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CompletedNCT05568251OpiStimUpdated Oct 6, 2022

TDCS Combined With CT In Opioid Use Disorder

An interventional study of transcranial Direct Current Stimulation and Cognitive training in Opioid Use Disorder, sponsored by Istanbul University. Completed at 2 sites in Turkey. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2022-10-06.

Sponsored by Istanbul University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 3 years 4 months after the study started (first participant enrolled Jun 2019, registered Oct 2022).
Phase
Not applicable
Study type
Interventional
Enrollment
38
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

The aim of the present study is to investigate the effect of prefrontal transcranial Direct Current Stimulation (tDCS) combined with cognitive training on cognitive functions in individuals with Opioid Use Disorder (OUD). The participants will be allocated into active/sham groups (1:1) and will receive a single session of prefrontal tDCS combined with cognitive training. Outcomes of the active and sham groups will be compared.

02

Conditions studied

  • Opioid Use Disorder

Keywords

  • brain stimulation
  • cognitive functions
  • neuropsychological evaluation
  • opioid use disorder
  • transcranial direct current stimulation
03

In context

Opioid-Related Disorders

1,411 studies on the registry are indexed under Opioid-Related Disorders; 290 are open to participants now.

This study's enrollment of 38 is below the median of 63 across 1,123 interventional studies indexed under Opioid-Related Disorders.

Browse Opioid-Related Disorders studies →

Lead sponsor

Istanbul University is the lead sponsor of 496 studies on the registry; 79 are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 1 (20%) have results posted.

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

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Being aged between 18-65 years
  • being in the maintenance phase of the OUD treatment
  • naivety to tDCS
  • at least 5 years of education

Exclusion criteria

Exclusion Criteria:

  • current diagnosis of major depressive disorder
  • current diagnosis or history of bipolar disorders, psychotic disorders, neurocognitive disorders, pervasive developmental disorders, mental retardation, severe neurological disorders,
  • common tDCS contraindications
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
38 participants (actual)

Study arms

  • Active comparator
    Active tDCS combined with Cognitive Training

    Device: transcranial Direct Current Stimulation · Procedure: Cognitive training

  • Sham comparator
    Sham tDCS combined with Cognitive Training

    Device: transcranial Direct Current Stimulation · Procedure: Cognitive training

Interventions

  • Devicetranscranial Direct Current Stimulation

    Participants will receive a single session of active/sham tDCS. During each session, 2 milliAmpers of active or sham tDCS will be applied for 20 minutes over the dorsolateral prefrontal cortex (right anodal/left cathodal).

  • ProcedureCognitive training

    Participants will be administered Game of Dice Task concurrent with the tDCS session

06

What researchers measure

Primary outcomes

  1. Changes in the Iowa Gambling Task net score

    Iowa Gambling Task net score is the total score of the task (between -100 and 100) that generally assesses the decision making under ambiguity, but also assesses the decision making under risk at the later stages. Higher scores in the task represents better decision making and healthy people generally have scores above 8-10 in the task.

    Time frame: Before and immediately after the intervention

  2. Changes in the Adjusted Number of Pumps in the Balloon Analogue Risk Task

    The Balloon Analogue Risk Task is the commonly used computerized measure of decision making under risk. Main outcome variable of the task is the Adjusted Number of Pumps which includes the mean number of pumps in the trials that not resulted with an explosion. Lower values mean lower impulsivity.

    Time frame: Before and immediately after the intervention

Secondary outcomes

  1. Changes in Interference Time in the Stroop Test

    The stroop effect (Interference Time) consists of both the semantic and the response conflict. Response conflict (time in milliseconds) is obtained by subtracting the semantic conflict (time in milliseconds obtained in the second step of the protocol) from the stroop effect (time in milliseconds obtained in the first step of the protocol). Minimum time difference is 0 and maximum time difference is 100 milliseconds. Lower time differences indicate better performance and higher time differences indicate worse performance.

    Time frame: Before and immediately after the intervention

  2. Changes in the Stop Signal Reaction time in the Stop Signal Test

    The Stop-Signal Task (SST) is a task requiring inhibition of a prepotent motor response. The SST requires participants to respond to a target stimulus as quickly and accurately as possible by pressing a button, but also to withhold their response when they hear an auditory signal. Thus, this task involves a competition between activating and inhibiting processes. The primary outcome variable is change in the stop signal reaction time (SSRT) for the task administered seconds to minutes before and seconds to minutes after stimulation. The theoretical minimum is zero seconds and there is no theoretical maximum. Higher SSRT scores reflect greater impulsivity.

    Time frame: Before and immediately after the intervention

  3. Changes in the verbal fluency performance

    Verbal fluency is a test that measure multiple domains of cognition such as executive functions and language functions. Phonemic Fluency assesses the number of words beginning with certain letters that participants can generate within 60 seconds, the semantic Fluency assesses the number of words within particular categories participants can generate within 60 seconds. Alternating fluency assesses the number of fruit-name pairs reported in a minute duration. Theoretical minimum is zero and there is no theoretical maximum . Lower scores indicate worse performance and higher scores indicate better performance.

    Time frame: Before and immediately after the intervention

  4. Changes in the digit span performance

    The Digit Span test is a measure of verbal short-term/working memory. Subjects must recall all digits either in forward (digit span forward) or backward (digit span backward) order. Digit span forward total score: 0-10; higher score indicate better performance, digit span backwards total score: 0-10; higher score indicate better performance

    Time frame: Before and immediately after the intervention

  5. Changes in the Trail Making Test A Time

    Trail Making A Test is a widely used as a quick and easy to administer measure of attention. Lower reaction times indicate better performance and higher reaction times indicate worse performance. Minimum time is 10 milliseconds and maximum time is 150 milliseconds.

    Time frame: Before and immediately after the intervention

  6. Changes in the Trail Making Test B Time

    Trail Making B Test is a widely used as a quick and easy to administer measure of executive functions. Lower reaction times indicate better performance and higher reaction times indicate worse performance. Minimum time is 10 milliseconds and maximum time is 150 milliseconds.

    Time frame: Before and immediately after the intervention

  7. Changes in the Letter Number Sequencing (LNS) Test performance

    Letter number is a test of working memory which involves ordering a series of up to 8 letters and numbers in which the numbers are repeated back first in order starting with the lowest number, then followed by the letters in alphabetical order. LNS consists of 10 items and each item has 3 trials rated as Incorrect (0) or Correct (1). The LNS total raw score (range 0 to 30) is auto-calculated by summing the 10 individual item scores (range 0 to 3 for each item). Higher number of correct items correlated to better performance and a negative change from baseline indicates worsening.

    Time frame: Before and immediately after the intervention

07

Study locations

2 sites
  • Istanbul University
    Istanbul, Turkey
  • Research, Treatment and Training Center for Alcohol and Substance Dependence (AMATEM)
    Istanbul, Turkey
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 6, 2022, 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
NCT05568251
Lead sponsor
Istanbul University
Collaborators
Research, Treatment and Training Center for Alcohol and Substance Dependence (AMATEM)
Responsible party
Serkan Aksu (Assistant Proffessor Doctor, Istanbul University) — Principal investigator
First posted
Oct 5, 2022
Start date
Jun 1, 2019
Primary completion
Jun 1, 2020
Completion
Jun 1, 2020
Last update
Oct 6, 2022

Study contacts

Serkan Aksu
principal investigator · Istanbul University

Oversight

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

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