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Clinical Trials/NCT03931512
NCT03931512CompletedNot Applicable

Transcranial Direct Current Stimulation Effects on Motor Learning and Motor Control in Healthy Subjetcs

Centro Universitario La Salle2 sites in 1 country33 target enrollmentStarted: April 30, 2019Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
33
Locations
2
Primary Endpoint
Change in trained manual dexterity of the dominant hand

Study Overview

Brief Summary

Clinical Trial with two groups, transcranial direct current stimulation aplication and sham; triple blinded. The protocol is applied 5 consecutive days during the training of a manual dexterity task. Manual dexterity and somatosensory variables are measured pre intervention, post one day of intervention, post 5 days of intervention, and 5 days after finish the intervention.

Detailed Description

Clinical Trial with two groups, transcranial direct current stimulation aplication (1 mA ) and sham (ramp up and down of 30 seconds in total) . Bouth interventions will last 20 minutes; at the same time of the aplication bouth are going to train the manual dexterity with Purdue Pegboard Test.

This protocol is applied 5 consecutive days, also it have a follow up of 5 days more.

It is triple blinded. Manual dexterity and somatosensory variables are measured pre intervention, post one day of intervention, post 5 days of intervention, and 5 days after finish the intervention.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 35 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • healthy volunteers

Exclusion Criteria

  • metal or skin lesions on the head
  • brain stimulation in the last 6 months
  • family history of epilepsy or seizures
  • pacemaker or any cardiac involvement
  • inability to understand or execute the task
  • taking drugs that may influence cognition
  • pregnancy

Outcomes

Primary Outcomes

Change in trained manual dexterity of the dominant hand

Time Frame: pre intervention, post one day of intervention, post 5 days of intervention, 5 days after finish the intervention

One hand manual dexterity is measured with Perdue Pegboard test

Secondary Outcomes

  • Changes in two points discrimination(pre intervention, post one day of intervention, post 5 days of intervention, 5 days after finish the intervention)
  • Sleep Quality(5 days after finish the intervention)
  • Changes in trained manual dexterity of bouth hands(pre intervention, post one day of intervention, post 5 days of intervention, 5 days after finish the intervention)
  • Changes in maximal isometric hand grip force(pre intervention, post one day of intervention, post 5 days of intervention, 5 days after finish the intervention)
  • Physical activity(5 days after finish the intervention)
  • Changes in nontrained manual dexterity of bouth hands(pre intervention, post one day of intervention, post 5 days of intervention, 5 days after finish the intervention)
  • Changes in pain detection treshold(pre intervention, post one day of intervention, post 5 days of intervention, 5 days after finish the intervention)
  • Changes in nontrained manual dexterity of the dominant hand(pre intervention, post one day of intervention, post 5 days of intervention, 5 days after finish the intervention)
  • Changes in pressure detection treshold(pre intervention, post one day of intervention, post 5 days of intervention, 5 days after finish the intervention)

Investigators

Sponsor
Centro Universitario La Salle
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Laura Flix Díez

Physiotherapyst, Msc

Centro Universitario La Salle

Study Sites (2)

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