- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04018196
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".
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Saint-Étienne, France
- CHU Saint-Etienne
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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:
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:
|
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:
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:
|
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
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 18CH128
- 2018-A02365-50 (Other Identifier: ANSM)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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