Effect of Vitamin D Supplementation on Balance in CKD
Primary Purpose
Renal Insufficiency, Chronic, Kidney Failure, Chronic
Status
Terminated
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Vitamin D
Sponsored by
About this trial
This is an interventional treatment trial for Renal Insufficiency, Chronic focused on measuring dialysis, end stage renal disease
Eligibility Criteria
Inclusion Criteria:
- must be likely to be able to complete the study
- must be able to walk without a walking aid
- must be able to complete questionnaires interactively research staff
- must have been on dialysis for greater than 3 months
- all patients must be receiving standard of care per their nephrologist
Exclusion Criteria:
- peritoneal dialysis
- an allergy to vitamin D
- liver disease
- intestinal disorders that would interfere with vitamin D absorption
- taking vitamin D supplements >800 IU per day, glucocorticoids, anticonvulsants, or other drug therapies for osteoporosis
- are pregnant
Sites / Locations
- University of Nebraska at Omaha
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
4000 IU Vitamin D
800 IU Vitamin D
Arm Description
4000 IU Vitamin D taken daily for six months
800 IU Vitamin D taken daily for six months
Outcomes
Primary Outcome Measures
Timed up and go
This measures fall risk. The measure is a length of time it takes to complete a walking test. A longer score indicates a longer amount of time to complete the test. A shorter amount of time is considered better.
Fullerton Advanced Balance Scale
This 10 item assessment measures one's balance. Scores can range between 0-40. A score of 40 is considered the best performance.
Gait Speed Over 20 Meters
Walking speed is measured over distance of 20 meters. Walking speed is measured in meters per second. A faster walking speed is considered better. Time in seconds needed to cover 20 meters while walking is reported.
Secondary Outcome Measures
Strength of the Quadriceps (Right Leg)
Muscle strength of the muscles in the thigh will be measured using an isokinetic dynamometer. Strength is measured by the amount of force (peak torque) and will be divided by body mass (kg). Strength is reported as a percent of body weight. A greater peak torque percentage is considered better.
Full Information
NCT ID
NCT03710161
First Posted
October 15, 2018
Last Updated
August 24, 2023
Sponsor
University of Nebraska
1. Study Identification
Unique Protocol Identification Number
NCT03710161
Brief Title
Effect of Vitamin D Supplementation on Balance in CKD
Official Title
Effect of Vitamin D Supplementation on Balance in Patients With Chronic Kidney Disease
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Terminated
Why Stopped
Study was stopped due to the COVID pandemic
Study Start Date
July 8, 2019 (Actual)
Primary Completion Date
March 13, 2020 (Actual)
Study Completion Date
March 13, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Nebraska
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Patients with end-stage renal disease on dialysis (ESRD5D) are 4-5x more likely to suffer from a fracture. Fractures can occur spontaneously but typically occur after a fall. Further, 70-90% of patients with ESRD5D are vitamin D deficient. Vitamin D supplementation has become routine care for many in this patient population, but evidence is lacking to support this practice. The proposed projects objective is to gather needed preliminary data regarding the effects of vitamin D supplementation on balance and muscle strength in patients with ESRD5D.
Detailed Description
In 2009, ~6% of the annual Medicare budget was spent to treat people with end-stage renal disease on dialysis (ESRD5D), making chronic kidney disease (CKD) an important and costly health problem affecting the United States. These patients are 4-5x more likely to suffer from a fracture. Fractures can occur spontaneously but typically occur after a fall. Further, 70-90% of patients with ESRD5D are vitamin D deficient. Vitamin D supplementation has become routine care for many in this patient population; without evidence to support this practice. While studies on the elderly document the effect of vitamin D in decreasing fall risk, findings are inconclusive for those elderly individuals with ESRD5D. The proposed projects objective is to gather needed preliminary data regarding the effects of vitamin D supplementation on balance and muscle strength in patients with ESRD5D. Thirty patients with ESRD5D will be recruited and randomized into two groups: 1) 4000 or 2) 800 IU oral, vitamin D taken daily. Men and women (ages 21-70 years) will be recruited from among patients receiving hemodialysis at a UNMC-directed dialysis facility. Other inclusion criteria include 1) likely to be able to complete the study; 2) ambulatory, without a walking aid; 3) able to complete questionnaires interactively with a research nurse; and 4) greater than 3 months on hemodialysis. Exclusion criteria include patients on peritoneal dialysis, allergy to vitamin D, liver disease, intestinal disorders that would interfere with vitamin D absorption; vitamin D supplements >800 IU per day, glucocorticoids, anticonvulsants, drug therapies for osteoporosis. All patients will be receiving standard of care per their nephrologist. Functional data will be collected at baseline, three, and six months. Data collected will include balance, muscle strength, and falls. Data to monitor vitamin D levels and calcium will be pulled from their medical record. There is no follow up after the six month long study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Insufficiency, Chronic, Kidney Failure, Chronic
Keywords
dialysis, end stage renal disease
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
5 (Actual)
8. Arms, Groups, and Interventions
Arm Title
4000 IU Vitamin D
Arm Type
Experimental
Arm Description
4000 IU Vitamin D taken daily for six months
Arm Title
800 IU Vitamin D
Arm Type
Active Comparator
Arm Description
800 IU Vitamin D taken daily for six months
Intervention Type
Drug
Intervention Name(s)
Vitamin D
Other Intervention Name(s)
25(OH)D
Intervention Description
Vitamin D taken in two different dosages daily for six months.
Primary Outcome Measure Information:
Title
Timed up and go
Description
This measures fall risk. The measure is a length of time it takes to complete a walking test. A longer score indicates a longer amount of time to complete the test. A shorter amount of time is considered better.
Time Frame
Baseline
Title
Fullerton Advanced Balance Scale
Description
This 10 item assessment measures one's balance. Scores can range between 0-40. A score of 40 is considered the best performance.
Time Frame
Baseline
Title
Gait Speed Over 20 Meters
Description
Walking speed is measured over distance of 20 meters. Walking speed is measured in meters per second. A faster walking speed is considered better. Time in seconds needed to cover 20 meters while walking is reported.
Time Frame
Baseline
Secondary Outcome Measure Information:
Title
Strength of the Quadriceps (Right Leg)
Description
Muscle strength of the muscles in the thigh will be measured using an isokinetic dynamometer. Strength is measured by the amount of force (peak torque) and will be divided by body mass (kg). Strength is reported as a percent of body weight. A greater peak torque percentage is considered better.
Time Frame
Baseline
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
must be likely to be able to complete the study
must be able to walk without a walking aid
must be able to complete questionnaires interactively research staff
must have been on dialysis for greater than 3 months
all patients must be receiving standard of care per their nephrologist
Exclusion Criteria:
peritoneal dialysis
an allergy to vitamin D
liver disease
intestinal disorders that would interfere with vitamin D absorption
taking vitamin D supplements >800 IU per day, glucocorticoids, anticonvulsants, or other drug therapies for osteoporosis
are pregnant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jenna Yentes, PhD
Organizational Affiliation
University of Nebraska
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Nebraska at Omaha
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
68182
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
De -identified data will be published as supplementary data to manuscripts.
Learn more about this trial
Effect of Vitamin D Supplementation on Balance in CKD
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