CBD is not active at the CB1 or CB2 receptors. It has very low affinity for them. It has moderate affinity for the serotonin-1a autoreceptor (that the anti-anxiety medication buspirone also targets). But only at very high dosages (ie, 300mg+).
So... this study has only really tested the placebo effect.
edit: I finished reading the journal article and it turns out they didn't use clinically relevant doses because it'd cost too much. So they decided to just go the placebo route.
>The doses used in this study (25 mg/d to 175 mg/d) were much lower than those reported in some of the clinical literature (300 mg/d to 600 mg/d)12–14,17 for 2 reasons. The first is that in our experience lower doses appear to elicit an adequate clinical response. Second, the current retail cost of CBD would make the use of 600 mg/d cost prohibitive.