- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05669131
Does Motor Imagery Training Enhance Control of Movement in Older Adults?
Motor Imagery Training, Force Steadiness and Neural Drive
The goal of this clinical trial is learn about motor imagery training (i.e. imagining a task) with healthy older adults. The main question this clinical trial aims to answer is:
• Will imagining a task improve control of force during an elbow flexion muscle contraction in healthy older adults?
Participants will:
- Complete questionaries about general activity levels and ability to imagine tasks
- Perform either motor imagery training or watch a documentary
- Perform maximal and submaximal elbow flexion contractions
Researchers will compare the motor imagery training with the control group to see if control of force is improved in the motor imagery training group.
Study Overview
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Jennifer Jakobi, PhD
- Phone Number: 250-807-9884
- Email: jennifer.jakobi@ubc.ca
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Healthy older adults aged 65 to 90 years old
Exclusion Criteria:
- have had an injury or orthopaedic surgery to the arm or shoulder in the prior 6 months
- are involved in high levels of upper-body strength training
- have history of training in fine motor tasks (i.e., musicians)
- have a history of MIT
- have systemic diseases and/or nerve damage affecting neuromuscular function
- have severe cognitive impairment
- are unable to read or speak English fluently
- are left hand dominant
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Motor Imagery Training
Participants will do motor imagery training in 5 minute blocks for a total of 20 minutes.
|
Participants imagine themselves through their own eyes performing submaximal elbow flexion contractions.
|
|
No Intervention: Control
Participants will watch a documentary in 5 minute blocks for a total of 20 minutes.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Force steadiness
Time Frame: Within one session: Change from baseline (immediately before session) to 20 minutes after the session
|
Measured as the the coefficient in variation of force
|
Within one session: Change from baseline (immediately before session) to 20 minutes after the session
|
|
Corticospinal excitability
Time Frame: Within one session: Change from baseline (immediately before session) to 20 minutes after the session
|
Measured as the peak-to-peak amplitude of a motor evoked potential
|
Within one session: Change from baseline (immediately before session) to 20 minutes after the session
|
|
Common synaptic input
Time Frame: Within one session: Change from baseline (immediately before session) to 20 minutes after the session
|
Estimated from motor unit discharge times.
|
Within one session: Change from baseline (immediately before session) to 20 minutes after the session
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Maximal elbow flexion force
Time Frame: Within one session: Change from baseline (immediately before session) to 20 minutes after the session
|
The total amount of force produced during a maximal contraction
|
Within one session: Change from baseline (immediately before session) to 20 minutes after the session
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Jennifer Jakobi, PhD, University of British Columbia- Okanagan
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
- MIT&ForceSteadiness
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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