Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07016061

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

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.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

65 year–85 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Previous studies investigating motor imagery and action observation training have examined their long-term effects in both young and older adults. Existing evidence regarding the benefits of exercise training indicates positive effects in both populations. However, the number of studies focusing on the acute effects of motor imagery and action observation training in the literature is very limited. Individuals who meet the inclusion criteria will be randomly assigned-using the Research Randomizer application-into five groups: motor imagery, action observation, exercise, combined exercise, and control group. A total of 50 participants, with 10 individuals in each group, will be included in the study. Assessments will be conducted before and after the intervention.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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)

Treatment and study plan

Motor İmagery Group

Other

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

Other

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

Other

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)

Other

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.

Primary outcomes

  1. Timed Up and Go (TUG) Test

    Time frame: 2 weeks

    The Timed Up and Go (TUG) test is a simple and widely used clinical test to assess functional mobility, balance, and fall risk in older adults. It measures the time it takes for an individual to stand up from a chair, walk three meters, turn around, walk back, and sit down.

Secondary outcomes

  1. Functional Reach Test (FRT)

    Time frame: 2 weeks

    The Functional Reach Test (FRT) is a clinical assessment tool used to evaluate dynamic balance and stability. It measures the maximum distance an individual can reach forward beyond arm's length while standing in a fixed position without losing balance or taking a step.

  2. 10-Meter Walk Test (10MWT)

    Time frame: 2 weeks

    The 10-Meter Walk Test (10MWT) is a standardized assessment used to measure walking speed over a short distance. It evaluates functional mobility, gait performance, and lower extremity motor function by recording the time taken to walk a distance of 10 meters at a comfortable or maximum pace.

  3. Computerized Serial Reaction Time Test (SRTT)

    Time frame: 2 weeks

    The Computerized Serial Reaction Time Test (SRTT) is a cognitive-motor task used to assess implicit motor learning, reaction time, and attention. In this test, participants respond as quickly and accurately as possible to visual stimuli that appear in a specific sequence on a computer screen, allowing for the measurement of both response speed and learning patterns

  4. Five Times Sit-to-Stand Test (FTSST)

    Time frame: 2 weeks

    The Five Times Sit-to-Stand Test (FTSST) is a simple and reliable clinical assessment used to evaluate lower limb muscle strength, functional mobility, and fall risk. It measures the time it takes for an individual to rise from a chair and sit back down five times as quickly as possible without using their arms for support

  5. Back Scratch Test

    Time frame: 2 weeks

    The Back Scratch Test is a flexibility assessment used to measure the range of motion and flexibility of the upper body, particularly the shoulders. It involves reaching one hand over the shoulder and the other behind the back to see how close the fingers can come to each other, or whether they overlap.

  6. Falls Efficacy Scale International, FES-I

    Time frame: 2 weeks

    The Falls Efficacy Scale-International (FES-I) is a validated questionnaire designed to assess fear of falling in older adults. It measures the level of concern individuals have about falling during a range of daily activities, both inside and outside the home. Higher scores indicate greater fear of falling.

  7. Montreal Cognitive Assessment (MoCA)

    Time frame: 2 weeks

    The Montreal Cognitive Assessment (MoCA) is a widely used screening tool designed to detect mild cognitive impairment. It assesses various cognitive domains including attention, executive functions, memory, language, visuospatial skills, and orientation. The test provides a total score out of 30, with higher scores indicating better cognitive performance.

  8. Trail Making Test

    Time frame: 2 weeks

    The Trail Making Test (TMT) is a neuropsychological assessment used to evaluate visual attention, processing speed, and executive function. It consists of two parts: Part A requires connecting numbered dots in sequence, while Part B involves alternating between numbers and letters in order. The time taken to complete each part is recorded, with longer times indicating potential cognitive impairment

  9. Verbal Memory Processes Test

    Time frame: 2 weeks

    The Verbal Memory Processes Test is a neuropsychological assessment designed to evaluate various aspects of verbal memory, including encoding, storage, and retrieval of verbal information. It typically involves tasks such as recalling word lists, story recall, or recognizing verbal stimuli to assess immediate and delayed memory performance

Study contacts

Contact information is provided by the study sponsor or research team.

Nursen İlçin, Professor

CONTACT

[email protected]

+90 0505 525 1313

Tolunay Keskin, Phd Student

CONTACT

[email protected]

+905367773239

Sponsors and collaborators

Lead sponsor

Dokuz Eylul University

Other

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Jun 11, 2025
Registry last updated
Jun 11, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.