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NCT06492967Completed

LatAm-FINGERS Initiative for Cognitive Change

Latin American Lifestyle Intervention Initiative to Reduce the Risk and Prevent Cognitive Impairment.

Source: ClinicalTrials.gov · Last updated 4 May 2026

Brief summary (registry, in English)

Currently, 40% of global dementia cases can be prevented through lifestyle changes, with Latin America having a 56% potential reduction due to its high-risk factors. At the moment, there are no medications that halt the clinical expression of dementia. LatAm-FINGERS, a multicenter study across 12 Latin American countries, aims to study the feasibility of an intervention modifying lifestyle in individuals aged 60 to 77 at risk of dementia. Success could influence public policy on clinical care for older adults.

Status (registry)
Completed
Study type
Interventional
Enrollment
1065 (actual)
First submitted
30 May 2023
Start date
27 Oct 2021
Primary completion date
7 Nov 2025
Lead sponsor
Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia
NCT number
NCT06492967

What you commit to

  • Study type: Interventional
  • Participants enrolled: 1065
  • From 27 Oct 2021 to the primary completion date, 7 Nov 2025
  • 13 sites in 12 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Use of psychoactive medications within the past 3 months, including tricyclic antidepressants, antipsychotics, psychotropic mood-stabilizing agents (e.g., lithium salts), psychostimulants, opioid analgesics, antiparkinsonian medications, anticonvulsant medications (except gabapentin and pregabalin for non-convulsant indications), systemic corticosteroids, or medications with significant central anticholinergic activity; in the absence of major depression, stable doses of selective serotonin reuptake inhibitors or serotonin and norepinephrine reuptake inhibitors are permitted.

Other illness

  • Dementia
  • Any medical condition that affects the participant's safety.
  • Significant neurological disease, including dementia, cognitive impairment, Parkinson's disease, Huntington's disease, normal pressure hydrocephalus, brain tumor, progressive supranuclear palsy, seizure disorder, subdural hematoma, multiple sclerosis or history of significant head injury with persistent neurological sequelae or structural brain abnormalities, major depressive disorder within the last 2 months, history of bipolar disorder or schizophrenia according to Diagnostic and Statistical Manual of Mental Disorders V (DSM V) criteria.
  • Cerebral vascular disease in the last 2 years.
  • Insulin-dependent diabetes mellitus.
  • Pulmonary disease requiring oxygen and/or steroids.
  • History within the last 2 years of treatment for primary or recurrent malignant disease.
  • History of hip fracture, knee replacement, or spinal surgery within the last 6 months.
  • History of bariatric surgery.
  • Cardiac surgery in the last year.
  • History of alcoholism or substance abuse in the last 2 years, according to DSM V criteria.

Lab values

  • Severe cardiovascular disease, including heart failure, clinically significant aortic stenosis, history of uncontrolled acute myocardial infarction (AMI) or angina and Cardiac rhythm disorders: g3 conduction block, uncontrolled arrhythmia, alterations in Q wave, S waver and T wave segment or QT segment and auricular fibrillation (AF) of less than one year of evolution, venous thrombosis or pulmonary thromboembolism (PTE) of less than 6 months of evolution and any pathology that in clinical judgment compromises the intervention of physical activity.
  • Renal disease defined as increased renal glomerular filtration rate \<60ml/min/1.73mt2 or albumin excretion rate (AER) \> 30mg/24 hrs.
  • Clinically significant laboratory abnormalities as judged by the investigator.

Other

  • MMSE \< 20
  • Severe osteoarticular problems that preclude the implementation of the physical activity intervention outlined in the protocol, such as, for example: osteoarthrosis of the knee(s), coxofemoral, or other.
  • Body Mass Index \>40
  • Being in cardiopulmonary rehabilitation.
  • Severe sensory loss or loss of communication skills.
  • No schooling.
  • Active participation in another intervention study.

Who the study is looking for

  • Age: 60-77 years.
  • Cardiovascular Risk Factors, Aging, and Incidence of Dementia (CAIDE) Risk Score \> 6.
  • Mini-Mental State Examination (MMSE) z score between 0 and -1.5 OR
  • CERAD Word List Learning Task (10 word x 3 repetitions) \< 0 z score OR
  • CERAD (delayed word list recall) \< z score \< 0

Age in the registry: 60 years to 77 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (13)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Fleni
Coordinator of this site? Confirm its status
Ciudad Autonoma de Buenos AireArgentinaUnknown status
Centro Neurológico Mente Activa
Coordinator of this site? Confirm its status
La PazBoliviaUnknown status
Universidade Federal de Minas Gerais
Coordinator of this site? Confirm its status
Belo HorizonteBrazilUnknown status
University of Sao Paulo School of Medicine
Coordinator of this site? Confirm its status
São PauloBrazilUnknown status
Hospital Clínico Universidad de Chile
Coordinator of this site? Confirm its status
SantiagoChileUnknown status
Antioquia University
Coordinator of this site? Confirm its status
AntioquiaColombiaUnknown status
Hospital Clínica Bíblica
Coordinator of this site? Confirm its status
San JoséCosta RicaUnknown status
Universidad Nacional Pedro Henriquez Urena (UNPHU)
Coordinator of this site? Confirm its status
Santo DomingoDominican RepublicUnknown status
Neuromedicenter - Cognitive Disorders Unit
Coordinator of this site? Confirm its status
QuitoEcuadorUnknown status
Instituto Nacional de Neurología y Neurocirugía "Manuel Velasco Suarez"
Coordinator of this site? Confirm its status
Mexico CityMexicoUnknown status
Instituto Peruano de Neurociencas
Coordinator of this site? Confirm its status
LimaPeruUnknown status
Universidad de Puerto Rico
Coordinator of this site? Confirm its status
San JuanPuerto RicoUnknown status
Clínica de la Memoria - Hospital Británico
Coordinator of this site? Confirm its status
MontevideoUruguayUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.