Calcium and Vitamin D Malnutrition in Elderly Women
Primary Purpose
Osteoporosis, Secondary Hyperparathyroidism
Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
calcium supplementation
calcium and vitamin D3 supplementation
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Osteoporosis focused on measuring calcium, vitamin D, secondary hyperparathyroidism, osteoporotic fractures
Eligibility Criteria
Inclusion Criteria: healthy women ages 55 and older who were at least four years postmenopausal living independently in a nine-county rural area of Nebraska - Exclusion Criteria: 1) chronic kidney disease, 2) Paget's metabolic bone disease, and 3) history of cancer except for superficial basal or squamous cell carcinoma of the skin and -
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Experimental
Arm Label
1
2
3
Arm Description
calcium supplementation
calcium and vitamin D3 supplementation
placebo
Outcomes
Primary Outcome Measures
fractures
Secondary Outcome Measures
changes in bone mass and density
changes in serum dihydroxyvitamin D
changes in serum parathyroid hormone
cancer
Falls
Full Information
NCT ID
NCT00352170
First Posted
July 12, 2006
Last Updated
August 8, 2008
Sponsor
Creighton University
Collaborators
GlaxoSmithKline
1. Study Identification
Unique Protocol Identification Number
NCT00352170
Brief Title
Calcium and Vitamin D Malnutrition in Elderly Women
Official Title
Calcium and Vitamin D Malnutrition in Elderly Women
Study Type
Interventional
2. Study Status
Record Verification Date
August 2008
Overall Recruitment Status
Completed
Study Start Date
May 2000 (undefined)
Primary Completion Date
July 2005 (Actual)
Study Completion Date
July 2005 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Creighton University
Collaborators
GlaxoSmithKline
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study is designed to test whether calcium supplementation alone or calcium plus vitamin D reduces the incidence of fractures, reduces high parathyroid secretory activity, and halts bone loss in a population-based sample of women 55+ years of age.
A calcium supplement of 1400 mg/d will significantly reduce the cumulative incidence of spine and appendicular fractures over four years for independently living, rural women 55 years of age and older compared to similar women on their usual diets.
A calcium supplement of 1400 mg/d plus 1100 IU vitamin D/d will significantly reduce the cumulative incidence of spine and appendicular fractures compared to a calcium supplement only.
Detailed Description
We are conducting a 4-year randomized, double-blind, placebo controlled trial of calcium or calcium with vitamin D supplementation. We randomly sampled the population of healthy, independent living women 55+ years in nine rural counties. We randomly assigned 1180 women to one of three groups: Group 1 receives calcium (1400 mg/d) and vitamin D placebo, Group 2 receives both calcium (1400 mg/d) and vitamin D (1100 IU/d) and Group 3 receives both placebos.
A full-service market research firm randomly selected telephone numbers from all households with listed numbers in the nine-county rural sample area. The firm continued calling until 1180 women were selected who met the inclusion and exclusion criteria and were willing to participate in a four year prospective study of calcium and vitamin D supplementation. The participants were enrolled into study between May 2000 and July 2001.
Participants have study visits every six months. Annually the following are performed: bone density scans, height and weight, brief medical history including medicine changes, fracture surveillance, and compliance with calcium and vitamin D. At baseline and end of study, spine x-rays and dietary recall were obtained.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoporosis, Secondary Hyperparathyroidism
Keywords
calcium, vitamin D, secondary hyperparathyroidism, osteoporotic fractures
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
1180 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
calcium supplementation
Arm Title
2
Arm Type
Experimental
Arm Description
calcium and vitamin D3 supplementation
Arm Title
3
Arm Type
Experimental
Arm Description
placebo
Intervention Type
Dietary Supplement
Intervention Name(s)
calcium supplementation
Intervention Description
calcium carbonate 1500 mg/day
Intervention Type
Dietary Supplement
Intervention Name(s)
calcium and vitamin D3 supplementation
Intervention Description
calcium carbonate 1500 mg/day vitamin D3 1000 IU/day
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
calcium and vitamin D3 placebo
Primary Outcome Measure Information:
Title
fractures
Time Frame
4 years
Secondary Outcome Measure Information:
Title
changes in bone mass and density
Time Frame
4 years
Title
changes in serum dihydroxyvitamin D
Time Frame
one year and four years
Title
changes in serum parathyroid hormone
Time Frame
one year and four years
Title
cancer
Time Frame
four years
Title
Falls
Time Frame
four years
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: healthy women ages 55 and older who were at least four years postmenopausal living independently in a nine-county rural area of Nebraska
-
Exclusion Criteria:
1) chronic kidney disease, 2) Paget's metabolic bone disease, and 3) history of cancer except for superficial basal or squamous cell carcinoma of the skin and
-
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joan M Lappe, Ph.D
Organizational Affiliation
Creighton University
Official's Role
Principal Investigator
12. IPD Sharing Statement
Citations:
PubMed Identifier
17556697
Citation
Lappe JM, Travers-Gustafson D, Davies KM, Recker RR, Heaney RP. Vitamin D and calcium supplementation reduces cancer risk: results of a randomized trial. Am J Clin Nutr. 2007 Jun;85(6):1586-91. doi: 10.1093/ajcn/85.6.1586. Erratum In: Am J Clin Nutr. 2008 Mar;87(3):794.
Results Reference
result
PubMed Identifier
24128439
Citation
Zhou Y, Zhao LJ, Xu X, Ye A, Travers-Gustafson D, Zhou B, Wang HW, Zhang W, Lee Hamm L, Deng HW, Recker RR, Lappe JM. DNA methylation levels of CYP2R1 and CYP24A1 predict vitamin D response variation. J Steroid Biochem Mol Biol. 2014 Oct;144 Pt A:207-14. doi: 10.1016/j.jsbmb.2013.10.004. Epub 2013 Oct 12.
Results Reference
derived
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Calcium and Vitamin D Malnutrition in Elderly Women
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