Diet, Exercise, Metabolism, and Obesity in Older Women (DEMO)
Primary Purpose
Abdominal Obesity, Metabolic Syndrome
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Caloric Restriction
Caloric Restriction + Low-Intensity aerobic exercise
Caloric Restriction plus High-intensity aerobic exercise
Sponsored by
About this trial
This is an interventional treatment trial for Abdominal Obesity focused on measuring Abdominal, obesity, exercise, intensity, weight loss, women
Eligibility Criteria
Inclusion Criteria:
- Currently 50 - 70 years of age (at screening)
- Post-menopausal at least 1 year
- Waist diameter of at least 34"
- Able to attend exercise classes 3 times per week
- BMI between 25 & 40 kg/m2
- MMSE > 25
Exclusion Criteria:
- Exercises regularly (ie- more than twice a week for more than 15 minutes per session)?
- Uncontrolled diabetes mellitus or insulin-controlled diabetes?
- Does not drive and does not have a reliable way to pick up meals once a week
- Cancer in past 5 years except skin cancer
- Unwilling or unable to eat prepared foods (non-compliant during test week)
- Unwilling or unable to record food intake accurately
- Self-reported weight loss or gain >5% in past 6 months
- Smoking within past year, or use of tobacco or nicotine product
- Coronary artery disease, liver disease, renal disease, or other systemic disorders
- Pulmonary disease
- Current use of thiazide diuretics, beta blockers or steroids
- Current use of more than one anti-hypertensive medication
- Current use of anti-depressants or hormone replacement therapy
- Gross physical impairment
- Blindness or retinopathy
- Triglyceride level >400 mg/dl
- Anemia (Hct < 37%)
- Contraindication to exercise by ECG or GXT
Sites / Locations
- Wake Forest University Health Sciences
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Experimental
Experimental
Arm Label
1
2
3
Arm Description
Caloric Restriction
Caloric restriction + Moderate-intensity aerobic exercise
Caloric restriction + Vigorous-intensity aerobic exercise
Outcomes
Primary Outcome Measures
Abdominal visceral fat volume
Secondary Outcome Measures
HDL cholesterol Triglyceride concentrations Glucose tolerance
Full Information
NCT ID
NCT00664729
First Posted
April 21, 2008
Last Updated
July 30, 2018
Sponsor
Wake Forest University Health Sciences
Collaborators
National Institute on Aging (NIA)
1. Study Identification
Unique Protocol Identification Number
NCT00664729
Brief Title
Diet, Exercise, Metabolism, and Obesity in Older Women
Acronym
DEMO
Official Title
Diet, Exercise, Metabolism, and Obesity in Older Women:DEMO
Study Type
Interventional
2. Study Status
Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
November 2002 (undefined)
Primary Completion Date
November 2008 (Actual)
Study Completion Date
November 2008 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wake Forest University Health Sciences
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
Reductions in fat oxidation and resting metabolic rate (RMR) are associated with normal aging and are accelerated with menopause. As a result, postmenopausal women have an increased risk of abdominal obesity and ultimately the metabolic complications that lead to the insulin resistance syndrome and its associated risks (hyperlipidemia, type 2 diabetes, and coronary heart disease). Thus, there is a need to determine the most successful treatment to reduce visceral obesity in postmenopausal women. The purpose of this study is to determine if dietary-induced weight loss alone and/or weight loss combined with exercise at low and high- intensities differentially affect the reduction in visceral adipose tissue in postmenopausal women with abdominal obesity.
Detailed Description
Design Overview:
This study's protocol will last approximately 18 months. Phase 1 involves recruitment and screening followed by baseline research testing (Phase 2). Next, subjects will be randomly assigned to one of three 5-month treatments (Phase 3): diet and high-intensity exercise, diet and low-intensity exercise, or diet only. In the Maintenance Phase, subjects will return for visits at 6 & 12 months following the completion of their 5 month intervention.
Interventions:
All treatment groups will experience the same total weekly caloric deficit (-2800 kcal/wk), but will derive this deficit by different reductions in dietary intake and exercise energy expenditure. The weekly caloric deficit will be accomplished as follows: 1) the diet alone group will reduce dietary intake by ~2800 kcal/week (~400 kcal/day); 2) both exercise groups will expend ~400 kcal/wk in exercise energy expenditure and will reduce dietary intake by ~2400 kcal/wk (~340 kcal/day) to achieve the 2800 kcal/wk deficit.
The exercise will take place in an exercise facility at the Geriatric Research Center on the campus of the Wake Forest University/Baptist Medical Center. Two study personnel, including at least one trained technician, will supervise all exercise sessions. Emergency equipment will be kept on site during exercise sessions. Blood pressure and heart rate will be measured and recorded before each exercise session and participants will warm-up by walking for 3-5 min at a slow pace. Women will use the treadmill to exercise at an intensity of 45-50% (low-intensity AEX) or 70-75% (high-intensity AEX) of VO2max. Both groups will exercise 3 d/wk and duration of exercise will progress from 10-15 min the 1st week to 55 min by the end of the 6th week and thereafter for the low-intensity AEX group. The duration of exercise for the high-intensity AEX group will progress from 10-15 min the 1st week to 30 min by the end of the 6th week and thereafter. Injuries are minimized by a feasible progression of exercise duration as well as careful monitoring of proper footwear and stretching exercises.
The diet intervention will consist of monthly meetings with a registered dietitian along with consuming a hypocaloric diet provided by the GCRC metabolic kitchen. Subjects will be asked to pick up their food three times a week. Two meals per day will be provided. In addition, a calcium supplement (1000mg) will be provided. Subjects will be required to keep a diary of other foods consumed including the calcium supplement. The diets will be composed of 50-60% carbohydrate, 15-20% protein, and 25-30% fat with adequate amounts of essential nutrients. The number of calories given to each subject will be estimated from energy expenditure estimates in combination with an activity factor. The diet only group will be provided with an approximate 400 kcal/day energy deficit diet, while both exercise groups will be provided with an approximate 340 kcal/day energy deficit diet. Menus and specific food choices will be determined by GCRC dietitians in consultation with each research subject.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Abdominal Obesity, Metabolic Syndrome
Keywords
Abdominal, obesity, exercise, intensity, weight loss, women
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
112 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Description
Caloric Restriction
Arm Title
2
Arm Type
Experimental
Arm Description
Caloric restriction + Moderate-intensity aerobic exercise
Arm Title
3
Arm Type
Experimental
Arm Description
Caloric restriction + Vigorous-intensity aerobic exercise
Intervention Type
Behavioral
Intervention Name(s)
Caloric Restriction
Other Intervention Name(s)
Diet Only
Intervention Description
Reduced calorie diet (400 kcal/day deficit)
Intervention Type
Behavioral
Intervention Name(s)
Caloric Restriction + Low-Intensity aerobic exercise
Other Intervention Name(s)
Diet+Low-Intensity AEX
Intervention Description
400 kcal/day deficit plus 3 days/week aerobic exercise at 45-50% maximal aerobic fitness
Intervention Type
Behavioral
Intervention Name(s)
Caloric Restriction plus High-intensity aerobic exercise
Other Intervention Name(s)
Diet+High-intensity AEX
Intervention Description
400 kcal/day deficit and 3 d/week of aerobic exercise at 65-75% maximal fitness
Primary Outcome Measure Information:
Title
Abdominal visceral fat volume
Time Frame
Baseline, follow-up
Secondary Outcome Measure Information:
Title
HDL cholesterol Triglyceride concentrations Glucose tolerance
Time Frame
Baseline and Follow-up
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Currently 50 - 70 years of age (at screening)
Post-menopausal at least 1 year
Waist diameter of at least 34"
Able to attend exercise classes 3 times per week
BMI between 25 & 40 kg/m2
MMSE > 25
Exclusion Criteria:
Exercises regularly (ie- more than twice a week for more than 15 minutes per session)?
Uncontrolled diabetes mellitus or insulin-controlled diabetes?
Does not drive and does not have a reliable way to pick up meals once a week
Cancer in past 5 years except skin cancer
Unwilling or unable to eat prepared foods (non-compliant during test week)
Unwilling or unable to record food intake accurately
Self-reported weight loss or gain >5% in past 6 months
Smoking within past year, or use of tobacco or nicotine product
Coronary artery disease, liver disease, renal disease, or other systemic disorders
Pulmonary disease
Current use of thiazide diuretics, beta blockers or steroids
Current use of more than one anti-hypertensive medication
Current use of anti-depressants or hormone replacement therapy
Gross physical impairment
Blindness or retinopathy
Triglyceride level >400 mg/dl
Anemia (Hct < 37%)
Contraindication to exercise by ECG or GXT
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Barbara J Nicklas, PhD
Organizational Affiliation
Wake Forest University Health Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Wake Forest University Health Sciences
City
Winston-Salem
State/Province
North Carolina
ZIP/Postal Code
27157
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
16446745
Citation
You T, Murphy KM, Lyles MF, Demons JL, Lenchik L, Nicklas BJ. Addition of aerobic exercise to dietary weight loss preferentially reduces abdominal adipocyte size. Int J Obes (Lond). 2006 Aug;30(8):1211-6. doi: 10.1038/sj.ijo.0803245. Epub 2006 Jan 31.
Results Reference
result
PubMed Identifier
15562250
Citation
You T, Yang R, Lyles MF, Gong D, Nicklas BJ. Abdominal adipose tissue cytokine gene expression: relationship to obesity and metabolic risk factors. Am J Physiol Endocrinol Metab. 2005 Apr;288(4):E741-7. doi: 10.1152/ajpendo.00419.2004. Epub 2004 Nov 23.
Results Reference
result
PubMed Identifier
25811948
Citation
Wang X, You T, Murphy K, Lyles MF, Nicklas BJ. Addition of Exercise Increases Plasma Adiponectin and Release from Adipose Tissue. Med Sci Sports Exerc. 2015 Nov;47(11):2450-5. doi: 10.1249/MSS.0000000000000670.
Results Reference
derived
PubMed Identifier
22035053
Citation
You T, Disanzo BL, Wang X, Yang R, Gong D. Adipose tissue endocannabinoid system gene expression: depot differences and effects of diet and exercise. Lipids Health Dis. 2011 Oct 28;10:194. doi: 10.1186/1476-511X-10-194.
Results Reference
derived
PubMed Identifier
19211823
Citation
Nicklas BJ, Wang X, You T, Lyles MF, Demons J, Easter L, Berry MJ, Lenchik L, Carr JJ. Effect of exercise intensity on abdominal fat loss during calorie restriction in overweight and obese postmenopausal women: a randomized, controlled trial. Am J Clin Nutr. 2009 Apr;89(4):1043-52. doi: 10.3945/ajcn.2008.26938. Epub 2009 Feb 11.
Results Reference
derived
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Diet, Exercise, Metabolism, and Obesity in Older Women
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