Calcium, Dairy, and Body Fat in Adolescents
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Purpose
Lifestyle choices,including diet,are conducive to healthy body weights in children. Dairy products and calcium supplementation have been associated with moderation of body weight and body fat. This study was designed to test the following hypotheses with overweight and obese adolescents consuming a controlled diet:
- Dietary calcium supplementation as calcium carbonate or dairy calcium modulates energy balance in adolescents.
- Increased calcium in the diet of adolescents will increase fecal fat excretion and thereby decrease fat absorption.
- Calcium and dairy product supplementation will increase lipid oxidation resulting in an increase in energy expenditure.
| Condition | Intervention |
|---|---|
|
Obesity Energy Metabolism |
Dietary Supplement: C (smoothies based on soy protein containing no additional calcium) Dietary Supplement: B (smoothies based on soy protein containing calcium) Dietary Supplement: A (smoothies based on dairy protein containing calcium) |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Crossover Assignment Masking: Double Blind (Subject, Caregiver, Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | Calcium, Dairy, and Body Fat in Adolescents |
- Energy balance will be calculated by quantitating the kilocalories represented by the following components: dietary intake, excreta, physical activity, resting energy expenditure, thermic effect of food, and thermogenesis. [ Time Frame: After equilibration on a controlled diet for one week, measurements will be taken over an additional two week period. ] [ Designated as safety issue: No ]
- Serum biochemical measures of calcium metabolism (PTH, Vitamin D, and calcium) [ Time Frame: Serial meausures over a 10 hour period following a meal containing calcium from the placebo, dairy or calcium carbonate supplement ] [ Designated as safety issue: No ]
- Calcium retention [ Time Frame: Two weeks on a controlled diet following one week of equilibration on the same diet ] [ Designated as safety issue: No ]
| Enrollment: | 43 |
| Study Start Date: | April 2004 |
| Study Completion Date: | August 2004 |
| Primary Completion Date: | August 2004 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Placebo Comparator: C
During one three week session of a controlled diet subjects will receive a smoothie based on soy protein two times per day that does not contain any additional calcium
|
Dietary Supplement: C (smoothies based on soy protein containing no additional calcium)
Two smoothies per day based on soy protein containing no additional calcium
|
|
Active Comparator: B
During one three week period half of the participants will receive two smoothies per day based on soy protein that contain 650 mg Ca as calcium carbonate
|
Dietary Supplement: B (smoothies based on soy protein containing calcium)
Two smoothies daily based on soy protein containing 650 mg calcium as calcium carbonate
|
|
Active Comparator: A
During one three week session subjects will receive two smoothies per day based on dairy protein containing 650 mg calcium
|
Dietary Supplement: A (smoothies based on dairy protein containing calcium)
Two smoothies daily based on dairy protein containing 650 mg calcium
|
Detailed Description:
Subjects will consume a controlled diet containing 800 mg calcium for two three week periods. During one period they will also receive a frozen ice cream like product (smoothie) twice a day based on soy protein that contains no additional calcium. During the other period they will receive a similar product twice a day based on either dairy protein that contains 650 mg calcium or based on soy protein that contains 650 mg calcium as calcium carbonate
Eligibility| Ages Eligible for Study: | 12 Years to 15 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Over weight (>85th percentile BMI for age)
Exclusion Criteria:
- > 180% of ideal body weight for height
- Malabsorptive disorders
- Bone disease
- Liver disease
- Kidney disease
- Anemia
- Smoking or illegal drugs
- Oral contraceptives
- Pregnancy
- Medications that influence calcium metabolism
Contacts and Locations| United States, Indiana | |
| Department of Foods and Nutrition | |
| W. Lafayette, Indiana, United States, 47907 | |
| Principal Investigator: | Connie Weaver, PHD | Department Foods and Nutrition, Purdue University |
| Study Director: | Berdine R Martin, PhD | Department Foods and Nutrition, Purdue University |
More Information
No publications provided by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Connie Weaver/Professor and Head of Department, Department of Foods and Nutrition, Purdue University |
| ClinicalTrials.gov Identifier: | NCT00592137 History of Changes |
| Other Study ID Numbers: | DK66108 (completed), 5 R01 DK066108 |
| Study First Received: | December 26, 2007 |
| Last Updated: | January 12, 2010 |
| Health Authority: | United States: Federal Government |
Keywords provided by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK):
|
calcium carbonate obesity dairy energy expenditure |
Additional relevant MeSH terms:
|
Obesity Overnutrition Nutrition Disorders Overweight Body Weight Signs and Symptoms Calcium, Dietary |
Calcium Carbonate Bone Density Conservation Agents Physiological Effects of Drugs Pharmacologic Actions Antacids Molecular Mechanisms of Pharmacological Action |
ClinicalTrials.gov processed this record on May 19, 2013