Treatment of Cannabis Use Disorder Among Adults With Comorbid Attention-Deficit/Hyperactivity Disorder



Status:Recruiting
Conditions:Neurology, Psychiatric, Psychiatric
Therapuetic Areas:Neurology, Psychiatry / Psychology
Healthy:No
Age Range:18 - 65
Updated:11/2/2018
Start Date:July 2016
End Date:September 2019
Contact:Amy Mahony, LMHC
Email:Amy.mahony@nyspi.columbia.edu
Phone:646-774-8183

Use our guide to learn which trials are right for you!

The proposed protocol is a double-blind, placebo-controlled outpatient study of the safety
and benefit of Extended-release mixed amphetamine salt (Adderall-XR, MAS-XR) in the treatment
of individuals with Cannabis Use Disorder (CUD) and Attention-deficit/Hyperactivity Disorder
(ADHD). The investigators plan to enroll 50 and randomize 40 of these patients in the trial.
The primary objective of the study is to determine the efficacy of MAS-XR in promoting
cannabis abstinence among individuals with CUD and in promoting a decrease of ADHD symptoms.

ADHD is common in substance use disorder patients in general and cannabis use disorder (CUD)
in particular, occurring at rates substantially greater than in the general population. A
meta-analysis found that approximately 23% of substance abusers seeking treatment have
childhood and/or adult ADHD. Moreover, ADHD was overrepresented in adults with CUD compared
to other substance use disorder patients seeking treatment. The importance in treating CUD
individuals who also have ADHD is underscored by findings demonstrating that individuals with
co-occurring ADHD and substance use disorders are a particularly intractable group: they
exhibit earlier onset of use, more severe use, a more complicated pattern of
remission/relapse, and poorer treatment outcomes relative to those without ADHD. Yet, to
date, ADHD individuals with CUD have not been adequately studied. The investigators have
found that in their treatment research studies targeting cannabis dependence that a
substantial percentage (35%) have screened positive for adult ADHD, rates that are higher
than participants in their cocaine use disorder clinical trial and almost 8x greater than
rates found in the general population. Thus, this appears to be a sizable cannabis-abusing
group warranting much greater clinical attention than they are currently receiving.

The goal is to demonstrate feasibility, tolerability, and estimate effect size for purposes
of planning future more definitive trials. Because of the research team's extensive
experience in working with stimulant medication in treating ADHD in cocaine-dependent
populations, the large effect size of amphetamine in treating adult ADHD, and notable
reduction in cocaine use and ADHD symptoms in cocaine-dependent ADHD adults, the
investigators will explore the efficacy of Adderall-XR (MAS-XR) for the treatment of cannabis
use disorder and ADHD. The study is a 12 week placebo controlled double-blind trial. The
maximum maintained dose will be 80 mg of MAS-XR daily.

Inclusion Criteria:

- Individuals who meet criteria for cannabis use disorder (CUD) and report that
marijuana is their primary drug of abuse

- Individuals must report using marijuana at least 5 days a week over the past 28 days
and have a positive urine test for THC on the day of study entry

- Individuals must meet DSM-5 criteria for adult ADHD

- Individuals who score > 22 on the AISRS scale

- Individuals between the ages of 18-65 capable of giving informed consent and capable
of complying with study procedures

- Women of child-bearing age will be included if they: a) are not pregnant, b) agree to
use an effective method of contraception, c) agree not to become pregnant during the
study and d) are not breastfeeding. To confirm this, urine pregnancy tests will be
repeated every month after screening. Women will be provided a full explanation of the
potential dangers of pregnancy while taking MAS-XR. If a woman becomes pregnant, she
will be taken off medication and continue standard treatment at STARS. At the end of
the study, patients will be offered treatment at STARS until an appropriate referral
can be made to a community clinic.

Exclusion Criteria:

- Individuals meeting DSM-5 criteria for schizophrenia, schizoaffective illness,
psychotic disorder other than transient psychosis due to drug abuse, current major
depression, bipolar illness or psychiatric disorders (other than substance abuse)
which require psychiatric intervention or would interfere with study participation

- Individuals who are medically unstable based on laboratory tests, electrocardiogram,
medical history, physical examination that would make participation hazardous

- Use of synthetic cannabinoids in the past month and meeting CUD diagnosis based on
synthetic cannabinoids use alone in the past year

- Individuals with liver enzyme function tests greater than 3 times normal

- Individuals with significant current suicidal risk

- Individuals with systolic blood pressure > 140; diastolic blood pressure >90; pulse
>100

- Individuals who are cognitively impaired to impede study participation

- Nursing mothers and pregnant women

- Individuals who are physiologically dependent on any other drugs (excluding nicotine)
that would require a medical intervention

- Individuals with known sensitivity/allergy to MAS-XR or amphetamine analogs

- Individuals currently being prescribed psychotropic medication (including sleep
medication)

- Individuals with history of seizures

- Individuals who are mandated to treatment

- Individuals with a history of amphetamine use disorders, including amphetamines such
as methamphetamine and MDMA.

- Individuals with a current cocaine use disorder
We found this trial at
1
site
New York, New York 10032
Principal Investigator: Frances R Levin, MD
Phone: 212-923-3031
?
mi
from
New York, NY
Click here to add this to my saved trials