NCT07268001

Brief Summary

The goal of this clinical trial is to examine the differential effect of continuous TBS (cTBS) over the left and right dorsolateral prefrontal cortex (DLPFC) on the facilitation of attention towards emotional (i.e., pleasant and distress-ing) versus neutral stimuli in healthy young adults. The main questions it aims to answer are:

  1. 1.To what extend a temporary modulation of DLPFC activity through cTBS influences attentional responses to emotional stimuli?
  2. 2.To what extend the effects of cTBS on attentional responses to emotional stimuli differ depending on whether the left or right dorsolateral prefrontal cortex (DLPFC) is stimulated?

Trial Health

87
On Track

Trial Health Score

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

Enrollment
91

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Apr 2020

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 15, 2020

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 16, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 16, 2020

Completed
5.5 years until next milestone

First Submitted

Initial submission to the registry

November 24, 2025

Completed
11 days until next milestone

First Posted

Study publicly available on registry

December 5, 2025

Completed
Last Updated

December 5, 2025

Status Verified

November 1, 2025

Enrollment Period

1 month

First QC Date

November 24, 2025

Last Update Submit

November 24, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Response times in the dot-probe task

    Response times to distressing, pleasant, and neutral stimuli were assessed using the dot-probe paradigm.

    From enrollment to the end of dot-probe task, that was performed in 1 session (1 day).

Study Arms (4)

cTBS over the left DLPFC

EXPERIMENTAL

Participants receive 1 session of continuous theta burst stimulation (cTBS) over the left dorsolateral prefrontal cortex (DLPFC; F3, following standard coordinates from the EEG International 10-20 system). The TBS sesssion consisted of 3 pulses at 50 Hz, with each train being repeated every 200 ms (5 Hz) for 40 seconds (600 pulses). After stimulation, attentional responses to pleasant and distressing images are assessed using the dot-probe task, which measures attentional bias toward emotional stimuli by presenting pairs of pleasant-neutral, distressing-neutral and neutral-neutral images. After each image pair, a dot appears in the location of one image, and participants must quickly indicate its position.

Device: Continuous theta burst stimulation

cTBS over the right DLPFC

EXPERIMENTAL

Participants receive 1 session of continuous theta burst stimulation (cTBS) over the right dorsolateral prefrontal cortex (DLPFC; F4, following standard coordinates from the EEG International 10-20 system). The TBS sesssion consisted of 3 pulses at 50 Hz, with each train being repeated every 200 ms (5 Hz) for 40 seconds (600 pulses). After stimulation, attentional responses to pleasant and distressing images are assessed using the dot-probe task, which measures attentional bias toward emotional stimuli by presenting pairs of pleasant-neutral, distressing-neutral and neutral-neutral images. After each image pair, a dot appears in the location of one image, and participants must quickly indicate its position.

Device: Continuous theta burst stimulation

sham cTBS over the left DLPFC

SHAM COMPARATOR

Participants receive 1 session of sham continuous theta burst stimulation (cTBS) over the left dorsolateral prefrontal cortex (DLPFC; F3, following standard coordinates from the EEG International 10-20 system). Sham stimulation was delivered using a sham coil that produced the same stimulation noise, but inducing nearly zero electric-field under the coil's center. After sham stimulation, attentional responses to pleasant and distressing images are assessed using the dot-probe task, which measures attentional bias toward emotional stimuli by presenting pairs of pleasant-neutral, distressing-neutral and neutral-neutral images. After each image pair, a dot appears in the location of one image, and participants must quickly indicate its position.

Device: Sham Control

sham cTBS over the right DLPFC

SHAM COMPARATOR

Participants receive 1 session of sham continuous theta burst stimulation (cTBS) over the right dorsolateral prefrontal cortex (DLPFC; F3, following standard coordinates from the EEG International 10-20 system). Sham stimulation was delivered using a sham coil that produced the same stimulation noise, but inducing nearly zero electric-field under the coil's center. After sham stimulation, attentional responses to pleasant and distressing images are assessed using the dot-probe task, which measures attentional bias toward emotional stimuli by presenting pairs of pleasant-neutral, distressing-neutral and neutral-neutral images. After each image pair, a dot appears in the location of one image, and participants must quickly indicate its position.

Device: Sham Control

Interventions

A TBS session burst consist of 3 pulses at 50 Hz, with each train being repeated every 200 ms (5 Hz) for 40 seconds (600 pulses).

Also known as: Non invasive brain stimulation
cTBS over the left DLPFCcTBS over the right DLPFC

Sham stimulation was delivered using an identical with the real Magstim figure of eight focal sham coil (70 mm diameter) that produced the same stimulation noise. Sham Magstim figure-of-eight coil have been found to induce nearly zero electric-field under the coil's center.

sham cTBS over the left DLPFCsham cTBS over the right DLPFC

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Medication-free, right-handed, normal vision, without ant estabished risk factor to rTMS (screening performed with Transcranial Magnetic Stimulation Safety Questionnaire).

You may not qualify if:

  • History of psychiatric/neurological disorders, such as epilepsy, head trauma and migraine.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Cyprus

Nicosia, 2109, Cyprus

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Prof. Dr.

Study Record Dates

First Submitted

November 24, 2025

First Posted

December 5, 2025

Study Start

April 15, 2020

Primary Completion

May 16, 2020

Study Completion

May 16, 2020

Last Updated

December 5, 2025

Record last verified: 2025-11

Data Sharing

IPD Sharing
Will not share

Locations