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Clinical Trials in Portugal / NCT07411833
Enrolling by invitation Not applicable

tDCS for Stress and Burnout in Higher Education

NCT07411833 · tracked via the Priya Life Science Portugal tracker
Phase
Not applicable
Started
2026-02-18
Last updated
2026-02-20

Condition(s) studied

Occupational Stress or Workplace StressBurnout SyndromeBurnout

Investigational drug(s) / intervention(s)

Transcranial Direct Current Stimulation (tDCS)Sham Transcranial Direct Current Stimulation

Transcranial Direct Current Stimulation (tDCS): Active transcranial direct current stimulation will be administered using the PlatoWork tDCS Headset device, developed by PlatoScience, with 20-minute stimulation sessions. The intervention consists of 10 sessions distributed over 4 weeks, with the anode electrode positioned over the left prefrontal cortex (F3 position) and cathode electrode over the right prefrontal cortex (F4 position).

Sham Transcranial Direct Current Stimulation: Sham transcranial direct current stimulation will be administered using the PlatoWork tDCS Headset device configured in sham mode. The sham procedure mimics the active tDCS intervention in all aspects (electrode placement, session duration, device operation) but does not deliver therapeutic stimulation. This serves as a placebo control to assess the specific effects of active tDCS.

Study summary

The goal of this clinical trial is to evaluate if transcranial direct current stimulation (tDCS) works to reduce occupational stress and burnout in university professors. The main questions it aims to answer are:

Does tDCS reduce levels of occupational stress in university professors?

Does tDCS reduce burnout levels in university professors?

Researchers will compare active tDCS to a sham stimulation (a look-alike procedure that contains no active stimulation) and a control group to see if tDCS effectively reduces stress and burnout.

Participants will:

* Complete questionnaires assessing stress and burnout levels before the intervention
* Complete follow-up assessments immediately after the intervention and 5 weeks later

During intervention, participans of active tDCS and Sham gruops will:

* Receive 10 sessions of tDCS over 4 weeks (excluding weekends), 20 minutes each

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * University staff in active functions * Age equal to or greater than 18 years * Availability for the 10 intervention sessions and subsequent assessments * Voluntary participation with informed consent Exclusion Criteria: * Contraindications for tDCS, namely pregnancy, history of seizures or epilepsy, neurological or anatomical contraindications, metal implants or brain surgeries * Initiation or change in prescription of psychotropic drugs or anticonvulsants in the last 3 months * Recent active psychotherapy * Diagnosis of psychiatric condition in the last year

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Egas Moniz School of Health and Science Almada Setúbal District

More Egas Moniz - Cooperativa de Ensino Superior, CRL trials in Portugal

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07411833 on ClinicalTrials.gov ↗ ← All trials in Portugal