ANVITAD: Prevention of Falls and Fractures in Old People by Administration of Calcium and Vitamin D. Randomized Clinical Trial

Sponsor
Gerencia de Atención Primaria, Albacete (Other)
Overall Status
Unknown status
CT.gov ID
NCT01452243
Collaborator
Instituto de Salud Carlos III (Other)
704
1
1
41
17.2

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Drug: Vitamin D and calcium suplementation
Phase 3

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
704 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Prevention of Falls and Fractures in Old People by Administration of Calcium and Vitamin D. Randomized Clinical Trial (ANVITAD)
Study Start Date :
Nov 1, 2008
Anticipated Primary Completion Date :
Nov 1, 2011
Anticipated Study Completion Date :
Apr 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Experimental: Calcium and vitamin D

The pharmacological intervention will be the daily administration of chewable tablets containing vitamin D and calcium.

Drug: Vitamin D and calcium suplementation
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.

Outcome Measures

Primary Outcome Measures

  1. Incidence of spontaneous falls. [24 months.]

    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

  1. Consequence of falls. [24 months.]

    Bone fractures at any location, need for healthcare, need for hospitalization, bed-ridden.

  2. Change in calcidiol [25(OH)D3] plasma levels [18 months.]

    Determined by RIA (Vitamin D deficiency is defined as a calcidiol plasma level lower than 10ng/ml).

  3. Change in bone mass (bone density or mineral content). [24 months.]

    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.

  4. Change in muscle strength in the dominant hand. [24 months]

    Determined by dyanometry (with a mean of 3 attempts to obtain a muscle strength measurement).

  5. Changes in musculoskeletal function. [24 months]

    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.

  6. Serious adverse events or any other adverse event. [24 months.]

    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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Research Unit. Primary Care Head Office of Albacete Albacete Spain 02001

Sponsors and Collaborators

  • Gerencia de Atención Primaria, Albacete
  • Instituto de Salud Carlos III

Investigators

  • Principal Investigator: Jesús López-Torres, Hidalgo, Research Unit. Primary Care Head Office of Albacete
  • Study Chair: Ignacio Párraga Martínez, Dr., Research Unit. Primary Care Head Office of Albacete
  • Study Chair: Beatriz Navarro Bravo, Dr., Research Unit. Primary Care Head Office of Albacete
  • Study Chair: Fernando Andrés Pretel, Dr., Research Unit. Primary Care Head Office of Albacete

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Gerencia de Atención Primaria, Albacete
ClinicalTrials.gov Identifier:
NCT01452243
Other Study ID Numbers:
  • 2006001
First Posted:
Oct 14, 2011
Last Update Posted:
Oct 14, 2011
Last Verified:
Oct 1, 2011
Keywords provided by Gerencia de Atención Primaria, Albacete
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 14, 2011