Complex Motor Learning With Motor Imaginary

Learning Disturbance Clinical Trial

Official title:

Complex Motor Learning With Motor Imaginary

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02999516
• Other study ID #: CULaSalle
• Status: Recruiting
• Phase: N/A
• Start date: December 2016
• Est. completion date: December 2018

Study information

• Verified date: July 2018
• Source: Centro Universitario La Salle
• Contact: Daniel Muñoz, PhD
• Phone: 91401970
• Email: daniel.munoz[@]lasallecampus.es
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: December 2018
• Est. primary completion date: June 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 29 Years

Eligibility

Inclusion Criteria:

• Age between 18 and 29 years old

• Asymptomatic

Exclusion Criteria:

• Subjects with pain

• In medical treatment

• Diagnosed of any disease

Related Conditions & MeSH terms

• Learning Disorders
• Learning Disturbance

Intervention

Other:
• Motor imaginary
Participants imagine doing a motor task watching a video recording
• Non Motor imaginary
Participants watch a television documentary
• tDCS
transcranial direct current stimulation (tDCS) stimulation during 20 minutes in the motor cortex (bilaterally) at 1mA of intensity.
• tDCS sham
tDCS stimulation during 30 seconds in the motor cortex (bilaterally) at 1mA of intensity and then 19 minutes and 30 seconds without any stimulation.
• Neurofeedback
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.
• Neurofeedback sham
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.

Locations

Country	Name	City	State
Spain	Centro Superior de Estudios Universitarios La Salle	Madrid

Sponsors (1)

Lead Sponsor	Collaborator
Centro Universitario La Salle

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Time	Minutes of time when the task is learned	immediately during the intervention