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

NCT ID: NCT06299787

Last Updated: 2024-03-08

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-02-07
• Study Completion Date: 2025-07-01

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.

Detailed Description

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

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

Active Bilateral

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

Group Type: ACTIVE_COMPARATOR

intermittent theta burst stimulation

Intervention Type: DEVICE

Theta-burst stimulation

Sham

Sham TBS

Group Type: SHAM_COMPARATOR

Sham stimulation

Intervention Type: DEVICE

Stimulation with double-sided B70-type coil

Interventions

intermittent theta burst stimulation

Theta-burst stimulation

Intervention Type: DEVICE

Sham stimulation

Stimulation with double-sided B70-type coil

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. are outpatients;

2. are voluntary and competent to consent to treatment;

3. have a Diagnostic and Statistical Manual for Mental Disorders, 5th edition (DSM-5) diagnosis of AUD based on the MINI;

4. do not exhibit problematic use of any substances (excluding nicotine and caffeine), including alcohol, for >1 month;

5. are male or female between the ages of 18 - 59;

6. screened positive for an MDE based on the MINI without psychotic symptoms

7. are agreeable to keeping their current antidepressant medications and medications for alcohol use disorder constant during the study;

8. are reliably taking SUD agonist therapies if appropriate and managed by their clinical team;

9. are able to adhere to the study schedule;

10. meet the TMS safety criteria.

Exclusion Criteria

1. have a concomitant major unstable medical illness;

2. are pregnant or intend to get pregnant during the study;

3. 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);

4. have failed a course of ECT, due to the lower likelihood of response to rTMS;

5. 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.

6. 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);

7. 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;

8. 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];

9. have an inability to communicate in English fluently enough to complete the clinical assessments.

10. have a MINI diagnosis or active symptoms of Bipolar Disorder

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 59 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Centre for Addiction and Mental Health

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Centre for Addiction and Mental Health

Toronto, Ontario, Canada

Site Status: RECRUITING

Countries

Canada

Central Contacts

Daphne Voineskos, MD

Role: CONTACT

daphne.voineskos@camh.ca

416-535-8501 ext. 30176

Facility Contacts

Daphne Voineskos, MD

Role: primary

daphne.voineskos@camh.ca

416-535-8501 ext. 30176

Other Identifiers

058-2021

Identifier Type: -

Identifier Source: org_study_id