- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02999516
Complex Motor Learning With Motor Imaginary
July 30, 2018 updated by: Daniel Muñoz-Garcia, Centro Universitario La Salle
Subjects participate in a motor learning training with a special bicycle.
The experimental group proceed with 15 minutes of physical training with the bicycle and 15 minutes of rest where they use motor imaginary.
The control group proceed equal except for the motor imaginary intervention.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
Subjects participate in a motor learning training with a special bicycle. The experimental group proceed with 15 minutes of physical training with the bicycle and 15 minutes of rest where they use motor imaginary. The control group proceed equal except for the motor imaginary intervention.
Participants will be controlled for vestibular system previous participation.
Study Type
Interventional
Enrollment (Anticipated)
60
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
-
-
-
Madrid, Spain, 28660
- Recruiting
- Centro Superior de Estudios Universitarios La Salle
-
Contact:
- Daniel Muñoz
- Phone Number: 689049424
- Email: daniel.munoz@lasallecampus.es
-
Principal Investigator:
- Daniel Muñoz-Garcia, PhD
-
-
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
14 years to 25 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Age between 18 and 29 years old
- Asymptomatic
Exclusion Criteria:
- Subjects with pain
- In medical treatment
- Diagnosed of any disease
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: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Motor imaginary
Intervention with Motor imaginary with video
|
Participants imagine doing a motor task watching a video recording
|
|
Experimental: Non Motor imaginary
Intervention with Rest without motor imaginary
|
Participants watch a television documentary
|
|
Experimental: tDCS
tDCS stimulation during 20 minutes in the motor cortex.
|
transcranial direct current stimulation (tDCS) stimulation during 20 minutes in the motor cortex (bilaterally) at 1mA of intensity.
|
|
Sham Comparator: tDCS sham
tDCS stimulation during 30 seconds in the motor cortex and then 19 minutes and 30 seconds without any stimulation.
|
tDCS stimulation during 30 seconds in the motor cortex (bilaterally) at 1mA of intensity and then 19 minutes and 30 seconds without any stimulation.
|
|
Experimental: Neurofeedback
EEG monitoring in real time with positive feedback in the computer screen when participants motor cortex is activated.
|
EEG monitoring of the cerebral cortex in real time with positive feedback in the computer screen when participants motor cortex is activated.
The positive feedback consist in an object that moves to the top of the screen when activation occurs in the motor cortex.
This task last during 20 minutes.
|
|
Sham Comparator: Neurofeedback sham
EEG monitoring in real time with randomized feedback in the computer screen despite the motor cortex activation.
|
EEG monitoring of the cerebral cortex in real time with randomized feedback in the computer screen despite motor cortex activation.
The positive feedback consist in an object that moves to the top of the screen in a randomized time.
This task last during 20 minutes.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Time
Time Frame: immediately during the intervention
|
Minutes of time when the task is learned
|
immediately during the intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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
December 1, 2016
Primary Completion (Actual)
June 1, 2018
Study Completion (Anticipated)
December 1, 2018
Study Registration Dates
First Submitted
November 24, 2016
First Submitted That Met QC Criteria
December 19, 2016
First Posted (Estimate)
December 21, 2016
Study Record Updates
Last Update Posted (Actual)
July 31, 2018
Last Update Submitted That Met QC Criteria
July 30, 2018
Last Verified
July 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CULaSalle
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
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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