Rhythmic Exercise in Older Adults With Cognitive Impairment

NCT ID: NCT06130878

Last Updated: 2025-04-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

96 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-01-08

Study Completion Date

2024-04-05

Brief Summary

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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.

Detailed Description

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Conditions

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Cognitive Impairment

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Caregivers Investigators Outcome Assessors

Study Groups

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Control Group (CG)

This group does not receive any treatment.

Group Type NO_INTERVENTION

No interventions assigned to this group

EXPERIMENTAL GROUP (EG)

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

Group Type EXPERIMENTAL

Rhythmic exercise

Intervention Type OTHER

A multicomponent rhythmic physical training will be carried out, with a predominance of QMT, following the principles of "Animal Flow" \[46\] and including the following components: wrist mobilizations; activations; specific stretching positions; special locomotor movements or "traveling forms"; interruptions and transitions with dynamic movements and choreographic sequences of "Flow". Aspects related to the control of intensity, volume and progression strategy have yet to be defined.

Interventions

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Rhythmic exercise

A multicomponent rhythmic physical training will be carried out, with a predominance of QMT, following the principles of "Animal Flow" \[46\] and including the following components: wrist mobilizations; activations; specific stretching positions; special locomotor movements or "traveling forms"; interruptions and transitions with dynamic movements and choreographic sequences of "Flow". Aspects related to the control of intensity, volume and progression strategy have yet to be defined.

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Jaén

OTHER

Sponsor Role lead

Responsible Party

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Agustín Aibar Almazán

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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U.E.D. Virgen de la Capilla

Jaén, , Spain

Site Status

Countries

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Spain

Other Identifiers

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-UJAEN

Identifier Type: -

Identifier Source: org_study_id

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