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Tests an exercise program for memory-related mild cognitive impairment

Tests a combined-task exercise program in adults with mild memory-related cognitive impairment.

Plain-language title generated from the registry record
Registry title: Impact of a Multicomponent Exercise Program on Cognitive and Functional Outcomes in Patients With Mild Cognitive Impairment

Key facts

Where
Pátrai, GreeceSee the site

Where in Greece

  • Department of Physiotherapy, University of PatrasPátrai, GreeceTaking people

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  2. Are travel costs paid?
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  4. What happens if I want to stop?
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Trial details

Who runs it
University of Patras
Trial code
NCT07334392
Record updated
12 January 2026
Original description
The goal of this randomised clinical trial is to investigate the effectiveness of an innovative therapeutic exercise program emphasizing in dual-task exercises in people with amnestic Mild Cognitive Impairment. The main questions it aims to answer are:Read full original descriptionShow less

Effectiveness of an Innovative Therapeutic Exercise Program on Physical and Cognitive Function in Mild Cognitive Impairment Due to Alzheimer's Disease

The goal of this randomised clinical trial is to investigate the effectiveness of an innovative therapeutic exercise program emphasizing in dual-task exercises in people with amnestic Mild Cognitive Impairment. The main questions it aims to answer are:

Does the innovative therapeutic exercise program improve gait and balance? Does the innovative therapeutic exercise program improve cognition?

Researchers will compare the innovative therapeutic exercise program emphasizing in dual-task exercises to a therapeutic exercise program without emphasizing in dual-task exercises and to a control group (given instruction about the benefits of exercise).

Participants will:

* Perform the exercise program twice a week for three months. * Will be assessed before and after the intervention. * Will record The Borg Scale of Perceived Exertion every second week to monitor and assess the progression of exercise intensity.

Inclusion: individuals > 50 years old; people with confirmed cognitive impairment, as evidenced by values within normal limits on the Montreal Cognitive Assessment test (MOCA ) >20; stable medication in the last month; independent walking.

Exclusion: people who have had recent surgery; people with dementia; people suffering from chronic mental illness (e.g. schizophrenia, bipolar disorder); people suffering from a neurological disorder or injuries (e.g. multiple sclerosis, Parkinson's, traumatic brain injury); people with clinical depression (as determined by the Neuropsychiatric Inventory (NPI) assessment and medical diagnosis); people with insufficient knowledge of the Greek language.

ClinicalTrials.gov NCT07334392