Effects of Motor Imagery on Motor Learning and Motor Retention in Octogenarian. (IMAge-8)

Effects of Motor Imagery on Motor Learning and Motor Retention in Octogenarian "IMAge-8".

Aging is associated with impairments in cognitive function, particularly motor learning and memorizing, impacting functional capacities. Older adults are still able to learn new skills but at a slower rate, and they forget quickly the new-learned skill because of an alteration in motor memory. Motor imagery, which is a mental simulation of an action without actual execution, has been demonstrated to improve performance in young adults and stabilize performance after a short break in older adults. However, in very old adults (>80 years old) for whom the decline in motor and cognitive functions is greater, it is unknown whether motor imagery training during a short break is still efficient. Previous studies on old adults were performed on upper limb muscles. Because aging differentially affects upper and lower limb muscles, the present study will aim to explore the effects of motor imagery on motor memorizing in both upper and lower limb muscles.

Study Overview

Detailed Description

The primary purpose is to evaluate the effectiveness of motor imagery to improve the performance of very old people (> 80 years) through learning a task of the upper limbs.

Study Type

Interventional

Enrollment (Actual)

84

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Saint-Étienne, France
        • CHU Saint-Etienne

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

80 years and older (Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Being part of the Proof cohort
  • Signed written consent form
  • Affiliated to social security

Exclusion Criteria:

  • Pathology or chirurgical intervention causing locomotor disorder
  • Neurological or psychic pathology
  • Use psychotropic drugs
  • Mini-Mental State Examination (MMSE) < 20

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental group
Patient aged over 80 years old will be included. They will have motor imagery training of manual task and motor imagery training of motor task.
They will have a motor imagery as training manual task for 30 minutes. They will have 3 tests for performing manual task before training (pretest) and after training (post-test).
Other Names:
  • Nine Hole Peg Test (NHPT)

They will have a motor imagery as training motor task for 30 minutes before performing this task.

They will have 3 tests for performing motor task before training (pretest) and after training (post-test).

Other Names:
  • hopscotch
Active Comparator: Control group
Patient aged over 80 years old will be included. They will have emotionally neutral film as training of manual task and emotionally neutral film as training of motor task.

They will have to watch an emotionally neutral as training manual task for 30 minutes before performing this task.

They will have 3 tests for performing manual task before training (pretest) and after training (post-test).

Other Names:
  • Nine Hole Peg Test (NHPT)

They will have to watch an emotionally neutral as training motor task for 30 minutes before performing this task.

They will have 3 tests for performing motor task before training (pretest) and after training (post-test).

Other Names:
  • hopscotch

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Performance at the manual task (Nine Hole Peg Test (NHPT)) (s)
Time Frame: Day: 0
Comparison of performance at the manual task (Nine Hole Peg Test (NHPT)) results in post-test between experimental and control group. Measured in seconds when performing manual task.
Day: 0

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Performance at the motor task (s)
Time Frame: Day: 7

Comparison of performance at the motor task (hopscotch) results pre-test and post-test between experimental and control group.

Measured in number of tests.

Day: 7
Learning capacity of manual task (Nine Hole Peg Test (NHPT))
Time Frame: Day: 0

Comparison of manual task (Nine Hole Peg Test (NHPT)) results between pre-test and post-test.

Measured in seconds.

Day: 0
Learning capacity of motor task (hopscotch)
Time Frame: Day: 7
Comparison of motor task (hopscotch) results between pre-test and post-test. Measured in number of tests.
Day: 7
Test of 6 minutes walking (m)
Time Frame: Day: 0
Comparison of test of 6 minutes walking results between experimental and control group. Measured in meters.
Day: 0
Test of Get-up-and-Go (s)
Time Frame: Day: 0

Comparison of test of Get-up-and-Go results between experimental and control group.

For test of Get-up-and-Go, participants will be asked to stand from a seated position, walk 3 meters at their usual pace, turn around, walk back to the chair, and sit down.

Measured in seconds when performing test.

Day: 0

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 9, 2019

Primary Completion (Actual)

February 14, 2022

Study Completion (Actual)

February 15, 2022

Study Registration Dates

First Submitted

July 11, 2019

First Submitted That Met QC Criteria

July 11, 2019

First Posted (Actual)

July 12, 2019

Study Record Updates

Last Update Posted (Actual)

March 15, 2022

Last Update Submitted That Met QC Criteria

March 1, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 18CH128
  • 2018-A02365-50 (Other Identifier: ANSM)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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