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Clinical Trials in Turkey / NCT07016061
Starting soon Not applicable

Acute Effects of Motor Imagery and Action Observation in the Elderly: Single-Blind Randomized Controlled Trial

NCT07016061 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-06-15
Last updated
2025-06-11

Condition(s) studied

Elderly (People Aged 65 or More)

Investigational drug(s) / intervention(s)

Motor İmagery GroupAction Observation GroupExercise GroupCombined Group (Motor Imagery + Action Observation+Exercise)

Motor İmagery Group: Participants will engage in a motor imagery exercise program consisting of 5 minutes of warm-up, 20 minutes of motor imagery, and 5 minutes of cool-down, totaling 30 minutes. The intervention will be administered in three sessions per week for one week.

Action Observation Group: Participants will receive an action observation training program delivered by researchers, including 5 minutes of warm-up, 20 minutes of action observation, and 5 minutes of cool-down, totaling 30 minutes. The intervention will be administered in three sessions per week for one week.

Exercise Group: Participants will perform a standard physical exercise program. The session will last 30 minutes, including warm-up, exercise, and cool-down phases. The intervention will be administered in three sessions per week for one week.

Combined Group (Motor Imagery + Action Observation+Exercise): articipants will engage in a combined motor imagery and action observation program for a total of 30 minutes, incorporating elements of both interventions. The intervention will be administered in three sessions per week for one week.

Study summary

The aim of this study is to investigate the effects of acute action observation, motor imagery, exercise, and combined exercise training on parameters such as balance, reaction time, flexibility, fear of falling, cognitive status, attention, and memory in older adults.

Eligibility

Sex
FEMALE
Min age
65 Years
Max age
85 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Being aged 65 years or older, Female gender, Literate in Turkish, Scoring 21 or above on the Montreal Cognitive Assessment (MoCA) Version 7.1, No health conditions that would prevent participation in exercise Exclusion Criteria: * Presence of serious health problems that would prevent participation in the study (e.g., trauma, cancer, surgery, severe cardiac or musculoskeletal disorders) Participation in other intervention trials or observational studies during the intervention period, or initiation of a physical exercise program within 2 weeks following the intervention period Any medical condition or chronic medication use that may jeopardize safety or affect cognitive functions (e.g., neuroleptics)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Dokuz Eylül University Izmir İzmir

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07016061 on ClinicalTrials.gov ↗ ← All trials in Turkey