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2019-2545

A combined multidomain intervention to prevent cognitive decline associated with cardiovascular risk factors.
Source : Import from center

clinicaltrials.gov reference: NCT04962061
Aging
Cardiovascular Risk factor
Cognition
Combined Intervention
Cognitive Training
Physical Exercise
Brain Functions
Biomarkers
Source : Import from center

Target population

Medical condition (targeted specialty)

Data not available

Participants profils

Participants gender(s)

ALL

Source : Import from center
Subjects aptitude

Selection criterias

Inclusion criteria

Inclusion Criteria:

* Adult aged 60 and older,
* Normal or corrected vision and normal hearing for their age range,
* No cognitive impairment (Mini-Mental State Examination - MMSE ≥ 25),
* Inactive (\< 150 min of physical activity per week).

Exclusion Criteria:

* MMSE ≤ 24 or diagnosis of dementia,
* Uncontrolled psychological / psychiatric condition within the past 6 months,
* Neurological disease,
* Severe exercise intolerance,
* Respiratory disease (e.g., asthma, COPD),
* Excessive alcohol consumption (\> 15 drinks/week),
* Documented cerebral, peripheral or coronary atherosclerotic disease,
* Chronic systolic or diastolic heart failure,
* Symptomatic aortic stenosis,
* Atrial fibrillation,
* Automatic implantable defibrillator or permanent pacemaker,
* Malignant exertional arrhythmias,
* Non-cardiopulmonary limitation to exercise (e.g., arthritis).

Source : Import from center
Exclusion criteria

Score MMSE plus petit ou égale à 24, diagnostique de démence, état psychologique / psychiatrique non contrôlé au cours des 6 derniers mois, maladie neurologique, intolérance grave à l'exercice, maladie respiratoire (ex: asthme ou COPD), consommation excessive d'alcool (plus de 15 verres par semaine), athérosclérose cérébrale, périphérique ou coronaire documentée, insuffisance cardiaque systolique ou diastolique chronique, sténose aortique symptomatique, fibrillation auriculaire, défibrillateur automatique implantable ou stimulateur cardiaque permanent, arythmies malignes à l'effort, une limitation non cardiopulmonaire à l'exercice (ex: l'arthrite).

Source : Import from center

Proposed Therapy or Intervention

Cohorts
Name Medical condition Treatment Recruitment status
Multidomain intervention The multidomain intervention will combine a cognitive training with aerobic and resistance exercises training, three sessions per week for 46 weeks. Participants will be allowed to perform cognitive and exercise training sessions either home-based or centre-based. Data not available
  • Unknown
  • Physical exercise intervention The physical exercises intervention will include aerobic and resistance exercises training, three sessions per week for 46 weeks. Participants will be allowed to perform cognitive and exercise training sessions either home-based or centre-based. Data not available
  • Unknown
  • Active control intervention The active control intervention will include stretching and toning exercises, three sessions per week for 46 weeks. Participants will be allowed to perform cognitive and exercise training sessions either home-based or centre-based. Data not available
  • Unknown
  • Multidomain intervention
    Recruitment status
    unknown
    Physical exercise intervention
    Recruitment status
    unknown
    Active control intervention
    Recruitment status
    unknown
    Current data since : February 05, 2025 19:00

    Study description

    Study summary

    The ACTIONcardioRisk trial is designed to investigate the effect of aerobic and progressive resistance training exercises combined with cognitive training, on neurocognitive functioning of sedentary older adults with and without cardiovascular risk factors.

    Source : Import from center

    The proportion of older adults is on the rise in Canada, with the fastest growth recorded among those seventy years of age or older. The prevalence of cardiovascular risk factors (CVRF) such as diabetes, hypertension, and high cholesterol increases drastically with age. Individuals with CVRF often show impaired cognition, such as attention and memory deficits. In healthy older adults, exercise training and cognitive stimulation can help enhance cognitive performances. More precisely, combined intervention, including physical and cognitive training, has shown beneficial effects on cognition in older adults without cognitive impairment and with mild cognitive impairment. However, the effect of such programs on cognition in individuals with CVRF is not well documented. This project compares the effect of a physical exercise program, including aerobic and resistance training, alone or combined with cognitive training on cognitive performances and brain imaging outcomes in individuals with CVRF and healthy controls.

    Source : Import from center

    Locations

    Participating centers

      2 centers
    • INSTITUT DE CARDIOLOGIE DE MONTRÉAL *

      Montréal

      QUÉBEC, CANADA

      Local recruitment
      Recruiting status: OPEN
      Contact details for recruitment
      Local project contacts
      researchers:
      • L. Bherer

      co-researchers:
      • M. Juneau

      • M. Gayda

      • A. Nigam

      • É. Thorin

      • P. L'Allier

      • P. Vitali

      • M. Dubé

      • D. Gagnon

      • C. Gauthier

      • F. Lesage

      • S. Duchesne

      • J. Gagné

      • G. Ferland

      • S. Lupien

      • C. Gagnon

      • T. Vincent

      • C. Grégoire

      • J. Poirier

      • E. Dupuy

      • F. Besnier

      • D. Talamonti

      • H. Mohammadi

      • F. Simard

      click here for more information about this center
      Cohorts
      Institut de cardiologie de Montréal
      Data not available
      Current data since : February 09, 2025 00:28
    • PREVENTIVE MEDICINE AND PHYSICAL ACTIVITY CENTRE (CENTRE EPIC), MONTREAL HEART INSTITUTE

      Montreal

      QUEBEC, CANADA

      Local recruitment
      Recruiting status: OPEN
      Contact details for recruitment
      Data not available

    Last modification : February 05, 2025
    Current data since : 09 Feb 00:29
    Data source : clinicaltrials.gov, Nagano
    Nagano reference: 2019-2545
    clinicaltrials.gov reference: NCT04962061