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Clinical Trials/NCT05986578
NCT05986578
Recruiting
Not Applicable

Identifying Electrophysiological Targets for Transcranial Magnetic Stimulation in Cocaine Use Disorder

The University of Texas Health Science Center, Houston1 site in 1 country75 target enrollmentNovember 8, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cocaine Use Disorder
Sponsor
The University of Texas Health Science Center, Houston
Enrollment
75
Locations
1
Primary Endpoint
Change in the amplitude of the Late Positive Potential (LPP) in microvolts in response to visual stimuli on the Picture Viewing Task.
Status
Recruiting
Last Updated
11 months ago

Overview

Brief Summary

The purpose of this study is to assess effects of intermittent theta burst stimulation (iTBS) to left dorsolateral prefrontal cortex (dlPFC) and dorsomedial prefrontal cortex (dmPFC) compared to sham on electrophysiological indices of reward sensitivity and motivated attention in adults with cocaine use disorder.

Registry
clinicaltrials.gov
Start Date
November 8, 2024
End Date
June 30, 2028
Last Updated
11 months ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Heather E. Webber, PhD

Instructor

The University of Texas Health Science Center, Houston

Eligibility Criteria

Inclusion Criteria

  • non-treatment-seeking adults
  • meet Diagnostic and Statistical Manual of Mental Disorders (DSM)-5 criteria for current cocaine use disorder of at least moderate severity (≥ 4 symptoms)
  • have at least 1 positive urine Benzoylecgonine (BE) specimen (≥ 300 ng/mL) during intake
  • be able to understand the consent form and provide written informed consent
  • be able to provide the following verifiable information for a minimum of 2 contact persons: full legal name,email address, local mailing address, and as applicable, home, work, and cell phone numbers

Exclusion Criteria

  • current DSM-5 diagnosis for substance use disorder (of at least moderate severity) other than cocaine, marijuana, or nicotine
  • in the opinion of the principal investigator (PI), the presence of any medical, neurological, psychiatric, or physical condition, disease, or illness that, may: (a) compromise interfere, limit, effect or reduce the subject's ability to complete the study; or (b) adversely impact the safety of the subject or the integrity of the data
  • has current or recent (within 3 months of potential enrollment) suicidal ideation, suicidal behavior, homicidal ideation or a homicidal plan sufficient to raise subject safety concerns based on the following assessments according to the PI:
  • Structured Clinical Interview for DSM-5 (SCID-5)
  • Columbia Suicide Severity Rating Scale (C-SSRS) Screener - Answers YES to Questions 3, 4, 5, or 6
  • Assault \& Homicidal Danger Assessment Tool - Key to Danger \> 1
  • medical implants contraindicating TMS (i.e., aneurysm clips or coils, stents, implanted stimulators, implanted vagus nerve or deep brain stimulators, implanted electrical devices such as pacemakers or medication pumps electrodes for monitoring brain activity, cochlear implants for hearing, any magnetic implants, bullet fragments, any other metal device or object implanted in your body closer than 30 cm from the coil)
  • history of brain surgery
  • history of an intracranial lesion or any medical or neurological diagnosis/condition associated with increased intracranial pressure (i.e., Idiopathic Intracranial Hypertension/Pseudotumor Cerebri) OR any of the following symptoms within 30 days of enrollment: headaches \> 15 days/month, loss of vision or decreased vision
  • moderate-to-severe heart disease

Outcomes

Primary Outcomes

Change in the amplitude of the Late Positive Potential (LPP) in microvolts in response to visual stimuli on the Picture Viewing Task.

Time Frame: Baseline(before iTBS session),immediately after iTBS session

The Picture Viewing Task will be used to elicit the LPP, reflecting the motivational salience of a stimulus. During this task, participants are asked to view a slide show of images including pleasant, unpleasant, neutral, and cocaine-related images.

Change in the amplitude of the Reward Positivity (RewP) component in microvolts in response to feedback on the Doors Task

Time Frame: Baseline(before iTBS session),immediately after iTBS session

The Doors Task will be used to elicit the RewP component, representing reward sensitivity. The task is a guessing game, where participants guess which door contains a reward behind it. After selecting a door, the participants are notified if they found the prize by a green arrow pointing up or if they did not find the prize by a red arrow pointing down.

Secondary Outcomes

  • Change in craving as assessed by the Minnesota Cocaine Craving Scale (MCCS)(Baseline(before iTBS session),immediately after iTBS session)
  • Change in pain as assessed by the Visual Analogue Scale(Baseline(before iTBS session),immediately after iTBS session)
  • Change in cognitive function as assessed by the The Montreal Cognitive Assessment (MoCA)(Baseline(before iTBS session),immediately after iTBS session)
  • Change in behavioral reward learning as assessed by the Pavlovian Go/No-Go task(Baseline(before iTBS session),immediately after iTBS session)
  • Change in Anhedonia as assessed by the Snaith Hamilton Pleasure Scale (SHAPS)(Baseline(before iTBS session),immediately after iTBS session)

Study Sites (1)

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