Status:

COMPLETED

Effect of Calcium + Vitamin D Supplementation on Weight Management in Very-low Calcium Consumers

Lead Sponsor:

Changhai Hospital

Conditions:

Obesity

Overweight

Eligibility:

All Genders

18-25 years

Phase:

PHASE4

Brief Summary

The purpose of the study is to determine whether calcium plus vitamin D supplementation is conducive to weight and fat loss during energy restriction in very-low calcium consumers.

Detailed Description

Due to the contradicting findings in the hypothesis of calcium supplementation on weight and fat loss, which might be explained by the difference in initial calcium intake, the present study is aimed ...

Eligibility Criteria

Inclusion

  • Male or female 18 to 25 years of age, generally healthy
  • Habitual calcium intake below 600mg/d
  • Overweight or obese (BMI between 24 and 35kg/m2, refer to the Chinese standard)
  • Stable body weight (body weight change less than 1kg two months before screening)
  • Less than 3 times of 20min of physical exercise per week
  • Signed written informed consent

Exclusion

  • Coronary heart disease, hypertension, diabetes; hepatic insufficiency or renal insufficiency, hyper- or hypothyroidism, mal-absorption, cholesterol concentrations requiring pharmaceutical treatment
  • Pregnant or lactating woman
  • Use of calcium supplements, oral antidiabetic agents, antihyperlipidemics or any other medications affecting metabolism 30 days before randomization
  • Participating in another weight loss programs (i.e. taking oral pharmacotherapeutic agents and/or herbal preparations intended for the management of obesity; excessive physical activity; be on a diet)
  • On special diets (i.e. vegetarian)
  • Presently taking or have recently taken a prescription drug such as fluoroquinolone antibiotics, tetracycline, or levothyroxine (thyroid medication)
  • Participating in another clinical trial 6 months before randomization
  • Unlikely to be compliant (i.e. alcohol, drug abuse)
  • Refusal or inability to give informed consent to participate in the study

Key Trial Info

Start Date :

April 1 2011

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

February 1 2012

Estimated Enrollment :

53 Patients enrolled

Trial Details

Trial ID

NCT01447433

Start Date

April 1 2011

End Date

February 1 2012

Last Update

August 1 2012

Active Locations (1)

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Changhai Hospital

Shanghai, China, 200433