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Effects of tDCS in M1 and DLPFC on Pain Processing in Healthy Volunteers

U

Universidad Rey Juan Carlos

Status

Completed

Conditions

Pain Processing in Healthy Volunteers

Treatments

Device: Transcranial direct current stimulation

Study type

Interventional

Funder types

Other

Identifiers

NCT04432363
30012020204820

Details and patient eligibility

About

The purpose of this study is to evaluate the effects of a direct current applied transcranial over two cortical areas on healthy volunteers' pain processing.

Enrollment

30 patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age between 18 and 40 years
  • Comprehension of the study tasks

Exclusion criteria

  • Presence of pain in the previous 6 months
  • Altered sensitivity in the tested regions
  • Intolerance to electrotherapy
  • Presence of pacemakers or any other implanted device
  • Ulcers or scars in the skin at the location of the electrodes
  • Treatment with direct current stimulation within one week
  • Pregnancy
  • Frequent headaches
  • Epilepsy
  • History of neuromuscular disease
  • Previous clinical history of cervical surgery
  • Injuries or surgery affecting the upper limb
  • diabetes mellitus
  • Cardiovascular diseases
  • Oncological diseases
  • Consumption of analgesic drugs 7 days before the study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Quadruple Blind

30 participants in 3 patient groups

M1 stimulation
Active Comparator group
Description:
A 20 minutes 1mA direct current stimulation over left M1.
Treatment:
Device: Transcranial direct current stimulation
M1+DLPFC stimulation
Active Comparator group
Description:
A 20 minutes 1mA direct current stimulation over left M1 and 1mA direct current stimulation over left DLPFC.
Treatment:
Device: Transcranial direct current stimulation
Sham stimulation
Sham Comparator group
Description:
A 20 minutes sham stimulation where the device only is working first 30s and last 30s of the intervention and have a 10 seconds fade out in intensity at each ramp.
Treatment:
Device: Transcranial direct current stimulation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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