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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02375503
Other study ID # 15-07-HC
Secondary ID
Status Completed
Phase N/A
First received February 24, 2015
Last updated May 12, 2017
Start date April 2015
Est. completion date June 2015

Study information

Verified date May 2017
Source United States Army Research Institute of Environmental Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary objective of this randomized, double-blind, placebo controlled trial is to determine the efficacy of a once per day calcium (1000mg) and vitamin D (1000IU) fortified food product on bone turnover markers, including parathyroid hormone (PTH) and microarchitecture during Army basic military training (BCT). The investigators hypothesize that consumption of a once daily calcium and vitamin D fortified food product will stabilize PTH and contribute to improved bone microarchitecture compared to placebo. The results will determine the efficacy of daily supplementation with calcium and vitamin D on bone turnover markers as well as provide novel data regarding microarchitectural changes during BCT as assessed by high resolution peripheral computed tomography (HRpQCT) scanning.


Description:

Stress fractures may affect up to 2-5% of male and 8-21% of female Soldiers during training, resulting in attrition in up to 60% of affected personnel. A recent report indicates that supplemental calcium (2000mg) and vitamin D (800-1000IU) stabilizes PTH, increases tibia volumetric bone mineral density in male and female recruits undergoing Army BCT, and reduces stress fracture incidence by up to 20% in female Nacy recruits. Bone macroarchitecture has been measured in response to basic training however, the resolution of standard peripheral quantitative computed tomography (pQCT) is insufficient for assessment of microarchitectural changes, which may underlie the pathophysiology of stress fracture. With the use of HRpQCT this study will allow the investigators to evaluate microarchitectural changes within the bone tissue and assess the efficacy of a moderate daily dose of calcium and vitamin D to support bone health during BCT.


Recruitment information / eligibility

Status Completed
Enrollment 175
Est. completion date June 2015
Est. primary completion date June 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 17 Years to 42 Years
Eligibility Inclusion Criteria:

- Female or male US Army recruits beginning Army basic combat training at Fort Jackson, South Carolina

Exclusion Criteria:

- Pregnant or breastfeeding

- History of kidney stones or kidney disease

- History of amenorrhea

- History or endocrine disorders

- History of bone modifying disorders

- Currently taking, or have taken glucocorticoid drugs in the 2 years prior to study participation

- Currently diagnosed as anemic by healthcare professional

- Those allergic to any component of the snack bar

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Calcium/Vitamin D
Daily, calcium and vitamin D fortified snack bar
Placebo


Locations

Country Name City State
United States Fort Jackson Columbia South Carolina

Sponsors (2)

Lead Sponsor Collaborator
United States Army Research Institute of Environmental Medicine United States Department of Defense

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Bone Turnover Markers Participants will have a pre- and post- BCT blood draw 8-10 weeks
Secondary Bone Microarchitecture Participants will receive a bone scan pre- and post- BCT in order to determine changes in bone microarchitecture 8-10 weeks
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