Clinical Trials Directory

Trials / Completed

CompletedNCT00472654

The Effect of Vitamin D Supplementation During Caloric Restriction on Intestinal Calcium Absorption

Nutritional Regulation of Bone - Aim 3

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
83 (actual)
Sponsor
Rutgers University · Academic / Other
Sex
Female
Age
50 Years – 72 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to learn how the amount of vitamin D supplementation influences intestinal fractional calcium absorption (a measure of the amount of calcium absorbed).

Detailed description

The extent of change in the amount of calcium that is absorbed with an increase in vitamin D supplementation is not known. This information is important for determining appropriate vitamin D requirements for optimal calcium absorption. During caloric restriction in postmenopausal women, we found that serum parathyroid hormone (PTH) explains 22% of the variance for the reduced calcium absorption (equivalent to 400 IU of Vitamin D per day). It is possible that higher dietary Vitamin D will increase serum 25-hydroxy-Vitamin D (25(OH)D) levels, offset serum PTH and thereby prevent a reduction in calcium absorption. This study seeks to determine if a high Vitamin D intake (a supplement of 2500 IU per day) can increase true fractional calcium absorption (TFCA) in postmenopausal women on a standard high-carbohydrate weight loss diet compared to weight maintenance, with the hypothesis that a high Vitamin D intake will raise serum 25(OH)D and offset the decline in TFCA during caloric restriction (vs. an increase in weight-stable women), and serum PTH will no longer be a major factor explaining changes in TFCA. Participants will be recruited for both weight loss and weight maintenance, and all will be randomly assigned to take either 2500 IU per day vitamin D supplement or matching placebo. All weight loss participants will attend 5-6 weekly counseling sessions (about 50 minutes per session). All participants will be asked to take a daily vitamin/mineral supplement and, depending on their usual food intake, they may be asked to take a calcium tablet to meet the recommended intake throughout the study period. To measure calcium absorption before and after the 6 weeks of weight loss, participants will go to the study site after an overnight fast where an IV will be placed and the participant will receive an infusion of a stable calcium isotope and consume a 4 oz beverage that also contains a stable isotope of calcium. Blood will be drawn, and then the participant will be asked to collect all urine for the next 24 hours. Body composition (fat, muscle mass, and bone mineral density) will be measured by a dual-energy x-ray absorptiometry (DXA) machine and peripheral quantitative computer tomography (pQCT). Participants will only be recruited in the winter and spring of each year.

Conditions

Interventions

TypeNameDescription
BEHAVIORALWeight LossDiet for weight loss for 6 weeks; all weight loss participants will attend 6 weekly counseling sessions (about 50 minutes per session)
DIETARY_SUPPLEMENTVitamin D 2500 IUDaily Vitamin D 2500 IU supplement for 6 weeks
BEHAVIORALWeight MaintenanceDiet for weight maintenance for 6 weeks

Timeline

Start date
2007-03-01
Primary completion
2010-05-01
Completion
2011-03-01
First posted
2007-05-14
Last updated
2023-03-28

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00472654. Inclusion in this directory is not an endorsement.