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RecruitingNCT05972200Updated Aug 4, 2023

V5/MT Stimulation on Reading and Reading-related Measures in Developmental Dyslexia

An interventional study of Active HD-tDCS over V5/MT and Active HD-tDCS over V1 in Developmental Dyslexia, sponsored by Bambino Gesù Hospital and Research Institute. Recruiting at 1 site in Italy. Open to participants aged 8 Years to 13 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-08-04.

Sponsored by Bambino Gesù Hospital and Research Institute · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
36
Allocation
Randomized
Ages
8 Years to 13 Years
Sex
All
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Study summary

The present study grounds on the absence of evidence-based treatment in individuals with developmental dyslexia (DD). At this topic, the present study will explore the potential effect of transcranial direct current stimulation (tDCS) over left hemispheric direct Lateral Geniculate Nucleus (LGN)-V5/MT pathway, cerebral areas usually disrupted in individuals with DD.

The investigators hypothesized that active tDCS over V5/MT will boost reading skills in children and adolescents with DD. On the contrary, sham (placebo condition) tDCS over V5/MT or active (control condition) tDCS over V1 will not have significant effect in improving reading skills. Further, both active and sham tDCS will be safe and well tolerated.

Read the detailed description

Over the last few decades, a huge number of studies has revealed that Developmental Dyslexia (DD), a brain-based neurodevelopmental disorder characterized by a severe and persistent impairment in the acquisition of reading skills may depend on multiple neurocognitive impairments, ranging from language-specific to cognitive-general deficits. Besides the most influential hypothesis of a phonological core deficit, there is also evidence for difficulties in low-level visual-temporal information processing, as the magnocellular deficit theory supports, as well as for visual-spatial attentional deficits, visual-perceptual impairments, and rapid automatized naming (RAN)-speed deficits.

Replicated structural/functional neuroimaging studies have demonstrated a DD hypoactivation relative to typical readers in the left temporo-occipital regions-critical for the automatic visual processing of word strings or print-and in the left temporo-parietal regions-important for grapheme-to-phoneme mapping.

Moreover, findings from animal models and post mortem studies in humans suggest that DD might also be associated with structural alterations in subcortical sensory pathways, particularly in visual and auditory thalamic nuclei and in their connections with high-order sensory cortices (i.e., the left hemispheric direct Lateral Geniculate Nucleus (LGN)-V5/MT pathway and the left hemispheric direct Medial Geniculate Body (MGB)-mPT pathway). In addition, in adults with DD, left V5/MT-LGN connectivity strength correlated with RAN abilities - a key deficit in DD.

A number of studies have demonstrated the positive effect of transcranial direct current stimulation (tDCS), a non-invasive brain stimulation used for transiently modifying neural activity of target areas, on reading and, particularly, in DD.

However, the few non-invasive brain stimulation studies on improving reading in DD yielded heterogeneous results and this variability might be partly due to the lack of neurobiological understanding of the underlying DD mechanism or to the use of traditional tDCS rather than a more focal technique such as the high-definition tDCS (HD-tDCS).

Starting from this, the aim of the current study is testing the effectiveness of a cutting-edge stimulation technique (i.e., HD-tDCS) in a within-subject experiment involving children and adolescents with DD. Especially, we will work to test i) the specific effect of HD-tDCS over high-order sensory cortices (i.e., V5/MT vs V1) on reading in children with DD; ii) the preconditions and neurobiological mechanisms that lead to high treatment outcomes.

If the stimulation over V5/MT is effective and specifically related to reading improvement, our results could help to i) understand the contribution and neurobiological mechanism of V5/MT in reading of children and adolescents with DD; ii) select criteria for potential responders to non-invasive brain stimulation; iii) develop evidence-based interventions in DD.

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Conditions studied

  • Developmental Dyslexia

Keywords

  • Children
  • Adolescents
  • tDCS
  • transcranial direct current stimulation
  • neurodevelopmental disorders
  • non-invasive brain stimulation
  • transcranial electrical stimulation
  • EEG
  • reading abilities
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In context

Dyslexia

127 studies on the registry are indexed under Dyslexia; 27 are open to participants now.

This study's planned enrollment of 36 is below the median of 71 across 106 interventional studies indexed under Dyslexia.

Browse Dyslexia studies →

Lead sponsor

Bambino Gesù Hospital and Research Institute is the lead sponsor of 54 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
8 Years to 13 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Italian speakers right-handed children and adolescents with dyslexia (, APA 2013);
  • Word/nonword/text reading accuracy and/or speed at least 2 Standard Deviations below the mean for school-age;
  • nv IQ ≥ 85;
  • normal hearing and normal or corrected-to-normal vision.

Exclusion criteria

Exclusion Criteria:

  • Having a comorbidity with other primary psychiatric/neurological diagnosis (e.g., depression, anxiety, autism, ADHD);
  • Having a personal history of neurological/medical/genetic diseases;
  • Having ongoing drug treatment influencing brain function;
  • Having epilepsy o family history of epilepsy.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

DSM diagnostic criteria

The American Psychiatric Association’s manual of mental health diagnoses. DSM-5 (2013, revised as DSM-5-TR in 2022) replaced DSM-IV, and some studies still name the older edition. “Meets DSM criteria for …” means diagnosed by that edition’s diagnostic criteria, usually by a clinician in an interview.

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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
36 participants (estimated)

Study arms

  • Experimental
    HD-tDCS V5/MT, HD-tDCS V1, Sham

    1. Active HD-tDCS over V5/MT 2. Active HD-tDCS over V1 3. Sham HD-tDCS over V5/MT or V1

    Device: Active HD-tDCS over V5/MT · Device: Active HD-tDCS over V1 · Device: Sham HD-tDCS over V5/MT or V1

  • Experimental
    HD-tDCS V5/MT, Sham, HD-tDCS V1

    1. Active HD-tDCS over V5/MT 2. Sham HD-tDCS over V5/MT or V1 3. Active HD-tDCS over V1

    Device: Active HD-tDCS over V5/MT · Device: Active HD-tDCS over V1 · Device: Sham HD-tDCS over V5/MT or V1

  • Experimental
    HD-tDCS V1, HD-tDCS V5/MT, Sham

    1. Active HD-tDCS over V1 2. Active HD-tDCS over V5/MT 3. Sham HD-tDCS over V5/MT or V1

    Device: Active HD-tDCS over V5/MT · Device: Active HD-tDCS over V1 · Device: Sham HD-tDCS over V5/MT or V1

  • Experimental
    HD-tDCS V1, Sham, HD-tDCS V5/MT

    1. Active HD-tDCS over V1 2. Sham HD-tDCS over V5/MT or V1 3. Active HD-tDCS over V5/MT

    Device: Active HD-tDCS over V5/MT · Device: Active HD-tDCS over V1 · Device: Sham HD-tDCS over V5/MT or V1

  • Experimental
    Sham, HD-tDCS V5/MT, HD-tDCS V1

    1. Sham HD-tDCS over V5/MT or V1 2. Active HD-tDCS over V5/MT 3. Active HD-tDCS over V1

    Device: Active HD-tDCS over V5/MT · Device: Active HD-tDCS over V1 · Device: Sham HD-tDCS over V5/MT or V1

  • Experimental
    Sham, HD-tDCS V1, HD-tDCS V5/MT

    1. Sham HD-tDCS over V5/MT or V1 2. Active HD-tDCS over V1 3. Active HD-tDCS over V5/MT

    Device: Active HD-tDCS over V5/MT · Device: Active HD-tDCS over V1 · Device: Sham HD-tDCS over V5/MT or V1

Interventions

  • DeviceActive HD-tDCS over V5/MT

    For HD-tDCS a 4 × 1 montage (Kessler et al., 2013), small circular electrodes (diameter 1 cm) will be used with the anode placed centrally with a current intensity of 1 mA for a total of 20 minutes (30 s ramp up/down). Hereby, the anodal electrode modulates the excitability of the targeted area left V5/MT, whereas the other 4 electrodes return electrical currents that flow away from that area. V5/MT will be localised via published procedures and electrode's placement will be done according to the 10-20 International EEG 10-20 System for electrode placement.

  • DeviceActive HD-tDCS over V1

    For HD-tDCS a 4 × 1 montage (Kessler et al., 2013), small circular electrodes (diameter 1 cm) will be used with the anode placed centrally with a current intensity of 1 mA for a total of 20 minutes (30 s ramp up/down). Hereby, the anodal electrode modulates the excitability of the targeted area left V1, whereas the other 4 electrodes return electrical currents that flow away from that area. V1 will be localised via published procedures and electrode's placement will be done according to the 10-20 International EEG 10-20 System for electrode placement.

  • DeviceSham HD-tDCS over V5/MT or V1

    Sham HD-tDCS will be delivered over left V5/MT or left V1. The same electrodes placement as well as the stimulation set-up will be used as in the active stimulation conditions, but the current will be applied for 30 s and will be ramped down (0 mA) during the rest of the session without the participants awareness. .

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What researchers measure

Primary outcomes

  1. Text reading accuracy (Experimental reading task)

    Change in text reading accuracy from baseline compared after to Active HD-tDCS over V5/MT sessions than after Active HD-tDCS over V1 and Sham sessions. Text reading accuracy is considered as the percentage (%) of accuracy and computed as the ratio between the number of correctly read stimuli and the total number of stimuli presented multiplied by 100. The time points will be pre- (baseline) vs post-stimulation session.

    Time frame: during procedure

  2. Text reading speed (Experimental reading task)

    Change in text reading speed from baseline compared to after Active HD-tDCS over V5/MT sessions than after Active HD-tDCS over V1 and Sham sessions. Text reading speed is considered as the syllables/seconds ratio and calculated dividing the total number of syllables pronounced by the total time spent to complete the reading (in seconds). The time points will be pre- (baseline) vs post-stimulation session.

    Time frame: during procedure

Secondary outcomes

  1. Word reading accuracy (Experimental reading task)

    Change in word reading accuracy from baseline compared to after Active HD-tDCS over V5/MT sessions than after Active HD-tDCS over V1 and Sham sessions. Word reading accuracy is considered as the percentage (%) of accuracy and computed as the ratio between the number of correctly read stimuli and the total number of stimuli presented multiplied by 100. The time points will be pre- (baseline) vs post-stimulation session.

    Time frame: during procedure

  2. Word reading speed (Experimental reading task)

    Change in word reading speed from baseline compared to after Active HD-tDCS over V5/MT sessions than during Active HD-tDCS over V1 and Sham sessions. Word reading speed is considered as the syllables/seconds ratio and calculated dividing the total number of syllables pronounced by the total time spent to complete the reading (in seconds). The time points will be pre- (baseline) vs post-stimulation session.

    Time frame: during procedure

  3. Non-word reading accuracy (Experimental reading task)

    Change in non-word reading accuracy from baseline compared to after Active HD-tDCS over V5/MT sessions than after Active HD-tDCS over V1 and Sham sessions. Non-word reading accuracy is considered as the percentage (%) of accuracy and computed as the ratio between the number of correctly read stimuli and the total number of stimuli presented multiplied by 100. The time points will be pre- (baseline) vs post-stimulation session.

    Time frame: during procedure

  4. Non-word reading speed (Experimental reading task)

    Change in non-word reading speed from baseline compared to after Active HD-tDCS over V5/MT sessions than after Active HD-tDCS over V1 and Sham sessions. Non-word reading speed is considered as the syllables/seconds ratio and calculated dividing the total number of syllables pronounced by the total time spent to complete the reading (in seconds). The time points will be pre- (baseline) vs post-stimulation session.

    Time frame: during procedure

  5. Right visual hemisphere-motion perception (Experimental reading task)

    Change in right visual hemisphere-motion perception from baseline compared to after Active HD-tDCS over V5/MT sessions than after Active HD-tDCS over V1 and Sham sessions. Right visual hemisphere-motion perception is considered as the number of correct saccades. The time points will be pre- (baseline) vs post-stimulation session.

    Time frame: during procedure

  6. Rapid automatized naming letter and number (Experimental reading task)

    Change in rapid automatized naming letter and number from baseline compared to after Active HD-tDCS over V5/MT sessions than after Active HD-tDCS over V1 and Sham sessions. Rapid automatized naming letter and number is considered as the total time spent (in seconds) to complete the task. The time points will be pre- (baseline) vs post-stimulation session.

    Time frame: during procedure

  7. Phoneme blending (Experimental reading task)

    Change in phoneme blending from baseline compared to after Active HD-tDCS over V5/MT sessions than after Active HD-tDCS over V1 and Sham sessions. Phoneme blending is considered as the number of correctly blended phonemes. The time points will be pre- (baseline) vs post-stimulation session.

    Time frame: during procedure

  8. Eye-movements during reading (Experimental reading task)

    Change in eye-movements from baseline compared to after reading during Active HD-tDCS over V5/MT sessions than after Active HD-tDCS over V1 and Sham sessions. Eye-movements during reading is considered as the number of saccades and the number of dwells. The time points will be pre- (baseline) vs post-stimulation session.

    Time frame: during procedure

  9. Spontaneous EEG (Experimental reading task)

    Change in spontaneous EEG from baseline compared to after Active HD-tDCS over V5/MT sessions than after Active HD-tDCS over V1 and Sham sessions. Spontaneous EEG is considered as the individual alpha-peak frequency and the beta and theta/gamma oscillations. The time points will be pre- (baseline) vs post-stimulation session.

    Time frame: during procedure

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Study locations

1 of 1 sites recruiting
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References and documents

Publications

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  • Snowling, M. Dyslexia, 2nd ed.; Blackwell Publishing: Oxford, UK. 2000.
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  • Giovagnoli G, Vicari S, Tomassetti S, Menghini D. The Role of Visual-Spatial Abilities in Dyslexia: Age Differences in Children's Reading? Front Psychol. 2016 Dec 21;7:1997. doi: 10.3389/fpsyg.2016.01997. eCollection 2016. PubMed 28066311 ↗
  • Wang Z, Cheng-Lai A, Song Y, Cutting L, Jiang Y, Lin O, Meng X, Zhou X. A perceptual learning deficit in Chinese developmental dyslexia as revealed by visual texture discrimination training. Dyslexia. 2014 Aug;20(3):280-96. doi: 10.1002/dys.1475. Epub 2014 Mar 18. PubMed 24643918 ↗
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  • Livingstone MS, Rosen GD, Drislane FW, Galaburda AM. Physiological and anatomical evidence for a magnocellular defect in developmental dyslexia. Proc Natl Acad Sci U S A. 1991 Sep 15;88(18):7943-7. doi: 10.1073/pnas.88.18.7943. Erratum In: Proc Natl Acad Sci U S A 1993 Mar 15;90(6):2556. PubMed 1896444 ↗
  • Galaburda AM, Menard MT, Rosen GD. Evidence for aberrant auditory anatomy in developmental dyslexia. Proc Natl Acad Sci U S A. 1994 Aug 16;91(17):8010-3. doi: 10.1073/pnas.91.17.8010. PubMed 8058748 ↗
  • Giraldo-Chica M, Hegarty JP 2nd, Schneider KA. Morphological differences in the lateral geniculate nucleus associated with dyslexia. Neuroimage Clin. 2015 Mar 20;7:830-6. doi: 10.1016/j.nicl.2015.03.011. eCollection 2015. PubMed 26082892 ↗
  • Muller-Axt C, Anwander A, von Kriegstein K. Altered Structural Connectivity of the Left Visual Thalamus in Developmental Dyslexia. Curr Biol. 2017 Dec 4;27(23):3692-3698.e4. doi: 10.1016/j.cub.2017.10.034. Epub 2017 Nov 16. PubMed 29153326 ↗
  • Tschentscher N, Ruisinger A, Blank H, Diaz B, von Kriegstein K. Reduced Structural Connectivity Between Left Auditory Thalamus and the Motion-Sensitive Planum Temporale in Developmental Dyslexia. J Neurosci. 2019 Feb 27;39(9):1720-1732. doi: 10.1523/JNEUROSCI.1435-18.2018. Epub 2019 Jan 14. PubMed 30643025 ↗
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  • Costanzo F, Varuzza C, Rossi S, Sdoia S, Varvara P, Oliveri M, Koch G, Vicari S, Menghini D. Reading changes in children and adolescents with dyslexia after transcranial direct current stimulation. Neuroreport. 2016 Mar 23;27(5):295-300. doi: 10.1097/WNR.0000000000000536. PubMed 26848997 ↗
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  • Lazzaro G, Costanzo F, Varuzza C, Rossi S, De Matteis ME, Vicari S, Menghini D. Individual differences modulate the effects of tDCS on reading in children and adolescents with dyslexia. Scientific Studies of Reading. 2021; 25(6): 1-17.
  • Lazzaro G, Costanzo F, Varuzza C, Rossi S, Vicari S, Menghini D. Effects of a short, intensive, multi-session tDCS treatment in developmental dyslexia: Preliminary results of a sham-controlled randomized clinical trial. Prog Brain Res. 2021;264:191-210. doi: 10.1016/bs.pbr.2021.01.015. PubMed 34167656 ↗
  • Battisti A, Lazzaro G, Costanzo F, Varuzza C, Rossi S, Vicari S, Menghini D. Effects of a short and intensive transcranial direct current stimulation treatment in children and adolescents with developmental dyslexia: A crossover clinical trial. Front Psychol. 2022 Sep 9;13:986242. doi: 10.3389/fpsyg.2022.986242. eCollection 2022. PubMed 36160506 ↗

Individual participant data

Plan to share: No

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 4, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05972200
Lead sponsor
Bambino Gesù Hospital and Research Institute
Responsible party
Deny Menghini (Head of Psychology Unit, Bambino Gesù Hospital and Research Institute) — Principal investigator
First posted
Aug 2, 2023
Start date
Sep 1, 2023 (estimated)
Primary completion
Aug 31, 2026 (estimated)
Completion
Aug 31, 2026 (estimated)
Last update
Aug 4, 2023

Study contacts

Deny Menghini
Contact
deny.menghini@opbg.net
06.6859.2875
Giulia Lazzaro
Contact
giulia.lazzaro@opbg.net

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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