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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02999516
Other study ID # CULaSalle
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
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
Health authority
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

Study Design


Related Conditions & MeSH terms


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
See also
  Status Clinical Trial Phase
Not yet recruiting NCT06212726 - RTL Concussion Communication N/A