NCT07411833

Brief 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

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
2mo left

Started Feb 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress58%
Feb 2026Aug 2026

First Submitted

Initial submission to the registry

February 9, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

February 17, 2026

Completed
1 day until next milestone

Study Start

First participant enrolled

February 18, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2026

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2026

Last Updated

February 20, 2026

Status Verified

February 1, 2026

Enrollment Period

3 months

First QC Date

February 9, 2026

Last Update Submit

February 18, 2026

Conditions

Keywords

Occupational StressBurnoutTranscranial Direct Current StimulationtDCSHigher EducationNeuromodulationNon-invasive brain stimulationHigher Education Staff

Outcome Measures

Primary Outcomes (2)

  • Change in Burnout levels measured by the Burnout Assessment Tool (BAT-12)

    The BAT-12 assesses burnout in four dimensions (Exhaustion, Mental Distance, Cognitive and Emotional Impairment Control) with 12 items on a 5-point Likert scale (1 = Never; 5 = Always). Higher scores indicate greater burnout. The Portuguese version presents good internal consistency with α=0.85.

    Baseline (pre-intervention), immediately after intervention completion (approximately 4 weeks), and at 5-week follow-up (approximately 9 weeks from baseline)

  • Change in Perceived Stress measured by the Perceived Stress Scale (PSS)

    The PSS assesses perceived stress in recent weeks. Contains 10 items on a 5-point Likert scale (0 = Never; 4 = Very frequently). The Portuguese version presents good internal consistency with α=0.79.

    Baseline (pre-intervention), immediately after intervention completion (approximately 4 weeks), and at 5-week follow-up (approximately 9 weeks from baseline)

Study Arms (3)

Active tDCS

EXPERIMENTAL

Participants will receive 10 sessions of active transcranial direct current stimulation (tDCS) over 4 weeks (excluding weekends), 20 minutes each session. The current intensity will be 1.2 mA, with the anode electrode positioned over the left prefrontal cortex (F3 position) and cathode electrode over the right prefrontal cortex (F4 position). Sessions will be conducted using the PlatoWork tDCS Headset device. There will be no less than 24 hours and no more than 72 hours between sessions.

Device: Transcranial Direct Current Stimulation (tDCS)

Sham tDCS

SHAM COMPARATOR

Participants will receive 10 sessions of sham transcranial direct current stimulation over 4 weeks (excluding weekends), 20 minutes each session. The sham condition will mimic the active tDCS intervention but without delivering therapeutic stimulation. Sessions will be conducted using the PlatoWork tDCS Headset device configured in sham mode. There will be no less than 24 hours and no more than 72 hours between sessions.

Device: Sham Transcranial Direct Current Stimulation

Control Group

NO INTERVENTION

Participants will complete all assessment protocols (pre-intervention, post-intervention, and follow-up) without receiving any intervention. This group serves to identify potential effects of environmental variables on the results.

Interventions

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).

Also known as: (tDCS)
Active tDCS

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.

Also known as: Sham tDCS
Sham tDCS

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Egas Moniz School of Health and Science

Almada, Setúbal District, 2829 - 511, Portugal

Location

Related Publications (8)

  • Stanton MP, Houser RA, Riechel MEK, Burnham JJ, McDougall G. The Effect of Transcranial Direct Current Stimulation (tDCS) on Resilience, Compassion Fatigue, Stress and Empathy in Professional Nurses. Adv Res. 2015;5(2):10.9734/AIR/2015/16842. doi: 10.9734/AIR/2015/16842. Epub 2015 Jun 8.

    PMID: 31663011BACKGROUND
  • Sudbrack-Oliveira P, Razza LB, Brunoni AR. Non-invasive cortical stimulation: Transcranial direct current stimulation (tDCS). Int Rev Neurobiol. 2021;159:1-22. doi: 10.1016/bs.irn.2021.01.001. Epub 2021 Mar 2.

    PMID: 34446242BACKGROUND
  • Quick JC, Henderson DF. Occupational Stress: Preventing Suffering, Enhancing Wellbeing. Int J Environ Res Public Health. 2016 Apr 29;13(5):459. doi: 10.3390/ijerph13050459.

    PMID: 27136575BACKGROUND
  • Herrera-Melendez AL, Bajbouj M, Aust S. Application of Transcranial Direct Current Stimulation in Psychiatry. Neuropsychobiology. 2020;79(6):372-383. doi: 10.1159/000501227. Epub 2019 Jul 24.

    PMID: 31340213BACKGROUND
  • Desouky D, Allam H. Occupational stress, anxiety and depression among Egyptian teachers. J Epidemiol Glob Health. 2017 Sep;7(3):191-198. doi: 10.1016/j.jegh.2017.06.002. Epub 2017 Jul 18.

    PMID: 28756829BACKGROUND
  • Brosschot JF, Pieper S, Thayer JF. Expanding stress theory: prolonged activation and perseverative cognition. Psychoneuroendocrinology. 2005 Nov;30(10):1043-9. doi: 10.1016/j.psyneuen.2005.04.008.

    PMID: 15939546BACKGROUND
  • Ahmadizadeh MJ, Rezaei M, Fitzgerald PB. Transcranial direct current stimulation (tDCS) for post-traumatic stress disorder (PTSD): A randomized, double-blinded, controlled trial. Brain Res Bull. 2019 Nov;153:273-278. doi: 10.1016/j.brainresbull.2019.09.011. Epub 2019 Sep 24.

    PMID: 31560945BACKGROUND
  • Acquadro Maran D, Varetto A, Zedda M, Ieraci V. Occupational stress, anxiety and coping strategies in police officers. Occup Med (Lond). 2015 Aug;65(6):466-73. doi: 10.1093/occmed/kqv060. Epub 2015 Jun 4.

    PMID: 26048331BACKGROUND

MeSH Terms

Conditions

Occupational StressBurnout, Psychological

Interventions

Transcranial Direct Current Stimulation

Condition Hierarchy (Ancestors)

Occupational DiseasesStress, PsychologicalBehavioral SymptomsBehavior

Intervention Hierarchy (Ancestors)

Electric Stimulation TherapyTherapeuticsConvulsive TherapyPsychiatric Somatic TherapiesBehavioral Disciplines and ActivitiesElectroshockPsychological Techniques

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Masking Details
The PlatoScience company will remotely configure user accounts as either experimental or sham condition without providing information about participants to the company. The research team will not have knowledge of which accounts are experimental and which are sham until the end of the study, ensuring double-blind conditions. The outcomes assessor role is also masked as assessments are conducted through self-report questionnaires administered identically across all groups.
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: Double-blind randomized controlled trial with three parallel arms: active tDCS intervention, sham tDCS intervention, and control group (assessment only). The active and sham tDCS groups will receive 10 sessions over 4 weeks.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 9, 2026

First Posted

February 17, 2026

Study Start

February 18, 2026

Primary Completion (Estimated)

June 1, 2026

Study Completion (Estimated)

August 1, 2026

Last Updated

February 20, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will not share

Individual participant data (IPD) will not be shared because the informed consent obtained for this study did not include permission to share de-identified participant-level data with external researchers. If an ethics/IRB amendment and participant authorization (e.g., re-consent) are obtained in the future, the study team may update this record and make a de-identified dataset available under controlled access.

Locations