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Impact of Protein and Alkali Supplementation on Skeletal Muscle in Older Adults

Primary Purpose

Age-Related Sarcopenia, Muscle Loss

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
whey protein isolate
potassium bicarbonate (KHCO3)
microcrystalline cellulose
maltodextrin powder
Sponsored by
Tufts University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Age-Related Sarcopenia

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. ability to sign informed consent form
  2. ambulatory community-dwelling men and women
  3. age 65 years and over
  4. habitual dietary intake of protein of ≤0.8 g/kg/d
  5. underactive
  6. estimated glomerular filtration rate ≥ 50 ml/min/1.73 m2

Exclusion Criteria:

  1. participation in a diet or intensive exercise program during the study
  2. vegetarian (no animal protein)
  3. oral glucocorticoid use for > 10 days in the last 3 months
  4. anabolic and gonadal hormones in the last 6 months
  5. Tamoxifen/raloxifene in the last 6 months
  6. regular use of alkali-producing antacids (> 3 times per week)
  7. potassium-containing supplements or products
  8. non-steroidal anti-inflammatory medications >3 times per week
  9. antacids containing calcium carbonate, aluminum hydroxide, magnesium hydroxide, or calcium acetate
  10. insulin
  11. sulfonylureas
  12. SGLT2 inhibitors
  13. a lower extremity fracture in the last year
  14. kidney stones in the past 5 years
  15. hyperkalemia
  16. elevated serum bicarbonate
  17. hypercalcemia
  18. uncontrolled diabetes mellitus defined as having fasting blood >150 or hemoglobin A1c >8%
  19. untreated thyroid or parathyroid disease
  20. significant immune disorder
  21. current unstable heart disease
  22. Crohn's disease
  23. active malignancy or cancer therapy in the last year
  24. alcohol use exceeding 2 drinks/day
  25. current peptic ulcers or esophageal stricture
  26. other condition or abnormality in screening labs, at discretion of the study physician

Sites / Locations

  • Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

whey protein isolate + KHCO3

whey protein isolate + microcrystalline cellulose

maltodextrin powder + KHCO3

maltodextrin powder + microcrystalline cellulose

Arm Description

1.5 gm/kg/day of whey protein and 81 mmol/day of KHCO3

1.5 gm/kg/day of whey protein and identical placebo microcrystalline cellulose capsules

isocaloric placebo maltodextrin powder and 81 mmol/day of KHCO3

isocaloric placebo maltodextrin powder and identical placebo microcrystalline cellulose capsules

Outcomes

Primary Outcome Measures

lower extremity muscle power
measure of muscle power using a double leg press

Secondary Outcome Measures

lower extremity muscle power
measure muscle power using double leg press
isokinetic leg extension strength and endurance
measure knee extension strength, torque and fatigability using Biodex Isokinetic Dynamometer
handgrip strength
measure strength using grip strength dynamometer
appendicular lean body mass
Dual energy X-ray absorptiometry (DXA) lean mass of arms plus legs divided by height squared
physical performance battery
measure performance based on Health Aging and Body Composition-Physical Performance Battery
24 hour urinary nitrogen excretion to nitrogen intake
measure based on 24 hour urine and 24 hour diet recall

Full Information

First Posted
August 5, 2019
Last Updated
August 9, 2023
Sponsor
Tufts University
Collaborators
National Institute on Aging (NIA)
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1. Study Identification

Unique Protocol Identification Number
NCT04048616
Brief Title
Impact of Protein and Alkali Supplementation on Skeletal Muscle in Older Adults
Official Title
Impact of Protein and Alkali Supplementation on Skeletal Muscle in Older Adults
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 1, 2019 (Actual)
Primary Completion Date
September 1, 2024 (Anticipated)
Study Completion Date
February 28, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tufts University
Collaborators
National Institute on Aging (NIA)

4. Oversight

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

5. Study Description

Brief Summary
Whether higher dietary protein benefits skeletal muscle health in older adults remains an ongoing area of investigation. This study will determine whether adding an alkaline salt supplement, potassium bicarbonate, to reduce the dietary acid load of a high protein diet can further enhance the beneficial impact of a high protein diet alone on muscle performance and mass in older underactive adults on baseline low protein diet.
Detailed Description
With aging, skeletal muscle mass and performance decline leading to an increased risk of falls and physical disability. There is ongoing research on whether increasing dietary protein intake in older adults improves indices of muscle health and thus translates to a reduction in physical disability. A main concern is that high protein results in a large dietary acid load from the breakdown of protein to acidogenic byproducts, which could in turn promote muscle degradation particularly in older adults with age-related declines in renal excretion of acid. The scientific premise of this project is that the balance between the amount of protein in the diet (anabolic component) and the net acid load of the diet (catabolic component) in part determines whether the diet as a whole has a net anabolic or catabolic effect on muscle. Preliminary data have suggested that a daily alkaline salt supplement (potassium bicarbonate, KHCO3) lowered the dietary acid load and improved lower extremity muscle power in postmenopausal women. The investigator's central hypothesis is that higher protein intake plus a neutralizing alkaline salt will have additive effects on muscle performance and mass in older adults to either intervention alone. To test the hypothesis, the investigators will conduct a randomized, double-blind, placebo-controlled, 2x2 factorial study in which underactive men and women age 65 and older on baseline lower protein diets will be enrolled. Participants will assigned to one of four groups: either a whey protein supplement (to raise protein intake to 1.5 g/kg/d) with or without KHCO3 81 mmol/d or an isocaloric placebo supplement with or without KHCO3 81 mmol/d for 24 wks. The primary outcome is lower extremity muscle power at 24 weeks. Secondary outcomes are lower extremity muscle power at 12 weeks, muscle endurance at 12 and 24 weeks, physical performance at 24 weeks, lean mass at 24 weeks, and 24-hr urinary nitrogen excretion adjusted for nitrogen intake at 24 weeks. Exploratory outcomes will include a measure of muscle mass - D3-creatine dilution - and how it correlates with lean mass. Changes in these outcomes will be compared in the 4 groups. If successful, this research would represent a meaningful step in defining the circumstances under which protein has its greatest anabolic benefit.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Age-Related Sarcopenia, Muscle Loss

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Model Description
double blind randomized placebo controlled 2x2 factorial design
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
whey protein isolate + KHCO3
Arm Type
Active Comparator
Arm Description
1.5 gm/kg/day of whey protein and 81 mmol/day of KHCO3
Arm Title
whey protein isolate + microcrystalline cellulose
Arm Type
Active Comparator
Arm Description
1.5 gm/kg/day of whey protein and identical placebo microcrystalline cellulose capsules
Arm Title
maltodextrin powder + KHCO3
Arm Type
Active Comparator
Arm Description
isocaloric placebo maltodextrin powder and 81 mmol/day of KHCO3
Arm Title
maltodextrin powder + microcrystalline cellulose
Arm Type
Placebo Comparator
Arm Description
isocaloric placebo maltodextrin powder and identical placebo microcrystalline cellulose capsules
Intervention Type
Dietary Supplement
Intervention Name(s)
whey protein isolate
Intervention Description
one 15-25 gm (based on body weight) protein packet three times a day with each meal
Intervention Type
Dietary Supplement
Intervention Name(s)
potassium bicarbonate (KHCO3)
Intervention Description
two 13.5 mmol capsules three times a day with each meal
Intervention Type
Other
Intervention Name(s)
microcrystalline cellulose
Intervention Description
identical placebo capsule
Intervention Type
Other
Intervention Name(s)
maltodextrin powder
Intervention Description
isocaloric placebo powder
Primary Outcome Measure Information:
Title
lower extremity muscle power
Description
measure of muscle power using a double leg press
Time Frame
24 weeks
Secondary Outcome Measure Information:
Title
lower extremity muscle power
Description
measure muscle power using double leg press
Time Frame
12 weeks
Title
isokinetic leg extension strength and endurance
Description
measure knee extension strength, torque and fatigability using Biodex Isokinetic Dynamometer
Time Frame
12 and 24 weeks
Title
handgrip strength
Description
measure strength using grip strength dynamometer
Time Frame
24 weeks
Title
appendicular lean body mass
Description
Dual energy X-ray absorptiometry (DXA) lean mass of arms plus legs divided by height squared
Time Frame
24 weeks
Title
physical performance battery
Description
measure performance based on Health Aging and Body Composition-Physical Performance Battery
Time Frame
24 weeks
Title
24 hour urinary nitrogen excretion to nitrogen intake
Description
measure based on 24 hour urine and 24 hour diet recall
Time Frame
24 weeks
Other Pre-specified Outcome Measures:
Title
D3-creatine dilution (exploratory)
Description
measure of total body muscle mass
Time Frame
24 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: ability to sign informed consent form ambulatory community-dwelling men and women age 65 years and over habitual dietary intake of protein of ≤0.8 g/kg/d underactive estimated glomerular filtration rate ≥ 50 ml/min/1.73 m2 Exclusion Criteria: participation in a diet or intensive exercise program during the study vegetarian (no animal protein) oral glucocorticoid use for > 10 days in the last 3 months anabolic and gonadal hormones in the last 6 months Tamoxifen/raloxifene in the last 6 months regular use of alkali-producing antacids (> 3 times per week) potassium-containing supplements or products non-steroidal anti-inflammatory medications >3 times per week antacids containing calcium carbonate, aluminum hydroxide, magnesium hydroxide, or calcium acetate insulin sulfonylureas SGLT2 inhibitors a lower extremity fracture in the last year kidney stones in the past 5 years hyperkalemia elevated serum bicarbonate hypercalcemia uncontrolled diabetes mellitus defined as having fasting blood >150 or hemoglobin A1c >8% untreated thyroid or parathyroid disease significant immune disorder current unstable heart disease Crohn's disease active malignancy or cancer therapy in the last year alcohol use exceeding 2 drinks/day current peptic ulcers or esophageal stricture other condition or abnormality in screening labs, at discretion of the study physician
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lisa Ceglia, MD MS
Organizational Affiliation
Tufts Medical Center and Tufts University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02111
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Impact of Protein and Alkali Supplementation on Skeletal Muscle in Older Adults

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