 21 or previously diagnosed dementia or cognitive impairment limiting ability to participate in rehabilitation and follow study protocols Chronic anemia with hemoglobin <10 gm/dl for males, <9 gm/dl for females or acute anemia requiring transfusion Significant impairment from a prior stroke or other neurologic disease or injury that would preclude participation Severe peripheral arterial disease that is the primary limitation to ambulation Medical condition that would limit exercise High risk for non-adherence as determined by screening evaluation Patients who have undergone renal transplantation Currently taking bicarbonate supplementation Current or recent (within the last 3 months) participation in an exercise program Carbon Dioxide level greater than the middle of the normal range i.e. 27mmol/L and thus predisposing to metabolic alkalosis Moderate 2+ or greater lower extremity edema Active congestive heart failure Ejection fraction less than 35% Patients using walkers and canes
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Killian Robinson, MD
Organizational Affiliation
Wake Forest University Health Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Wake Forest Baptist Health Cardiac Rehab
City
Winston-Salem
State/Province
North Carolina
ZIP/Postal Code
27157
Country
United States

12. IPD Sharing Statement

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Pathways to Improving Functional Capacity in Older Patients With Chronic Kidney Disease and Cardiovascular Disease

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