Rhythmic Exercise in Older Adults With Cognitive Impairment

University of Jaén

Status: Completed

Conditions: Cognitive Impairment

Treatments: Other: Rhythmic exercise

Study type: Interventional

Funder types: Other

Identifiers

NCT06130878

-UJAEN

Details and patient eligibility

About

Rhythmic physical exercise is a very promising non-pharmaceutical tool to prevent or reduce cognitive decline that occurs in people sixty years of age or older. The main objective is to determine the effect of a rhythmic exercise program on the physical, mental and cognitive performance of older adults with cognitive impairment. The main variables of the study will be: global cognitive function evaluated by the Mini Mental State Examination (MMSE) and the Montreal Cognitive Assessment (MoCA); attention and executive functions evaluated using the Trail Making Test (TMT) part A and B. As secondary variables, the functional abilities evaluated using the Senior Fitness Test (SFT) will be taken into account. Additionally, sociodemographic variables and variables related to health status will be evaluated. These will take into account the quality of sleep evaluated with the Pittsburgh index, the nutritional status evaluated using the Mini Nutritional Assessment-Short Form (MNA-SF) scale, and the Stress and anxiety levels will be assessed using the Depression Anxiety Stress Scales-21 (DASS-21). All variables will be evaluated before the intervention and after it. After the intervention, it is expected that the exercise program will improve the neurocognitive performance, as well as the functional and psychological abilities of older adults.

Enrollment: 96 patients

Sex: All

Ages: 60+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Be 60 years old or older
• Do not participate in any physical exercise program
• Present physical autonomy to participate in the physical activities required by the study.
• Present scores of > 25 on the MMSE
• Present current affiliation to the social health security system.
• Sign the informed consent
• Understand the instructions, programs and protocols of this project.
• Complete more than 90% of the intervention with exercise.

Exclusion criteria

• Present medical contraindications for performing physical tests.
• Present diseases that limit cognitive performance and physical activity.
• Present vestibular diseases
• Present rheumatological diseases that can be exacerbated by stress articulate.
• Refusing to sign the informed consent

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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96 participants in 2 patient groups

Control Group (CG)

No Intervention group

Description:

This group does not receive any treatment.

EXPERIMENTAL GROUP (EG)

Experimental group

Description:

People assigned to this group will undergo a 12-week physical training intervention

Treatment:

Other: Rhythmic exercise