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Visual Stimulus-Based Cognitive-Motor Agility Exercise in Older Adults

18 juillet 2026 mis à jour par: Gulsah Sahin, Çanakkale Onsekiz Mart University

Effects of Visual Stimulus-Based Cognitive-Motor Agility Exercise on Cognitive, Psychomotor, and Functional Performance in Older Adults: A Randomized Controlled Trial

This randomized controlled trial examined the effects of adding a brief visual stimulus-based cognitive-motor agility exercise component to a multicomponent exercise program in community-dwelling older adults. Participants were randomized to either an experimental group or an active control group. Both groups participated in supervised multicomponent exercise sessions twice weekly for 8 weeks. Each session lasted 45 minutes. During the final 10 minutes of each session, the experimental group performed the visual stimulus-based cognitive-motor agility exercises, whereas the active control group performed time-matched low-intensity activities. The primary outcome was global cognitive performance assessed using the Montreal Cognitive Assessment. Secondary outcomes included hand and foot visual-motor response time, visual working memory, and functional performance.

Aperçu de l'étude

Description détaillée

This study was designed as an 8-week, parallel-group randomized controlled exercise intervention in community-dwelling older adults. The study aimed to determine whether adding a brief Light Trainer-assisted visual stimulus-based cognitive-motor agility exercise component to a multicomponent exercise program would provide additional benefits for cognitive, psychomotor, and functional performance.

After completion of baseline assessments, eligible participants were randomized to either an experimental group or an active control group. Both groups participated in supervised exercise sessions twice weekly for 8 weeks, for a total of 16 sessions. Each session lasted 45 minutes. The first 35 minutes of each session consisted of the same multicomponent exercise program in both groups. This program included light-paced walking, mobility exercises, multidirectional stepping, balance tasks, agility exercise, coordination exercises, low-resistance strengthening exercises, and functional movement combinations.

During the final 10 minutes of each session, participants in the experimental group completed visual stimulus-based cognitive-motor agility exercises using the Light Trainer system. These tasks required participants to perceive randomized visual stimuli, select an appropriate motor response, and respond as quickly and accurately as possible using hand or foot movements. The Light Trainer component included 13 repetitions of 30-second task intervals separated by 15-second rest periods. Task difficulty progressed across the 8-week intervention by increasing the number of modules from two to six and by increasing task complexity, stimulus randomness, movement direction changes, response speed requirements, and cognitive-motor demands.

Participants in the active control group completed the same 35-minute multicomponent exercise program followed by a time-matched 10-minute low-intensity activity period. These activities included supervised stretching, mobility, agility, balance, or recovery exercises and did not include visual stimulus-based response tasks, rapid decision-making, reactive agility tasks, or Light Trainer-assisted exercises.

Assessments were performed at baseline and after the 8-week intervention period. The primary outcome was global cognitive performance assessed using the Montreal Cognitive Assessment. Secondary outcomes included hand and foot visual-motor response time, visual working memory performance time and accuracy, Ten-Step Test, 30-second Chair Stand Test, 30-second Arm Curl Test, and 8-Foot Up-and-Go Test. The study was conducted in community-dwelling older adults aged 60 years or older who were able to ambulate independently and follow basic exercise and testing instructions.

Type d'étude

Interventionnel

Inscription (Réel)

41

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

      • Çanakkale, Turquie (Türkiye), 17100
        • Çanakkale Onsekiz Mart University

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Oui

La description

Inclusion Criteria:

  • Community-dwelling older adults aged 60 years or older
  • Able to ambulate independently
  • Able to understand and follow basic exercise and testing instructions
  • Montreal Cognitive Assessment score of 23 or higher
  • No health condition that would limit safe participation in exercise
  • Able to participate regularly in the 8-week exercise program

Exclusion Criteria:

  • Serious cardiovascular, neurological, orthopedic, or vestibular disease that could prevent safe participation in exercise
  • Recent surgery
  • Uncontrolled hypertension
  • Severe visual or hearing problems
  • Montreal Cognitive Assessment score below 23
  • Use of medications known to substantially affect cognitive, psychomotor, balance, or motor performance
  • Very low physical function preventing safe participation in the exercise program

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Autre
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Visual stimuli Cognitive-Motor Agility Exercise
Participants in this arm completed supervised exercise sessions twice weekly for 8 weeks. Each 45-minute session included the same 35-minute multicomponent exercise program performed by both groups, followed by 10 minutes of Light Trainer-assisted visual stimulus-based cognitive-motor agility exercise. The Light Trainer component included reactive visual-motor tasks requiring participants to respond to randomized visual stimuli using hand and foot movements.
Participants completed a supervised 35-minute multicomponent exercise program twice weekly for 8 weeks. The program included light-paced walking, mobility exercises, multidirectional stepping, balance tasks, coordination exercises, low-resistance strengthening exercises, and functional movement combinations. This component was performed by both the experimental and active control groups.
The experimental group completed a 10-minute Light Trainer-assisted visual stimulus-based cognitive-motor agility exercise component during the final part of each supervised session. Tasks required participants to perceive randomized visual stimuli, select an appropriate motor response, and respond as quickly and accurately as possible using hand or foot movements. Each session included 13 repetitions of 30-second task intervals separated by 15-second rest periods. Task difficulty progressed across 8 weeks by increasing the number of modules from two to six and increasing task complexity.
Comparateur actif: Active Control: Multicomponent Exercise With Low-Intensity Activities
Participants in this arm completed supervised exercise sessions twice weekly for 8 weeks. Each 45-minute session included the same 35-minute multicomponent exercise program performed by the experimental group, followed by 10 minutes of time-matched low-intensity activities. These activities included supervised stretching, mobility, balance, or recovery exercises and did not include visual stimulus-based response tasks, rapid decision-making, reactive agility tasks, or Light Trainer-assisted exercises.
Participants completed a supervised 35-minute multicomponent exercise program twice weekly for 8 weeks. The program included light-paced walking, mobility exercises, multidirectional stepping, balance tasks, coordination exercises, low-resistance strengthening exercises, and functional movement combinations. This component was performed by both the experimental and active control groups.
The active control group completed a 10-minute time-matched low-intensity activity period during the final part of each supervised session. These activities included stretching, mobility, balance, or recovery exercises and did not include visual stimulus-based response tasks, rapid decision-making, reactive agility tasks, or Light Trainer-assisted exercises.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Change in Montreal Cognitive Assessment Score
Délai: Baseline and 8 weeks
The Montreal Cognitive Assessment was used to assess global cognitive function. Scores range from 0 to 30, with higher scores indicating better cognitive performance. Change from baseline to 8 weeks was evaluated. The Montreal Cognitive Assessment was used to assess global cognitive function. Scores range from 0 to 30, with higher scores indicating better cognitive performance. Change from baseline to 8 weeks was evaluated.
Baseline and 8 weeks

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Change in Ten-Step Test Time
Délai: Baseline and after 8 weeks
Lower-extremity rapid stepping and agility performance were assessed using the Ten-Step Test. Participants completed 10 alternating stepping movements on a 10-cm step block as quickly as possible. Test duration was recorded in seconds. Shorter time indicates better performance.
Baseline and after 8 weeks
Change in Hand Visual-Motor Response Time
Délai: Baseline and 8 weeks
Hand visual-motor response performance was assessed using the Light Trainer system. Participants responded to randomized visual stimuli by touching illuminated modules with either hand during a 30-second task. Fastest and mean response times were recorded in seconds. Shorter response times indicate better performance.
Baseline and 8 weeks
Change in Foot Visual-Motor Response Time
Délai: Baseline and 8 weeks
Foot visual-motor response performance was assessed using the Light Trainer system. Participants responded to randomized visual stimuli by stepping on illuminated modules with either foot during a 30-second task. Fastest and mean response times were recorded in seconds. Shorter response times indicate better performance.
Baseline and 8 weeks
Change in Visual Working Memory Performance Time
Délai: Baseline and 8 weeks
Visual working memory response time was assessed using the memory mode of the Light Trainer system. Participants memorized the color and position of illuminated modules and then identified the module corresponding to a target color. Fastest times were recorded in seconds, with shorter values indicating better visual working memory performance. Change from baseline to 8 weeks was evaluated.
Baseline and 8 weeks
Change in Visual Working Memory Accuracy
Délai: Baseline and 8 weeks
Visual working memory accuracy was assessed using the memory mode of the Light Trainer system. Participants memorized the color and position of illuminated modules and then identified the module corresponding to a target color. Accuracy was expressed as the device-recorded percentage of correct responses across all trials and ranged from 0% to 100%, with higher values indicating better visual working memory performance. Change from baseline to 8 weeks was evaluated.
Baseline and 8 weeks
Change in 30-Second Chair Stand Test Performance
Délai: Baseline and 8 weeks
Lower-body functional strength was assessed using the 30-second Chair Stand Test. Participants were instructed to stand up fully and sit down as many times as possible within 30 seconds. The total number of correctly completed repetitions was recorded. Higher repetition count indicates better performance.
Baseline and 8 weeks
Change in 30-Second Arm Curl Test Performance
Délai: Baseline and 8 weeks
Upper-body functional strength was assessed using the 30-second Arm Curl Test. Participants performed as many controlled elbow flexion-extension repetitions as possible within 30 seconds while seated. The test was performed separately for the right and left arms. Higher repetition count indicates better performance.
Baseline and 8 weeks
Change in 8-Foot Up-and-Go Test Time
Délai: Baseline and 8 weeks
Functional mobility, agility, and dynamic balance were assessed using the 8-Foot Up-and-Go Test. Participants rose from a chair, walked around a marker placed 2.44 meters away, returned to the chair, and sat down again. Test duration was recorded in seconds. Shorter time indicates better performance.
Baseline and 8 weeks

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

1 avril 2026

Achèvement primaire (Réel)

8 juin 2026

Achèvement de l'étude (Réel)

8 juin 2026

Dates d'inscription aux études

Première soumission

15 juillet 2026

Première soumission répondant aux critères de contrôle qualité

15 juillet 2026

Première publication (Réel)

20 juillet 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

21 juillet 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

18 juillet 2026

Dernière vérification

1 juillet 2026

Plus d'information

Termes liés à cette étude

Termes MeSH pertinents supplémentaires

Autres numéros d'identification d'étude

  • 2026-YONP-0051

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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