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Substance-Related DisordersNCT05350033

Transcranial Direct Current Stimulation on Inhibitory Control in Addictions.

A study testing tDCS - tDCS in people with Substance-Related Disorders, run by Universidad de Almeria at 1 site in Spain.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The research in neuroscience of the last 20 years is defined, in addition to continuing to advance in the field of behavioral and pharmacological therapy, by the birth and development of a new therapeutic category, called neuromodulation. Read more about this study

Who is it for?
Ages 18 years and older, men only
Conditions the study is for
Substance-Related Disorders
What is being tested?
tDCS - tDCS
Type of treatment
Medical device
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
200 participants
Where
1 siteSpain
Study dates
5 Apr 2021to 31 Dec 2022
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Men only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Substance abuse
  • Under clinical treatment at the Noesso Addiction Rehabilitation Center La Quinta, Laujar de Andarax, Spain
  • Participation approved by the clinical team
  • Participation approved by the experimental team by means of the Göttingen screening questionnaire
  • Signed informed consent
  • At least 26 points in the Montreal Cognitive Assessment (MOCA) evaluation

Who cannot join

  • Epilepsy or history of epilepsy (convulsions due compsumtion not included)
  • Cardiopathy or cardiac electronic devices
  • Skin reaction or high sensitivity to tDCS
  • Head metallic implant
  • Serious mental disease
  • Exclusion because of clinical criteria (physician, psychologist)

Trial locations and contacts

1 site in 1 country.

Spain1 site
  • Psychobiology Lab

    Almería, 04120

Other trials in Spain

About this study

Official title: Transcranial Direct Current Stimulation on Inhibitory Control in Addictions: a Triple-blinded, Sham-controlled Clinical Trial.

The research in neuroscience of the last 20 years is defined, in addition to continuing to advance in the field of behavioral and pharmacological therapy, by the birth and development of a new therapeutic category, called neuromodulation. Neuromodulation offers the possibility of producing changes in the Nervous System (SN) and therefore, in behavior, in addition to lasting over time. One of the most used non-invasive neuromodulation techniques is transcranial direct current stimulation (tDCS). The benefits of tDCS are promising and varied, so it is a potential neurorehabilitation tool, which has also shown its greatest effectiveness when accompanied by complementary rehabilitation treatment. The present study focuses on the effect of tDCS on addiction. Specifically, there is a great problem with the high rates of relapse presented by those individuals who try to abandon addictive behavior. Therefore, the maintenance of the abstinence period is the central theme of addiction research and the main challenge of rehabilitation at present. For that aim, the intervention will be carried out in a sample in the intermediate phase (internal) in the NOESSO (No EstáS Sólo) therapeutic community (Almería, Spain), between day 15 after arrival and the first day to leave on leave (day 45-60). The research will be made up of a previous period of selection and collection of data related to addiction, together with two phases or moments of correlative intervention and evaluation. Users will receive a bilateral (F3/F4) and repeated stimulation of 2 mA intensity for 20 min each, that is, every 24h for 5 consecutive days in each phase. Through this procedure, the aim is to seek to increase adherence to treatment in the early intervention phase and decrease the dropout rate due to the enhancement of inhibitory control. On the other hand, in the second phase, advanced intervention is sought to reduce craving, through an improvement in inhibitory and emotional control at the time of returning to the context of real consumption. In order to increase the knowledge about intra-individual differences in the effect of tDCS, researchers will compare the early intervention (Phase 1, at the begging of the rehabilitation process) with the advanced intervention (Phase 2, right before the first leave).

Read the detailed description

The research in behavioral neuroscience of the last 20 years is defined, in addition to continuing to advance in the field of behavioral and pharmacological therapy, by the birth and development of a new therapeutic category, called neuromodulation. Neuromodulation, especially non-invasive neuromodulation, has had a great impact on the current scientific landscape, encompassing the participation and interest of different disciplines such as medicine, bioengineering, psychology, and neuroscience. Scientific publications, as well as the media impact of this type of technique, have been increasing and continue to grow today. Neuromodulation offers the possibility of producing changes in the Nervous System (SN), and these also last over time. These techniques were born with the idea of avoiding the side effects of pharmacological therapy while offering a direct impact on the improvement of pathological symptoms. The changes produced by neuromodulation are promoted, among others, by ultrasound, microscale magnetic fields, and electricity. This last resource, electrical energy, is used by electrical neuromodulation techniques, one of the most studied branches of neuromodulation currently. Electrical neuromodulation starts from the basis that the neurons of our SN communicate with each other through chemical and electrical processes. By applying low-intensity electricity directly to the SN, it is possible to modulate the neuronal communication of the stimulated area by increasing or decreasing the excitability of the membrane of the target neuron field. Electrical neurostimulation encompasses different techniques, among which is Transcranial Direct Current Stimulation (tDCS). The present project focuses on tDCS since it is the technique that has demonstrated higher success rates as well as fewer, or no, side effects.

The tDCS consists of a device that contains a ≈9-volt battery. Two electrodes generally emanate from this device: the anode (positive pole), and the cathode (negative pole). Once placed non-invasively on the scalp, electricity flows between both electrodes at very low intensity (maximum 2 mA) for an approximate time of 20 minutes. This flow is barely noticeable to the user, who usually feels only a slight itch in the area of the electrodes that disappear after 60 seconds. However, under the skull, in the brain, electrical changes occur in the neurons in the area. Usually, under the anode there is a depolarization of the neuronal membrane, generating excitability, that is, the first step to greater activity. Under the cathode, most of the time, the opposite process occurs, a polarization that precedes a neuronal inhibition. This change in activity has been recorded by different studies and methods, directly measuring the change in cortical excitability, oxyhemoglobin level, white matter or the change in the levels of neurotransmitters such as gamma-aminobutyric acid (GABA) and Glutamate.

So far, tDCS has proven to be an effective yet safe technique, including relatively simple use causing the least discomfort to the user. The most common side effect that has been recorded is the slight itching in the area of the electrodes that also decreases after 60 seconds. This sensation can be controlled and reduced by using an adequate amount of conductive fluid, as well as by greater separation between both electrodes. In fact, tDCS has been shown to be a safe technique for use in children, adolescents, and older people. Administration of tDCS has been shown not to change indirect biomarkers of brain damage (N-acetyl-asperate), as well as levels of other related metabolites. In addition, no adverse effects on cardiac function have been found from stimulation and no convulsive effects have been associated with tDCS. However, to ensure effective and safe stimulation, possible skin sensitivity, medication, substance use, psychiatric disorders or a history of epilepsy should be recorded for each participant, thus controlling their possible interaction. A recent study conducted an updated tDCS safety exploration with more than 1,000 subjects, including participants from vulnerable populations, with an application of more than 33,200 sessions of tDCS, with stimulation of up to 4 mA and up to 40 minutes per session. The results showed no evidence of any serious adverse effects or irreversible damage.

The interesting thing about tDCS is not only the direct changes it produces on brain activity but those it produces directly on behavior and are perceptible. In a recent review on tDCS conducted by our research team, it was found that tDCS produces beneficial effects on human motor function when the motor cortex and cerebellum are stimulated. In addition, it has been found that the application of tDCS can reduce neuropathic pain, improve psychopathologies such as depression, schizophrenia and anxiety, as well as improving cognitive processes such as learning, perception and memory. The benefits of tDCS are promising and varied, so it is a potential neurorehabilitation tool, which has also shown its greatest effectiveness when accompanied by complementary rehabilitation treatment.

The excitatory or inhibitory effect of a single session of tDCS has been shown to last up to 90 minutes after stimulation. However, what makes this neurorehabilitation technique really interesting is its long-term effect. It has been proven that when stimulation is performed continuously, in repeated sessions, there is a therapeutic benefit that has been maintained up to 3 months after the last stimulation session. In fact, the alteration produced by tDCS in the glutamatergic system has been shown to be related to an increase in brain-derived neurotrophic factor (BDNF), a key molecule for synaptic plasticity. That is, there are changes in the brain that last over time.

tDCS and addiction The present study focuses on the effect of tDCS on addiction. Substance addiction is one of the most important mental health problems today. Specifically, there is a great problem with the high rates of relapse presented by those individuals who try to abandon addictive behavior. Therefore, the maintenance of the abstinence period is the central theme of addiction research and the main challenge of rehabilitation in the present. In this line, it has been found that stimulating through tDCS areas related to the circuits of addiction and decision making, preferably the dorsolateral prefrontal cortex (DLPFC) has been possible to modulate the processes of addiction. Anodal stimulation with tDCS over DLPFC has been shown to improve cognitive processes, such as working memory and decision making. This is because this brain area is involved in key processes of addiction, such as impulse control and stimulus salience. Neuroimaging studies have shown that DLPFC dysfunction is related, in addition to these processes, directly to compulsive drug use. To date, stimulation of this brain region has been found to decrease craving for the substance of addiction, relapse rate, and level of substance use such as alcohol, tobacco, cocaine and methamphetamine. Therefore, tDCS is presented as a potential rehabilitation tool that can produce great benefits for addiction, especially in the withdrawal phase, preventing relapse.

In addition to addiction-related behaviors, such as craving, relapse, and the emotions that accompany addiction, such as depressive or anxiety symptoms, the present study aims to deeply analyze the psychological process underlying addiction: inhibitory control. Inhibitory control is the ability to contain or stop an inappropriate behavior or response, and its alteration leads to maladaptive behaviors such as impulsivity and compulsivity. Previous studies have found a direct relationship between addiction and high impulsivity, high compulsivity, and a preference for risky decision-making. With tDCS, it has been possible to improve impulsivity and compulsivity, not only in addiction, but also in behaviors related, such as pathological gambling and binge eating disorders.

Although there are increasingly consolidated literature on the therapeutic benefits of tDCS applied to DLPFC (F3/F4) on addiction, the latest review on tDCS and addiction points out the need to study its effect on polyaddiction to different substances, which constitutes a population much closer to reality, addiction to a single substance being uncommon. In addition, it is postulated that the samples used in tDCS studies are too small. Finally, a determining limitation is that the opportune moment to apply tDCS is not yet known, if in a more initial phase of addiction rehabilitation, or in a later phase when the rehabilitation process is in a more advanced state. Therefore, this study aims to cover in a longitudinal study an important sample of people with polyaddiction treated in their therapeutic context, to verify the effects of tDCS on the direct components of addiction, such as craving and relapse, as well as on the basic psychological process that underlies addiction: inhibitory control. The intervention will be applied in the initial phase of rehabilitation, as well as in an advanced phase of it. Through the sham condition of tDCS, a control group will be created. All patients will participate in an intervention program while receiving tDCS treatment. This procedure aims to study the efficacy of tDCS for the improvement of inhibitory control and addiction in a process of addiction rehabilitation.

It is expected, therefore, that through the neuromodulation of inhibitory control through the application of tDCS in DLPFC there will be a benefit in the rehabilitation of a population with polyaddiction, which is reflected in greater control of the levels of impulsivity and compulsiveness, better decision making, and therefore, lower rates of anxiety, craving for the substance, relapse rate and an increase in quality of life.

This project is proposed in collaboration and close coordination with the NOESSO (No EstáS Sólo) Association. NOESSO is dedicated, as a non-profit association, to the reception and treatment of people with addictions. It is integrated into the healthcare network for the treatment of addiction of the Junta de Andalucía, in Spain. It is composed of various rehabilitation and integration centers in the province of Almeria. In Laujar de Andarax there is located the center of primary rehabilitation reception (Cortijo La Quita Therapeutic Community), where patients referred from various centers are admitted. The rehabilitation process follows a strict protocol, in accordance with national and regional guidelines, which combines a multidisciplinary strategy. After the first period of detoxification of a minimum of 15 days, the patient enters a therapeutic program where doctors, psychologists, educators, and social workers work according to an individualized program. The rehabilitation process is completed with a progressive program of departures from the center so that patients gradually face their previous environment. The first departure occurs between 45 and 60 days after admission, at the discretion of the clinical team. NOESSO receives between 90-100 admissions annually. Of these, between 15-20% reach therapeutic discharge, and 25-30% achieve partially achieve objectives. They voluntarily abandon between 20-25% and the rest enter other casuistries without therapeutic success. Therefore, the percentage of dropouts and relapses is high. In fact, in the first scheduled departure from the center, about 20% of relapses are recorded, objectified by control of substances by urinalysis.

Hypothesis: Through the neuromodulation of inhibitory control through the application of tDCS in DLPFC there will be a benefit in the rehabilitation of a population with polyaddiction, which is reflected in greater control of the levels of impulsivity and compulsiveness, better decision making, and therefore, lower rates of anxiety, craving for the substance, relapse rate and an increase in quality of life.

General objective: to reduce the relapse rate, thus increasing the success rate, and increasing the quality of life of patients undergoing a rehabilitation process for substance addiction.

The objectives of this project are aimed at improving the inhibitory control of patients with polyaddiction through the repeated application of stimulation with tDCS. It is expected that the consequence of this improvement will be reflected in greater adherence to treatment, that is, in a significant reduction in the rate of relapse and abandonment. The objectives, therefore, can be divided into three different categories, although all of them are interrelated. Throughout the four evaluations that will be carried out (pre and post of each phase), the objective is to induce a progressive improvement of all the components of inhibitory control that will be measured by neurobehavioral tasks. That is, the goal is for participants who receive tDCS to show a lower rate of risky decisions, i.e. a higher Net Score in the Iowa Gambling Task and a lower number of false alarms in the Go/No Go task. It is expected for participants who have received tDCS to show lower scores on the compulsivity (MOCI) and impulsivity (BIS-11) questionnaires, as well as a better emotional state reflected in more favorable scores on symptoms of depression (BDI-BECK), anxiety (STAI-E/R), fatigue (VAS) and consequently, a higher score on the perceived quality of life (WHOQOL-BREF). The change that treatment with tDCS can suppose on these variables is expected to be reflected in the primary objective of this work, which is the reduction of substance craving (VAS), and therefore, greater adherence to treatment, reflected in a lower relapse rate and a greater number of patients who do not abandon therapy. These changes produced in a population with polyaddiction will be a novelty in the panorama of the scientific literature regarding neuromodulation, since to date there is still a demand for studies on tDCS in the rehabilitation of several substances, a situation closer to the reality of this health problem.

Being tested
tDCS - tDCS, tDCS - Sham, Sham - tDCS, Sham - Sham
Keywords
substance abuse, transcraneal electrical stimulation, tDCS, inhibitory control, drug craving, treatment adherence
Medical subject headings
Substance-Related Disorders, Treatment Adherence and Compliance

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • tDCS - tDCSDevice

    active-tDCS administered during 10 sessions, in Phase 1 and Phase 2

  • tDCS - ShamDevice

    active-tDCS administered during 5 sessions, in Phase 1

  • Sham - tDCSDevice

    active-tDCS administered during 5 sessions, in Phase 2

  • Sham - ShamDevice

    sham-tDCS administered during 10 sessions, in Phase 1 and Phase 2

Study groups in NCT05350033
Study groupRoleWhat they receive
Active-ActiveExperimentalParticipants will receive active-tDCS stimulation (anode F4 / cathode F3) at 2 mA during 20 min in Phase 1 (5 sessions, intersession time-24h) and in Phase 2 (5 sessions, intersession time-24h).
Receives: Device: tDCS - tDCS
Active-ShamExperimentalParticipants will receive active-tDCS stimulation (anode F4 / cathode F3) at 2 mA during 20 min in Phase 1 (5 sessions, intersession time-24h), and sham-tDCS at 2 mA (active-stimulation lasting for 1 min) in Phase 2 (5 sessions, intersession time-24h).
Receives: Device: tDCS - Sham
Sham-ActiveExperimentalParticipants will receive sham-tDCS stimulation (anode F4 / cathode F3) at 2 mA (active-stimulation lasting for 1 min) in Phase 1 (5 sessions, intersession time-24h), and active-tDCS at 2 mA during 20 min in Phase 2 (5 sessions, intersession time-24h).
Receives: Device: Sham - tDCS
Sham-ShamSham comparatorParticipants will receive sham-tDCS stimulation (anode F4 / cathode F3) at 2 mA (active-stimulation lasting for 1 min) in Phase 1 (5 sessions, intersession time-24h), and sham-tDCS at 2 mA (active-stimulation lasting for 1 min) in Phase 2 (5 sessions, intersession time-24h).
Receives: Device: Sham - Sham

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Dropouts phase 1: participants that abandon the treatment phase

    Number of participants that abandon the treatment phase before the first free weekend outside the center

    Measured: 45-60 days

  2. Dropouts phase 2: participants that abandon the treatment after the first free weekend outside the center

    Number of participants that abandon the treatment after the first free weekend outside the center

    Measured: 47-62 days

  3. Relapses:

    Number of relapses on drug comsuption during the first free weekend outside the center

    Measured: 41-62 days

Secondary outcomes (9)
  1. VAS - Craving

    Quantification fo drug craving by Visual Analogue Scale (VAS): This is a visual analog scale, which means that it does not present lexical items. On the contrary, the user only has to mark on the scale from 0 to 10 the degree of a perceived sensation or state of health, in this case the desire for drug (craving)

    Measured: Daily during the total ten days of intervention

  2. VAS - Fatigue

    Quantification fo drug craving by Visual Analogue Scale (VAS): This is a visual analog scale, which means that it does not present lexical items. On the contrary, the user only has to mark on the scale from 0 to 10 the degree of a perceived sensation or state of health, in this case fatigue.

    Measured: For each interventional phase: first and fifth day

  3. STAI-E/R

    Questionnaire of anxiety state / trait STAI-E / R, is one of the most used tests to measure anxiety, since it allows to differentiate between the stable anxiety in the own time of people with threatening attribution to a wide range of situations, and the anxiety that occurs at that specific moment or transitory emotional state, that the subject is conscious.

    Measured: For each interventional phase: first and fifth day

  4. WHOQOL-BREF

    WHOQOL-BREF is the Spanish version of the most used test in the field of health to evaluate quality of life in a generic and self-reported way. It consists of 26 items, classified into 4 dimensions (physical, psychological, social relations and environment). It is fast and effective, however it does not allow specific clinical areas to be evaluated in a concrete way.

    Measured: For each interventional phase: first and fifth day

  5. Beck BDI-BECK

    Beck BDI-BECK-II inventory is widely used to assess the degree of depression. It consists of 21 items indicative of symptoms such as sadness, crying, loss of pleasure, guilt, and desire for suicide according to the Diagnostic and Statistical Manual of Mental Disorders (DSM). Its administration is self-report and provides a measure of presence and severity in adults and adolescents. It is indicated for clinical psychology, neuropsychology, and forensics.

    Measured: For each interventional phase: first and fifth day

  6. BIS-11

    Barratt impulsivity scale (BIS-11). It evaluates impulsivity and its subtypes: cognitive impulsivity, motor impulsivity and impulsivity related to non-planning. The scale consists of 30 Likert-type items and its administration is self-reported. This scale is widely applied in research related to clinical population and substance abuse.

    Measured: For each interventional phase: first and fifth day

  7. MOCI

    Maudsley Obsessional-Compulsive Inventory (MOCI) (Spanish version). It evaluates compulsivity and its subtypes: (a) checking, (b) cleanliness, (c) slowness and repetition, and (d) doubt and awareness. It has been developed in order to investigate the traits of compulsivity. The questionnaire comprises 30 items with true/false answers. The results are interpreted as a measure of the intensity of compulsive behaviors since the high false alarms in the Go/no-go task are related to a high score in the MOCI questionnaire.

    Measured: For each interventional phase: first and fifth day

  8. IGT

    Iowa Gambling Task (IGT): is a neurobehavioral task that measures risky decision-making. Four decks of cards will appear on the computer screen. Each participant will have to choose a card from any deck by clicking on it. The task will consist of 100 essays. In each choice, decks A and B will generate a profit of 100 points and decks C and D of 50 points. However, every 10 trials the choice of the first deck will result in a net loss of 250 points, while the choice of the second will result in a net gain of the same amount. All participants will start with 2000 points and will be instructed to maximize their profits.

    The main variable Net Score: is the total score obtained by the participant. People with a low Net Score have shown a deficit in performing this task, such as people with substance addiction.

    Measured: For each interventional phase: first and fifth day

  9. Go/no-go

    Go/no-go task has been widely used to assess cognitive control, compulsion, and inhibitory control of behavior. A recently published version by our research group will be used. It consist of the presentation of circles of two different colors separated by a fixing point, during 200 tests. What participants should do is respond by pressing the computer's keyboard space bar as quickly as possible if the circle that appears is green (Go test), and avoid responding to the appearance of blue circles (No-Go test). 80% of the trials will be Go trials. Both stimuli will appear on the screen for 350ms. The presentation time will be adjusted to the participant's reaction time (+50ms or -50ms). The interval between stimuli will be variable, between 800ms and 1500ms. The main variable is "false alarms", pressing the key in No-Go trials.

    Measured: For each interventional phase: first and fifth day

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Apr 2022
  2. Study start5 Apr 2021
  3. Primary completion15 Jul 2022 (estimated)
  4. Study completion31 Dec 2022 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
* Group 1: Active-stimulation in Phase 1 and Phase 2 * Group 2: Active-stimulation in Phase 1 and Sham-stimulation in Phase 2 * Group 3: Sham-stimulation in Phase 1 and Active-stimulation in Phase 2 * Group 4: Sham-stimulation in Phase 1 and Phase 2
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
200 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05350033
Sponsor's protocol ID
TESADIC
Status last verified
Apr 2022
First submitted
14 Mar 2022
Last updated
27 Apr 2022
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: All collected Individual Participants Data (IPD) will be shared in .csv files together with readme.txt files describing data processing

Publications

  • Salling MC, Martinez D. Brain Stimulation in Addiction. Neuropsychopharmacology. 2016 Nov;41(12):2798-2809. doi: 10.1038/npp.2016.80. Epub 2016 May 31.

    PubMed 27240657
  • Bajbouj M, Padberg F. A perfect match: noninvasive brain stimulation and psychotherapy. Eur Arch Psychiatry Clin Neurosci. 2014 Nov;264 Suppl 1:S27-33. doi: 10.1007/s00406-014-0540-6. Epub 2014 Sep 25.

    PubMed 25253645
  • Page SJ, Cunningham DA, Plow E, Blazak B. It takes two: noninvasive brain stimulation combined with neurorehabilitation. Arch Phys Med Rehabil. 2015 Apr;96(4 Suppl):S89-93. doi: 10.1016/j.apmr.2014.09.019.

    PubMed 25813373
  • Hsu TY, Juan CH, Tseng P. Individual Differences and State-Dependent Responses in Transcranial Direct Current Stimulation. Front Hum Neurosci. 2016 Dec 21;10:643. doi: 10.3389/fnhum.2016.00643. eCollection 2016.

    PubMed 28066214
  • Dubljevic V, Saigle V, Racine E. The rising tide of tDCS in the media and academic literature. Neuron. 2014 May 21;82(4):731-6. doi: 10.1016/j.neuron.2014.05.003.

    PubMed 24853934
  • Lewis PM, Thomson RH, Rosenfeld JV, Fitzgerald PB. Brain Neuromodulation Techniques: A Review. Neuroscientist. 2016 Aug;22(4):406-21. doi: 10.1177/1073858416646707. Epub 2016 Apr 29.

    PubMed 27130839
  • De Ridder D, Perera S, Vanneste S. State of the Art: Novel Applications for Cortical Stimulation. Neuromodulation. 2017 Apr;20(3):206-214. doi: 10.1111/ner.12593. Epub 2017 Mar 28.

    PubMed 28371170
  • Nitsche MA, Cohen LG, Wassermann EM, Priori A, Lang N, Antal A, Paulus W, Hummel F, Boggio PS, Fregni F, Pascual-Leone A. Transcranial direct current stimulation: State of the art 2008. Brain Stimul. 2008 Jul;1(3):206-23. doi: 10.1016/j.brs.2008.06.004. Epub 2008 Jul 1.

    PubMed 20633386
  • Nitsche MA, Paulus W. Excitability changes induced in the human motor cortex by weak transcranial direct current stimulation. J Physiol. 2000 Sep 15;527 Pt 3(Pt 3):633-9. doi: 10.1111/j.1469-7793.2000.t01-1-00633.x.

    PubMed 10990547
  • McKendrick R, Parasuraman R, Ayaz H. Wearable functional near infrared spectroscopy (fNIRS) and transcranial direct current stimulation (tDCS): expanding vistas for neurocognitive augmentation. Front Syst Neurosci. 2015 Mar 9;9:27. doi: 10.3389/fnsys.2015.00027. eCollection 2015.

    PubMed 25805976
  • Zheng X, Schlaug G. Structural white matter changes in descending motor tracts correlate with improvements in motor impairment after undergoing a treatment course of tDCS and physical therapy. Front Hum Neurosci. 2015 Apr 30;9:229. doi: 10.3389/fnhum.2015.00229. eCollection 2015.

    PubMed 25983684
  • Kim S, Stephenson MC, Morris PG, Jackson SR. tDCS-induced alterations in GABA concentration within primary motor cortex predict motor learning and motor memory: a 7 T magnetic resonance spectroscopy study. Neuroimage. 2014 Oct 1;99:237-43. doi: 10.1016/j.neuroimage.2014.05.070. Epub 2014 Jun 3.

    PubMed 24904994
  • Bachtiar V, Near J, Johansen-Berg H, Stagg CJ. Modulation of GABA and resting state functional connectivity by transcranial direct current stimulation. Elife. 2015 Sep 18;4:e08789. doi: 10.7554/eLife.08789.

    PubMed 26381352
  • Poreisz C, Boros K, Antal A, Paulus W. Safety aspects of transcranial direct current stimulation concerning healthy subjects and patients. Brain Res Bull. 2007 May 30;72(4-6):208-14. doi: 10.1016/j.brainresbull.2007.01.004. Epub 2007 Jan 24.

    PubMed 17452283
  • Minhas P, Datta A, Bikson M. Cutaneous perception during tDCS: role of electrode shape and sponge salinity. Clin Neurophysiol. 2011 Apr;122(4):637-8. doi: 10.1016/j.clinph.2010.09.023. Epub 2010 Nov 12. No abstract available.

    PubMed 21075048

Questions about this trial

What is this clinical trial studying?

A study testing tDCS - tDCS in people with Substance-Related Disorders, run by Universidad de Almeria at 1 site in Spain.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 27 Apr 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Dropouts phase 1: participants that abandon the treatment phase (time frame: 45-60 days). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05350033, which also lists 66 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Apr 2022.

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