ADHD
Study register · detail RCT · ADHD · 2017

Cannabinoids in attention-deficit/hyperactivity disorder: A randomised-controlled trial.

Mixed GRADE Moderate 170 citations
Samplen = 30 Pat.
Duration17.07.14 to 18.06.15
ControlPlacebo spray
EndpointQbTest
Blindingdoppelblind
DesignRCT
Cannabinoidkombination
THC:CBD1:1
Routeoromukosal
Key finding

No significant differences in the primary outcome (cognition and activity level), but nominal improvements in secondary outcomes (hyperactivity/impulsivity, inhibition), which did not reach significance after correction for multiple testing.

Summary

n=30 adults with ADHD, randomised to Sativex oromucosal spray (n=15) vs. placebo (n=15). Primary outcome (cognitive performance/activity via QbTest): no significant ITT difference (Est=−0,17, 95% CI −0,40 to 0,07, p=0,16). Secondary outcomes: nominally significant improvement for hyperactivity/impulsivity (p=0,03) and cognitive inhibition (p=0,05), trend for inattention (p=0,10) and emotional lability (p=0,11). Effects not significant after correction for multiple testing. Per-protocol effects higher.

P
PopulationAdults with ADHD, n=30
I
InterventionSativex oromucosal spray (THC/CBD combination), oral spray
C
ControlPlacebo spray
O
OutcomePrimary endpoint (QbTest): no significant difference (Est=−0,17, 95%-KI −0,40 to 0,07, p=0,16); nominally significant improvement in hyperactivity/impulsivity (p=0,03) and cognitive inhibition (p=0,05)
Confidence in the evidence
Moderate

The third of four GRADE levels, the effect estimate is probably reliable.

Downgraded for
Imprecision
Quality profile
Sample size
Blinding Double-blind
Effect size Mixed
Citations / year
Authors
Cooper RE, Williams E, Seegobin S, Tye C, Kuntsi J, Asherson P
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Abstract
Adults with ADHD describe self-medicating with cannabis, with some reporting a preference for cannabis over ADHD medications. A small number of psychiatrists in the US prescribe cannabis medication for ADHD, despite there being no evidence from randomised controlled studies. The EMA-C trial (Experimental Medicine in ADHD-Cannabinoids) was a pilot randomised placebo-controlled experimental study of a cannabinoid medication, Sativex Oromucosal Spray, in 30 adults with ADHD. The primary outcome was cognitive performance and activity level using the QbTest. Secondary outcomes included ADHD and emotional lability (EL) symptoms. From 17.07.14 to 18.06.15, 30 participants were randomly assigned to the active (n=15) or placebo (n=15) group. For the primary outcome, no significant difference was found in the ITT analysis although the overall pattern of scores was such that the active group usually had scores that were better than the placebo group (Est=-0.17, 95%CI-0.40 to 0.07, p=0.16, n=15/11 active/placebo). For secondary outcomes Sativex was associated with a nominally significant improvement in hyperactivity/impulsivity (p=0.03) and a cognitive measure of inhibition (p=0.05), and a trend towards improvement for inattention (p=0.10) and EL (p=0.11). Per-protocol effects were higher. Results did not meet significance following adjustment for multiple testing. One serious (muscular seizures/spasms) and three mild adverse events occurred in the active group and one serious (cardiovascular problems) adverse event in the placebo group. Adults with ADHD may represent a subgroup of individuals who experience a reduction of symptoms and no cognitive impairments following cannabinoid use. While not definitive, this study provides preliminary evidence supporting the self-medication theory of cannabis use in ADHD and the need for further studies of the endocannabinoid system in ADHD.

The impediment to action advances action. — Marcus Aurelius