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

D

Dokuz Eylül University (DEU)

Status

Not yet enrolling

Conditions

Elderly (People Aged 65 or More)

Treatments

Other: Exercise Group
Other: Action Observation Group
Other: Motor İmagery Group
Other: Combined Group (Motor Imagery + Action Observation+Exercise)

Study type

Interventional

Funder types

Other

Identifiers

NCT07016061
2024/16-20

Details and patient eligibility

About

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.

Full description

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.

Enrollment

50 estimated patients

Sex

Female

Ages

65 to 85 years old

Volunteers

Accepts Healthy Volunteers

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)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 5 patient groups

Motor İmagery Group
Active Comparator group
Description:
Motor imagery is the mental simulation of movement without actual physical execution. 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.
Treatment:
Other: Motor İmagery Group
Action Observation Group
Active Comparator group
Description:
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.
Treatment:
Other: Action Observation Group
Exercise Group
Active Comparator group
Description:
Participants will perform a standard physical exercise program. The session will last 30 minutes, including warm-up, exercise, and cool-down phases.
Treatment:
Other: Exercise Group
Combined Group (Motor Imagery + Action Observation+Exercise)
Active Comparator group
Description:
Participants will engage in a combined motor imagery and action observation program for a total of 30 minutes, incorporating elements of both interventions.
Treatment:
Other: Combined Group (Motor Imagery + Action Observation+Exercise)
Control Group
No Intervention group
Description:
Participants will not receive any intervention during the study period. After the completion of the 3-session evaluation phase, they will be given the option to participate in the exercise program if they wish.

Trial contacts and locations

1

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Central trial contact

Tolunay Keskin, Phd Student; Nursen İlçin, Professor

Data sourced from clinicaltrials.gov

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