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Mod of Cognitive Flexibility by tDCS, Tyrosine Polymorphisms in the COMT Gene

Modulation of Cognitive Flexibility by Transcranial Direct Current Stimulation, Tyrosine Administration and Polymorphisms in the COMT Gene

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03845920
Enrollment
32
Registered
2019-02-19
Start date
2019-02-18
Completion date
2019-09-30
Last updated
2019-04-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Modulation of Cognitive Flexibility by Transcranial Direct Current Stimulation, Tyrosine Administration and Polymorphisms in the COMT Gene

Brief summary

The current study would examine whether increases in endogenous dopaminergic activity via tyrosine and the (presumed) excitation of these by anodal tDCS of the dlPFC could causally be related to cognitive flexibility as measured by task switching and reversal learning. Additionally, the study will test whether the Val158Met-polymorphism in the catechol- O-methyltransferase (COMT) gene could also predict the effect of TYR supplementation, as this gene is involved in DA degradation in the prefrontal cortex.

Interventions

COMBINATION_PRODUCTtdcs (sham/anodal) + drug (placebo/tyrosine)

tDCS= A DC Stimulator Plus (neuroConn, Germany) with one 5 cm x 7 cm rubber electrode (anode) and a 10 cm x 10 cm (cathode; reference electrode), encased in saline soaked sponges will be used. The anode will be positioned over the left dlPFC, centered on F3 in the 10e20 electroencephalography (EEG) system, while the cathode on the contralateral supraorbital ridge (Fp2).Current will be delivered at 1.5mA for 20 min plus 30 s fade in/fade out periods.For sham stimulation, the current will be faded in over 30 s, at 1.5mA and then will be switched off. Drugs= 2.0 g of L-Tyrosine and 2.0 g of the placebo microcrystalline cellulose will be dissolved in 400ml of orange juice as per previously published protocols.

Sponsors

Sheffield Hallam University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* • Either male or female * Between 18 and 30 years * You are in good health * You agree to fast overnight prior to testing

Exclusion criteria

* • Are suffering from cardiac, hepatic, renal, neurological disorders * Damaged or diseased skin on your face and scalp, or a sensitive scalp * A history of alcohol or drug addiction, or severe psychiatric illness * Drug treatment which may lower seizure threshold (i.e. epilepsy) * Pregnancy * Sleep deprivation (less than 6 hours a day) * A history of migraine or headaches * A history of taking antidepressants * A history of taking tyrosine supplements

Design outcomes

Primary

MeasureTime frameDescription
Wisconsin Card Sorting Test (WCST) performanceMeasured twice in each session (4 arms): at time 0 and 80 minutes into testing.Measuring change in perseverative errors in the WCST
Probabilistic Reversal Learning (PRL) performanceMeasured twice in each session (4 arms): at time 0 and 80 minutes into testing.Measuring change in reversal errors in the WCST
Flanker Task performanceMeasured twice in each session (4 arms): at time 0 and 80 minutes into testing.Measuring change in conflict cost (defined as the difference in reaction time between congruent and incongruent responses)

Countries

United Kingdom

Contacts

Primary ContactLuca Aquili, Ph.D.
luca.aquili@shu.ac.uk+ 44 (0) 114 225
Backup ContactAnn Macaskill, Ph.D.
a.macaskill@shu.ac.uk44 (0)114 225

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026