Evaluation of the Hypoalgesic Effects of Transcranial Direct Current (tDCS) in Healthy Subjects
NCT ID: NCT04127253
Last Updated: 2019-10-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
45 participants
INTERVENTIONAL
2020-01-01
2020-07-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Transcranial Direct Current Stimulation (tDCS) in the Primary Motor Cortex in Healthy Individuals
NCT04148547
Impact of Transcranial Direct Current Stimulation Intensity on Leg Muscle Fatigability in Healthy Adults
NCT04321304
Transcranial Direct Current Stimulation for Chronic Low Back Pain
NCT02768129
Intensity-Dependent Effects of 4-week Transcranial Direct Current Stimulation on Motor Learning in Healthy Young Adults
NCT07089069
Long-term Effect of tDCS in Patients With Disorders of Consciousness
NCT03114397
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
BASIC_SCIENCE
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
transcranial direct current plus Brain training tools
20 minutes of transcranial direct current stimulation along with the application of motor imagery and action observation
Sooma transcranial direct current stimulation device plus Brain training tools
This group will carry out an observation training of actions and motor imagery in combination with the stimulation of the transcranial direct current.
Placebo transcranial direct current plus Brain training tools
A placebo intervention of direct transcranial stimulation being active during 15 seconds and then it will be turned off the rest of the time until 20 minutes. This group will also carry out the training of action observation and motor imagery.
Placebo Sooma transcranial direct current stimulation deviceplus Brain training tools
This group will carry out an observation training of actions and motor imagery in combination with the placebo stimulation of the transcranial direct current, where it will be acrtivo during 15 seconds and then it will be turned off during the rest of the intervention.
Brain training tools in isolation
This group will act as a control, they will only carry out the training of action observation and motor imagery.
Brain training tools in isolation
This group will act as a control, they will only carry out the training of action observation and motor imagery.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Sooma transcranial direct current stimulation device plus Brain training tools
This group will carry out an observation training of actions and motor imagery in combination with the stimulation of the transcranial direct current.
Placebo Sooma transcranial direct current stimulation deviceplus Brain training tools
This group will carry out an observation training of actions and motor imagery in combination with the placebo stimulation of the transcranial direct current, where it will be acrtivo during 15 seconds and then it will be turned off during the rest of the intervention.
Brain training tools in isolation
This group will act as a control, they will only carry out the training of action observation and motor imagery.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* men and women aged 18 to 65 years
Exclusion Criteria
* nausea
* headache
* pregnant woman
* use of painkillers in the last twenty four hours
* presence of metal inside the head
* pacemaker
* wound on the area of electrodes' application
* drugs consumer
* recent application of transcranial direct stimulation
* psychiatric disease who lead the subject to a misunderstand of the study
18 Years
65 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Centro Universitario La Salle
OTHER
Universidad Autonoma de Madrid
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Roy La Touche Arbizu
Principal Investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
CSEU La Salle
Madrid, , Spain
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
uammadrid
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.