search
Back to results

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
Creighton University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoporosis focused on measuring calcium, vitamin D, secondary hyperparathyroidism, osteoporotic fractures

Eligibility Criteria

55 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

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

    First Posted
    July 12, 2006
    Last Updated
    August 8, 2008
    Sponsor
    Creighton University
    Collaborators
    GlaxoSmithKline
    search

    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

    Learn more about this trial

    Calcium and Vitamin D Malnutrition in Elderly Women

    We'll reach out to this number within 24 hrs