Cognitive Dysfunction in the Addictions Study - Project 4 (P4)

NCT06299787 | Recruiting

• 1 other identifier: 058-2021
• Study Type: interventional
• Target: 40
• Locations: 1 country
• Sites: 1

Brief Summary

The prefrontal cortex, although well established as an efficacious target for the treatment of major depressive disorder (MDD), has recently come into favour as a therapeutic target for alcohol use disorders (AUD). Depressive symptoms are also highly prevalent in individuals with AUD. A number of cognitive and psychological processes stemming from the prefrontal cortex, a common treatment target for repetitive transcranial magnetic stimulation (rTMS), are disrupted in both MDD and AUD. The proposed study will enhance the development of theta burst stimulation (TBS) as a new intervention for AUD in the context of depressive symptoms and uses integrated TMS-EEG to identify neurophysiological targets of executive dysfunction in this disorder.

Conditions

Major Depressive Disorder; Alcohol Use Disorder

Outcome Measures

Primary Outcomes (3)

• Executive Function Index - inhibition

  Flanker task

  baseline and 4 weeks after baseline (after 20 treatments of active/sham rTMS)

• Executive Function Index - working memory

  N-back task

  baseline and 4 weeks after baseline (after 20 treatments of active/sham rTMS)

• Executive Function Index - set shifting

  switch task

  baseline and 4 weeks after baseline (after 20 treatments of active/sham rTMS)

Secondary Outcomes (1)

• 17-Item Hamilton Depression Rating Scale (HRSD-17)

  baseline and 4 weeks after baseline (after 20 treatments of active/sham rTMS)

Other Outcomes (1)

• Columbia-Suicide Severity Rating Scale

  baseline and 4 weeks after baseline (after 20 treatments of active/sham rTMS)

Study Arms (2)

Active Bilateral

ACTIVE COMPARATOR

Bilteral TBS, applied as cTBS over the right DLPFC followed by iTBS over the left DLPFC

Device: intermittent theta burst stimulation

Sham

SHAM COMPARATOR

Sham TBS

Device: Sham stimulation

Interventions

intermittent theta burst stimulation DEVICE

Theta-burst stimulation

Active Bilateral

Sham stimulation DEVICE

Stimulation with double-sided B70-type coil

Sham

Eligibility Criteria

• Age: 18 Years - 59 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64)

You may qualify if:

• are outpatients;
• are voluntary and competent to consent to treatment;
• have a Diagnostic and Statistical Manual for Mental Disorders, 5th edition (DSM-5) diagnosis of AUD based on the MINI;
• do not exhibit problematic use of any substances (excluding nicotine and caffeine), including alcohol, for \>1 month;
• are male or female between the ages of 18 - 59;
• screened positive for an MDE based on the MINI without psychotic symptoms
• are agreeable to keeping their current antidepressant medications and medications for alcohol use disorder constant during the study;
• are reliably taking SUD agonist therapies if appropriate and managed by their clinical team;
• are able to adhere to the study schedule;
• meet the TMS safety criteria.

You may not qualify if:

• have a concomitant major unstable medical illness;
• are pregnant or intend to get pregnant during the study;
• have possible or probable dementia (based on the Informant Questionnaire on Cognitive Decline in the Elderly that will be administered to any participant with a baseline total score of \< 26 on the Montreal Cognitive Assessment (MoCA);
• have failed a course of ECT, due to the lower likelihood of response to rTMS;
• have any significant neurological disorder (e.g., a space occupying brain lesion, a history of stroke, a cerebral aneurysm, a seizure disorder, Parkinson's disease, Huntington's chorea, multiple sclerosis, significant history of head trauma with radiological evidence of intracranial trauma at the time of injury due to risk of possible seizure foci from prior intracranial lesions.
• present with a medical condition, a medication, or a laboratory abnormality that could cause a major depressive episode or significant cognitive impairment in the opinion of the investigator (e.g., hypothyroidism with low TSH, Cushing's disease);
• have an intracranial implant (e.g., aneurysm clips, shunts, cochlear implants) or any other metal object within or near the head, excluding the mouth, that cannot be safely removed;
• require a benzodiazepine with a dose equivalent to lorazepam 2 mg/day or higher or any anticonvulsant due to the potential of these medications to limit the efficacy of rTMS \[79\];
• have an inability to communicate in English fluently enough to complete the clinical assessments.
• have a MINI diagnosis or active symptoms of Bipolar Disorder

Sponsors & Collaborators

• Centre for Addiction and Mental Health: lead

Study Sites (1)

Centre for Addiction and Mental Health

Toronto, Ontario, M6J 1H4, Canada

RECRUITING

MeSH Terms

Conditions

Depressive Disorder, Major; Alcoholism

Condition Hierarchy (Ancestors)

Depressive Disorder; Mood Disorders; Mental Disorders; Alcohol-Related Disorders; Substance-Related Disorders; Chemically-Induced Disorders

Central Study Contacts

Daphne Voineskos, MD

CONTACT

416-535-8501; daphne.voineskos@camh.ca

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: TRIPLE
• Who Masked: PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 13, 2022
• First Posted: March 8, 2024
• Study Start: February 7, 2022
• Primary Completion: December 31, 2024
• Study Completion: July 1, 2025
• Last Updated: March 8, 2024

Record last verified: 2024-03

Locations

CA (1)