Skip to content

Prospective Population Based Cohort Study on Cognitive and Cardiovascular Aging (MonaLisaPredor)

Prospective Population Based Cohort Study on Cognitive and Cardiovascular Aging

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02566538
Acronym
MLP
Enrollment
520
Registered
2015-10-02
Start date
2013-05-22
Completion date
2018-06-30
Last updated
2020-07-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aging

Keywords

Cohort study, psychometric tests, cognitive function, cardiovascular risk, prediction algorithm

Brief summary

Aging is a long term process, starting early in life, and progressively affecting various functions and organs. Cardiovascular diseases and cognitive impairment are two conditions related to advancing age and sharing common risk factors. The Mona Lisa- PREDOR study is a population-based prospective cohort study carried out to develop risk prediction algorithms aimed at identifying people who are the most likely to develop impaired psychometric and cognitive functioning and impaired cardiovascular risk, in the coming years.

Detailed description

The study is aimed at identifying predictors of impaired changes in psychometric and cognitive performances and level of cardiovascular risk, over a seven-year period, and to develop risk prediction algorithms. Main secondary objectives are to study response to psychometric and cognitive tests according to age, and to estimate the prevalence of the frailty syndrome according to age. The design is a prospective cohort study carried out among 1500 men and women from the general population, aged 42-89 years, and living in South-western France. Except for participants aged 80-89 years, all participants have been previously assessed in 2005-2007, as regard to their psychometric and cognitive performances and level of cardiovascular risk, as part of the Mona Lisa study. Data collection includes a detailed questionnaire on previous medical history, drug intake, education level, and life habits; a standardised clinical examination; psychometric tests (word list learning test, digit symbol substitution test, word fluency test and Stroop test), and a fasting blood sample. Level of cardiovascular risk and frailty syndrome were assessed.

Interventions

None listed

Sponsors

Institut National de la Santé Et de la Recherche Médicale, France
CollaboratorOTHER_GOV
University Hospital, Toulouse
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
42 Years to 89 Years
Healthy volunteers
Yes

Inclusion criteria

* Men and women aged 42-79 years, living in South-western France, who participated in the Mona Lisa Study (2005-2007) (in the Mona Lisa study, participants were selected by drawing on polling lists) * Men and women aged 80-89 years, living in South-western France, selected by drawing on polling lists.

Exclusion criteria

* Subject who refuses to participate (who refuses to sign the inform consent) * Subject not affiliated to a health assurance system * Subject with altered cognitive functioning compromising the understanding of the information on the study, and not accompanied by a trusted third party.

Design outcomes

Primary

MeasureTime frameDescription
Test of memorizing and restitution of words7 years after the first assessmentFrench version of the Rey auditory verbal learning test

Secondary

MeasureTime frameDescription
Level of cardiovascular risk7 years after the first assessmentNumber of risk factors
WAIS-DSST7 years after the first assessmentWechsler Adult Intelligence Survey - Digit Symbol Substitution Subtest
Stroop test7 years after the first assessment

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026