Visual Stimulus-Based Cognitive-Motor Agility Exercise in Older Adults
Effects of Visual Stimulus-Based Cognitive-Motor Agility Exercise on Cognitive, Psychomotor, and Functional Performance in Older Adults: A Randomized Controlled Trial
1 other identifier
interventional
41
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 8, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
June 8, 2026
CompletedFirst Submitted
Initial submission to the registry
July 15, 2026
CompletedFirst Posted
Study publicly available on registry
July 20, 2026
CompletedJuly 21, 2026
July 1, 2026
2 months
July 15, 2026
July 18, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Montreal Cognitive Assessment Score
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
Secondary Outcomes (8)
Change in Hand Visual-Motor Response Time
Baseline and 8 weeks
Change in Foot Visual-Motor Response Time
Baseline and 8 weeks
Change in Visual Working Memory Performance Time
Baseline and 8 weeks
Change in Visual Working Memory Accuracy
Baseline and 8 weeks
Change in Ten-Step Test Time
Baseline and after 8 weeks
- +3 more secondary outcomes
Study Arms (2)
Visual stimuli Cognitive-Motor Agility Exercise
EXPERIMENTALParticipants 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.
Active Control: Multicomponent Exercise With Low-Intensity Activities
ACTIVE COMPARATORParticipants 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.
Interventions
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.
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.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Canakkale Onsekiz Mart University
Çanakkale, 17100, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor, Faculty of Sports Sciences, Çanakkale Onsekiz Mart University
Study Record Dates
First Submitted
July 15, 2026
First Posted
July 20, 2026
Study Start
April 1, 2026
Primary Completion
June 8, 2026
Study Completion
June 8, 2026
Last Updated
July 21, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will not share