tDCS for Stress and Burnout in Higher Education
tDCS4HESnB
Non-Invasive Neuromodulation as a Strategy for Reducing Occupational Stress and Burnout in Higher Education
1 other identifier
interventional
60
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2026
Shorter than P25 for not_applicable
1 active site
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
First Submitted
Initial submission to the registry
February 9, 2026
CompletedFirst Posted
Study publicly available on registry
February 17, 2026
CompletedStudy Start
First participant enrolled
February 18, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 1, 2026
February 20, 2026
February 1, 2026
3 months
February 9, 2026
February 18, 2026
Conditions
Keywords
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
EXPERIMENTALParticipants 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.
Sham tDCS
SHAM COMPARATORParticipants 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.
Control Group
NO INTERVENTIONParticipants 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).
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.
Eligibility Criteria
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
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: 31663011BACKGROUNDSudbrack-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: 34446242BACKGROUNDQuick 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: 27136575BACKGROUNDHerrera-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: 31340213BACKGROUNDDesouky 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: 28756829BACKGROUNDBrosschot 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: 15939546BACKGROUNDAhmadizadeh 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: 31560945BACKGROUNDAcquadro 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
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
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
- 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.