- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04076982
Effect of Supplementary Dietary Protein (21g Per Day) on Lean Mass and Strength in Sedentary, Adult Vegetarians (MungBean)
September 3, 2019 updated by: Carol Johnston, Arizona State University
It is possible that the lower protein intake in vegetarians and vegans may relate to a decrease in grip strength.
Furthermore, there is limited research examining the effects of plant-based protein intake on strength and LBM independent of an exercise training component.
The present study was designed to examine relationships between strength, protein intake, and LBM in underactive vegetarian and vegan adults, as well as the impact of protein supplementation (18 g mung bean protein daily) on these indices.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The American Dietetic Association states that based off of evidence, it is possible for a vegetarian to obtain the recommended amount of nutrients with a properly planned diet.
By mixing various sources of plant proteins throughout the day, a person can obtain all the amino acids needed for growth and tissue maintenance and repair.
Yet, many vegetarians struggle to eat a substantial diet, especially when it comes to protein.
This is because plant protein has protein bioavailability that is 10-30% lower than animal protein.
As a result, current research suggests that there needs to be a separate protein dietary reference intake (DRI) for vegetarians and it needs to be larger than the protein DRI for omnivores.
Whenever considering protein bioavailability, the quality must be assessed by analyzing the digestibility, chemical integrity, and freedom from interference in metabolism of the amino acid.
This is a major concern because inadequate protein intake can affect bone health and alter muscle mass.
Importantly, research has shown as a result of inadequate protein intake, vegetarians tend to have less lean body mass and less muscle strength than omnivores.
Currently, all research available on this topic included strength training as a variable for increasing lean muscle mass, and no research has been reported that analyzed the impact of increased dietary protein on lean body mass without a training component.
This parallel arm study will examine the effect of supplemental plant protein on strength and lean body mass in adult, non-athletic vegetarians in the Phoenix area.
Study Type
Interventional
Enrollment (Actual)
37
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Arizona
-
Phoenix, Arizona, United States, 85004
- Arizona State University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 55 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- vegetarian or vegan for at least one year
- healthy by self-report
Exclusion Criteria:
- supplement use such as protein powder or creatine
- previous diagnosis of heart disease, cancer, stroke, diabetes, autoimmune disorders, or thyroid condition
- competition in any athletic event in the past year
- moderate to strenuous exercise exceeding 150 minutes per week
- pregnant or planning to become pregnant.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: mung bean
daily oral administration of protein supplement
|
Participants were instructed to consume the test foods in the morning hours and to keep a record of the days the foods were consumed on a study calendar which was returned to investigators at the final visit and used to track protocol adherence.
|
|
Placebo Comparator: biscuit
daily oral administration of control supplement
|
Participants were instructed to consume the test foods in the morning hours and to keep a record of the days the foods were consumed on a study calendar which was returned to investigators at the final visit and used to track protocol adherence.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
grip strength
Time Frame: change in strength from baseline to week 8
|
Dominant handgrip strength was measured in triplicate in a seated position with the elbow flexed to 90 degrees and a neutral wrist position in triplicate using a handheld dynamometer
|
change in strength from baseline to week 8
|
|
leg strength
Time Frame: change in strength from baseline to week 8
|
Lower body strength was measured in the dominant leg using a multi-joint system dynamometer.
Isokinetic knee flexion and extension were measured from a seated position at a resistance of 90°/sec.
|
change in strength from baseline to week 8
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
lean body mass
Time Frame: change in LBM from baseline to week 8
|
LBM was measured via dual energy X-ray absorptiometry (DEXA) and was conducted by a trained X-ray technician.
|
change in LBM from baseline to week 8
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 3, 2018
Primary Completion (Actual)
January 12, 2019
Study Completion (Actual)
January 12, 2019
Study Registration Dates
First Submitted
August 29, 2019
First Submitted That Met QC Criteria
September 3, 2019
First Posted (Actual)
September 4, 2019
Study Record Updates
Last Update Posted (Actual)
September 4, 2019
Last Update Submitted That Met QC Criteria
September 3, 2019
Last Verified
September 1, 2019
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- MungBean00005383
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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