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Veterans Achieving Weight Loss and Optimizing Resilience-Using Protein (VALOR-UP)

Primary Purpose

Prediabetes, Obesity

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Foods rich in high quality protein
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Prediabetes focused on measuring obesity, prediabetic state, older person, diet, reducing, protein, muscle function

Eligibility Criteria

55 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Male Veterans
  • African American or Caucasian
  • Obese (BMI > 30 kg/m2)
  • Age > 60 years
  • Pre-diabetes (confirmed fasting plasma glucose 100 and <126 mg/dL) or HbA1c 5.7-6.4%
  • Short Physical Performance Battery score of 4 to 10 units
  • Age-normal renal function
  • English speaking
  • Able to record dietary intake or has a proxy who can record dietary intake
  • Willing and able to be randomized to either intervention group

Exclusion Criteria:

  • Presence of unstable or symptomatic life-threatening illness
  • Glomerular filtration rates (GFR) less than 45 mL/min

    • A GFR of 45-59 requires bi-monthly testing per the investigators' established algorithm
    • Those with a GFR <45 mL/min are excluded
  • Mini Cog score of <3

    --Vegetarian

  • Neurological conditions causing functional impairments, including:

    • Parkinson's Disease
    • multiple sclerosis
    • permanent disability due to stroke
  • Inability to complete physical function assessment
  • History of significant weight instability
  • Contraindicated medications, including narcotic mail-outs and active substance abuse
  • Any psychiatric condition that would prevent the subject from participating in a group intervention setting, including diagnosed personality disorders
  • Primary care provider disapproves participation

Sites / Locations

  • Durham VA Medical Center, Durham, NCRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

WL-Control

WL-Protein

Arm Description

0.8 g protein per kg body weight. Seven servings of whey protein powder (15 g/serving) per week will be provided to participants to support diet affordability.

>30 g of high quality protein per meal, 1.2 g protein/kg body weight/day. Fourteen servings of high quality (30 g/serving) protein (lean meats, low fat dairy products) provided to participants each week to increase compliance.

Outcomes

Primary Outcome Measures

Change in Short Physical Performance Battery (SPPB)
Three different Balance test-(side-by-side, semi-tandem, tandem). They hold each position for 10 seconds Possible Score for Balance Test: 0-4 Possible Score for whole SPPB Test 0-12
Change in Short Physical Performance Battery (SPPB)
Gait speed (4-meter timed walk)- we are measuring there normal walk speed. Possible Score for Gait Speed: 0-4 Possible Score for whole SPPB Test 0-12
Change in Short Physical Performance Battery (SPPB)
Lower Body Strength-5 Chair Stand as fast as they can do. Chair Stand- With arms across chest, stand up completely, returns to seated Possible Score for Chair Stands: 0-4 Possible Score for whole SPPB Test 0-12

Secondary Outcome Measures

Change in Body Weight
Same scale, light clothing and no shoes, measured to nearest 0.1 kg
Change in 6 Minutes Walk Test (aerobic endurance)
As many walking laps as possible in six minutes between cones placed 40 meters apart
Change in 8-ft Up and Go (agility/dynamic balance)
Begins seated. On word 'go' stands, walks around a cone 8 feet away, returns to seated.
Change in 30 second chair stands (lower body strength)
With arms across chest, stand up completely, returns to seated as many times as possible in 30 seconds.
Change in Isokinetic knee extension peak torque (muscle strength)
Knee extensor at 60 degrees with a dynamometer (HUMAC NORM Isokinetic Extremity System). Average peak torque for three trials will be recorded.
Change in Computerized Axial Tomography (CAT) scan
Cross sectional area of the thigh without contrast to determine muscle mass.
Change in Isometric hand grip (upper body strength)
Jamar Hand Dynamometer (Sammons Preston Rolyan). Highest of three trials/hand.
Change in Minimal Waist Circumference
At smallest horizontal circumference above umbilicus and below xiphoid process.
Change in Body Composition: BodPod
Air displacement plethysmography method (Life Measurement, Inc., Concord, CA). The Cardio Pulmonary, Metabolic and Body Composition (COSMED) BodPod has excellent sensitivity and test-to-test reliability, ease of use, and non-invasive nature, which is important for full participation from this population.
Change in number of falls and fear of falling
In-person interview with questionnaire. This is a open ended questionnaire to see the change in number of times a person falls between time points. Yes or no response to the question, "Do you have a fear of falling?"
Mini-Cog
Screens for cognitive impairment with minimal language content, reduces cultural and educational bias. A 3-item recall component plus a Clock Drawing Test. The items recall component Score: 3 The Normal Clock Drawing Score: 2 Eligible score to be in study is 3.
Change in Short Form-36 (SF-36) Health Survey
Quality of Life Questionnaires The SF-36 measures 8 QOL domains which are dichotomized into physical (functioning, role limitations-physical, pain, general health) and mental health (vitality, social functioning, role limitations-emotional, and emotional/mental health). Item scores were converted to a 0-100 point scale; domain scores were derived by averaging individual items within the subscale; and physical composite and mental health composite scores were derived by averaging the four component domains of each. Higher values are indicative of better QOL
Change in Profile of Mood States (POMS)
Mood Questionnaires The 30-item POMS measures mood and mood changes, has low respondent burden, and includes 6 subscales: tension, depression, anger, fatigue, confusion and vigor (all with range 0-20). Total mood disturbance (TMD) is derived from POMS using the following formula, TMD = (Sum of all subscales except vigor) - vigor (range -20 - 100).
Change in Center for Epidemiologic Studies Depression Scale (CES-D)
Depression Questionnaires Individuals were coded as positive for depression if they had a CES-D score of 16 and/or had self-report of depression diagnosis at baseline. In addition to the total score, the CES-D includes 4 subscales: depressed affect (range 0-21), positive affect (range 0-12), somatic (range 0-21), and interpersonal (range 0-6).
Change in Perceived Stress Scale (PSS)
Stress Questionnaires The PSS assesses the degree to which situations in one's life are considered stressful (range 0-40). Scores ranging from 0-13 would be considered low stress. Scores ranging from 14-26 would be considered moderate stress. Scores ranging from 27-40 would be considered high perceived stress.
Change in Pittsburgh Sleep Quality Index (PSQI)
Quality of sleep Questionnaires Reported PSQI values include only these six component scores: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, and use of sleeping medication (all with a range 0-3). The PSQI includes a scoring key for calculating a patient's seven subscores, each of which can range from 0 to 3. The subscores are tallied, yielding a "global" score that can range from 0 to 21. A global score of 5 or more indicates poor sleep quality; the higher the score, the worse the quality.
Change in Satisfaction with Life Scale (SWLS)
Life Satisfaction Questionnaires The SWLS evaluates global life satisfaction, an important component of subjective well-being (range 5-35). The SWLS is a 7-point Likert scale style response scale. The possible range of scores is 5-35, with a score of 20 representing a neutral point on the scale. Scores between 5-9 indicate the respondent is extremely dissatisfied with life, whereas scores between 31-35 indicate the respondent is extremely satisfied.
Change in 3-day diet record
3-day diet record by multiple pass; analyzed Food Processor (Version 10.13, 2013; ESHA Research);
Change in Protein Checklist Form
RedCap analysis for protein they have consumed
Change in Actigraph, Axis accelerometer (activity counts, step counts, physical activity intensity)
Actigraph WGT3X-BT activity counts at 1-s epoch from three orthogonal axes at 30 Hz sampling frequency.
Change in Metabolic Panel (LabCorp)- A Blood Draw and testing
Routine chemistries, blood testing
Change in Glucose Tolerance Test (OGTT) (78-80), blood
Ingestion of a 75 g glucose load with blood draws at 0, 10, 20, 30, 60, 90, 120, 150 and 180 minutes.
Change in Daily food journal (Adherence)
Daily food journal assessed by RD every week

Full Information

First Posted
January 29, 2019
Last Updated
January 23, 2023
Sponsor
VA Office of Research and Development
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1. Study Identification

Unique Protocol Identification Number
NCT03835416
Brief Title
Veterans Achieving Weight Loss and Optimizing Resilience-Using Protein
Acronym
VALOR-UP
Official Title
Enhanced Protein Intake During Obesity Reduction in Older Male Veterans: Differences in Physical Function and Muscle Quality Responses by Race
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 15, 2019 (Actual)
Primary Completion Date
February 28, 2024 (Anticipated)
Study Completion Date
March 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Diabetes is a major health concern in obese older Veterans, especially in those who are African American. The negative impact of diabetes on muscle and physical function contributes to metabolic as well as physical decline and is under-studied. This randomized controlled trial compares a higher-protein, weight loss regimen previously shown to improve physical function to an Recommended Dietary Allowance (RDA) protein intervention in obese older male Veterans with pre-diabetes and functional limitations. Equal numbers of white and black male Veterans will be studied, filling gaps in the investigators' knowledge of differential responses by race as well as obesity interventions for men in general. The primary outcome is functional performance by Short Physical Performance Battery and secondary measures include muscle quality, insulin sensitivity, lean body mass, physical activity, recent falls and fear of falling, instrumental activities of daily living, and quality of life measured at 0, 3 and 6 months. The goal of this research is to accelerate functional recovery and enhance independence in obese male Veterans, which is strongly aligned with the RR&D mission to "maximize the physical and social autonomy of Veterans".
Detailed Description
This study examines an evidence-based obesity intervention as a means of reducing the impact of prediabetes on muscle function in obese older men of white and black race. A total of 168 obese (BMI 30 kg/m2) male Veterans aged 55 + yrs, with mild to moderate functional impairments (Short Physical Performance Battery score of 4 to 10 units) and prediabetes, will be randomized to a higher-protein weight loss treatment (HP-WL) or an RDA-level protein control weight loss treatment (C-WL). All participants receive individualized calorie prescriptions calculated to achieve a weight loss of ~1-2 pounds per week and attend weekly group support sessions designed to enhance diet compliance with goal setting, self-monitoring, stress management, and daily diet journaling. They will also attend a weekly low impact, chair exercise class. HP-WL participants are provided a supply of chilled/frozen high-quality protein foods (lean meats, low fat dairy products) sufficient to give 30 g high quality protein for two of three meals daily to help assure diet compliance. C-WL participants are provided 1 serving per day of high quality protein to avoid unintentional bias. Treatment responses will be compared for the primary outcome of functional performance by Short Physical Performance Battery and important secondary measures, including muscle quality, insulin sensitivity, lean body mass, physical activity, recent falls and fear of falling, instrumental activities of daily living, and quality of life at 0, 3 and 6 months. An exploratory aim examines potential mediators of racial differences in treatment responses and documents the most successful intervention strategies. This will be the first randomized controlled trial of a balanced, higher-protein diet during a metabolic challenge (caloric restriction) in those with prediabetes and the first study to look at racial differences in responses of obese older men to this regimen. Study findings will fulfill the RR&D mission by advancing interventions to improve physical function in older Veterans, yield novel information about the impact of balanced, higher protein on muscle quality and insulin sensitivity, and explore racial differences in responses to obesity interventions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prediabetes, Obesity
Keywords
obesity, prediabetic state, older person, diet, reducing, protein, muscle function

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Two-armed Randomized Controlled Trial. Control group follows RDA-level (0.8 g/kg bw/d)protein weight loss diet. Protein follows higher protein (1.2 g/kg bw/d) weight loss diet with balanced protein at each meal.
Masking
Outcomes Assessor
Masking Description
Those responsible for outcomes assessment will be blinded from group treatment arm to every extent possible.
Allocation
Randomized
Enrollment
240 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
WL-Control
Arm Type
Experimental
Arm Description
0.8 g protein per kg body weight. Seven servings of whey protein powder (15 g/serving) per week will be provided to participants to support diet affordability.
Arm Title
WL-Protein
Arm Type
Experimental
Arm Description
>30 g of high quality protein per meal, 1.2 g protein/kg body weight/day. Fourteen servings of high quality (30 g/serving) protein (lean meats, low fat dairy products) provided to participants each week to increase compliance.
Intervention Type
Dietary Supplement
Intervention Name(s)
Foods rich in high quality protein
Intervention Description
Along with a weight reduction diet (by instruction), participants will receive high quality protein foods provided to them to include in their daily diet (see study arm description).
Primary Outcome Measure Information:
Title
Change in Short Physical Performance Battery (SPPB)
Description
Three different Balance test-(side-by-side, semi-tandem, tandem). They hold each position for 10 seconds Possible Score for Balance Test: 0-4 Possible Score for whole SPPB Test 0-12
Time Frame
0, 3 and 6 months
Title
Change in Short Physical Performance Battery (SPPB)
Description
Gait speed (4-meter timed walk)- we are measuring there normal walk speed. Possible Score for Gait Speed: 0-4 Possible Score for whole SPPB Test 0-12
Time Frame
0, 3, 6 months
Title
Change in Short Physical Performance Battery (SPPB)
Description
Lower Body Strength-5 Chair Stand as fast as they can do. Chair Stand- With arms across chest, stand up completely, returns to seated Possible Score for Chair Stands: 0-4 Possible Score for whole SPPB Test 0-12
Time Frame
0, 3, 6 months
Secondary Outcome Measure Information:
Title
Change in Body Weight
Description
Same scale, light clothing and no shoes, measured to nearest 0.1 kg
Time Frame
0, 3 and 6 months
Title
Change in 6 Minutes Walk Test (aerobic endurance)
Description
As many walking laps as possible in six minutes between cones placed 40 meters apart
Time Frame
0, 3 and 6 months
Title
Change in 8-ft Up and Go (agility/dynamic balance)
Description
Begins seated. On word 'go' stands, walks around a cone 8 feet away, returns to seated.
Time Frame
0,3, and 6 months
Title
Change in 30 second chair stands (lower body strength)
Description
With arms across chest, stand up completely, returns to seated as many times as possible in 30 seconds.
Time Frame
0, 3, and 6 months
Title
Change in Isokinetic knee extension peak torque (muscle strength)
Description
Knee extensor at 60 degrees with a dynamometer (HUMAC NORM Isokinetic Extremity System). Average peak torque for three trials will be recorded.
Time Frame
0, 3, and 6 months
Title
Change in Computerized Axial Tomography (CAT) scan
Description
Cross sectional area of the thigh without contrast to determine muscle mass.
Time Frame
0, 3, and 6 months
Title
Change in Isometric hand grip (upper body strength)
Description
Jamar Hand Dynamometer (Sammons Preston Rolyan). Highest of three trials/hand.
Time Frame
0, 3, and 6 months
Title
Change in Minimal Waist Circumference
Description
At smallest horizontal circumference above umbilicus and below xiphoid process.
Time Frame
0, 3, and 6 months
Title
Change in Body Composition: BodPod
Description
Air displacement plethysmography method (Life Measurement, Inc., Concord, CA). The Cardio Pulmonary, Metabolic and Body Composition (COSMED) BodPod has excellent sensitivity and test-to-test reliability, ease of use, and non-invasive nature, which is important for full participation from this population.
Time Frame
0, 3, and 6 months
Title
Change in number of falls and fear of falling
Description
In-person interview with questionnaire. This is a open ended questionnaire to see the change in number of times a person falls between time points. Yes or no response to the question, "Do you have a fear of falling?"
Time Frame
0, 3, 6 months
Title
Mini-Cog
Description
Screens for cognitive impairment with minimal language content, reduces cultural and educational bias. A 3-item recall component plus a Clock Drawing Test. The items recall component Score: 3 The Normal Clock Drawing Score: 2 Eligible score to be in study is 3.
Time Frame
Baseline
Title
Change in Short Form-36 (SF-36) Health Survey
Description
Quality of Life Questionnaires The SF-36 measures 8 QOL domains which are dichotomized into physical (functioning, role limitations-physical, pain, general health) and mental health (vitality, social functioning, role limitations-emotional, and emotional/mental health). Item scores were converted to a 0-100 point scale; domain scores were derived by averaging individual items within the subscale; and physical composite and mental health composite scores were derived by averaging the four component domains of each. Higher values are indicative of better QOL
Time Frame
0, 3, 6, 9, 12 months
Title
Change in Profile of Mood States (POMS)
Description
Mood Questionnaires The 30-item POMS measures mood and mood changes, has low respondent burden, and includes 6 subscales: tension, depression, anger, fatigue, confusion and vigor (all with range 0-20). Total mood disturbance (TMD) is derived from POMS using the following formula, TMD = (Sum of all subscales except vigor) - vigor (range -20 - 100).
Time Frame
0, 3, 6, 9, 12 months
Title
Change in Center for Epidemiologic Studies Depression Scale (CES-D)
Description
Depression Questionnaires Individuals were coded as positive for depression if they had a CES-D score of 16 and/or had self-report of depression diagnosis at baseline. In addition to the total score, the CES-D includes 4 subscales: depressed affect (range 0-21), positive affect (range 0-12), somatic (range 0-21), and interpersonal (range 0-6).
Time Frame
0, 3, 6, 9, 12 months
Title
Change in Perceived Stress Scale (PSS)
Description
Stress Questionnaires The PSS assesses the degree to which situations in one's life are considered stressful (range 0-40). Scores ranging from 0-13 would be considered low stress. Scores ranging from 14-26 would be considered moderate stress. Scores ranging from 27-40 would be considered high perceived stress.
Time Frame
0, 3, 6, 9, 12 months
Title
Change in Pittsburgh Sleep Quality Index (PSQI)
Description
Quality of sleep Questionnaires Reported PSQI values include only these six component scores: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, and use of sleeping medication (all with a range 0-3). The PSQI includes a scoring key for calculating a patient's seven subscores, each of which can range from 0 to 3. The subscores are tallied, yielding a "global" score that can range from 0 to 21. A global score of 5 or more indicates poor sleep quality; the higher the score, the worse the quality.
Time Frame
0, 3, 6, 9, 12 months
Title
Change in Satisfaction with Life Scale (SWLS)
Description
Life Satisfaction Questionnaires The SWLS evaluates global life satisfaction, an important component of subjective well-being (range 5-35). The SWLS is a 7-point Likert scale style response scale. The possible range of scores is 5-35, with a score of 20 representing a neutral point on the scale. Scores between 5-9 indicate the respondent is extremely dissatisfied with life, whereas scores between 31-35 indicate the respondent is extremely satisfied.
Time Frame
0, 3, 6, 9, 12 months
Title
Change in 3-day diet record
Description
3-day diet record by multiple pass; analyzed Food Processor (Version 10.13, 2013; ESHA Research);
Time Frame
0, 3, 6, [9, 12] months
Title
Change in Protein Checklist Form
Description
RedCap analysis for protein they have consumed
Time Frame
0,1,2,3,4,5,6 months
Title
Change in Actigraph, Axis accelerometer (activity counts, step counts, physical activity intensity)
Description
Actigraph WGT3X-BT activity counts at 1-s epoch from three orthogonal axes at 30 Hz sampling frequency.
Time Frame
0, 3, 6 months (7 days each time point)
Title
Change in Metabolic Panel (LabCorp)- A Blood Draw and testing
Description
Routine chemistries, blood testing
Time Frame
0, 3, 6 months
Title
Change in Glucose Tolerance Test (OGTT) (78-80), blood
Description
Ingestion of a 75 g glucose load with blood draws at 0, 10, 20, 30, 60, 90, 120, 150 and 180 minutes.
Time Frame
0, 3, 6 months
Title
Change in Daily food journal (Adherence)
Description
Daily food journal assessed by RD every week
Time Frame
we will collect the daily food journal Up to 36 weeks through study completation

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male Veterans African American or Caucasian Obese (BMI > 30 kg/m2) Age 55+ years Pre-diabetes (confirmed fasting plasma glucose 100 and <126 mg/dL) or HbA1c 5.7-6.4% Short Physical Performance Battery score of 4 to 10 units Age-normal renal function English speaking Able to record dietary intake or has a proxy who can record dietary intake Willing and able to be randomized to either intervention group Exclusion Criteria: Presence of unstable or symptomatic life-threatening illness Glomerular filtration rates (GFR) less than 45 mL/min A GFR of 45-59 requires bi-monthly testing per the investigators' established algorithm Those with a GFR <45 mL/min are excluded Mini Cog score of <3 --Vegetarian Neurological conditions causing functional impairments, including: Parkinson's Disease multiple sclerosis permanent disability due to stroke Inability to complete physical function assessment History of significant weight instability Contraindicated medications, including narcotic mail-outs and active substance abuse Any psychiatric condition that would prevent the subject from participating in a group intervention setting, including diagnosed personality disorders Primary care provider disapproves participation
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Connie W Bales, PhD RD
Phone
(919) 286-0411
Ext
6780
Email
connie.bales@va.gov
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Connie W Bales, PhD RD
Organizational Affiliation
Durham VA Medical Center, Durham, NC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Durham VA Medical Center, Durham, NC
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27705-3875
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Connie W Bales, PhD RD
Phone
919-286-0411
Ext
6780
Email
connie.bales@va.gov
First Name & Middle Initial & Last Name & Degree
Connie W Bales, PhD RD

12. IPD Sharing Statement

Plan to Share IPD
No

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Veterans Achieving Weight Loss and Optimizing Resilience-Using Protein

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