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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01327196
Other study ID # BIO39/SA04/10
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 2010
Est. completion date December 2012

Study information

Verified date September 2014
Source Fundacion para la Investigacion y Formacion en Ciencias de la Salud
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The objective of this project is to study cognitive yields in people of the town of Salamanca over 65, with particular emphasis on the acquisition of the initial symptoms of cognitive impairment in order to detect mild cognitive impairment and study the relationship between the clinical situation and cardiovascular risk factors. It will depart from a reference population of 420 people older than 65 years living in the municipality of Salamanca which took part in a survey prior to partner health needs of the elderly of 65 years in the municipality of Salamanca. This was a stratified sampling as stratum considering the area of health. The results of this study are expected to evidence the extent of the problem of cognitive decline in the population over 65 years. It is also expected to determine the relationship between the co-morbidity in this problem and specific factors of cardiovascular risk in this group of population.


Description:

A random sample population, the information obtained has a validity superior to other studies in which the sample has not followed very strict criteria of selection.

Protocol for measurement:

- variable demographic partner

- vascular risk factors

- co-morbidity

- functional level for the activities of daily life

- cognitive performance in attention, memory, language, praxias, gnosias (abbreviated neuropsychological battery)

Through a battery short neuropsychological specially adapted for the study of older people will carry out a study of the cognitive performance in people older than 65 years of age and will try to establish how much influence the controlled variables of cardiovascular risk.


Recruitment information / eligibility

Status Completed
Enrollment 327
Est. completion date December 2012
Est. primary completion date June 2012
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria:

- lives in the municipality of Salamanca

- over 65 years of age

Study Design


Locations

Country Name City State
Spain Fundacion INFOSALUD Salamanca

Sponsors (2)

Lead Sponsor Collaborator
Fundacion para la Investigacion y Formacion en Ciencias de la Salud Grupo de Investigación de Atención Primaria de Castilla y León

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Other neuropsychological assessment neuropsychological assessment
Primary Prevalence of risk factors cardiovascular Prevalence of risk factors cardiovascular
Secondary neuropsychological assessment neuropsychological assessment
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