Prevention of Falls and Fractures in Old People by Administration of Calcium and Vitamin D. Randomized Clinical Trial (ANVITAD)
Primary Purpose
Fall, Fractures
Status
Unknown status
Phase
Phase 3
Locations
Spain
Study Type
Interventional
Intervention
Vitamin D and calcium suplementation
Sponsored by
About this trial
This is an interventional prevention trial for Fall focused on measuring Vitamin D, Calcium, Elderly
Eligibility Criteria
Inclusion Criteria:
- Aged over 65 years with normal renal function
- Normal transaminase levels
- Normal calcium blood levels
- Not homebound (not immobilized) nor in socio-healthcare institutions.
Exclusion Criteria:
- Need for medical treatment with calcium or vitamin D
- Hypersensitivity to or contraindication for calcium or vitamin D
- Medical treatment that includes calcium or vitamin D
- Physical disability that impedes their collaboration
- Taking thiazide diuretics
- Oral anticoagulants
- Hormone replacement therapy
- Digitalis drugs
- Anticonvulsants or barbiturates
Having any of the following diseases:
- Lithiasis
- Renal impairment (serum creatinine >1.4 mg/dl)
- Hypo or hyperthyroidism
- Paget's disease
- Chronic liver disease
- Tumors
- Sarcoidosis
- Impaired intestinal absorption or chronic alcoholism (>40 g/day).
Sites / Locations
- Research Unit. Primary Care Head Office of Albacete
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Calcium and vitamin D
Arm Description
The pharmacological intervention will be the daily administration of chewable tablets containing vitamin D and calcium.
Outcomes
Primary Outcome Measures
Incidence of spontaneous falls.
The primary variable will be the incidence of spontaneous falls according to the FICSIT (Frailty and Injury: Cooperative Study of Intervention Techniques) definition: "Unintentionally coming to rest on the ground, floor, or other lower level. Coming to rest against furniture or a wall was not counted as a fall".
Secondary Outcome Measures
Consequence of falls.
Bone fractures at any location, need for healthcare, need for hospitalization, bed-ridden.
Change in calcidiol [25(OH)D3] plasma levels
Determined by RIA (Vitamin D deficiency is defined as a calcidiol plasma level lower than 10ng/ml).
Change in bone mass (bone density or mineral content).
By densitometry (risk of fracture). Osteoporosis will be diagnosed based on a densitometry T-score of less than 2.5 in the vertebral column, according to WHO criteria.
Change in muscle strength in the dominant hand.
Determined by dyanometry (with a mean of 3 attempts to obtain a muscle strength measurement).
Changes in musculoskeletal function.
By the timed up and go test (the elderly person gets up from a chair with arms, walks three meters, turns round, walks back and sits down again). Taking more than 20 seconds indicates a high risk for falls.
Serious adverse events or any other adverse event.
An adverse event is considered as any untoward medical occurrence in any patient included in the study which does not necessarily have a causal relationship with the treatment. An adverse event can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with the use of a medicinal product.
Full Information
NCT ID
NCT01452243
First Posted
October 9, 2011
Last Updated
October 11, 2011
Sponsor
Gerencia de Atención Primaria, Albacete
Collaborators
Instituto de Salud Carlos III
1. Study Identification
Unique Protocol Identification Number
NCT01452243
Brief Title
Prevention of Falls and Fractures in Old People by Administration of Calcium and Vitamin D. Randomized Clinical Trial
Acronym
ANVITAD
Official Title
Prevention of Falls and Fractures in Old People by Administration of Calcium and Vitamin D. Randomized Clinical Trial (ANVITAD)
Study Type
Interventional
2. Study Status
Record Verification Date
October 2011
Overall Recruitment Status
Unknown status
Study Start Date
November 2008 (undefined)
Primary Completion Date
November 2011 (Anticipated)
Study Completion Date
April 2012 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Gerencia de Atención Primaria, Albacete
Collaborators
Instituto de Salud Carlos III
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The first objective is to determine the efficacy of calcium and vitamin D supplementation at doses of 1200 mg and 800 IU, respectively, to reduce the incidence of falls and fractures in non-institutionalized elderly people.
The second objective is to measure and compare treatment groups (calcium and vitamin D vs placebo) as regards muscle strength and musculoskeletal function, bone mineral density, calcidiol level and treatment safety.
Detailed Description
Background:
There are many studies that associate vitamin D serum levels in older persons with muscle strength, physical performance and risk of fractures and falls. However, current evidence is insufficient to make a general recommendation for administrating calcium and vitamin D to older persons. The objective of this study is to determine the effectiveness of calcium and vitamin D supplementation in improving musculoskeletal function and decreasing the number of falls in person aged over 65 years.
Design:
Phase III, randomized, double blind, placebo-controlled trial to evaluate the efficacy of already marketed drugs in a new indication. It will be performed at Primary Care doctor visits at several Healthcare Centers in different Spanish Health Areas. A total of 704 non-institutionalized subjects aged 65 years or older will be studied (sample size calculated for a statistical power of 80%, alpha error 0.05, annual incidence of falls 30% and expected reduction of 30% to 20% and expected loss to follow up of 20%). The test drug containing 800 IU of vitamin D and 1000 mg of calcium will be administered daily. The control group will receive a placebo. The subjects will be followed up over two years. The primary variable will be the incidence of spontaneous falls. The secondary variables will include: consequences of the falls (fractures, need for hospitalization), change in calcidiol plasma levels and other analytical determinations (transaminases, PTH, calcium/phosphorous, albumin, creatinine, etc.), change in bone mass by densitometry, change in muscle strength in the dominant hand and change in musculoskeletal strength, risk factors for falls, treatment compliance, adverse effects and socio-demographic data.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fall, Fractures
Keywords
Vitamin D, Calcium, Elderly
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
704 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Calcium and vitamin D
Arm Type
Experimental
Arm Description
The pharmacological intervention will be the daily administration of chewable tablets containing vitamin D and calcium.
Intervention Type
Drug
Intervention Name(s)
Vitamin D and calcium suplementation
Intervention Description
The pharmacological intervention will be the daily administration of chewable tablets containing 800 IU of vitamin D and 1200 mg of calcium. They will be administered over 2 years during the months of November to April in order to avoid the influence of sunlight.
Primary Outcome Measure Information:
Title
Incidence of spontaneous falls.
Description
The primary variable will be the incidence of spontaneous falls according to the FICSIT (Frailty and Injury: Cooperative Study of Intervention Techniques) definition: "Unintentionally coming to rest on the ground, floor, or other lower level. Coming to rest against furniture or a wall was not counted as a fall".
Time Frame
24 months.
Secondary Outcome Measure Information:
Title
Consequence of falls.
Description
Bone fractures at any location, need for healthcare, need for hospitalization, bed-ridden.
Time Frame
24 months.
Title
Change in calcidiol [25(OH)D3] plasma levels
Description
Determined by RIA (Vitamin D deficiency is defined as a calcidiol plasma level lower than 10ng/ml).
Time Frame
18 months.
Title
Change in bone mass (bone density or mineral content).
Description
By densitometry (risk of fracture). Osteoporosis will be diagnosed based on a densitometry T-score of less than 2.5 in the vertebral column, according to WHO criteria.
Time Frame
24 months.
Title
Change in muscle strength in the dominant hand.
Description
Determined by dyanometry (with a mean of 3 attempts to obtain a muscle strength measurement).
Time Frame
24 months
Title
Changes in musculoskeletal function.
Description
By the timed up and go test (the elderly person gets up from a chair with arms, walks three meters, turns round, walks back and sits down again). Taking more than 20 seconds indicates a high risk for falls.
Time Frame
24 months
Title
Serious adverse events or any other adverse event.
Description
An adverse event is considered as any untoward medical occurrence in any patient included in the study which does not necessarily have a causal relationship with the treatment. An adverse event can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with the use of a medicinal product.
Time Frame
24 months.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Aged over 65 years with normal renal function
Normal transaminase levels
Normal calcium blood levels
Not homebound (not immobilized) nor in socio-healthcare institutions.
Exclusion Criteria:
Need for medical treatment with calcium or vitamin D
Hypersensitivity to or contraindication for calcium or vitamin D
Medical treatment that includes calcium or vitamin D
Physical disability that impedes their collaboration
Taking thiazide diuretics
Oral anticoagulants
Hormone replacement therapy
Digitalis drugs
Anticonvulsants or barbiturates
Having any of the following diseases:
Lithiasis
Renal impairment (serum creatinine >1.4 mg/dl)
Hypo or hyperthyroidism
Paget's disease
Chronic liver disease
Tumors
Sarcoidosis
Impaired intestinal absorption or chronic alcoholism (>40 g/day).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jesús López-Torres, Hidalgo
Organizational Affiliation
Research Unit. Primary Care Head Office of Albacete
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ignacio Párraga Martínez, Dr.
Organizational Affiliation
Research Unit. Primary Care Head Office of Albacete
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Beatriz Navarro Bravo, Dr.
Organizational Affiliation
Research Unit. Primary Care Head Office of Albacete
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Fernando Andrés Pretel, Dr.
Organizational Affiliation
Research Unit. Primary Care Head Office of Albacete
Official's Role
Study Chair
Facility Information:
Facility Name
Research Unit. Primary Care Head Office of Albacete
City
Albacete
ZIP/Postal Code
02001
Country
Spain
12. IPD Sharing Statement
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Prevention of Falls and Fractures in Old People by Administration of Calcium and Vitamin D. Randomized Clinical Trial
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