Prevention of physical disability represents a major priority for the public health system. Physical disability is the final result of a complex cascade of negative events occurring at different levels (i.e., environmental, social, biological, and clinical). The heterogeneity of the underlying mechanisms responsible for the onset of physical disability may require the adoption of preventive interventions affecting multiple domains. Although several studies suggest that single or different combinations of preventive interventions (in particular, physical activity, cognitive training, and healthy diet) might provide beneficial effects in preventing functional loss (and its related features, such as pain or reduced quality of life), very limited evidence coming from clinical trials is currently available on the topic. Intervention trials are usually designed to test the effect of a specific monodimensional intervention on a very selected population, so to reduce the risk of biased results. This approach, although legitimate and methodologically correct, may 1) be insufficient to target the multiple and heterogeneous physiopathological mechanisms underlying the onset of physical disability, and 2) cause a population selection bias leading to difficulties in implementing the study results to the overall older population (thus, determining the "evidence-based medicine" issue in the elderly). To our knowledge, there are no available data from clinical trials evaluating the effects of a multidomain intervention based on lifestyle modifications (e.g., physical activity, cognitive training, nutritional modification) for preventing mobility disability (a very early phase of the disabling process) in community-dwelling older persons. In the present project (Multidomain Intervention to preveNt Disability in ElDers, MINDED), we propose to conduct a pilot study aimed at estimating the effects of a multidomain person-tailored preventive intervention (based on physical activity, cognitive training, and nutritional modifications) on frailty status, physical performance, cognitive function, nutritional status, health-related quality of life, and use of health care services. In addition, we will perform cost-effectiveness analyses of the proposed intervention. The project will yield the necessary preliminary data to design a definitive full-scale Phase 3 randomized clinical trial. By providing a conclusive answer about the effectiveness of a multidimensional preventive program in the primary prevention of major health-related outcomes, the results of the full-scale trial will have relevant clinical and public health implications, and will promote the practicing of a truly evidence-based geriatric medicine.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Enrollment
210
Multidomain preventive intervention designed by a multidisciplinary team on the basis of results of a comprehensive geriatric assessment
Centre de Rééducation Fonctionnelle "La Roseraie"
Montfaucon, France
400-meter walk test
Incident inability to complete the 400-meter walk test in the two randomization groups
Time frame: 12 months
Participants' adherence/retention to the intervention protocol and control groups
Participants' adherence/retention to the intervention protocol
Time frame: 12 months
Intercurrent illnesses rates
Intercurrent illnesses rates in the two randomization groups
Time frame: 12 months
Serious fall injuries
Incident fall injuries occurred in the two randomization groups
Time frame: 12 months
Hospitalizations and institutionalization rates
Incidence of acute care hospitalizations and nursing home admissions in the two randomization groups
Time frame: 12 months
Mortality
Overall mortality rate in the two randomization groups
Time frame: 12 months
Health-related quality of life
Modifications of health-related quality of life in the two randomization groups
Time frame: 12 months
Body composition modifications
Body composition modifications (assessed using bioimpedance analysis) in the two randomization groups
Time frame: 12 months
Modification of Pain
Modification of pain symptoms in the two randomization groups
Time frame: 12 months
Fatigue
Modification of the fatigue symptom in the two randomization groups
Time frame: 12 months
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