Treatment With Transcranial Magnetic Stimulation for Cocaine Addiction: Clinical Response and Functional Connectivity.

Cocaine-Related Disorders Clinical Trial

— TMS_COC_CONN  

Official title:

Effects of Transcranial Magnetic Stimulation on Functional Connectivity and Response to Treatment of Cocaine Dependent Patients

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02986438
• Other study ID #: IC16036.0
• Status: Recruiting
• Phase: N/A
• Start date: May 1, 2017
• Est. completion date: December 31, 2020

Study information

• Verified date: June 2020
• Source: Instituto Nacional de Psiquiatría Dr. Ramón de la Fuente
• Contact: Ruth Alcala-Lozano, MD, MSc
• Phone: +52(55)41605065
• Email: ruthalcala_[@]hotmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to investigate the short and long term clinical and cognitive effects of repetitive Transcranial Magnetic Stimulation (rTMS) at 5 Hz and/or 10 Hz frequencies on the left dorsolateral prefrontal cortex in cocaine dependent patients and to examine possible changes in brain structure and functional connectivity associated with this intervention.

Description:

Repetitive transcranial magnetic stimulation (rTMS) has been shown to reduce craving in cocaine addicts in the short term. However, there are no studies on the long term clinical and cognitive effects of sustained rTMS therapy. Moreover, clinical improvement or decline could be related to long term changes in brain structure and function. The purpose of this study is to investigate the short and long term clinical and cognitive effects of repetitive Transcranial Magnetic Stimulation (rTMS) at 5 Hz and/or 10 Hz frequencies on the left dorsolateral prefrontal cortex in cocaine dependent patients and to examine possible changes in brain structure and functional connectivity associated with this intervention. For this purpose the investigators will recruit cocaine dependent patients and stimulate them using rTMS with a acute intervention (twice a day for 2 weeks) and a maintenance intervention (twice a week for 3 months). The investigators will follow the patients to determine clinical outcome. The investigators will also measure clinical, cognitive and brain structural and functional connectivity to asses changes related to the intervention in the short and long term (measurements at: baseline, 2 weeks and 3 months).

Procedure:

The projects consists of: Screening Visit, Part 1 and Part 2.

First, there will be a screening visit, where a clinical interview will be conducted and tests will be applied to select study participants who meet the inclusion and exclusion criteria.

Baseline clinical, cognitive and neuroimaging data will be acquired. The cognitive and neuroimaging data will be exploratory, to be associated with the outcome measures. Part 1 of the study entails the determination of the rTMS target frequency (5 or 10 Hz) for Part 2 (long term stimulation). In Part 1, all participants will be randomly assigned to one of the four treatment legs with rTMS (10Hz, 10Hz-Sham, 5Hz, 5Hz-Sham). Participants will receive 20 sessions of rTMS (intervention or sham), twice per day for 10 consecutive days. Each session lasts approximately 35 minutes.

At 2 weeks, the investigators will evaluate the short term effect of treatment by measuring clinical, cognitive and neuroimaging changes and select which frequency of stimulation is the most effective in terms of clinical improvement, but also in terms of the rate of secondary effects. Our hypothesis is that 5 Hz is as effective as 10 Hz without the high rate of secondary effects (i.e. seizures).

In Part 2 of the study, the sham groups will end and they will be invited to the treatment condition although they data not will be considered for later phases. Here the maintenance phase starts (long term), where rTMS will be performed twice a week for 12 months using the target frequency (5 or 10 Hz). Clinical, cognitive and neuroimaging data will be acquired at 2 weeks and 3 months.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 40
• Est. completion date: December 31, 2020
• Est. primary completion date: December 31, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• Minimum age of eighteen and maximum of fifty years.

• Cocaine users for at least 1 year, currently using at least 3 times a week, with abstinence periods continuing to be less than one month in the last year.

• The reading level of at least 6th grade of primary (equivalent to fifth grade of elementary school).

• The ability to give a valid informed consent.

• Right-handed (in order to control by cerebral laterality in Neuroimaging).

• If the subject is female and of childbearing age, she agrees to use a medically acceptable form of contraception, and to not become pregnant during the duration of the study. A woman is considered to have potential for pregnancy, unless she is postmenopause or surgically sterilized. Female patients of childbearing potential should use either: (1) contraceptive pill or hormone preparation IUD or deposit (ring, injection, implant); And / or (2) a barrier method of contraception, such as the diaphragm, spermicide sponge, or a condom.

Contraceptive measures will be reviewed with the female subjects at each visit prior to the rTMS treatment.

• Self-report of experiencing cocaine craving when exposed to cocaine-associated cues.

• Body mass index less or equal to 30, allowing them to safely enter the Magnetic Resonance.

Exclusion Criteria:

• Personal or first-degree family history of any clinically defined neurological disorder, including organic brain disease, epilepsy, brain events, brain injury, or multiple sclerosis; Or personal history of previous neurosurgery or traumatic brain injury that have produced loss of consciousness.

• Cardiac pacemakers, neural stimulators, implantable defibrillators, implanted medication pumps, intracardiac lines, or acute, unstable heart disease, with intracranial implants (eg, aneurysm clips, leads, stimulators, cochlear implants, or electrodes) or with any other Metallic object inside or near the head that can not be safely removed.

• Screw metal or metallic projectiles into the head or body.

• Current use of any investigational drug or any anti-proconvulsant drug such as tricyclic or neuroleptic antidepressants (which reduce the seizure threshold).

• Increased intracranial pressure (decreasing seizure threshold).

• History of schizophrenia, bipolar disorder, mania or hypomania.

• History of myocardial infarction, angina pectoris, congestive heart failure, cardiomyopathy, cerebrovascular events or transient ischemic attack, or any heart condition currently under medical care.

• Women with reproductive potential who do not use an acceptable form of contraception pregnant or who are lactating.

• Any history of seizures.

• The current dependence (DSM-V criteria) on substances other than cocaine and / or nicotine.

• Claustrophobia making them unable to tolerate lying inside the MRI scanner.

• History of HIV infection or HIV antibody test positive (Due to potential neuroinfection).

These data will be corroborated by a screening visit where the following instruments will be used:

Clinical Interview. Self-applicable demographic questionnaire. Mini International Neuropsychiatric Interview (MINI-Plus). Structured clinical interview for DSM Axis II, self report (SCID-II).

Elimination criteria:

The participation of all participants during the study will be suspended if:

• They express their desire to stop participating.

• They present abnormal radiological findings that require more attention outside the study to ensure the health of the participant.

• Worsening of clinical condition.

Related Conditions & MeSH terms

• Cocaine-Related Disorders

Intervention

Device:
• Repetitive Transcranial Magnetic Stimulation
The investigators will use a Magpro R-30 MagVenture quick stimulator, equipped with an 8-reel, 75 mm internal diameter in each spiral. Each patient will receive consistent treatment in 2 sessions a day for 10 consecutive business days in the first two weeks, then receive 2 weekly sessions, until the year of treatment is completed. Each session will consist of the application of 30 trains of 10 seconds duration separated by intervals of one minute, at a fixed frequency (5Hz or 10Hz), to 100% of the motor threshold.
• Repetitive Transcranial Magnetic Stimulation (Sham)
The investigators will use a Magpro R-30 MagVenture quick stimulator, equipped with an 8-reel, 75 mm internal diameter in each spiral with a coil that allows simulated stimulation (Coil AP). This condition will only last two weeks.

Locations

Country	Name	City	State
Mexico	Instituto Nacional de Psiquiatría "Ramón de la Fuente Muñiz"	Mexico City

Sponsors (2)

Lead Sponsor	Collaborator
Instituto Nacional de Psiquiatría Dr. Ramón de la Fuente	National Council of Science and Technology, Mexico

Country where clinical trial is conducted

Mexico, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Cocaine Craving (CCQ)	The craving will be measured using a craving questionnaire for cocaine validated in Mexican population (Cocaine Craving Questionnaire or CCQ).	Baseline, 2 weeks, 3 months
Primary	Change in Cocaine Craving (VAS)	The craving will be measured using a 100 mm visual analogue scales (VAS).	Baseline, 2 weeks, 3 months
Primary	Change in Cocaine Urine Test	Frequency of cocaine use will be measured using reagent strips from Instant View drug screening (> 300 ng/mL). Results are Positive or Negative.	Baseline, 2 weeks, 3 months
Secondary	Changes in Psychopathological Symptoms	Measured by the 90 Symptoms Questionnaire (SCL-90).	Baseline, 2 weeks, 3 months
Secondary	Changes in Depression	Measured by Hamilton Depression Rating Scale (HDRS) (21 items).	Baseline, 2 weeks, 3 months
Secondary	Changes in Anxiety	Measured by Hamilton Anxiety Rating Scale (HARS).	Baseline, 2 weeks, 3 months
Secondary	Changes in Drug Consumption and Related Problems	Measured by the Addiction Severity Index (ASI-lite).	Baseline, 2 weeks, 3 months
Secondary	Changes in Sleep Quality: PSQI	Measured by the Pittsburgh Sleep Quality Index (PSQI).	Baseline, 2 weeks, 3 months
Secondary	Changes in Impulsivity	Measured by the Barrat Impulsivity Scale-11 (BIS-11).	Baseline, 2 weeks, 3 months
Secondary	Lapse rate	Lapse is defined as at least one consumption event not in the same pattern as the baseline consumption. The report of self-consumption of cocaine and urine drug tests, with special attention to the presence of traces of cocaine.	Baseline, 2 weeks, 3 months
Secondary	Relapse rate	Relapse is defined as consumption events in the same pattern as the baseline consumption. The report of self-consumption of cocaine and urine drug tests, with special attention to the presence of traces of cocaine.	Baseline, 2 weeks, 3 months